This study presents a facile and rapid method for synthesizing novel Layered Double Hydroxide(LDH)nanoflakes,exploring their application as a photocatalyst,and investigating the influence of condensed phosphates'g...This study presents a facile and rapid method for synthesizing novel Layered Double Hydroxide(LDH)nanoflakes,exploring their application as a photocatalyst,and investigating the influence of condensed phosphates'geometric linearity on their photocatalytic properties.Herein,the Mg O film,obtained by plasma electrolysis of AZ31 Mg alloys,was modified by growing an LDH film,which was further functionalized using cyclic sodium hexametaphosphate(CP)and linear sodium tripolyphosphate(LP).CP acted as an enhancer for flake spacing within the LDH structure,while LP changed flake dispersion and orientation.Consequently,CP@LDH demonstrated exceptional efficiency in heterogeneous photocatalysis,effectively degrading organic dyes like Methylene blue(MB),Congo red(CR),and Methyl orange(MO).The unique cyclic structure of CP likely enhances surface reactions and improves the catalyst's interaction with dye molecules.Furthermore,the condensed phosphate structure contributes to a higher surface area and reactivity in CP@LDH,leading to its superior photocatalytic performance compared to LP@LDH.Specifically,LP@LDH demonstrated notable degradation efficiencies of 93.02%,92.89%,and 88.81%for MB,MO,and CR respectively,over a 40 min duration.The highest degradation efficiencies were observed in the case of the CP@LDH sample,reporting 99.99%for MB,98.88%for CR,and 99.70%for MO.This underscores the potential of CP@LDH as a highly effective photocatalyst for organic dye degradation,offering promising prospects for environmental remediation and water detoxification applications.展开更多
The hybridization of metal-organic framework(MOF)with inorganic layers would lead to the discovery of novel hybrid materials that can provide a compelling strategy for enhancing its photocatalytic and electrochemical ...The hybridization of metal-organic framework(MOF)with inorganic layers would lead to the discovery of novel hybrid materials that can provide a compelling strategy for enhancing its photocatalytic and electrochemical response.In the present study,a highly efficient multifunctional hybrid material was developed by exploiting the defective layer formed on AZ31 Mg alloy through plasma electrolytic oxidation(PEO)as a nucleation and growth site for Co-MOF.The concentrations of the organic linker 2-Methylimidazole(2,MIm)and cobalt nitrate as a source of Co^(2+) ions were varied to control the growth of the obtained Co-MOF.Lower concentrations of the 2,MIm ligand favored the formation of leaf-like MOF structures through an anisotropic,two-dimensional growth,while higher concentrations led to rapid,isotropic nucleation and the creation of polyhedral Co-MOF structures.The sample characterized by polyhedral Co-MOF structures exhibited superior electrochemical stability,with the lowest corrosion current density(3.11×10^(-9) A/cm^(2))and the highest top layer resistance(2.34×10^(6)Ωcm^(2)),and demonstrated outstanding photocatalytic efficiency,achieving a remarkable 99.98%degradation of methylene blue,an organic pollutant,in model wastewater.To assess the active adsorption sites of the Co-MOF,density functional theory(DFT)was utilized.This study explores the changes in morphologies of the coatings of Co-MOF with the change of solution concentration to form coatings with enhanced properties on the metallic substrate,which could establish the groundwork for the development of next-generation multifunctional frameworks with diverse applications.展开更多
Herein,cure characteristics,morphology,and mechanical properties of natural rubber filled with activated carbon-based materials were investigated.Carbon-based materials were prepared from bagasse,coffee grounds and pi...Herein,cure characteristics,morphology,and mechanical properties of natural rubber filled with activated carbon-based materials were investigated.Carbon-based materials were prepared from bagasse,coffee grounds and pineapple crowns by the pyrolysis method at temperatures in the range of 300℃.As-synthesized carbon materials were characterized by optical microscopy(OM),scanning electron microscopy(SEM),and Fourier-transform infrared spectroscopy(FTIR)to analyze size distribution,morphology,and functional groups,respectively.OM and SEM analysis revealed that particles,flakes,and a small quantity of fiber-like carbon were obtained using bagasse and pineapple crown as raw materials,while honeycomb-like carbon materials can be derived from coffee grounds.To investigate the mechanical properties,natural rubber was filled with carbon black and as-synthesized carbon materials by the internal mixing and compression molding process.Transmission electron microscopy(TEM)was utilized to characterize the dispersion of carbon materials in the rubber matrix.The results of tensile testing showed that the natural rubber mixed with as-synthesized carbon materials from pineapple crowns exhibited 54%and 74%improvement in the ultimate tensile strength and Young’s modulus,respectively,compared with natural rubber without filled carbon materials.The enhancement in mechanical properties by activated carbon materials derived from pineapple crowns can be attributed to the flake-and fiber-like structures and good dispersion of carbon materials in the rubber matrix.In addition,it is higher than that of rubber mixed with carbon black.The results demonstrated that as-synthesized carbon materials from pineapple crowns have the potential materials to substitute carbon black in the rubber compound industry.展开更多
