Transparent glass ceramics were prepared from the phosphosilicate system by melt-quenching devitrification（MQD） method, i.e., nanocrystals spontaneously form during cooling of the melts. Introduction of 2.5 wt.% Yb2...Transparent glass ceramics were prepared from the phosphosilicate system by melt-quenching devitrification（MQD） method, i.e., nanocrystals spontaneously form during cooling of the melts. Introduction of 2.5 wt.% Yb2O3 and 0.5 wt.% Er2O3 into the glass melt induced the change of type and concentration of crystals. The comparison of rheological and thermodynamic properties of both undoped and Yb^3＋/Er^3＋ doped melts showed that addition of Yb^3＋/Er^3＋ oxides caused increase of liquid fragility, and degree of medium-range order. In addition, the thermodynamic barriers for nucleation ΔG＊ as a function of reduced temperature T/Tm were calculated with an assumption of wetting angle θ=90o, Yb^3＋/Er^3＋ doped melt tended to firstly nucleate as compared to undoped melt at small undercooling.展开更多
The Yb3^＋ -doped silicate, phosphate and borophosphate laser glasses were prepared by means of conventional melt quenching technology. The physical and spectral properties of the glasses were investigated. The result...The Yb3^＋ -doped silicate, phosphate and borophosphate laser glasses were prepared by means of conventional melt quenching technology. The physical and spectral properties of the glasses were investigated. The results show that, due to the existence of OH^-, the fluorescence lifetime of phosphate glass is shorter than that of silicate glass, so silicate glass has better spectral properties than phosphate glass. Silicate glass has better mechanical and thermal properties than phosphate glass, but with the addition of B2O3, mechanical and thermal properties of phosphate glass are improved greatly without fluorescence quenching effect. This kind of borophosphate glass can be used in high average power solid state lasers.展开更多
The Er^3＋/Yb^3＋ co-doped TeO2-Nb2O5-Li2O glass is prepared by conventional melting method, and its upconversion spectra are measured. The intense green upconversion luminescence upon excitation with a 976 nm laser d...The Er^3＋/Yb^3＋ co-doped TeO2-Nb2O5-Li2O glass is prepared by conventional melting method, and its upconversion spectra are measured. The intense green upconversion luminescence upon excitation with a 976 nm laser diode is observed with the naked eyes. The dependence of luminescence intensity on the ratio of Yb^3＋/Er^3＋ is discussed in detail, and the relationship between the ratio of green luminescence intensity to red luminescence intensity and the ratio of Yb^3＋/Er^3＋ is also studied, The luminescence intensity increases with the ratio of Yb^3＋/Er^3＋ increasing. The ratio of Yb^3＋/Er^3＋ plays a more important role than the concentration of Er^3＋ in determining the upconversion luminescence intensity. The ratio of green luminescence intensity to red luminescence intensity reaches a maximum when ratio of Yb^3＋/Er^3＋ is 3. Thus the glass could be one of the potential candidates for LD pumping solid-state lasers.展开更多
Regulating lithium(Li)plating/stripping behavior in three-dimensional(3D)conductive scaffolds is critical to stabilizing Li metal batteries(LMBs).Surface protrusions and roughness in these scaffolds can induce uneven ...Regulating lithium(Li)plating/stripping behavior in three-dimensional(3D)conductive scaffolds is critical to stabilizing Li metal batteries(LMBs).Surface protrusions and roughness in these scaffolds can induce uneven distributions of the electric fields and ionic concentrations,forming“hot spots.”Hot spots may cause uncontrollable Li dendrites growth,presenting significant challenges to the cycle stability and safety of LMBs.To address these issues,we construct a Li ionic conductive-dielectric gradient bifunctional interlayer(ICDL)onto a 3D Li-injected graphene/carbon nanotube scaffold(LGCF)via in situ reaction of exfoliated hexagonal boron nitride(fhBN)and molten Li.Microscopic and spectroscopic analyses reveal that ICDL consists of fhBN-rich outer layer and inner layer enriched with Li_(3)N and Li-boron composites(Li-B).The outer layer utilizes dielectric properties to effectively homogenize the electric field,while the inner layer ensures high Li ion conductivity.Moreover,DFT calculations indicate that ICDL can effectively adsorb Li and decrease the Li diffusion barrier,promoting enhanced Li ion transport.The modulation of Li kinetics by ICDL increases the critical length of the Li nucleus,enabling suppression of Li dendrite growth.Attributing to these advantages,the ICDL-coated LGCF(ICDL@LGCF)demonstrates impressive long-term cycle performances in both symmetric cells and full cells.展开更多
