In 2025,the global rare earth exploration and development sector achieved breakthroughs across multiple fronts.Projects advanced intensively across the Americas,Oceania,Africa,and Europe,with significant growth in res...In 2025,the global rare earth exploration and development sector achieved breakthroughs across multiple fronts.Projects advanced intensively across the Americas,Oceania,Africa,and Europe,with significant growth in resources,continuous emergence of new deposits,and strong impetus injected into the industry by technological innovation and policy support.The global rare earth resource supply pattern was further optimized (Table 1).1.Fruitful results in resource growth and new deposit discoveriesBrazil emerged as a core region for resource growth.The Colossus rare earth deposit saw a 150%increase in resources and announced its first reserve estimate.The Caldeira rare earth deposit’s resource estimate grew by 50%.The combined ore resources in the Caladão rare earth deposit’s Zones A and B reached 5.72×10~8 tonnes,with a total rare earth oxide(TREO) grade of 0.1506%,concurrently hosting 2.29×10~4tonnes of gallium metal resources.展开更多
Phosphorus (P) is an essential nutrient element that is critical for plant growth and ecosystem functionality.The soil P cycle plays multiple roles,such as sustaining plant growth and productivity,regulating nutrient ...Phosphorus (P) is an essential nutrient element that is critical for plant growth and ecosystem functionality.The soil P cycle plays multiple roles,such as sustaining plant growth and productivity,regulating nutrient balance within ecosystems,and enhancing ecosystem adaptability and resilience.This cycle is influenced by factors such as the restoration approach and microbial community dynamics.However,the extent to which the restoration approach alters the P cycle in karst ecosystems and the underlying microbial mechanisms remain poorly understood.The P-cycle multifunctionality index (P-cycle MFI) serves as a comprehensive indicator for evaluating soil P cycle function,and it provides insights into changes in the P cycle between different restoration approaches.To investigate the shifts in soil P-cycle MFI and microbial mechanisms between different restoration approaches,we analyzed soil available P (AP),total P (TP),microbial biomass P (MBP),and the activities of acid phosphatase (ACP) and alkaline phosphatase (ALP).These data were used to calculate the P-cycle MFI by averaging the Z-scores between two restoration approaches(artificial restoration of forest (AF) and natural restoration of forest (NF)) and a control (cropland,CP) at six subtropical karst ecosystem sites in China.We also determined the soil organic carbon (SOC),exchangeable calcium (Ca) and magnesium (Mg),pH,bulk density (BD),microbial biomass C (MBC),and microbial biomass nitrogen (MBN),as well as the community structure,relative abundance,diversity indices,and co-occurrence networks of phoD-harboring bacteria.The results showed that the community structure of phoD-harboring bacteria varied significantly among AF,NF,and CP and across different temperature gradients.These bacteria exhibited increasing complexity and tightness in co-occurrence networks from CP to AF and then to NF,along with the ACP and ALP activities,but not the TP and AP contents.The P-cycle MFI values were significantly higher in NF compared to AF and CP,and the variation was significantly explained by restoration approach,temperature,MBC,MBN,SOC,exchangeable Ca,BD,community structure of phoD-harboring bacteria,and exchangeable Mg.Furthermore,natural restoration had a more substantial impact on the P-cycle MFI than temperature by enhancing SOC,microbial biomass,the complexity and co-occurrence network tightness of the phoD-harboring bacterial community structure,and ACP and ALP activities,but it reduced soil BD.The rare genera of phoD-harboring bacteria significantly influenced the variation of soil P-cycle MFI compared to the dominant genera.This study highlights the importance of rare genera of phoD-harboring bacteria in driving soil P-cycle multifunctionality in karst ecosystems,with natural restoration being more effective than artificial methods for enhancing soil organic matter and microbial community complexity.展开更多
Ln@MOFs by anchoring rare metal ions(Ln) into metal-organic frameworks(MOFs) are proved to have great potential in the field of luminescent molecular thermometer.Nevertheless,the current research indicated that the po...Ln@MOFs by anchoring rare metal ions(Ln) into metal-organic frameworks(MOFs) are proved to have great potential in the field of luminescent molecular thermometer.Nevertheless,the current research indicated that the poor structural stability and low sensitivity hindered their application scope.In this work,a new MOF Zn-450 luminescent thermometer with multiple emission fluorescence characteristics was synthesized by the combination of 3,3,5,5-biphenyl tetracarboxylic acid(H_(4)L) and Zn^(2+) ion under solvothermal conditions.Interestingly,a high relative sensitivity of 1.43 % K^(-1) was found within 80-300 K based on Zn-450.Subsequently,two high-sensitivity luminescent Ln@MOFs(Ln = Eu and Tb) were further fabricated by doping rare earth ions into Zn-450 based on the post-synthesis strategy.Among them,the Eu@Zn-450 demonstrates various luminous behaviors while achieving an increased relative sensitivity of 1.63 % K^(-1).In addition,the continuously visible red,pink,and purple luminescent emissions at the same temperature range were observed,suggesting that the Eu@Zn-450 could be utilized as a luminescent colorimetric molecular thermometer.Importantly,this work can present new possibilities for the development of rare earth-doped luminescence and its temperature sensing properties.展开更多
Carbonatite is a rare but highly prospective rock that plays a significant role as a source of critical metals,notably rare earth elements(REE)and niobium(Nb).The widespread occurrence of fluorine-bearing minerals(e.g...Carbonatite is a rare but highly prospective rock that plays a significant role as a source of critical metals,notably rare earth elements(REE)and niobium(Nb).The widespread occurrence of fluorine-bearing minerals(e.g.,fluorite,fluorapatite,and bastnäsite)in carbonatites indicates that their parent magmas are rich in fluorine.Nevertheless,the mechanisms by which fluorine controls REE and Nb mineralization remain unclear.Building on previous work,we systematically synthesize the regulatory role of fluorine in REE and Nb mineralization throughout the entire magmatic evolution of carbonatites.Our key findings are:(1)during partial melting,fluorine decreases the solidus of carbonated peridotite,thereby enhancing the generation and stability of carbonatitic melt.(2)In the mantle melting stage,it lowers the partition coefficients of REE and Nb between mantle minerals and melt,effectively promoting their extraction.(3)Throughout magmatic crystallization,fluorine significantly enriches REE and Nb in the residual melt.(4)During liquid immiscibility,fluorine exerts limited influence,as the partition behaviors of REE and Nb are primarily governed by structural differences between the conjugate melts.(5)In the hydrothermal stage,fluorine facilitates the mobilization,transport,and ultimate precipitation of REE-and Nb-bearing minerals,directly driving mineralization.The presented evidence implies that carbonatitic melts and fluoride-bearing minerals exert primary control over the spatial distribution and mineralization potential of REE and Nb.Future studies should focus on(1)clarifying how fluorine promotes REE and Nb enrichment in late-stage brine melts and(2)investigating its effect on the solubility and precipitation mechanisms of REE-and Nb-bearing minerals during the late stages of magma evolution.展开更多
Coal serves not only as a crucial energy resource but also as a significant reservoir of critical metal elements,including Lithium(Li),Gallium(Ga),Germanium(Ge),and rare earth elements(REE).This paper provides a syste...Coal serves not only as a crucial energy resource but also as a significant reservoir of critical metal elements,including Lithium(Li),Gallium(Ga),Germanium(Ge),and rare earth elements(REE).This paper provides a systematic review of the enrichment characteristics,occurrence modes,and comprehensive utilization potential of these critical metals in coal.Globally,the distribution of these metal resources exhibits significant regional heterogeneity.While the concentration in most coals falls below industrial cut-off grades,anomalous enrichment in specific coal basins results in Li,Ga,Ge,and REE concentrations far exceeding global averages,highlighting their considerable potential as unconventional metal deposits.The occurrence modes of these metals are diverse:Li is primarily hosted in mineral phases;Ga exists in inorganic,organic,and complex forms;Ge shows a strong association with organic matter;and REE are mainly present in adsorbed/isomorphic forms within clay minerals,while also displaying organic affinity.Direct extraction of metals from raw coal is often cost-prohibitive;effective recovery is therefore more feasible when integrated with coal processing.Metals are further enriched in solid wastes such as coal gangue,fly ash,and bottom ash,from which recovery is more economically and technically viable.Current comprehensive utilization primarily employs integrated mineral processing-hydrometallurgy approaches.Future research should focus on elucidating the precise occurrence forms of metals in coal and solid wastes,optimizing pre-treatment methods,and selecting effective activators and leachants.Advancing the synergistic extraction and green recovery of multiple associated resources from coal and its by-products is essential for achieving high-value,comprehensive utilization of coal-based resources.展开更多