MXenes,the most recent addition to the 2D material family,have attracted significant attention owing to their distinctive characteristics,including high surface area,conductivity,surface characteristics,mechanical str...MXenes,the most recent addition to the 2D material family,have attracted significant attention owing to their distinctive characteristics,including high surface area,conductivity,surface characteristics,mechanical strength,etc.This review begins by presenting MXenes,providing insights into their structural characteristics,synthesis methods,and surface functional groups.The review covers a thorough analysis of MXene surface properties,including surface chemistry and termination group impacts.The properties of MXenes are influenced by their synthesis,which can be fluorine-based or fluorinedependent.Fluorine-based synthesis techniques involve etching with fluorine-based reagents,mainly including HF or LiF/HCl,while fluorine-free methods include electrochemical etching,chemical vapor deposition(CVD),alkaline etching,Lewis acid-based etching,etc.These techniques result in the emergence of functional groups such as-F,-O,-OH,-Cl,etc.on the MXenes surface,depending on the synthesis method used.Properties of MXenes,such as electrical conductivity,electronic properties,catalytic activity,magnetic properties,mechanical strength,and chemical and thermal stability,are examined,and the role of functional groups in determining these properties is explored.The review delves into the diverse applications of MXenes,encompassing supercapacitors,battery materials,hydrogen storage,fuel cells,electromagnetic interference(EMI) shielding,pollutant removal,water purification,flexible electronics,sensors,additive manufacturing,catalysis,biomedical and healthcare fields,etc.Finally,this article outlines the challenges and opportunities in the current and future development of MXenes research,addressing various aspects such as synthesis scalability,etching challenges,and multifunctionality,and exploring novel applications.The review concludes with future prospects and conclusions envisioning the impact of MXenes on future technologies and innovation.展开更多
Heteroatom-doped transition metal oxides have attracted great attention as advanced anode materials for lithium-ion batteries due to their high theoretical capacity and superior properties.However,the limited resource...Heteroatom-doped transition metal oxides have attracted great attention as advanced anode materials for lithium-ion batteries due to their high theoretical capacity and superior properties.However,the limited resource availability has led to a substantial rise in prices for valuable metals such as Ni and Co,posing a significant challenge for their application.To address this issue,recycling of these metals from waste materials have gained prominence,and particularly the recovery of Co has been mostly focused on its economic benefits.Herein,we introduced a novel recycling strategy for fabrication of heteroatomdoped CoO_(x)(comprising mainly Co_(3)O_(4)with a minor CoO phase)anode with a yolk–shell structure for lithium-ion batteries,by separating Co from cemented tungsten carbide waste.By employing a simple leaching process and subsequent spray pyrolysis,the yolk–shell structured microsphere comprising CoO_(x)was successfully synthesized.Moreover,the presence of other waste metals in the leachate facilitated multi-heteroatom doping during synthesis.Interestingly,the introduction of various dopants into CoO_(x)induced oxygen vacancy formation,thereby enhancing the electrochemical properties of the CoO_(x)anode.As a result,compared with the phase-pure(undoped)CoO_(x)yolk–shell,the heteroatom-doped CoO_(x)yolk–shell exhibited robust cycling stability(602 mAh·g^(-1)for 200 cycles at 1 A·g^(-1))and excellent rate capability(210 mAh·g^(-1)at 10 A·g^(-1)).展开更多
Advanced hybrid materials with unique properties are essential for addressing the demands of increasingly complex applications.Despite their importance,the self-assembly of layered double hydroxides(LDH)with metallic ...Advanced hybrid materials with unique properties are essential for addressing the demands of increasingly complex applications.Despite their importance,the self-assembly of layered double hydroxides(LDH)with metallic oxide nanoparticles and dicarboxylic acids is constrained by a limited understanding of the formation mechanisms and difficulties in evaluating their anticorrosive performance.In this study,we developed a novel anticorrosive system by intercalating CeNiLDH with a complex of vanadium pentoxide(V2O5)nanoparticles and(2E)-but-2-enedioic acid((2E)-BDA)on a MgO layer created through plasma-electrolysis of AZ31 Mg alloy.This system was compared with LDH films intercalated with either V2O5 or(2E)-BDA alone.The intercalation of LDH with V_(2)O_(5)and(2E)-BDA resulted