Oxy-fluoride glasses with composition of 25SiO2-65PbF2-9.4AlF3-0.1HoF3-0.5YbF3 were prepared. Their up-conversion fluorescence characteristics were investigated by 980 nm laser. Two emission peaks were observed at 540...Oxy-fluoride glasses with composition of 25SiO2-65PbF2-9.4AlF3-0.1HoF3-0.5YbF3 were prepared. Their up-conversion fluorescence characteristics were investigated by 980 nm laser. Two emission peaks were observed at 540 and 650 nm. The up-conversion mechanism and processes were analyzed. The relationship between pumping power and relative intensity of emissions was discussed. From the dependence, it is known that the emissions centered at 540 and 650 nm are both attributed to two-photon process.展开更多
The three host glasses doped with Yb 3+ were prepared by means of conventional melt quenching technology, and the influence on physical and spectral properties of phosphate glass due to addition of B2O3 was investigat...The three host glasses doped with Yb 3+ were prepared by means of conventional melt quenching technology, and the influence on physical and spectral properties of phosphate glass due to addition of B2O3 was investigated and compared with silicate glass. The results show that due to the existence of OH- impurities which induce the non-radiative route, the fluorescence lifetime of phosphate glass is shorter, so silicate glass has better spectral properties than phosphate glass. Silicate glass has more excellent thermal-mechanical properties than phosphate glass, but with the addition of B2O3, thermal-mechanical properties of phosphate glass are improved greatly without fluorescence quenching effect, and this kind of borophosphate glass will be the candidate to be used in high average power solid state laser.展开更多
Polydiacetylene(PDA)is one kind of the conjugated polymer with layered structure,which can serve as a host to accommodate the vip components through intercalation.In these intercalated PDAs,some of them were reporte...Polydiacetylene(PDA)is one kind of the conjugated polymer with layered structure,which can serve as a host to accommodate the vip components through intercalation.In these intercalated PDAs,some of them were reported to have a nearly perfect organized structure and perform completely reversible thermochromism.Till now,these reported intercalated PDAs were made by only introducing a single component for intercalation.Here,we chose 10,12-pentacosadiynoic acid(PCDA)as the monomer,of which the carboxyl-terminal groups can interact with either Tb^3+ ions or melamines(MAs).When the feeding molar ratio of PCDA,MA,and Tb^3+ ion was 3:267:1,only Tb^3+ ions were intercalated though excess MAs existed.Such Tb^3+- intercalated poly-PCDA exhibited completely reversible thermochromism,where almost all the carboxyl groups interacted with Tb^3+ ions to form the nearly perfect structure.When the feeding molar ratio of PCDA,MA,and Tb^3+ ion was 3:267:0.6,both Tb^3+ ions and MAs were intercalated.There existed some defects in the imperfect MA-intercalated domains and at the domain boundaries.The MA/Tb^3+- intercalated poly-PCDA exhibits partially reversible thermochromism,where the backbones near the defects are hard to return the initial conformation,while the rest,those at nearly perfect organized domains,are still able to restore the initial conformation.展开更多
A series of CaFCl：Tb3＋ and CaFCI：Tb3＋,A＋ （A=Li, Na and K） nanophosphors were synthesized by the one-step sol-gel method, which were reported for the first time. The sample consisted of monodisperse particles, t...A series of CaFCl：Tb3＋ and CaFCI：Tb3＋,A＋ （A=Li, Na and K） nanophosphors were synthesized by the one-step sol-gel method, which were reported for the first time. The sample consisted of monodisperse particles, the average size of which was 37 nm. The emissions of Tb3＋ ions and oxygen defects OF＇ were demonstrated in the CaFCl：Tb3＋ samples. The former was made up of several peaks at 488, 545, 587 and 623 nm, ascribed to 5D4→7FJ （j=6-3） transitions of Tb3＋ ions. The latter was shown as a broad band peaked at about 450 nm. Alkali metal ions A＋ （A=Li, Na and K） were introduced as the charge compensators to improve the luminescence of samples. The influence of charge compensators on the emissions of Tb3＋ ions and oxygen defects OF＇ was investigated by the measurement of fluorescence spectra and luminescence decay curves. The results indicated that all the charge compensators weakened the defects emission. Furthermore, Li＋ ion was the best charge compensator, because it not only reduced the defects emission but also increased the emission intensity of Tb3＋ significantly. Our results suggested that this nanophosphor sensitized by the charge compensator might broaden potential applications of rare-earth doped CaFCl.展开更多