This review provides a comprehensive overview of recent advancements in aluminum-based conductor alloys engineered to achieve superior mechanical strength and thermal stability without sacrificing electrical conductiv...This review provides a comprehensive overview of recent advancements in aluminum-based conductor alloys engineered to achieve superior mechanical strength and thermal stability without sacrificing electrical conductivity.Particular emphasis is placed on the role of microalloying elements—particularly Sc and Zr-in promoting the formation of coherent nanoscale precipitates such as Al_(3)Zr,Al_(3)Sc,and core-shell Al_(3)(Sc,Zr)with metastable L1_(2)crystal structures.These precipitates contribute significantly to high-temperature performance by enabling precipitation strengthening and stabilizing grain boundaries.The review also explores the emerging role of other rare earth elements(REEs),such as erbium(Er),in accelerating precipitation kinetics and improving thermal stability by retarding coarsening.Additionally,recent advancements in thermomechanical processing strategies are examined,with a focus on scalable approaches to optimize the strength-conductivity balance.These approaches involve multi-step heat treatments and carefully controlled manufacturing sequences,particularly the combination of cold drawing and aging treatment to promote uniform and effective precipitation.This review offers valuable insights to guide the development of cost-effective,high-strength,heat-resistant aluminum alloys beyond conductor applications,particularly those strengthened through microalloying with Sc and Zr.展开更多
Aluminum is the main impurity of the weathered crust elution-deposited rare earth ore(WCED-REO).Efficient leaching of rare earths and low leaching of aluminum are of great importance for the leaching of the WCED-REO.T...Aluminum is the main impurity of the weathered crust elution-deposited rare earth ore(WCED-REO).Efficient leaching of rare earths and low leaching of aluminum are of great importance for the leaching of the WCED-REO.The effects of pH,MgSO_(4) concentration and Al^(3+)concentration of the leaching agent solution on the column leaching behaviors of WCED-REO using magnesium sulfate were investigated.Experimental data show that controlling the MgSO_(4) concentration to 0.15 mol/L,pH of the leaching agent solution to 2,the leaching amount of aluminum from the rare earth ore gradually decreases with the increase of Al^(3+)concentration in the leaching agent solution,indicating that Al^(3+)in the leaching agent solution may act as leaching agent to participate in the ion exchange of RE3+,but the leaching amounts of rare earths change insignificantly as the Al^(3+)concentration is increased.Increasing the MgSO_(4) concentration is beneficial to the leaching of aluminum,and when the Al^(3+)concentration is 0.04 mol/L(Al accumulation),the amount of Al^(3+)leached from the rare earth ore increased gradually with increasing the MgSO_(4) concentration.The pH of the leaching agent solution has a significant influence on the leaching of aluminum in the rare earth ore,and the leaching amount of aluminum from the rare earth ore increases gradually with decreasing the pH.When the Al^(3+)conce ntration is 0.04 mol/L(Al accumulation)and the pH of the leaching agent solution is above 2.0,the aluminum in the leaching agent solution can be back-adsorbed onto the rare earth ore,and the amount of the back-adsorbed Al^(3+)increases with increasing the pH of the leaching agent solution.The injection rate of the leaching agent solution has slight effect on the leaching behavior of rare earths and aluminum.In summary,leaching of Al^(3+)and consumption of MgSO_(4) can be reduced by regulating the accumulation of aluminum,MgSO_(4) concentration and pH.展开更多
Modification of 6061 aluminum alloy was conducted through composite addition of cerium-rich rare earths and Al-Ti-B.Results show that the composite addition of Al-Ti-B and Ce/La element at a specific ratio notably pro...Modification of 6061 aluminum alloy was conducted through composite addition of cerium-rich rare earths and Al-Ti-B.Results show that the composite addition of Al-Ti-B and Ce/La element at a specific ratio notably promotes the refinement of the alloy's grains.Ce and La elements are combined with Si and other elements to form rare earth phases,improving the morphology and distribution of precipitates and mitigating the adverse effects ofβ-Fe phases on the microstructure and mechanical properties of alloy.However,excessive rare earth content poses challenges;it not only leads to a decrease in Mg-Si strengthening phase by binding with Si but also promotes the formation of larger or numerous rare earth phases that may act as initiation points for cracks,thereby impeding the improvement of the structure and performance of alloy.The composite addition of cerium-rich rare earths and Al-Ti-B not only preserves the strength of the alloy but also significantly enhances the plasticity of the 6061 as-cast alloy.At a composite addition ratio of Al-Ti-B:RE=2:1,the newly developed 6061-RE aluminum alloy exhibits increased average elongation by 50%and 45%in its as-cast and homogenized states,respectively,compared to the baseline 6061 alloy,facilitating subsequent deformation processing.After solution treatment at 540℃for 1 h and aging at 180℃for 5 h,the average ultimate tensile strength and yield strength of 6061-RE alloys reach 313.2 and 283.1 MPa,increased by 12.3%and 14.5%compared with those of the original alloy,respectively,and the average elongation is improved by 41%.展开更多
The rare earth elements(REEs)extraction by chemical leaching from ion-adsorption type rare earth ores(IAREO)has led to serious ecological and environmental risks.Conversely,demand for bioleaching is on the rise with t...The rare earth elements(REEs)extraction by chemical leaching from ion-adsorption type rare earth ores(IAREO)has led to serious ecological and environmental risks.Conversely,demand for bioleaching is on the rise with the advantage of being environmental-friendly.As one of the organic acids produced by biological metabolism,citric acid was used to leach REEs and explore the performance and process.The results demonstrate that citric acid exhibits higher leaching efficiency(96.00%)for REEs at a relatively low concentration of 0.01 mol/L compared with(NH_(4))_(2)SO_(4)(84.29%,0.1 mol/L)and MgSO_(4)(83.99%,0.1 mol/L).Citric acid shows a preference for leaching heavy rare earth elements,with 99%leaching efficiency in IAREO,which shows higher capacity than(NH_(4))_(2)SO_(4)and MgSO_(4)(as inorganic leaching agents).Kinetic analysis indicates that the leaching process of REEs with citric acid is controlled by both the internal diffusion kinetics and chemical reaction kinetics,which is different from inorganic leaching agents.Visual Minteq calculations confirm that RE-Citrate is the main constituent of the extract solution in the leaching process of the IAREO,thereby enhancing the leaching efficiency of REEs from the IAREO.It suggests that citric acid may be used as a promising organic leaching agent for the environmentalfriendly extraction of REEs from IAREO.展开更多
Solvent extraction is the main method used to separate and purify rare earth elements.In the process of rare earths extraction,emulsification often generated due to the instability of the aqueous and organic phases or...Solvent extraction is the main method used to separate and purify rare earth elements.In the process of rare earths extraction,emulsification often generated due to the instability of the aqueous and organic phases or improper operating conditions.Once emulsification occurs,it would not only lead to low rare earths recovery efficiency,small product quantities,high production costs and the losing of extractant and rare earth resources,but also result in serious environmental pollution.Therefore,it is very important to study the micro-mechanisms of emulsification and establish new methods to prevent emulsification at the source.In this paper,possible factors resulting in emulsification,such as the compositions and properties of the organic and aqueous phases,the operating conditions of the rare earths extraction are reviewed.The micro-mechanisms of emulsification are summarized basing on the microscopic structures in the bulk phase,aggregations of the extractants at the organic-aqueous interface,spectral characterizations and computational simulations.On this basis,new formation mechanisms are proposed for emulsification.Preliminary explorations are employed to verify the correctness of these new viewpoints.Finally,future directions for studies of the emulsification micro-mechanism are proposed.This study provides a theoretical basis for further understanding the micro-mechanisms of interfacial instability resulting in emulsification in the process of rare earths extraction.展开更多