in a flower-like structure,while modification with their complex led to a more compact,cloud-like formation.These cloud-like structures,driven by enhanced absorption and robust hydrogen bonding throughout the hierarchical network,effectively suppress corrosion by delaying the movement of corrosive anions.This was reflected in a polarization resistance of 1.51×10^(10)Ω·cm^(2),which is approximately two orders of magnitude times higher than the resistance of the unmodified LDH film(3.41×10^(8)Ω·cm^(2)).Additionally,the corrosion current density(icorr)of the VOBDA sample showed a decrease by four orders of magnitude compared to the unmodified LDH sample,emphasizing the superior anticorrosive performance of this hybrid coating.Density functional theory(DFT)was used to elucidate the bonding and formation mechanisms between LDH and the inorganic-organic complex.展开更多
The high compacted density LiNi<sub>0.5-x</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub>Mg<sub>x</sub>O<sub>2</sub> cathode material for lithium-ion batteries was syn...The high compacted density LiNi<sub>0.5-x</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub>Mg<sub>x</sub>O<sub>2</sub> cathode material for lithium-ion batteries was synthesized by high temperature solid-state method, taking the Mg element as a doping element and the spherical Ni<sub>0.5</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub> (OH)<sub>2</sub>, Li<sub>2</sub>CO<sub>3</sub> as raw materials. The effects of calcination temperature on the structure and properties of the products were investigated. The structure and morphology of cathode materials powder were analyzed by X-ray diffraction spectroscopy (XRD) and scanning electronmicroscopy (SEM). The electrochemical properties of the cathode materials were studied by charge-discharge test and cyclic properties test. The results show that LiNi<sub>0.4985</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub> Mg<sub>0.0015</sub>O<sub>2</sub> cathode material prepared at calcination temperature 930°C has a good layered structure, and the compacted density of the electrode sheet is above 3.68 g/cm<sup>3</sup>. The discharge capacity retention rate is more than 97.5% after 100 cycles at a charge-discharge rate of 1C, displaying a good cyclic performance.展开更多
(2E,6E)-4-methyl-2,6-bis(pyridin-3-ylmethylene)cyclohexan-1-one(L_(1))and 4-methyl-2,6-bis[(E)-4-(pyridin-4-yl)benzylidene]cyclohexan-1-one(L_(2))were synthesized and combined with isophthalic acid(H_(2)IP),then under...(2E,6E)-4-methyl-2,6-bis(pyridin-3-ylmethylene)cyclohexan-1-one(L_(1))and 4-methyl-2,6-bis[(E)-4-(pyridin-4-yl)benzylidene]cyclohexan-1-one(L_(2))were synthesized and combined with isophthalic acid(H_(2)IP),then under solvothermal conditions,to react with transition metals achieving four novel metal-organic frameworks(MOFs):[Zn(IP)(L_(1))]_(n)(1),{[Cd(IP)(L_(1))]·H_(2)O}_(n)(2),{[Co(IP)(L_(1))]·H_(2)O}_(n)(3),and[Zn(IP)(L_(2))(H_(2)O)]_(n)(4).MOFs 1-4 have been characterized by single-crystal X-ray diffraction,powder X-ray diffraction,thermogravimetry,and elemental analysis.Single-crystal X-ray diffraction shows that MOF 1 crystallizes in the monoclinic crystal system with space group P2_(1)/n,and MOFs 2-4 belong to the triclinic system with the P1 space group.1-3 are 2D sheet structures,2 and 3 have similar structural characters,whereas 4 is a 1D chain structure.Furthermore,1-3 exhibited certain photocatalytic capability in the degradation of rhodamine B(Rh B)and pararosaniline hydrochloride(PH).4could be used as a heterogeneous catalyst for the Knoevenagel reaction starting with benzaldehyde derivative and malononitrile.4 could promote the reaction to achieve corresponding products in moderate yields within 3 h.Moreover,the catalyst exhibited recyclability for up to three cycles without significantly dropping its activity.A mechanism for MOF 4 catalyzed Knoevenagel condensation reaction of aromatic aldehyde and malononitrile has been initially proposed.CCDC:2356488,1;2356497,2;2356499,3;2356498,4.展开更多
K–Se batteries have been identified as promising energy storage systems owing to their high energy density and cost-effectiveness.However,challenges such as substantial volume changes and low Se utilization require f...K–Se batteries have been identified as promising energy storage systems owing to their high energy density and cost-effectiveness.However,challenges such as substantial volume changes and low Se utilization require further investigation.In this study,novel N-doped multichannel carbon nanofibers(h-NMCNFs)with hierarchical porous structures were successfully synthesized as efficient cathode hosts for K–Se batteries through the carbonization of two electrospun immiscible polymer nanofibers and subsequent chemical activation.Mesopores originated from the decomposition of the polymer embedded in the carbon nanofibers,and micropores were introduced via KOH activation.During the activation step,hierarchical porous carbon nanofibers with enhanced pore volumes were formed because of the micropores in the carbon nanofibers.Owing to the mesopores that enabled easy access to the electrolyte and the high utilization of chain-like Se within the micropores,the Se-loaded hierarchical porous carbon nanofibers(60 wt%Se)exhibited a high discharge capacity and excellent rate performance.The discharge capacity of the nanofibers at the 1,000th cycle was 210.8 mA.h.g^(-1)at a current density of 0.5C.The capacity retention after the initial activation was 64%.In addition,a discharge capacity of 165 mA.h.g^(-1)was obtained at an extremely high current density of 3.0C.展开更多