Different concentrations of Mg^（2＋） -doped hexagonal phase NaGdF_4：Yb^（3＋）, Er^（3＋）nanocrystals（NCs） were synthesized by a modified solvothermal method. Successful codoping of Mg^（2＋）ions in upconversio...Different concentrations of Mg^（2＋） -doped hexagonal phase NaGdF_4：Yb^（3＋）, Er^（3＋）nanocrystals（NCs） were synthesized by a modified solvothermal method. Successful codoping of Mg^（2＋）ions in upconversion nanoparticles（UCNPs） was supported by XRD, SEM, EDS, and PL analyses. The effects of Mg^（2＋）doping on the morphology and the intensity of the upconversion（UC） emission were discussed in detail. It turned out that with the concentration of Mg^（2＋）increasing, the morphology of the nanoparticles turn to change gradually and the UC emission was increasing gradually as well. Notably the UC fluorescence intensities of Er^（3＋）were gradually improved owing to the codoped Mg^（2＋）and then achieved a maximum level as the concentration of Mg^（2＋）ions was 60 mol% from the amendment of the crystal structure of β-NaGdF_4：Yb^（3＋）,Er^（3＋）nanoparticles. Moreover, the UC luminescence properties of the rare-earth（Yb3＋, Er^（3＋）） ions codoped NaGdF_4 nanocrystals were investigated in detail under 980-nm excitation.展开更多
In this work,for the first time,it is demonstrated that during the insertion/extraction of Na ions,the structural evolution at the Na_(4)site at a voltage range of 3-4 V is a key factor for the capacity decay of Na_(4...In this work,for the first time,it is demonstrated that during the insertion/extraction of Na ions,the structural evolution at the Na_(4)site at a voltage range of 3-4 V is a key factor for the capacity decay of Na_(4)Fe_(3)(PO_(4))_(2)P_(2)O_(7)(NFPP).Herein,a strategy of introducing columnar potassium ions at the Na_(4)site is proposed to address the aforementioned challenge.As a cathode material for sodium-ion batteries,the K_(0.12)Na_(3.88)Fe_(3)(PO_(4))_(2)P_(2)O_(7)/C(K-NFPP)composite enhances the reversibility of Na_(4)extraction.Specifically,the K-NFPP exhibits an initial discharge capacity of 107.8 mAh g^(-1)at a high current density of 5 C,with a capacity retention of 91.4% after 2000 cycles,outperforming the pristine NFPP material(81.1 m Ah g^(-1)and 67.1%).At 5 C,the K-NFPP also retains 81.5% of the reversible capacity at 0.1 C,whereas the NFPP only retains 68.3%.Moreover,the K-NFPP-based full-cell delivers an initial capacity of 110.1 m Ah g^(-1)at 1 C,with a capacity retention of 90% after 100 cycles.It is found that in comparison to K-doping of the Na1,Na2,and Na3 sites,K-doping at the Na4 site effectively optimizes the band gap and stabilizes the crystal structure,thereby reducing lattice changes of FeO_(6)evolution during Na^(+)insertion/extraction.As a result,the introduction of columnar potassium ions significantly enhances the capacity contribution of the Na_(4)site,optimizes reaction kinetics,and effectively mitigates the capacity decay of NFPP cathodes.It is believed that this study offers a new entry point for the application of NFPP in high-voltage sodium storage.展开更多
The sodium-ion battery(SIB)cathode material,Na_(4)Fe_(3)(PO_(4))_(2)(P_(2)O_(7))(NFPP),has become a focal material in both academia and industry due to its low cost,long lifespan,and high safety.In the recent three ye...The sodium-ion battery(SIB)cathode material,Na_(4)Fe_(3)(PO_(4))_(2)(P_(2)O_(7))(NFPP),has become a focal material in both academia and industry due to its low cost,long lifespan,and high safety.In the recent three years,substantial efforts have been devoted to promoting the practical applications of NFPP by optimizing its electrochemical performance and disclosing the reaction mechanisms.Various modification strategies and their effect mechanisms have been explored,and the performance evaluation of NFPP has progressively advanced from laboratory-scale coin cells to practical pouch cell configurations.Nevertheless,there remains a lack of systematic reviews comprehensively assessing the developmental status and application readiness of NFPP.This review critically examines NFPP's fundamental structural characteristics and proposes four key development issues.Then,the latest research advances are introduced with explicit differentiation of design strategies and their mechanistic impacts.Notably,we provide a dedicated discussion on NFPP's current pouch cell performance metrics,while highlighting two critical yet underexplored research directions(enhancing air stability and improving tap density)for commercial viability.展开更多
A pseudocapacitance dominated anode material assembled from Li_(3)VO_(4)nanocrystals encapsulated in the interlayers of N-doped graphene has been developed via a facile 2D nanospace confined strategy for lithium ion c...A pseudocapacitance dominated anode material assembled from Li_(3)VO_(4)nanocrystals encapsulated in the interlayers of N-doped graphene has been developed via a facile 2D nanospace confined strategy for lithium ion capacitors(LICs).In this contribution,the N-doped graphene synthesized by a faicle solid state reaction using C_(3)N_(4)nanosheets as template and glucose as carbon source provides sufficient 2D nanospace for the confined and homogeneous growth of Li_(3)VO_(4)at the nanoscale,and simultaneously efficiently anchors each nanobuilding block inside the interlayers,thus realizing the utilizaiton of full potential of active components.The so-formed 3D hybrids not only ensure intimate electronic coupling between active materials and N-doped graphene,but also realize robust structure integrity.Owing to these unique advantages,the resulting hybrids show pseudocapacitance dominated lithium storage behaviors with capacitive contributions of over 90%at both low and high current rates.The LVO@C@NG delivers reversible capacities of 206 mAh/g at 10 A/g,capacity retention of 92.7%after 1000 cycles at 2 A/g,and a high energy density of 113.6 Wh/kg at 231.8 W/kg for LICs.展开更多