Metal-organic frameworks(MOFs)and their derivatives have gained significant attention in recent years for their ability to catalyze the advanced oxidation of persulfates.Cerium-doped MOFs,in particular,have shown prom...Metal-organic frameworks(MOFs)and their derivatives have gained significant attention in recent years for their ability to catalyze the advanced oxidation of persulfates.Cerium-doped MOFs,in particular,have shown promise due to their high catalytic efficiency,practical applicability,and cost-effectiveness.However,their structure,catalytic properties,and mechanisms are not yet fully understood.ZIF-8 was chosen as the raw material to prepare cerium-doped hollow carbon nano fibers(Ce-HCNFs)using the electrostatic spinning-calcination method.The objective is to investigate the structure,catalytic performance,and catalytic mechanism of Ce-HCNFs.The results show that Ce-HCNFs catalyzed the degradation of tetracycline(TC)by persulfate up to 76.9%,Quenching experiments and electron paramagnetic resonance experiments indicate the dominant role of single-linear oxygen.Furthermore,the experiments on the influence factor and cycling demonstrate the exceptional stability and recycling capability of Ce-HCNFs in real-world water environments.展开更多
Lanthanide ions(Ln^(3+))doping provides a potential strategy to control over the luminescent properties of lead-free halide double perovskite nanocrystals(DP NCs).However,due to the low energy transfer efficiency betw...Lanthanide ions(Ln^(3+))doping provides a potential strategy to control over the luminescent properties of lead-free halide double perovskite nanocrystals(DP NCs).However,due to the low energy transfer efficiency between self-trapped exciton(STE)and Ln^(3+)ions,the characteristic emissions of Ln^(3+)ions are not prominent.Furthermore,the energy transfer mechanism between STE and Ln^(3+)ions is also elusive and requires in-depth study.We chose trace Bi^(3+)-doped Cs_(2)Ag_(0.6)Na_(0.4)InCl_(6-x)Br_(x) as a representative DP matrix to demonstrate that by tuning the bromide concentration,the Ln^(3+)emission can be greatly enhanced.Such enhanced STE and Ln^(3+)ions energy transfer originates from the high covalency of Ln-Br bond,which contributes to improve ment of the characteristic emission of Ln^(3+)ions.Furthermo re,optical spectroscopy reveals that the energy transfer mechanism from DP to Eu^(3+)ions is different from all the other doped Ln^(3+)ions.The energy transfer from DP to Eu^(3+)ions is mostly through Eu-Br charge transfer while the other Ln^(3+)ions are excited by energy transfer from STE.The distinct energy transfer mechanism has resulted from the energy separation between the excited energy level of Ln^(3+)ions and the bottom of conduction band of DP.With increasing the energy separation,the energy transfer from STE to Ln^(3+)ions is less efficient because of the generation of a larger number of phonons and finally becomes impossible for Eu^(3+)ions.Our results provide new insight into tuning the energy transfer of Ln^(3+)-doped DP NCs.展开更多
Rare-earth(RE) magnesium alloys have attracted lots of attention due to their excellent mechanical properties.In this work,the microstructure and mechanical properties of as-extruded 8.5Gd-4.5Y-0.8Zn-0.4Zr magnesium a...Rare-earth(RE) magnesium alloys have attracted lots of attention due to their excellent mechanical properties.In this work,the microstructure and mechanical properties of as-extruded 8.5Gd-4.5Y-0.8Zn-0.4Zr magnesium alloy under different solution treatment were examined with the optical microscope(OM),scanning electron microscope(SEM),high resolution transmission electron microscope(HRTEM),electron back-scattered diffraction(EBSD) and Instron testing machine.The results show that the ES12alloy(solution treatment for 12 h at 520℃) has the highest ultimate tensile strength(UTS) of 390 MPa with a fracture elongation of 24.5% at the co st of a minor drop in yielding strength(YS) compared to the asextruded alloy.During solution treatment,the block-shaped long period stacking ordered(LPSO) in asextruded alloy evolves into plate-shaped LPSO,which disperses at grain boundaries(GBs),and lamellar LPSO,which distributes in grains.The coexistence of plate-shaped and lamellar LPSO,which impedes the dislocations movement,and the activated dislocations are regarded as the primary reasons for mechanical properties improvement.Furthermore,the(11-21) <1-100> texture in as-extruded alloy transforms into the(11-20) <0001> texture in ES12 alloy.The average grain size increases from 3.45 μm in as-extruded alloy to 18.70 μm in ES12 alloy.The Schmid factors of {0001} <11-20>,{10-10} <11-20>,{10-11} <11-20>,and {11-22} <11-23> increase,which indicate that slip systems are more easily activated in plastic deformation.The dynamic recrystallization(DRX) grains fraction increase to 92.8% for ES12 alloy due to the particle-stimulated nucleation(PSN) mechanism triggered by block-shaped and plate-shaped LPSO.The freshly DRXed grains further weaken the texture,and reduce the dislocation density.All of these factors increase elongation of RE magnesium alloy.展开更多
Rare earth-doped inorganic compounds contribute mostly to the family of persistent luminescent materials due to the versatile energy levels of rare earth ions.One of the key research aims is to match the trap level st...Rare earth-doped inorganic compounds contribute mostly to the family of persistent luminescent materials due to the versatile energy levels of rare earth ions.One of the key research aims is to match the trap level stemming from the doped rare earth ion or intrinsic defects to the electronic structure of the host,and therefore thermoluminescence measurement becomes a radical technology in studying trap depth,which is one of the significant parameters that determine the properties of persistent luminescence and photostimulated luminescence.However,the results of trap depth obtained by different thermoluminescence methods are quite different so that they are not comparable.Herein,we analyzed different thermoluminescence methods,selected and improved the traditional peak position method of T_(m)/500 to be E=(-0.94Inβ+30.09)kT_(m).Only the experimental heating rate(β)is needed additionally,but the accuracy is improved greatly in most cases.This convenient and accurate method will accelerate the discovery of novel rare earth-doped materials.展开更多
Precipitation is often used for the preparation of La(OH)_(3)with precipitants of liquid alkali and ammonia.To solve the problems of high cost and wastewater pollution caused by common precipitants,the active MgO synt...Precipitation is often used for the preparation of La(OH)_(3)with precipitants of liquid alkali and ammonia.To solve the problems of high cost and wastewater pollution caused by common precipitants,the active MgO synthesized by pyrolysis was used as the precipitant to prepare La(OH)_(3).The species distribution of LaCl_(3)and LaCl_(3)-MgCl_(2)mixed system solution was calculated,and the kinetic analysis of the precipi-tation process was carried out to confirm the key factors influencing the precipitation of La(OH)_(3).The results show that La(OH)_(3)with D_(50)of 5.57μm,a specific surface area of 25.70 m^(2)/g,a rod-like shape,and MgO content of 0.044 wt%,was successfully prepared by adding active MgO.The precipitation ratio of La reaches 99.92%.The La(OH)_(3)precipitation is controlled by the diffusion process.The activity of MgO has a significant influence on MgO content in the precipitate.The preparation of La(OH)_(3)by active MgO provides a potential way for an eco-friendly preparation method of rare earth.展开更多
The reaction of carbon-free oxide-based(corundum,spinel,zirconia,and mullite)submerged entry nozzle(SEN)lining with rare earth inclusions and its anti-clogging effects under near working conditions were systematically...The reaction of carbon-free oxide-based(corundum,spinel,zirconia,and mullite)submerged entry nozzle(SEN)lining with rare earth inclusions and its anti-clogging effects under near working conditions were systematically studied.A variety of lining composite test methods were innovatively used to ensure the consistency of test conditions.The experimental results showed that the mullite(acidic oxide)has strong reactivity with rare earth inclusions,and the spinel(basic oxide)has stable chemical properties and weak reactivity with rare earth inclusions.Because alumina is one of the main reactants of clogging formation,corundum is not suitable for SEN lining.There are less clogs on the surface of zirconia,but it will be exsoluted and unstable.Therefore,solving the problem of zirconia exsolution will greatly strengthen its application in SEN lining.展开更多