This study presents a novel approach to improving the anticorrosive performance of AZ31 Mg alloy by exploiting the role of the hydration reaction to induce interactions between Quinolin-8-ol(8HQ)molecules and the poro...This study presents a novel approach to improving the anticorrosive performance of AZ31 Mg alloy by exploiting the role of the hydration reaction to induce interactions between Quinolin-8-ol(8HQ)molecules and the porous MgO layer formed via plasma electrolytic oxidation(PEO).The AZ31 Mg alloy,initially coated with a PEO layer,underwent a dipping treatment in an ethanolic solution of 0.05 M 8HQ at 50℃ for 3 h.The results were compared with those from a different procedure where the PEO layer was subjected to a hydration reaction for 2 h at 90℃ before immersion in the 8HQ solution under the same conditions.The hydration treatment played a crucial role by converting MgO to Mg(OH)_(2),significantly enhancing the surface reactivity.This transformation introduced hydroxyl groups(−OH)on the surface,which facilitated donor-acceptor interactions with the electron-accepting sites on 8HQ molecules.The calculated binding energy(Ebinding)from DFT indicated that the interaction energy of 8HQ with Mg(OH)_(2) was lower compared to 8HQ with MgO,suggesting easier adsorption of 8HQ molecules on the hydrated surface.This,combined with the increased number of active sites and enhanced surface area,allowed for extensive surface coverage by 8HQ,leading to the formation of a stable,flake-like protective layer that sealed the majority of pores on the PEO layer.DFT calculations further suggested that the hydration treatment provided multiple active sites,enabling effective contact with 8HQ and rapid electron transfer,creating ideal conditions for charge-transfer-induced physical and chemical bonding.This study shows that hydration and 8HQ treatments significantly enhance the corrosion resistance of Mg alloys,highlighting their potential for advanced anticorrosive coatings.展开更多
Recently,hollow carbon nanospheres(HCSs)have garnered significant attention as potential Li metal hosts owing to their unique large voids and ease of fabrication.However,similar to other nanoscale hosts,their practica...Recently,hollow carbon nanospheres(HCSs)have garnered significant attention as potential Li metal hosts owing to their unique large voids and ease of fabrication.However,similar to other nanoscale hosts,their practical performance is limited by inhomogeneous agglomeration,increased binder requirements,and high tortuosity within the electrode.To overcome these problems and high tortuosity within the electrode,this study introduces a pomegranate-like carbon microcluster composed of primary HCSs(P-CMs)as a novel Li metal host.This unique nanostructure can be easily prepared using the spray-drying technique,enabling its mass production.Comprehensive analyses with various tools demonstrate that compared with HCS hosts,the P-CM host requires a smaller amount of binder to fabricate a sufficiently robust and even surface electrode.Furthermore,owing to reduced tortuosity,the well-designed P-CM electrode can provide continuous and shortened pathways for electron/ion transport,accelerating the Li-ion transfer kinetics and prohibiting preferential Li plating at the upper region of the electrode.Due to these characteristics,Li metal can be effectively encapsulated in the large inner voids of the primary HCSs constituting the P-CM,thereby enhancing the electrochemical performance of P-CM hosts in Li metal batteries.Specifically,the Coulombic efficiency of the P-CM host can be maintained at 97%over 100 cycles,with a high Li deposition areal capacity of 3 mAh·cm^(-2)and long cycle life(1000 h,1 mA·cm^(-2),and 1.0 mAh·cm^(-2)).Furthermore,a full cell incorporating a LiFePO4 cathode exhibits excellent cycle life.展开更多
Microalloying addition plays a significant role in controlling the characteristics of precipitates in Al alloys.This study investigates the effects of Ag and Sc microalloying addition on the thermal stability of Al–Z...Microalloying addition plays a significant role in controlling the characteristics of precipitates in Al alloys.This study investigates the effects of Ag and Sc microalloying addition on the thermal stability of Al–Zn–Mg–Cu alloys,via differential scanning calorimetry,transmission electron microscopy,and atom-probe tomography.The results demonstrate that Ag and Sc additions increase the number density ofη-MgZn_(2) type nano-precipitates(formed during heat treatment)by forming direct(Mg–Ag phase,prototype of precipitate)or indirect precursors(Al_(2) Sc phase,constituent of precipitate)for the precipitate.In addition,the Ag and Sc elements can effectively prevent the coarsening ofηprecipitates and facilitate the high-density distribution of fineηprecipitates,during the over-aging period,improving the thermal stability of the Al–Zn–Mg–Cu alloys.The thermal stability is particularly improved by Ag addition because Ag atoms directly prevent the coarsening ofηprecipitates by hindering Zn diffusion into the precipitate.On the contrary,Sc addition indirectly prevents the coarsening ofηprecipitates by depleting the solute species from the Al matrix,enabling abundant precipitates limited growth.Thus Ag addition improves precipitation strengthening by preventing the coarsening of precipitates during over-aging.展开更多