All-inorganic perovskite CsPbX_(3)(X=Cl,Br,I)nanocrystals(NCs)have emerged as promising candidates for light-emitting diode(LED)displays due to their outstanding photophysical properties.However,their practical applic...All-inorganic perovskite CsPbX_(3)(X=Cl,Br,I)nanocrystals(NCs)have emerged as promising candidates for light-emitting diode(LED)displays due to their outstanding photophysical properties.However,their practical application remains hindered by poor stability and the inherent toxicity of Pb2+.In this study,we present a two-step heating method to synthesize CsPb_(1-x)Zn_(x)Br_(3)NCs with enhanced optoelectronic performance and uniform dispersion.The optimized Zn^(2+)-doped NCs achieve a photoluminescence quantum yield(PLQY)of 86%,with a reduction in lattice spacing from 0.384 to 0.365 nm,attributed to increased perovskite lattice formation energy and effective surface passivation.To further improve stability,a silica(SiO_(2))shell is introduced via surface modification with(3-aminopropyl)triethoxysilane(APTES),forming CsPb_(0.7)Zn_(0.3)Br_(3)@SiO_(2)core–shell NCs.At an optimal APTES/B-site metal ion molar ratio of 1.8,the PLQY increases to 96%.The SiO2encapsulation significantly enhances environmental stability,with coated NCs retaining 43%of their initial photoluminescence(PL)intensity after immersion in water for 36 h,compared to only 5%for uncoated NCs.Furthermore,after ethanol treatment for 210 min,the coated NCs retain 39%of their initial PL intensity,while the uncoated counterparts retain merely7%.The enhanced stability and luminescence performance of CsPb_(0.7)Zn_(0.3)Br_(3)@SiO_(2)NCs make them highly promising for LED applications.White light-emitting diodes(WLEDs)fabricated using these NCs exhibit a color rendering index(CRI)of 78.2,a correlated color temperature(CCT)of 5470 K,and a luminous efficiency(LE)of 54.2 lm/W,demonstrating significant potential for next-generation display and lighting technologies.展开更多
Rare-earth ion-doped garnets with excellent luminescent properties show great potential for temperature sensing,displays,and nondestructive detection.However,their limited luminescent modes and low photoluminescence q...Rare-earth ion-doped garnets with excellent luminescent properties show great potential for temperature sensing,displays,and nondestructive detection.However,their limited luminescent modes and low photoluminescence quantum yields(PLQY)restrict further applications.In this study,we synthesized Al^(3+),Er^(3+)-co-doped Gd_(3)Ga_(5)O_(12) garnets with multimode luminescence via a high-temperature solid-state method.Notably,the preferential substitution of Al^(3+)ion at octahedral-coordinated GaI sites significantly enhanced the charge density and electron transition probability,achieving a PLQY enhancement of the downshifting luminescence from 35.1%to 68.5%.Al^(3+)ion also influences electron relaxation during up-conversion luminescence,resulting in a color shift from red to yellow to green.Additionally,Al^(3+)incorporation increased the photoelectric conversion efficiency of light-emitting diodes from 2.9%to 6.3%and improved temperature sensing sensitivity from 2.7%to 5.1%K⁻1.This work provides new insights into the photophysical mechanisms and underscores the key role of Al^(3+)ion in optimizing the optical properties of garnet-based materials.展开更多
基金Project supported by the Natural Science Fund of Elite Young Researchers of Shandong Province(2008BS04004)
文摘Transparent glass ceramics were prepared from the phosphosilicate system by melt-quenching devitrification（MQD） method, i.e., nanocrystals spontaneously form during cooling of the melts. Introduction of 2.5 wt.% Yb2O3 and 0.5 wt.% Er2O3 into the glass melt induced the change of type and concentration of crystals. The comparison of rheological and thermodynamic properties of both undoped and Yb^3＋/Er^3＋ doped melts showed that addition of Yb^3＋/Er^3＋ oxides caused increase of liquid fragility, and degree of medium-range order. In addition, the thermodynamic barriers for nucleation ΔG＊ as a function of reduced temperature T/Tm were calculated with an assumption of wetting angle θ=90o, Yb^3＋/Er^3＋ doped melt tended to firstly nucleate as compared to undoped melt at small undercooling.