Ferroelastic rare earth tantalates(RETaO_(4))are widely researched as the next-generation thermal barrier coatings(TBCs),and RETaO_(4)powders are hugely significant for synthesizing their coatings.The current research...Ferroelastic rare earth tantalates(RETaO_(4))are widely researched as the next-generation thermal barrier coatings(TBCs),and RETaO_(4)powders are hugely significant for synthesizing their coatings.The current research used chemical co-precipitation within an automated experimental device to synthesize RETaO_(4)(RE=Nd,Sm,Gd,Ho,Er)powders.The device automatically monitored and controlled the solutions'pH,improving the chemical co-precipitation efficiency.The crystal structure and microstructure of the RETaO_(4)powders can be controlled by changing the annealing temperature,and the materials undergo an m'-m phase transition.The m'-RETaO_(4)powders exhibit nano-size grains,while m-RETaO_(4)powders evince micron-size grains,altered by the annealing temperatures.A simultaneous thermal analysis es-timates the reversive ferroelastic tetragonal-monoclinic phase transition temperatures.Overall,this research focuses on the synthesis,crystal structures,microstructures,and phase transition of the fabricated RETaO_(4)powders.展开更多
Improving and optimizing the target properties of ceramics via the high entropy strategy has attracted significant attention.Rare earth niobate is a potential thermal barrier coating(TBCs)material,but its poor high-te...Improving and optimizing the target properties of ceramics via the high entropy strategy has attracted significant attention.Rare earth niobate is a potential thermal barrier coating(TBCs)material,but its poor high-temperature phase stability limits its further application.In this work,four sets of TBCs high-entropy ceramics,(Sm_(1/5)Dy_(1/5)Ho_(1/5)Er_(1/5)Yb_(1/5))(Nb_(1/2)Ta_(1/2))O_(4)(5NbTa),(Sm_(1/6)Dy_(1/6)Ho_(1/6)Er_(1/6)Yb_(1/6)Lu_(1/6))(Nb_(1/2)Ta_(1/2))O_(4)(6NbTa),(Sm_(1/7)Gd_(1/7)Dy_(1/7)Ho_(1/7)Er_(1/7)Yb_(1/7)Lu_(1/7))(Nb_(1/2)Ta_(1/2))O_(4)(7NbTa),(Sm_(1/8)Gd_(1/8)Dy_(1/8)Ho_(1/8)Er_(1/8)Tm_(1/8)Yb_(1/8)Lu_(1/8))(Nb_(1/2)Ta_(1/2))O_(4)(8NbTa)are synthesized using a solid-state reaction method at 1650℃for 6 h.Firstly,the X-ray diffractometer(XRD)patterns display that the samples are all single-phase solid solution structures(space group C 2/c).Differential scanning calorimetry(DSC)and the high-temperature XRD of 8NbTa cross-check that the addition of Ta element in 8HERN increases the phase transition temperature above 1400℃,which can be attributed to that the Ta/Nb co-doping at B site introduces the fluctuation of the bond strength of Ta-O and Nb-O.Secondly,compared to high-entropy rare-earth niobates,the introduction of Ta atoms at B site substantially reduce thermal conductivity(re-duced by 44%,800℃)with the seven components high entropy ceramic as an example.The low thermal conductivity means strong phonon scattering,which may originate from the softening acoustic mode and flattened phonon dispersion in 5–8 principal element high entropy rare earth niobium tantalates(5–8NbTa)revealed by the first-principles calculations.Thirdly,the Ta/Nb co-doping in 5–8NbTa systems can further optimize the insulation performance of oxygen ions.The oxygen-ion conductivity of 8NbTa(3.31×10^(−6)S cm^(−1),900℃)is about 5 times lower than that of 8HERN(15.8×10^(−6)S cm^(−1),900℃)because of the sluggish diffusion effect,providing better oxygen barrier capacity in 5–8NbTa systems to inhibit the overgrowth of the thermal growth oxide(TGO)of TBCs.In addition,influenced by lattice dis-tortion and solid solution strengthening,the samples possess higher hardness(7.51–8.15 GPa)and TECs(9.78×10^(−6)K−1^(-1)0.78×10^(−6)K^(−1),1500℃)than the single rare-earth niobates and tantalates.Based on their excellent overall properties,it is considered that 5–8NbTa can be used as auspicious TBCs.展开更多
This study focuses on the impact of Gd^(3+),Sm^(3+),Er^(3+).Y^(3+),and Bi^(3+)multi-doping on the crystal structure,microscopic surface features,and ionic conductivity of cerium dioxide in the Ce_(1-x)(Gd_(1/5)Sm_(1/5...This study focuses on the impact of Gd^(3+),Sm^(3+),Er^(3+).Y^(3+),and Bi^(3+)multi-doping on the crystal structure,microscopic surface features,and ionic conductivity of cerium dioxide in the Ce_(1-x)(Gd_(1/5)Sm_(1/5)Er_(1/5)Y_(1/)_5Bi_(1/5))_(x)O_(2-δ)(GSEYB)system.This system holds promise as a solid electrolyte material for low and medium-temperature solid oxide fuel cells.The powders of Ce_(1-x)(Gd_(1/5)Sm_(1/5)Er_(1/5)Y_(1/5)Bi_(1/5))_(x)O_(2-δ)(x=0,0.10,0.15,0.20,0.25,0.30)were synthesized using the solid-phase reaction method.The GSEYB electrolytes were comprehensively investigated for their phase structure,microstructure,oxygen vacancy concentration,and ionic conductivity using X-ray diffraction(XRD),scanning electron microscopy(SEM),energy dispersive spectroscopy(EDS),transmission electron microscopy(TEM),X-ray photoelectron spectroscopy(XPS),and impedance spectroscopy.XRD diffraction patterns confirm a cubic fluorite-type structure with Fm3m space groups in all multi-doped systems.After sintering at 1400℃for 10 h,the relative density of doped samples exceeds 96%.In terms of electrical properties,the Ce_(0.75)Gd_(0.05)Sm_(0.05)Er_(0.05)Y_(0.05)Bi_(0.05)O_(2-δ)(x=0.25)electrolyte exhibits the highest ionic conductivity(σ_(t)=4.45×10^(-2)S/cm)and the lowest activation energy(E_(a)=0.79 eV)at 800℃.The coefficient of thermal expansion of the developed electrolyte aligns well with that of the commonly used electrode materials.This compatibility positions it as a highly promising candidate for utilization as an electrolyte material in solid oxide fuel cells(SOFCs).展开更多
In recent years,photochromic(PC)materials have garnered widespread interest due to their potential applications in next-generation optical storage devices and photocatalysis.These materials,which control luminescence ...In recent years,photochromic(PC)materials have garnered widespread interest due to their potential applications in next-generation optical storage devices and photocatalysis.These materials,which control luminescence intensity via PC reactions,are not only suitable for optical switches and information storage but also play a crucial role in enhancing catalytic efficiency in photocatalytic applications.However,quantifying the PC effect on performance in these applications is challenging,complicating the material design needed to meet performance specifications.This study reports on a multifunctional Na_(0.5)Bi_(4.5)Ti_(4)O_(15)(NBT)material that achieves adjustable photoluminescence(PL)and photocatalytic(PCA)performance through precise control of the PC reaction.Under alternating exposure to 405 nm light and thermal annealing,the Er/Yb co-doped NBT samples display remarkable photochromic(PC)behavior,capable of reversible color transitions between yellow and gray.After 30 s of 405 nm irradiation,strong energy transfer facilitates a high up-conversion(UC)luminescence contrast of 78.02%.Additionally,the PC reaction promotes the ideal separation of photoexcited carriers and significantly enhances the utilization of electron-hole pairs,nearly doubling the PCA efficiency of the NBT samples by 1.9 times.Furthermore,the luminescence contrast and PCA efficiency controlled by PC can be regulated through varying Er/Yb doping levels,maintaining consistent trends.This study provides theoretical and experimental foundations for the performance modulation of rare-earth-doped multifunctional photochromic materials.展开更多
文摘In 2025,the global rare earth exploration and development sector achieved breakthroughs across multiple fronts.Projects advanced intensively across the Americas,Oceania,Africa,and Europe,with significant growth in resources,continuous emergence of new deposits,and strong impetus injected into the industry by technological innovation and policy support.The global rare earth resource supply pattern was further optimized (Table 1).1.Fruitful results in resource growth and new deposit discoveriesBrazil emerged as a core region for resource growth.The Colossus rare earth deposit saw a 150%increase in resources and announced its first reserve estimate.The Caldeira rare earth deposit’s resource estimate grew by 50%.The combined ore resources in the Caladão rare earth deposit’s Zones A and B reached 5.72×10~8 tonnes,with a total rare earth oxide(TREO) grade of 0.1506%,concurrently hosting 2.29×10~4tonnes of gallium metal resources.