This study presents a novel photocatalytic system exploiting the unique properties of ZrO_(2) and its integration with layered double hydroxide(LDH)films on porous coatings produced via plasma electrolytic oxidation(PE...This study presents a novel photocatalytic system exploiting the unique properties of ZrO_(2) and its integration with layered double hydroxide(LDH)films on porous coatings produced via plasma electrolytic oxidation(PEO).Herein,CoFe-LDHfilms were created on the porous surface of PEO-coated AZ31 Mg alloy using a hydrothermal treatment in cobalt and iron nitrate solutions,followed by a secondary hydrothermal process in a ZrO_(2) solution for 10 h at 70℃.The impact of ZrO_(2) on the morphological,compositional,and photocatalytic performance was then compared to the case where ZrO_(2) nanoparticles were electrophoretically incorporated into the porous PEO coating.Characterization results revealed that the ZrO_(2)-modified LDH coatings exhibited a dispersedflake-like structure with an increased surface area,a reduced band gap energy of 3.14 eV,and enhanced electron-hole separation.Experimental results demonstrated an outstanding 99.8%degradation of indigo carmine within 15 mins,with remarkable multi-cycle stability overfive consecutive cycles without significant performance decline.This system demonstrates faster degradation rates and greater durability compared to previously reported catalysts,underscoring its potential for effective and sustainable environmental remediation.The synergistic integration of ZrO_(2),LDH,and PEO highlights a promising strategy for wastewater treatment,particularly for the removal of persistent organic dyes like indigo carmine.展开更多
Seawater is the most abundant source of molecular hydrogen.Utilizing the hydrogen reserves present in the seawater may inaugurate innovative strategies aimed at advancing sustainable energy and environmental preservat...Seawater is the most abundant source of molecular hydrogen.Utilizing the hydrogen reserves present in the seawater may inaugurate innovative strategies aimed at advancing sustainable energy and environmental preservation endeavors in the future.Recently,there has been a surge in study in the field addressing the production of hydrogen through the electrochemical seawater splitting.However,the performance and durability of the electrode have limitations due to the fact that there are a few challenges that need to be addressed in order to make the technology suitable for the industrial purpose.The active site blockage caused by chloride ions that are prevalent in seawater and chloride corrosion is the most significant issue;it has a negative impact on both the activity and the durability of the anode component.Addressing this particular issue is of upmost importance in the seawater splitting area.This review concentrates on the newly developed materials and techniques for inhibiting chloride ions by blocking the active sites,simultaneously preventing the chloride corrosion.It is anticipated that the concept will be advantageous for a large audience and will inspire researchers to study on this particular area of concern.展开更多
This study explores the development of an organic-inorganic hybrid coating to enhance the corrosion resistance and photocatalytic properties of AZ31 Mg alloy modified by plasma electrolytic oxidation(PEO).The PEO proc...This study explores the development of an organic-inorganic hybrid coating to enhance the corrosion resistance and photocatalytic properties of AZ31 Mg alloy modified by plasma electrolytic oxidation(PEO).The PEO process typically generates a porous oxide layer,which can reduce corrosion protection by allowing corrosive agents to penetrate the substrate.To address this limitation,phenopyridine(PHEN)and 2-methylimidazole(2-IMD)were incorporated into the PEO surface to form a robust organic layer on the Mg alloy.Potassium hydroxide(KOH)was used to adjust the pH,improving the interaction and solubility between the organic molecules and the PEO coating.The hybrid coating exhibited unique twig-like surface structures that contributed to forming a multifunctional coating with high corrosion resistance and superior photocatalytic activity.The PEO-PHEN-2IMD sample on the Mg alloy demonstrated exceptional corrosion resistance,with the lowest corrosion current density(I_(corr))of 1.92×10^(-10) A/cm^(2),a high corrosion potential(E_(corr)),and the highest top layer resistance(R_(top))of 2.57×10^(6)Ω·cm^(2),indicating excellent barrier properties.Additionally,the coating achieved complete(100%)degradation of methylene blue(MB)within 30 min under visible light.Density Functional Theory(DFT)calculations provide deeper insights into the bonding mechanisms and interaction stability between PHEN,2-IMD,and the PEO layer on the Mg alloy and MB dye.These findings confirmed the enhanced performance of the hybrid coating in both corrosion resistance and photocatalytic applications.展开更多