文摘The Yb3^＋ -doped silicate, phosphate and borophosphate laser glasses were prepared by means of conventional melt quenching technology. The physical and spectral properties of the glasses were investigated. The results show that, due to the existence of OH^-, the fluorescence lifetime of phosphate glass is shorter than that of silicate glass, so silicate glass has better spectral properties than phosphate glass. Silicate glass has better mechanical and thermal properties than phosphate glass, but with the addition of B2O3, mechanical and thermal properties of phosphate glass are improved greatly without fluorescence quenching effect. This kind of borophosphate glass can be used in high average power solid state lasers.
基金Project supported by the National Natural Science Foundation of China （Grant No 60307004） and the Science and Technology Program of Guangzhou, Guangdong province, China （Grant No 2004Z2-D0131）.
文摘The Er^3＋/Yb^3＋ co-doped TeO2-Nb2O5-Li2O glass is prepared by conventional melting method, and its upconversion spectra are measured. The intense green upconversion luminescence upon excitation with a 976 nm laser diode is observed with the naked eyes. The dependence of luminescence intensity on the ratio of Yb^3＋/Er^3＋ is discussed in detail, and the relationship between the ratio of green luminescence intensity to red luminescence intensity and the ratio of Yb^3＋/Er^3＋ is also studied, The luminescence intensity increases with the ratio of Yb^3＋/Er^3＋ increasing. The ratio of Yb^3＋/Er^3＋ plays a more important role than the concentration of Er^3＋ in determining the upconversion luminescence intensity. The ratio of green luminescence intensity to red luminescence intensity reaches a maximum when ratio of Yb^3＋/Er^3＋ is 3. Thus the glass could be one of the potential candidates for LD pumping solid-state lasers.
基金the financial support from the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (NRF-2023R1A2C2007699 and 2022R1A6A1A0306303912)the Nano Material Technology Development Program through the NRF funded by the Ministry of Science and ICT (NRF-2015M3A7B6027970)the Technology Innovation Program by the Ministry of Trade, Industry & Energy (RS-202300236794)
文摘Regulating lithium(Li)plating/stripping behavior in three-dimensional(3D)conductive scaffolds is critical to stabilizing Li metal batteries(LMBs).Surface protrusions and roughness in these scaffolds can induce uneven distributions of the electric fields and ionic concentrations,forming“hot spots.”Hot spots may cause uncontrollable Li dendrites growth,presenting significant challenges to the cycle stability and safety of LMBs.To address these issues,we construct a Li ionic conductive-dielectric gradient bifunctional interlayer(ICDL)onto a 3D Li-injected graphene/carbon nanotube scaffold(LGCF)via in situ reaction of exfoliated hexagonal boron nitride(fhBN)and molten Li.Microscopic and spectroscopic analyses reveal that ICDL consists of fhBN-rich outer layer and inner layer enriched with Li_(3)N and Li-boron composites(Li-B).The outer layer utilizes dielectric properties to effectively homogenize the electric field,while the inner layer ensures high Li ion conductivity.Moreover,DFT calculations indicate that ICDL can effectively adsorb Li and decrease the Li diffusion barrier,promoting enhanced Li ion transport.The modulation of Li kinetics by ICDL increases the critical length of the Li nucleus,enabling suppression of Li dendrite growth.Attributing to these advantages,the ICDL-coated LGCF(ICDL@LGCF)demonstrates impressive long-term cycle performances in both symmetric cells and full cells.