基金supported by the National Key Research and Development Program of China (2022YFF1300705)the Key Research and Development Project of Guangxi,China (Guike AB24010051)+1 种基金the National Natural Science Foundation of China (42261011,32271730 and U20A2011)the Central Public Welfare Research Institutes,Chinese Academy of Geological Sciences (2023020)。
文摘Phosphorus (P) is an essential nutrient element that is critical for plant growth and ecosystem functionality.The soil P cycle plays multiple roles,such as sustaining plant growth and productivity,regulating nutrient balance within ecosystems,and enhancing ecosystem adaptability and resilience.This cycle is influenced by factors such as the restoration approach and microbial community dynamics.However,the extent to which the restoration approach alters the P cycle in karst ecosystems and the underlying microbial mechanisms remain poorly understood.The P-cycle multifunctionality index (P-cycle MFI) serves as a comprehensive indicator for evaluating soil P cycle function,and it provides insights into changes in the P cycle between different restoration approaches.To investigate the shifts in soil P-cycle MFI and microbial mechanisms between different restoration approaches,we analyzed soil available P (AP),total P (TP),microbial biomass P (MBP),and the activities of acid phosphatase (ACP) and alkaline phosphatase (ALP).These data were used to calculate the P-cycle MFI by averaging the Z-scores between two restoration approaches(artificial restoration of forest (AF) and natural restoration of forest (NF)) and a control (cropland,CP) at six subtropical karst ecosystem sites in China.We also determined the soil organic carbon (SOC),exchangeable calcium (Ca) and magnesium (Mg),pH,bulk density (BD),microbial biomass C (MBC),and microbial biomass nitrogen (MBN),as well as the community structure,relative abundance,diversity indices,and co-occurrence networks of phoD-harboring bacteria.The results showed that the community structure of phoD-harboring bacteria varied significantly among AF,NF,and CP and across different temperature gradients.These bacteria exhibited increasing complexity and tightness in co-occurrence networks from CP to AF and then to NF,along with the ACP and ALP activities,but not the TP and AP contents.The P-cycle MFI values were significantly higher in NF compared to AF and CP,and the variation was significantly explained by restoration approach,temperature,MBC,MBN,SOC,exchangeable Ca,BD,community structure of phoD-harboring bacteria,and exchangeable Mg.Furthermore,natural restoration had a more substantial impact on the P-cycle MFI than temperature by enhancing SOC,microbial biomass,the complexity and co-occurrence network tightness of the phoD-harboring bacterial community structure,and ACP and ALP activities,but it reduced soil BD.The rare genera of phoD-harboring bacteria significantly influenced the variation of soil P-cycle MFI compared to the dominant genera.This study highlights the importance of rare genera of phoD-harboring bacteria in driving soil P-cycle multifunctionality in karst ecosystems,with natural restoration being more effective than artificial methods for enhancing soil organic matter and microbial community complexity.
基金supported by the National Natural Science Foundation of China (No.21801111)the Training Plan for Young Core Teachers in Higher Education of Henan Province (No.2021GGJS131)+1 种基金Natural Science Foundation of Henan Province (No.232300421232)the Heluo Young Talent Lifting Project (No.2023HLTJ02)。
文摘Ln@MOFs by anchoring rare metal ions(Ln) into metal-organic frameworks(MOFs) are proved to have great potential in the field of luminescent molecular thermometer.Nevertheless,the current research indicated that the poor structural stability and low sensitivity hindered their application scope.In this work,a new MOF Zn-450 luminescent thermometer with multiple emission fluorescence characteristics was synthesized by the combination of 3,3,5,5-biphenyl tetracarboxylic acid(H_(4)L) and Zn^(2+) ion under solvothermal conditions.Interestingly,a high relative sensitivity of 1.43 % K^(-1) was found within 80-300 K based on Zn-450.Subsequently,two high-sensitivity luminescent Ln@MOFs(Ln = Eu and Tb) were further fabricated by doping rare earth ions into Zn-450 based on the post-synthesis strategy.Among them,the Eu@Zn-450 demonstrates various luminous behaviors while achieving an increased relative sensitivity of 1.63 % K^(-1).In addition,the continuously visible red,pink,and purple luminescent emissions at the same temperature range were observed,suggesting that the Eu@Zn-450 could be utilized as a luminescent colorimetric molecular thermometer.Importantly,this work can present new possibilities for the development of rare earth-doped luminescence and its temperature sensing properties.
基金supported by the Guangdong S&T Program(Grant No.2024B0303390002)the National Natural Science Foundation of China(Grant Nos.42173024,92162106)+2 种基金the National Key Research and Development Program of China(Grant No.2021YFC2901705)the Director’s Fund of Guangzhou Institute of Geochemistry,Chinese Academy of Sciences(Grant No.2022SZJJZD-02)the East China University of Technology Graduate Student Innovation Grant(Grant No.YC2025-B156).
文摘Carbonatite is a rare but highly prospective rock that plays a significant role as a source of critical metals,notably rare earth elements(REE)and niobium(Nb).The widespread occurrence of fluorine-bearing minerals(e.g.,fluorite,fluorapatite,and bastnäsite)in carbonatites indicates that their parent magmas are rich in fluorine.Nevertheless,the mechanisms by which fluorine controls REE and Nb mineralization remain unclear.Building on previous work,we systematically synthesize the regulatory role of fluorine in REE and Nb mineralization throughout the entire magmatic evolution of carbonatites.Our key findings are:(1)during partial melting,fluorine decreases the solidus of carbonated peridotite,thereby enhancing the generation and stability of carbonatitic melt.(2)In the mantle melting stage,it lowers the partition coefficients of REE and Nb between mantle minerals and melt,effectively promoting their extraction.(3)Throughout magmatic crystallization,fluorine significantly enriches REE and Nb in the residual melt.(4)During liquid immiscibility,fluorine exerts limited influence,as the partition behaviors of REE and Nb are primarily governed by structural differences between the conjugate melts.(5)In the hydrothermal stage,fluorine facilitates the mobilization,transport,and ultimate precipitation of REE-and Nb-bearing minerals,directly driving mineralization.The presented evidence implies that carbonatitic melts and fluoride-bearing minerals exert primary control over the spatial distribution and mineralization potential of REE and Nb.Future studies should focus on(1)clarifying how fluorine promotes REE and Nb enrichment in late-stage brine melts and(2)investigating its effect on the solubility and precipitation mechanisms of REE-and Nb-bearing minerals during the late stages of magma evolution.
基金supported by the Key Support Project of Regional Innovation and Development Joint Fund of the National Natural Science Foundation of China(No.U24A2095).
文摘Coal serves not only as a crucial energy resource but also as a significant reservoir of critical metal elements,including Lithium(Li),Gallium(Ga),Germanium(Ge),and rare earth elements(REE).This paper provides a systematic review of the enrichment characteristics,occurrence modes,and comprehensive utilization potential of these critical metals in coal.Globally,the distribution of these metal resources exhibits significant regional heterogeneity.While the concentration in most coals falls below industrial cut-off grades,anomalous enrichment in specific coal basins results in Li,Ga,Ge,and REE concentrations far exceeding global averages,highlighting their considerable potential as unconventional metal deposits.The occurrence modes of these metals are diverse:Li is primarily hosted in mineral phases;Ga exists in inorganic,organic,and complex forms;Ge shows a strong association with organic matter;and REE are mainly present in adsorbed/isomorphic forms within clay minerals,while also displaying organic affinity.Direct extraction of metals from raw coal is often cost-prohibitive;effective recovery is therefore more feasible when integrated with coal processing.Metals are further enriched in solid wastes such as coal gangue,fly ash,and bottom ash,from which recovery is more economically and technically viable.Current comprehensive utilization primarily employs integrated mineral processing-hydrometallurgy approaches.Future research should focus on elucidating the precise occurrence forms of metals in coal and solid wastes,optimizing pre-treatment methods,and selecting effective activators and leachants.Advancing the synergistic extraction and green recovery of multiple associated resources from coal and its by-products is essential for achieving high-value,comprehensive utilization of coal-based resources.