Reducing the Ir loading while preserving catalytic performance and mechanical robustness in anodic catalyst layers remains a critical challenge for the large-scale implementation of proton exchange membrane water elec...Reducing the Ir loading while preserving catalytic performance and mechanical robustness in anodic catalyst layers remains a critical challenge for the large-scale implementation of proton exchange membrane water electrolysis(PEMWE).Herein,we present a structural engineering strategy involving neodymium-doped Ir/IrO_(2)(Nd-Ir/IrO_(2))hollow nanospheres with precisely adjustable shell thickness and cavity dimensions.The optimized catalyst demonstrates excellent oxygen evolution reaction(OER)performance in acidic media,achieving a remarkably low overpotential of 259 mV at a benchmark current density of 10 mA cm^(-2) while exhibiting substantially enhanced durability compared to commercial IrO_(2) and Ir/IrO_(2) counterparts.Notably,the Nd-Ir/IrO_(2) catalyst delivers a mass activity of 541.6 A gIr^(-1) at 1.50 V vs RHE,representing a 74.5-fold enhancement over conventional IrO_(2).Through comprehensive electrochemical analysis and advanced characterization techniques reveal that,the hierarchical hollow architecture simultaneously addresses multiple critical requirements:(i)abundant exposed active sites enabled by an enhanced electrochemical surface area,(ii)optimized mass transport pathways through engineered porosity,and(iii)preserved structural integrity via a continuous conductive framework,collectively enabling significant Ir loading reduction without compromising catalytic layer performance.Fundamental mechanistic investigations further disclose that Nd doping induces critical interfacial Nd-O-Ir configurations that stabilize lattice oxygen,together with intensified electron effect among mixed valent Ir that inhibits the overoxidation of Ir active sites during the OER process,synergistically ensuring enhanced catalytic durability.Our work establishes a dual-modulation paradigm integrating nanoscale architectural engineering with atomic-level heteroatom doping,providing a viable pathway toward high-performance PEMWE systems with drastically reduced noble metal requirements.展开更多
Pyrochlore oxide(Y_(2)Ru_(2)O_(7))has been identified as a promising catalyst for the oxygen evolution reaction(OER)in advanced green energy strategies.However,its electrochemical inertness necessitates the exploratio...Pyrochlore oxide(Y_(2)Ru_(2)O_(7))has been identified as a promising catalyst for the oxygen evolution reaction(OER)in advanced green energy strategies.However,its electrochemical inertness necessitates the exploration of an effective strategy to facilitate electronic modulation.This study proposes a surface modification approach involving the integration of defective NiFe(D-NiFe)nanoparticles onto a Y_(2)Ru_(2)O_(7)(YRO)support(YRO@D-NiFeP/Ru)using a Prussian blue analog(PBA).Numerous cyanide(CN)vacancies are generated through the oxidation treatment of the NiFe PBA grown on the YRO support,yielding a defective PBA precursor(YRO@D-PBA).Subsequent annealing facilitates the transformation to the D-NiFe nanoparticles on the YRO support(YRO@D-NiFeP/Ru),which augments the exposure of Ni3+active sites beneficial for the OER.Moreover,the reduction of Ru cations from YRO results in the exsolution of Ru nanoparticles,which promotes synergistic charge transfer from the nanoparticles to the interior of Y_(2)Ru_(2)O_(7).Consequently,YRO@D-NiFeP/Ru exhibits a remarkable voltage of 1.49 V at 10 mA·cm^(−2) and the lowest Tafel slope of 42.4 mV·dec^(−1).In addition,a Zn–air battery constructed with YRO@D-NiFeP/Ru exhibits an outstanding power density of 136.2 mW·cm^(−2) and high charge–discharge stability,confirming the applicability of YRO@D-NiFeP/Ru in metal-air batteries.展开更多
Aqueous zinc-ion batteries(AZIBs)have emerged as promising,practical energy storage devices based on their non-toxic nature,environmental friendliness,and high energy density.However,excellent rate characteristics and...Aqueous zinc-ion batteries(AZIBs)have emerged as promising,practical energy storage devices based on their non-toxic nature,environmental friendliness,and high energy density.However,excellent rate characteristics and stable long-term cycling performance are essential.These essential aspects create a need for superior cathode materials,which represents a substantial challenge.In this study,we used MXenes as a framework for NH_(4)V_(4)O_(10)(NVO)construction and developed electrodes that combined the high capacity of NVO with the excellent conductivity of MXene/carbon nanofibers(MCNFs).We explored the electrochemical characteristics of electrodes with varying NVO contents.Considering the distinctive layered structure of NVO,the outstanding conductivity of MCNFs,and the strong synergies between the two components.NVO-MCNFs exhibited better charge transfer compared with earlier materials,as well as more ion storage sites,excellent conductivity,and short ion diffusion pathways.A composite electrode with optimized NVO content exhibited an excellent specific capacitance of 360.6mAh g^(-1) at 0.5 A g^(-1) and an outstanding rate performance.In particular,even at a high current density of 10 A g^(-1),the 32NVO-MCNF exhibited impressive cycling stability:88.6%over 2500 cycles.The mechanism involved was discovered via comprehensive characterization.We expect that the fabricated nanofibers will be useful in energy storage and conversion systems.展开更多