文摘Oxy-fluoride glasses with composition of 25SiO2-65PbF2-9.4AlF3-0.1HoF3-0.5YbF3 were prepared. Their up-conversion fluorescence characteristics were investigated by 980 nm laser. Two emission peaks were observed at 540 and 650 nm. The up-conversion mechanism and processes were analyzed. The relationship between pumping power and relative intensity of emissions was discussed. From the dependence, it is known that the emissions centered at 540 and 650 nm are both attributed to two-photon process.
文摘The three host glasses doped with Yb 3+ were prepared by means of conventional melt quenching technology, and the influence on physical and spectral properties of phosphate glass due to addition of B2O3 was investigated and compared with silicate glass. The results show that due to the existence of OH- impurities which induce the non-radiative route, the fluorescence lifetime of phosphate glass is shorter, so silicate glass has better spectral properties than phosphate glass. Silicate glass has more excellent thermal-mechanical properties than phosphate glass, but with the addition of B2O3, thermal-mechanical properties of phosphate glass are improved greatly without fluorescence quenching effect, and this kind of borophosphate glass will be the candidate to be used in high average power solid state laser.
基金supported by the Programs of the Shanghai Pujiang Program(No.18PJ1401500)the National Natural Science Foundation of China(No.21801046,No.51721002,No.21574025 and No.21871057)the Ministry of Science and Technology(2016YFA0203302)。
文摘Polydiacetylene(PDA)is one kind of the conjugated polymer with layered structure,which can serve as a host to accommodate the vip components through intercalation.In these intercalated PDAs,some of them were reported to have a nearly perfect organized structure and perform completely reversible thermochromism.Till now,these reported intercalated PDAs were made by only introducing a single component for intercalation.Here,we chose 10,12-pentacosadiynoic acid(PCDA)as the monomer,of which the carboxyl-terminal groups can interact with either Tb^3+ ions or melamines(MAs).When the feeding molar ratio of PCDA,MA,and Tb^3+ ion was 3:267:1,only Tb^3+ ions were intercalated though excess MAs existed.Such Tb^3+- intercalated poly-PCDA exhibited completely reversible thermochromism,where almost all the carboxyl groups interacted with Tb^3+ ions to form the nearly perfect structure.When the feeding molar ratio of PCDA,MA,and Tb^3+ ion was 3:267:0.6,both Tb^3+ ions and MAs were intercalated.There existed some defects in the imperfect MA-intercalated domains and at the domain boundaries.The MA/Tb^3+- intercalated poly-PCDA exhibits partially reversible thermochromism,where the backbones near the defects are hard to return the initial conformation,while the rest,those at nearly perfect organized domains,are still able to restore the initial conformation.
基金Project supported by the National Natural Science Foundation of China(11204039,51202033)the Science Foundation of the Educational Department of Fujian Province of China(JA13084)the Natural Science Foundation of Fujian Province of China(2015J01243)
文摘A series of CaFCl：Tb3＋ and CaFCI：Tb3＋,A＋ （A=Li, Na and K） nanophosphors were synthesized by the one-step sol-gel method, which were reported for the first time. The sample consisted of monodisperse particles, the average size of which was 37 nm. The emissions of Tb3＋ ions and oxygen defects OF＇ were demonstrated in the CaFCl：Tb3＋ samples. The former was made up of several peaks at 488, 545, 587 and 623 nm, ascribed to 5D4→7FJ （j=6-3） transitions of Tb3＋ ions. The latter was shown as a broad band peaked at about 450 nm. Alkali metal ions A＋ （A=Li, Na and K） were introduced as the charge compensators to improve the luminescence of samples. The influence of charge compensators on the emissions of Tb3＋ ions and oxygen defects OF＇ was investigated by the measurement of fluorescence spectra and luminescence decay curves. The results indicated that all the charge compensators weakened the defects emission. Furthermore, Li＋ ion was the best charge compensator, because it not only reduced the defects emission but also increased the emission intensity of Tb3＋ significantly. Our results suggested that this nanophosphor sensitized by the charge compensator might broaden potential applications of rare-earth doped CaFCl.