文摘This review provides a comprehensive overview of recent advancements in aluminum-based conductor alloys engineered to achieve superior mechanical strength and thermal stability without sacrificing electrical conductivity.Particular emphasis is placed on the role of microalloying elements—particularly Sc and Zr-in promoting the formation of coherent nanoscale precipitates such as Al_(3)Zr,Al_(3)Sc,and core-shell Al_(3)(Sc,Zr)with metastable L1_(2)crystal structures.These precipitates contribute significantly to high-temperature performance by enabling precipitation strengthening and stabilizing grain boundaries.The review also explores the emerging role of other rare earth elements(REEs),such as erbium(Er),in accelerating precipitation kinetics and improving thermal stability by retarding coarsening.Additionally,recent advancements in thermomechanical processing strategies are examined,with a focus on scalable approaches to optimize the strength-conductivity balance.These approaches involve multi-step heat treatments and carefully controlled manufacturing sequences,particularly the combination of cold drawing and aging treatment to promote uniform and effective precipitation.This review offers valuable insights to guide the development of cost-effective,high-strength,heat-resistant aluminum alloys beyond conductor applications,particularly those strengthened through microalloying with Sc and Zr.
基金Project supported by the Major Research Plan of the National Natural Science Foundation of China(91962211)the National Key Research and Development Program of China(2021YFC2902202)the Key Research and Development Program of Guangxi Province(Guike-AB22080056)。
文摘Aluminum is the main impurity of the weathered crust elution-deposited rare earth ore(WCED-REO).Efficient leaching of rare earths and low leaching of aluminum are of great importance for the leaching of the WCED-REO.The effects of pH,MgSO_(4) concentration and Al^(3+)concentration of the leaching agent solution on the column leaching behaviors of WCED-REO using magnesium sulfate were investigated.Experimental data show that controlling the MgSO_(4) concentration to 0.15 mol/L,pH of the leaching agent solution to 2,the leaching amount of aluminum from the rare earth ore gradually decreases with the increase of Al^(3+)concentration in the leaching agent solution,indicating that Al^(3+)in the leaching agent solution may act as leaching agent to participate in the ion exchange of RE3+,but the leaching amounts of rare earths change insignificantly as the Al^(3+)concentration is increased.Increasing the MgSO_(4) concentration is beneficial to the leaching of aluminum,and when the Al^(3+)concentration is 0.04 mol/L(Al accumulation),the amount of Al^(3+)leached from the rare earth ore increased gradually with increasing the MgSO_(4) concentration.The pH of the leaching agent solution has a significant influence on the leaching of aluminum in the rare earth ore,and the leaching amount of aluminum from the rare earth ore increases gradually with decreasing the pH.When the Al^(3+)conce ntration is 0.04 mol/L(Al accumulation)and the pH of the leaching agent solution is above 2.0,the aluminum in the leaching agent solution can be back-adsorbed onto the rare earth ore,and the amount of the back-adsorbed Al^(3+)increases with increasing the pH of the leaching agent solution.The injection rate of the leaching agent solution has slight effect on the leaching behavior of rare earths and aluminum.In summary,leaching of Al^(3+)and consumption of MgSO_(4) can be reduced by regulating the accumulation of aluminum,MgSO_(4) concentration and pH.
基金Subproject of Inner Mongolia Autonomous Region Key Research and Development and Achievement Transformation Plan Project(2023YFDZ0064,2023KJHZ0020,2022YFDZ0097)Natural Science Foundation of Inner Mongolia Autonomous Region of China(2022QN05040)+1 种基金Basic Research Funds for Directly Affiliated Universities in Inner Mongolia Autonomous Region(JY20220093)Program for Young Talents of Science and Technology in Universities of Inner Mongolia Autonomous Region(NJYT24008)。
文摘Modification of 6061 aluminum alloy was conducted through composite addition of cerium-rich rare earths and Al-Ti-B.Results show that the composite addition of Al-Ti-B and Ce/La element at a specific ratio notably promotes the refinement of the alloy's grains.Ce and La elements are combined with Si and other elements to form rare earth phases,improving the morphology and distribution of precipitates and mitigating the adverse effects ofβ-Fe phases on the microstructure and mechanical properties of alloy.However,excessive rare earth content poses challenges;it not only leads to a decrease in Mg-Si strengthening phase by binding with Si but also promotes the formation of larger or numerous rare earth phases that may act as initiation points for cracks,thereby impeding the improvement of the structure and performance of alloy.The composite addition of cerium-rich rare earths and Al-Ti-B not only preserves the strength of the alloy but also significantly enhances the plasticity of the 6061 as-cast alloy.At a composite addition ratio of Al-Ti-B:RE=2:1,the newly developed 6061-RE aluminum alloy exhibits increased average elongation by 50%and 45%in its as-cast and homogenized states,respectively,compared to the baseline 6061 alloy,facilitating subsequent deformation processing.After solution treatment at 540℃for 1 h and aging at 180℃for 5 h,the average ultimate tensile strength and yield strength of 6061-RE alloys reach 313.2 and 283.1 MPa,increased by 12.3%and 14.5%compared with those of the original alloy,respectively,and the average elongation is improved by 41%.
基金Project supported by the Thousand Talents Program of Jiangxi Province,China(JXSQ2023201003)National Natural Science Foundation of China(42107254)+4 种基金Science and Technology Major Program of Ordos City(2022EEDSKJZDZX014-2)Technological Innovation Guidance Program of Jiangxi Province(20212BDH81029)Rare Earth Industry Fund(IAGM2020DB06)Selfdeployed Projects of Ganjiang Innovation Academy,Chinese Academy of Sciences(E055A01)the Key Research Program of the Chinese Academy of Sciences(ZDRW-CN-2021-3-3)。
文摘The rare earth elements(REEs)extraction by chemical leaching from ion-adsorption type rare earth ores(IAREO)has led to serious ecological and environmental risks.Conversely,demand for bioleaching is on the rise with the advantage of being environmental-friendly.As one of the organic acids produced by biological metabolism,citric acid was used to leach REEs and explore the performance and process.The results demonstrate that citric acid exhibits higher leaching efficiency(96.00%)for REEs at a relatively low concentration of 0.01 mol/L compared with(NH_(4))_(2)SO_(4)(84.29%,0.1 mol/L)and MgSO_(4)(83.99%,0.1 mol/L).Citric acid shows a preference for leaching heavy rare earth elements,with 99%leaching efficiency in IAREO,which shows higher capacity than(NH_(4))_(2)SO_(4)and MgSO_(4)(as inorganic leaching agents).Kinetic analysis indicates that the leaching process of REEs with citric acid is controlled by both the internal diffusion kinetics and chemical reaction kinetics,which is different from inorganic leaching agents.Visual Minteq calculations confirm that RE-Citrate is the main constituent of the extract solution in the leaching process of the IAREO,thereby enhancing the leaching efficiency of REEs from the IAREO.It suggests that citric acid may be used as a promising organic leaching agent for the environmentalfriendly extraction of REEs from IAREO.
基金Project supported by the National Natural Science Foundation of China(52074031)the Key Research and Development Program of Shandong Province(ZR2021MB051,ZR2020ME256)the Open Project of Key Laboratory of Green Chemical Engineering Process of Ministry of Education(GCP202117)。
文摘Solvent extraction is the main method used to separate and purify rare earth elements.In the process of rare earths extraction,emulsification often generated due to the instability of the aqueous and organic phases or improper operating conditions.Once emulsification occurs,it would not only lead to low rare earths recovery efficiency,small product quantities,high production costs and the losing of extractant and rare earth resources,but also result in serious environmental pollution.Therefore,it is very important to study the micro-mechanisms of emulsification and establish new methods to prevent emulsification at the source.In this paper,possible factors resulting in emulsification,such as the compositions and properties of the organic and aqueous phases,the operating conditions of the rare earths extraction are reviewed.The micro-mechanisms of emulsification are summarized basing on the microscopic structures in the bulk phase,aggregations of the extractants at the organic-aqueous interface,spectral characterizations and computational simulations.On this basis,new formation mechanisms are proposed for emulsification.Preliminary explorations are employed to verify the correctness of these new viewpoints.Finally,future directions for studies of the emulsification micro-mechanism are proposed.This study provides a theoretical basis for further understanding the micro-mechanisms of interfacial instability resulting in emulsification in the process of rare earths extraction.