This study investigates zinc’s(Zn)key role in enhancing the precipitation kinetics and refinement of Mg_(17)Al_(12)and Mg_(2)Sn phases in magnesium alloys through trace sodium(Na)additions.Magnesium alloys with varyi...This study investigates zinc’s(Zn)key role in enhancing the precipitation kinetics and refinement of Mg_(17)Al_(12)and Mg_(2)Sn phases in magnesium alloys through trace sodium(Na)additions.Magnesium alloys with varying compositions of aluminum(Al),tin(Sn),Zn,and Na were prepared and aged at 453 K.Microstructural analyses were conducted using transmission electron microscopy(TEM),scanning transmission electron microscopy(STEM),and atom probe tomography(APT).Trace additions of Na significantly enhanced the precipitation responses of both Mg_(17)Al_(12)and Mg_(2)Sn phases.When Zn was co-added with Na,as in the ATZ641N3 alloy(Mg–6Al–4Sn–1Zn–0.3Na),there was a pronounced refinement in precipitate morphology and acceleration of precipitation kinetics.The ATZ641N3 alloy achieved a peak hardness of 103 Hv at 36 hours,compared to 91 Hv at 72 hours for the ATZ641 alloy without Na.The simultaneous addition of Zn and Na led to the formation of Sn–Na–Zn particles that acted as effective nucleation sites for Mg_(2)Sn,promoting aluminum partitioning and accelerating the precipitation of Mg_(17)Al_(12)through Al-rich regions.Additionally,Zn and Na co-segregated within the Mg_(17)Al_(12)phase,reducing misfit strain caused by Zn substitution and improving precipitate stability and refinement.These findings highlight Zn’s critical role,alongside trace Na additions,in refining and accelerating the precipitation of Mg_(17)Al_(12)and Mg_(2)Sn phases,thereby enhancing the age-hardening response of magnesium alloys.展开更多
Piezoelectric and triboelectric effects are of growing interest for facilitating high-sensitivity and self-powered tactile sensor applications.The working principles of piezoelectric and triboelectric nanogenerators p...Piezoelectric and triboelectric effects are of growing interest for facilitating high-sensitivity and self-powered tactile sensor applications.The working principles of piezoelectric and triboelectric nanogenerators provide strategies for enhancing output voltage signals to achieve high sensitivity.Increasing the piezoelectric constant and surface triboelectric charge density are key factors in this enhancement.Methods such as annealing processes,doping techniques,grain orientation controls,crystallinity controls,and composite structures can effectively enhance the piezoelectric constant.For increasing triboelectric output,surface plasma treatment,charge injection,microstructuring,control of dielectric constant,and structural modification are effective methods.The fabrication methods present significant opportunities in tactile sensor applications.This review article summarizes the overall piezoelectric and triboelectric fabrication processes from materials to device aspects.It highlights applications in pressure,touch,bending,texture,distance,and material recognition sensors.The conclusion section addresses challenges and research opportunities,such as limited flexibility,stretchability,decoupling from multi-stimuli,multifunctional sensors,and data processing.展开更多
基金the National Research Foundation of Korea(NRF)funded by the Korean Government(MSIT)(No.2022R1A2C1006743)。
文摘This study presents a facile and rapid method for synthesizing novel Layered Double Hydroxide(LDH)nanoflakes,exploring their application as a photocatalyst,and investigating the influence of condensed phosphates'geometric linearity on their photocatalytic properties.Herein,the Mg O film,obtained by plasma electrolysis of AZ31 Mg alloys,was modified by growing an LDH film,which was further functionalized using cyclic sodium hexametaphosphate(CP)and linear sodium tripolyphosphate(LP).CP acted as an enhancer for flake spacing within the LDH structure,while LP changed flake dispersion and orientation.Consequently,CP@LDH demonstrated exceptional efficiency in heterogeneous photocatalysis,effectively degrading organic dyes like Methylene blue(MB),Congo red(CR),and Methyl orange(MO).The unique cyclic structure of CP likely enhances surface reactions and improves the catalyst's interaction with dye molecules.Furthermore,the condensed phosphate structure contributes to a higher surface area and reactivity in CP@LDH,leading to its superior photocatalytic performance compared to LP@LDH.Specifically,LP@LDH demonstrated notable degradation efficiencies of 93.02%,92.89%,and 88.81%for MB,MO,and CR respectively,over a 40 min duration.The highest degradation efficiencies were observed in the case of the CP@LDH sample,reporting 99.99%for MB,98.88%for CR,and 99.70%for MO.This underscores the potential of CP@LDH as a highly effective photocatalyst for organic dye degradation,offering promising prospects for environmental remediation and water detoxification applications.