基金supported by the National High Technology Research and Development Program of China(Grant No.2013AA032205)the Key Project of Beijing Scientific Committee,China(Grant No.D161100003416001)+1 种基金the Fundamental Research Funds for the Central Universities,China(Grant No.2016JBM066)the National Natural Science Foundation of China(Grant Nos.51272022 and 11474018)
文摘Different concentrations of Mg^（2＋） -doped hexagonal phase NaGdF_4：Yb^（3＋）, Er^（3＋）nanocrystals（NCs） were synthesized by a modified solvothermal method. Successful codoping of Mg^（2＋）ions in upconversion nanoparticles（UCNPs） was supported by XRD, SEM, EDS, and PL analyses. The effects of Mg^（2＋）doping on the morphology and the intensity of the upconversion（UC） emission were discussed in detail. It turned out that with the concentration of Mg^（2＋）increasing, the morphology of the nanoparticles turn to change gradually and the UC emission was increasing gradually as well. Notably the UC fluorescence intensities of Er^（3＋）were gradually improved owing to the codoped Mg^（2＋）and then achieved a maximum level as the concentration of Mg^（2＋）ions was 60 mol% from the amendment of the crystal structure of β-NaGdF_4：Yb^（3＋）,Er^（3＋）nanoparticles. Moreover, the UC luminescence properties of the rare-earth（Yb3＋, Er^（3＋）） ions codoped NaGdF_4 nanocrystals were investigated in detail under 980-nm excitation.
基金financial support from the National Natural Science Foundation of China(52272237,22279101 and 22172117)the Natural Science Foundation of Shaanxi(2020JC-41 and 2024JC-YBQN-0141)+2 种基金the Scientific Research Program Funded by the Education Department of Shaanxi Provincial Government(22JP056)the S&T Program of Energy Shaanxi Laboratory(ESLB202402)the Foshan Science and Technology Innovation Team Project(1920001004098)。
文摘In this work,for the first time,it is demonstrated that during the insertion/extraction of Na ions,the structural evolution at the Na_(4)site at a voltage range of 3-4 V is a key factor for the capacity decay of Na_(4)Fe_(3)(PO_(4))_(2)P_(2)O_(7)(NFPP).Herein,a strategy of introducing columnar potassium ions at the Na_(4)site is proposed to address the aforementioned challenge.As a cathode material for sodium-ion batteries,the K_(0.12)Na_(3.88)Fe_(3)(PO_(4))_(2)P_(2)O_(7)/C(K-NFPP)composite enhances the reversibility of Na_(4)extraction.Specifically,the K-NFPP exhibits an initial discharge capacity of 107.8 mAh g^(-1)at a high current density of 5 C,with a capacity retention of 91.4% after 2000 cycles,outperforming the pristine NFPP material(81.1 m Ah g^(-1)and 67.1%).At 5 C,the K-NFPP also retains 81.5% of the reversible capacity at 0.1 C,whereas the NFPP only retains 68.3%.Moreover,the K-NFPP-based full-cell delivers an initial capacity of 110.1 m Ah g^(-1)at 1 C,with a capacity retention of 90% after 100 cycles.It is found that in comparison to K-doping of the Na1,Na2,and Na3 sites,K-doping at the Na4 site effectively optimizes the band gap and stabilizes the crystal structure,thereby reducing lattice changes of FeO_(6)evolution during Na^(+)insertion/extraction.As a result,the introduction of columnar potassium ions significantly enhances the capacity contribution of the Na_(4)site,optimizes reaction kinetics,and effectively mitigates the capacity decay of NFPP cathodes.It is believed that this study offers a new entry point for the application of NFPP in high-voltage sodium storage.
基金financial support from the Hong Kong Polytechnic University(1-YWC6)the Scientific Research Project of Hubei University of Science and Technology,China(BK202018)。
文摘The sodium-ion battery(SIB)cathode material,Na_(4)Fe_(3)(PO_(4))_(2)(P_(2)O_(7))(NFPP),has become a focal material in both academia and industry due to its low cost,long lifespan,and high safety.In the recent three years,substantial efforts have been devoted to promoting the practical applications of NFPP by optimizing its electrochemical performance and disclosing the reaction mechanisms.Various modification strategies and their effect mechanisms have been explored,and the performance evaluation of NFPP has progressively advanced from laboratory-scale coin cells to practical pouch cell configurations.Nevertheless,there remains a lack of systematic reviews comprehensively assessing the developmental status and application readiness of NFPP.This review critically examines NFPP's fundamental structural characteristics and proposes four key development issues.Then,the latest research advances are introduced with explicit differentiation of design strategies and their mechanistic impacts.Notably,we provide a dedicated discussion on NFPP's current pouch cell performance metrics,while highlighting two critical yet underexplored research directions(enhancing air stability and improving tap density)for commercial viability.