基金Project supported by the National Natural Science Foundation of China(22206080)the Natural Science Foundation of Jiangsu(SBK2022041070)+1 种基金the Science and Technology Project of Henan Province(232102321050,232102321035)the International Science,Innovators,Technology Cooperation Projects of Henan Province(232102521009)。
文摘Metal-organic frameworks(MOFs)and their derivatives have gained significant attention in recent years for their ability to catalyze the advanced oxidation of persulfates.Cerium-doped MOFs,in particular,have shown promise due to their high catalytic efficiency,practical applicability,and cost-effectiveness.However,their structure,catalytic properties,and mechanisms are not yet fully understood.ZIF-8 was chosen as the raw material to prepare cerium-doped hollow carbon nano fibers(Ce-HCNFs)using the electrostatic spinning-calcination method.The objective is to investigate the structure,catalytic performance,and catalytic mechanism of Ce-HCNFs.The results show that Ce-HCNFs catalyzed the degradation of tetracycline(TC)by persulfate up to 76.9%,Quenching experiments and electron paramagnetic resonance experiments indicate the dominant role of single-linear oxygen.Furthermore,the experiments on the influence factor and cycling demonstrate the exceptional stability and recycling capability of Ce-HCNFs in real-world water environments.
基金Project supported by the Research Project of Mindu Innovation Laboratory(2021ZZ114)Natural Science Foundation of Xiamen(3502Z20227255)+1 种基金Major Research Project of Xiamen(3502Z20191015)the Science and Technology Major Project of Fujian Province(2021HZ021013)。
文摘Lanthanide ions(Ln^(3+))doping provides a potential strategy to control over the luminescent properties of lead-free halide double perovskite nanocrystals(DP NCs).However,due to the low energy transfer efficiency between self-trapped exciton(STE)and Ln^(3+)ions,the characteristic emissions of Ln^(3+)ions are not prominent.Furthermore,the energy transfer mechanism between STE and Ln^(3+)ions is also elusive and requires in-depth study.We chose trace Bi^(3+)-doped Cs_(2)Ag_(0.6)Na_(0.4)InCl_(6-x)Br_(x) as a representative DP matrix to demonstrate that by tuning the bromide concentration,the Ln^(3+)emission can be greatly enhanced.Such enhanced STE and Ln^(3+)ions energy transfer originates from the high covalency of Ln-Br bond,which contributes to improve ment of the characteristic emission of Ln^(3+)ions.Furthermo re,optical spectroscopy reveals that the energy transfer mechanism from DP to Eu^(3+)ions is different from all the other doped Ln^(3+)ions.The energy transfer from DP to Eu^(3+)ions is mostly through Eu-Br charge transfer while the other Ln^(3+)ions are excited by energy transfer from STE.The distinct energy transfer mechanism has resulted from the energy separation between the excited energy level of Ln^(3+)ions and the bottom of conduction band of DP.With increasing the energy separation,the energy transfer from STE to Ln^(3+)ions is less efficient because of the generation of a larger number of phonons and finally becomes impossible for Eu^(3+)ions.Our results provide new insight into tuning the energy transfer of Ln^(3+)-doped DP NCs.
基金supported by the Key Research and Development Program of Heilongjiang (2022ZX01A01)National Natural Science Foundation of China (51975167)Natural Science Foundation of Heilongjiang Province(LH2022E080)。
文摘Rare-earth(RE) magnesium alloys have attracted lots of attention due to their excellent mechanical properties.In this work,the microstructure and mechanical properties of as-extruded 8.5Gd-4.5Y-0.8Zn-0.4Zr magnesium alloy under different solution treatment were examined with the optical microscope(OM),scanning electron microscope(SEM),high resolution transmission electron microscope(HRTEM),electron back-scattered diffraction(EBSD) and Instron testing machine.The results show that the ES12alloy(solution treatment for 12 h at 520℃) has the highest ultimate tensile strength(UTS) of 390 MPa with a fracture elongation of 24.5% at the co st of a minor drop in yielding strength(YS) compared to the asextruded alloy.During solution treatment,the block-shaped long period stacking ordered(LPSO) in asextruded alloy evolves into plate-shaped LPSO,which disperses at grain boundaries(GBs),and lamellar LPSO,which distributes in grains.The coexistence of plate-shaped and lamellar LPSO,which impedes the dislocations movement,and the activated dislocations are regarded as the primary reasons for mechanical properties improvement.Furthermore,the(11-21) <1-100> texture in as-extruded alloy transforms into the(11-20) <0001> texture in ES12 alloy.The average grain size increases from 3.45 μm in as-extruded alloy to 18.70 μm in ES12 alloy.The Schmid factors of {0001} <11-20>,{10-10} <11-20>,{10-11} <11-20>,and {11-22} <11-23> increase,which indicate that slip systems are more easily activated in plastic deformation.The dynamic recrystallization(DRX) grains fraction increase to 92.8% for ES12 alloy due to the particle-stimulated nucleation(PSN) mechanism triggered by block-shaped and plate-shaped LPSO.The freshly DRXed grains further weaken the texture,and reduce the dislocation density.All of these factors increase elongation of RE magnesium alloy.
基金Project supported by the National Natural Science Foundation of China(52372134,12274023)the Fundamental Re search Funds for the Central Universities(FRF-EYIT-23-04)。
文摘Rare earth-doped inorganic compounds contribute mostly to the family of persistent luminescent materials due to the versatile energy levels of rare earth ions.One of the key research aims is to match the trap level stemming from the doped rare earth ion or intrinsic defects to the electronic structure of the host,and therefore thermoluminescence measurement becomes a radical technology in studying trap depth,which is one of the significant parameters that determine the properties of persistent luminescence and photostimulated luminescence.However,the results of trap depth obtained by different thermoluminescence methods are quite different so that they are not comparable.Herein,we analyzed different thermoluminescence methods,selected and improved the traditional peak position method of T_(m)/500 to be E=(-0.94Inβ+30.09)kT_(m).Only the experimental heating rate(β)is needed additionally,but the accuracy is improved greatly in most cases.This convenient and accurate method will accelerate the discovery of novel rare earth-doped materials.
基金the National Key Research and Development Program of China(2022YFB3504503)the National Natural Science Foundation of China(52274355)the Gansu Province Science and Technology Major Special Project,China(22ZD6GD061).
文摘Precipitation is often used for the preparation of La(OH)_(3)with precipitants of liquid alkali and ammonia.To solve the problems of high cost and wastewater pollution caused by common precipitants,the active MgO synthesized by pyrolysis was used as the precipitant to prepare La(OH)_(3).The species distribution of LaCl_(3)and LaCl_(3)-MgCl_(2)mixed system solution was calculated,and the kinetic analysis of the precipi-tation process was carried out to confirm the key factors influencing the precipitation of La(OH)_(3).The results show that La(OH)_(3)with D_(50)of 5.57μm,a specific surface area of 25.70 m^(2)/g,a rod-like shape,and MgO content of 0.044 wt%,was successfully prepared by adding active MgO.The precipitation ratio of La reaches 99.92%.The La(OH)_(3)precipitation is controlled by the diffusion process.The activity of MgO has a significant influence on MgO content in the precipitate.The preparation of La(OH)_(3)by active MgO provides a potential way for an eco-friendly preparation method of rare earth.
基金supported by the National Outstanding Youth Science Fund Project of National Natural Science Foundation of China(52302031)National Natural Science Foundation of China(51932008 and 51772277)Central China Thousand Talents Project(204200510011).
文摘The reaction of carbon-free oxide-based(corundum,spinel,zirconia,and mullite)submerged entry nozzle(SEN)lining with rare earth inclusions and its anti-clogging effects under near working conditions were systematically studied.A variety of lining composite test methods were innovatively used to ensure the consistency of test conditions.The experimental results showed that the mullite(acidic oxide)has strong reactivity with rare earth inclusions,and the spinel(basic oxide)has stable chemical properties and weak reactivity with rare earth inclusions.Because alumina is one of the main reactants of clogging formation,corundum is not suitable for SEN lining.There are less clogs on the surface of zirconia,but it will be exsoluted and unstable.Therefore,solving the problem of zirconia exsolution will greatly strengthen its application in SEN lining.
基金the Rare and Precious Metals Material Genetic Engineering Project of Yunnan Province(202102AB080019-1)National Key Research and Development Program of China(2022YFB3708600)the National Natural Science Foundation of China(91960103).
文摘Ferroelastic rare earth tantalates(RETaO_(4))are widely researched as the next-generation thermal barrier coatings(TBCs),and RETaO_(4)powders are hugely significant for synthesizing their coatings.The current research used chemical co-precipitation within an automated experimental device to synthesize RETaO_(4)(RE=Nd,Sm,Gd,Ho,Er)powders.The device automatically monitored and controlled the solutions'pH,improving the chemical co-precipitation efficiency.The crystal structure and microstructure of the RETaO_(4)powders can be controlled by changing the annealing temperature,and the materials undergo an m'-m phase transition.The m'-RETaO_(4)powders exhibit nano-size grains,while m-RETaO_(4)powders evince micron-size grains,altered by the annealing temperatures.A simultaneous thermal analysis es-timates the reversive ferroelastic tetragonal-monoclinic phase transition temperatures.Overall,this research focuses on the synthesis,crystal structures,microstructures,and phase transition of the fabricated RETaO_(4)powders.
基金support from Yunnan Major Scientific and Technological Projects(No.202302AG050010)Yunnan Fundamental Research Projects(Nos.202101AW070011 and202101BE070001–015)+1 种基金National Natural Science Foundation of China(No.52303295)Project Funds of“Xingdian Talent Support Program”.
文摘Improving and optimizing the target properties of ceramics via the high entropy strategy has attracted significant attention.Rare earth niobate is a potential thermal barrier coating(TBCs)material,but its poor high-temperature phase stability limits its further application.In this work,four sets of TBCs high-entropy ceramics,(Sm_(1/5)Dy_(1/5)Ho_(1/5)Er_(1/5)Yb_(1/5))(Nb_(1/2)Ta_(1/2))O_(4)(5NbTa),(Sm_(1/6)Dy_(1/6)Ho_(1/6)Er_(1/6)Yb_(1/6)Lu_(1/6))(Nb_(1/2)Ta_(1/2))O_(4)(6NbTa),(Sm_(1/7)Gd_(1/7)Dy_(1/7)Ho_(1/7)Er_(1/7)Yb_(1/7)Lu_(1/7))(Nb_(1/2)Ta_(1/2))O_(4)(7NbTa),(Sm_(1/8)Gd_(1/8)Dy_(1/8)Ho_(1/8)Er_(1/8)Tm_(1/8)Yb_(1/8)Lu_(1/8))(Nb_(1/2)Ta_(1/2))O_(4)(8NbTa)are synthesized using a solid-state reaction method at 1650℃for 6 h.Firstly,the X-ray diffractometer(XRD)patterns display that the samples are all single-phase solid solution structures(space group C 2/c).Differential scanning calorimetry(DSC)and the high-temperature XRD of 8NbTa cross-check that the addition of Ta element in 8HERN increases the phase transition temperature above 1400℃,which can be attributed to that the Ta/Nb co-doping at B site introduces the fluctuation of the bond strength of Ta-O and Nb-O.Secondly,compared to high-entropy rare-earth niobates,the introduction of Ta atoms at B site substantially reduce thermal conductivity(re-duced by 44%,800℃)with the seven components high entropy ceramic as an example.The low thermal conductivity means strong phonon scattering,which may originate from the softening acoustic mode and flattened phonon dispersion in 5–8 principal element high entropy rare earth niobium tantalates(5–8NbTa)revealed by the first-principles calculations.Thirdly,the Ta/Nb co-doping in 5–8NbTa systems can further optimize the insulation performance of oxygen ions.The oxygen-ion conductivity of 8NbTa(3.31×10^(−6)S cm^(−1),900℃)is about 5 times lower than that of 8HERN(15.8×10^(−6)S cm^(−1),900℃)because of the sluggish diffusion effect,providing better oxygen barrier capacity in 5–8NbTa systems to inhibit the overgrowth of the thermal growth oxide(TGO)of TBCs.In addition,influenced by lattice dis-tortion and solid solution strengthening,the samples possess higher hardness(7.51–8.15 GPa)and TECs(9.78×10^(−6)K−1^(-1)0.78×10^(−6)K^(−1),1500℃)than the single rare-earth niobates and tantalates.Based on their excellent overall properties,it is considered that 5–8NbTa can be used as auspicious TBCs.
基金supported by the Guangdong Provincial Basic and Applied Basic Research Foundation(2021A1515010671,2020A1515011221)the Guangdong Provincial Key Discipline Research Capacity Enhancement Project(2021ZDJS071)the Guangdong Provincial College Innovation Project(2021KTSCX122,2022KQNCX077)。
文摘This study focuses on the impact of Gd^(3+),Sm^(3+),Er^(3+).Y^(3+),and Bi^(3+)multi-doping on the crystal structure,microscopic surface features,and ionic conductivity of cerium dioxide in the Ce_(1-x)(Gd_(1/5)Sm_(1/5)Er_(1/5)Y_(1/)_5Bi_(1/5))_(x)O_(2-δ)(GSEYB)system.This system holds promise as a solid electrolyte material for low and medium-temperature solid oxide fuel cells.The powders of Ce_(1-x)(Gd_(1/5)Sm_(1/5)Er_(1/5)Y_(1/5)Bi_(1/5))_(x)O_(2-δ)(x=0,0.10,0.15,0.20,0.25,0.30)were synthesized using the solid-phase reaction method.The GSEYB electrolytes were comprehensively investigated for their phase structure,microstructure,oxygen vacancy concentration,and ionic conductivity using X-ray diffraction(XRD),scanning electron microscopy(SEM),energy dispersive spectroscopy(EDS),transmission electron microscopy(TEM),X-ray photoelectron spectroscopy(XPS),and impedance spectroscopy.XRD diffraction patterns confirm a cubic fluorite-type structure with Fm3m space groups in all multi-doped systems.After sintering at 1400℃for 10 h,the relative density of doped samples exceeds 96%.In terms of electrical properties,the Ce_(0.75)Gd_(0.05)Sm_(0.05)Er_(0.05)Y_(0.05)Bi_(0.05)O_(2-δ)(x=0.25)electrolyte exhibits the highest ionic conductivity(σ_(t)=4.45×10^(-2)S/cm)and the lowest activation energy(E_(a)=0.79 eV)at 800℃.The coefficient of thermal expansion of the developed electrolyte aligns well with that of the commonly used electrode materials.This compatibility positions it as a highly promising candidate for utilization as an electrolyte material in solid oxide fuel cells(SOFCs).
基金Project supported by the Jiangsu Province Graduate Research and Innovation Program(KYCX24_0329)。
文摘In recent years,photochromic(PC)materials have garnered widespread interest due to their potential applications in next-generation optical storage devices and photocatalysis.These materials,which control luminescence intensity via PC reactions,are not only suitable for optical switches and information storage but also play a crucial role in enhancing catalytic efficiency in photocatalytic applications.However,quantifying the PC effect on performance in these applications is challenging,complicating the material design needed to meet performance specifications.This study reports on a multifunctional Na_(0.5)Bi_(4.5)Ti_(4)O_(15)(NBT)material that achieves adjustable photoluminescence(PL)and photocatalytic(PCA)performance through precise control of the PC reaction.Under alternating exposure to 405 nm light and thermal annealing,the Er/Yb co-doped NBT samples display remarkable photochromic(PC)behavior,capable of reversible color transitions between yellow and gray.After 30 s of 405 nm irradiation,strong energy transfer facilitates a high up-conversion(UC)luminescence contrast of 78.02%.Additionally,the PC reaction promotes the ideal separation of photoexcited carriers and significantly enhances the utilization of electron-hole pairs,nearly doubling the PCA efficiency of the NBT samples by 1.9 times.Furthermore,the luminescence contrast and PCA efficiency controlled by PC can be regulated through varying Er/Yb doping levels,maintaining consistent trends.This study provides theoretical and experimental foundations for the performance modulation of rare-earth-doped multifunctional photochromic materials.