基金financially supported by the National Natural Science Foundation of China(Nos.52001059,52072119)Hunan Provincial Natural Science Foundation(No.2023JJ50015)the 111 Project(No.D20015)。
文摘A pseudocapacitance dominated anode material assembled from Li_(3)VO_(4)nanocrystals encapsulated in the interlayers of N-doped graphene has been developed via a facile 2D nanospace confined strategy for lithium ion capacitors(LICs).In this contribution,the N-doped graphene synthesized by a faicle solid state reaction using C_(3)N_(4)nanosheets as template and glucose as carbon source provides sufficient 2D nanospace for the confined and homogeneous growth of Li_(3)VO_(4)at the nanoscale,and simultaneously efficiently anchors each nanobuilding block inside the interlayers,thus realizing the utilizaiton of full potential of active components.The so-formed 3D hybrids not only ensure intimate electronic coupling between active materials and N-doped graphene,but also realize robust structure integrity.Owing to these unique advantages,the resulting hybrids show pseudocapacitance dominated lithium storage behaviors with capacitive contributions of over 90%at both low and high current rates.The LVO@C@NG delivers reversible capacities of 206 mAh/g at 10 A/g,capacity retention of 92.7%after 1000 cycles at 2 A/g,and a high energy density of 113.6 Wh/kg at 231.8 W/kg for LICs.
基金supported by the National Natural Science Foundation of China(No.52062019)the Natural Science Research Project of Higher Education Institutions in Jiangsu Province,China(No.24KJA430013)the Natural Science Foundation of Jiangsu Province for Youths,China(No.BK20230662)。
文摘All-inorganic perovskite CsPbX_(3)(X=Cl,Br,I)nanocrystals(NCs)have emerged as promising candidates for light-emitting diode(LED)displays due to their outstanding photophysical properties.However,their practical application remains hindered by poor stability and the inherent toxicity of Pb2+.In this study,we present a two-step heating method to synthesize CsPb_(1-x)Zn_(x)Br_(3)NCs with enhanced optoelectronic performance and uniform dispersion.The optimized Zn^(2+)-doped NCs achieve a photoluminescence quantum yield(PLQY)of 86%,with a reduction in lattice spacing from 0.384 to 0.365 nm,attributed to increased perovskite lattice formation energy and effective surface passivation.To further improve stability,a silica(SiO_(2))shell is introduced via surface modification with(3-aminopropyl)triethoxysilane(APTES),forming CsPb_(0.7)Zn_(0.3)Br_(3)@SiO_(2)core–shell NCs.At an optimal APTES/B-site metal ion molar ratio of 1.8,the PLQY increases to 96%.The SiO2encapsulation significantly enhances environmental stability,with coated NCs retaining 43%of their initial photoluminescence(PL)intensity after immersion in water for 36 h,compared to only 5%for uncoated NCs.Furthermore,after ethanol treatment for 210 min,the coated NCs retain 39%of their initial PL intensity,while the uncoated counterparts retain merely7%.The enhanced stability and luminescence performance of CsPb_(0.7)Zn_(0.3)Br_(3)@SiO_(2)NCs make them highly promising for LED applications.White light-emitting diodes(WLEDs)fabricated using these NCs exhibit a color rendering index(CRI)of 78.2,a correlated color temperature(CCT)of 5470 K,and a luminous efficiency(LE)of 54.2 lm/W,demonstrating significant potential for next-generation display and lighting technologies.
基金supported by the Guangxi Natural Science Foundation(Grant No.2025GXNSFDA069038)The Guangxi Science and Technology Plan Project(Grant No.AA23073018)+1 种基金the National Natural Science Foundation of China(Grant Nos.22175043 and 52162021)the Open Foundation of State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures(Grant No.MMCS2023OF05).
文摘Rare-earth ion-doped garnets with excellent luminescent properties show great potential for temperature sensing,displays,and nondestructive detection.However,their limited luminescent modes and low photoluminescence quantum yields(PLQY)restrict further applications.In this study,we synthesized Al^(3+),Er^(3+)-co-doped Gd_(3)Ga_(5)O_(12) garnets with multimode luminescence via a high-temperature solid-state method.Notably,the preferential substitution of Al^(3+)ion at octahedral-coordinated GaI sites significantly enhanced the charge density and electron transition probability,achieving a PLQY enhancement of the downshifting luminescence from 35.1%to 68.5%.Al^(3+)ion also influences electron relaxation during up-conversion luminescence,resulting in a color shift from red to yellow to green.Additionally,Al^(3+)incorporation increased the photoelectric conversion efficiency of light-emitting diodes from 2.9%to 6.3%and improved temperature sensing sensitivity from 2.7%to 5.1%K⁻1.This work provides new insights into the photophysical mechanisms and underscores the key role of Al^(3+)ion in optimizing the optical properties of garnet-based materials.