基金supported by the National Research Foundation of Korea(NRF)funded by the Korean government(MSIT)(No.2022R1A2C1006743).
文摘The hybridization of metal-organic framework(MOF)with inorganic layers would lead to the discovery of novel hybrid materials that can provide a compelling strategy for enhancing its photocatalytic and electrochemical response.In the present study,a highly efficient multifunctional hybrid material was developed by exploiting the defective layer formed on AZ31 Mg alloy through plasma electrolytic oxidation(PEO)as a nucleation and growth site for Co-MOF.The concentrations of the organic linker 2-Methylimidazole(2,MIm)and cobalt nitrate as a source of Co^(2+) ions were varied to control the growth of the obtained Co-MOF.Lower concentrations of the 2,MIm ligand favored the formation of leaf-like MOF structures through an anisotropic,two-dimensional growth,while higher concentrations led to rapid,isotropic nucleation and the creation of polyhedral Co-MOF structures.The sample characterized by polyhedral Co-MOF structures exhibited superior electrochemical stability,with the lowest corrosion current density(3.11×10^(-9) A/cm^(2))and the highest top layer resistance(2.34×10^(6)Ωcm^(2)),and demonstrated outstanding photocatalytic efficiency,achieving a remarkable 99.98%degradation of methylene blue,an organic pollutant,in model wastewater.To assess the active adsorption sites of the Co-MOF,density functional theory(DFT)was utilized.This study explores the changes in morphologies of the coatings of Co-MOF with the change of solution concentration to form coatings with enhanced properties on the metallic substrate,which could establish the groundwork for the development of next-generation multifunctional frameworks with diverse applications.
基金funded by Faculty of Engineering,Burapha University,grant number 003/2567.
文摘Herein,cure characteristics,morphology,and mechanical properties of natural rubber filled with activated carbon-based materials were investigated.Carbon-based materials were prepared from bagasse,coffee grounds and pineapple crowns by the pyrolysis method at temperatures in the range of 300℃.As-synthesized carbon materials were characterized by optical microscopy(OM),scanning electron microscopy(SEM),and Fourier-transform infrared spectroscopy(FTIR)to analyze size distribution,morphology,and functional groups,respectively.OM and SEM analysis revealed that particles,flakes,and a small quantity of fiber-like carbon were obtained using bagasse and pineapple crown as raw materials,while honeycomb-like carbon materials can be derived from coffee grounds.To investigate the mechanical properties,natural rubber was filled with carbon black and as-synthesized carbon materials by the internal mixing and compression molding process.Transmission electron microscopy(TEM)was utilized to characterize the dispersion of carbon materials in the rubber matrix.The results of tensile testing showed that the natural rubber mixed with as-synthesized carbon materials from pineapple crowns exhibited 54%and 74%improvement in the ultimate tensile strength and Young’s modulus,respectively,compared with natural rubber without filled carbon materials.The enhancement in mechanical properties by activated carbon materials derived from pineapple crowns can be attributed to the flake-and fiber-like structures and good dispersion of carbon materials in the rubber matrix.In addition,it is higher than that of rubber mixed with carbon black.The results demonstrated that as-synthesized carbon materials from pineapple crowns have the potential materials to substitute carbon black in the rubber compound industry.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korean government(MSIT)(NRF-2020R1A6A1A03043435 and 2020R1A2C1099862)supported by the Korea Institute for Advancement of Technology(KIAT)grant funded by the Korean Government(MOTIE)(P0012451,The Competency Development Program for Industry Specialist)。
文摘MXenes,the most recent addition to the 2D material family,have attracted significant attention owing to their distinctive characteristics,including high surface area,conductivity,surface characteristics,mechanical strength,etc.This review begins by presenting MXenes,providing insights into their structural characteristics,synthesis methods,and surface functional groups.The review covers a thorough analysis of MXene surface properties,including surface chemistry and termination group impacts.The properties of MXenes are influenced by their synthesis,which can be fluorine-based or fluorinedependent.Fluorine-based synthesis techniques involve etching with fluorine-based reagents,mainly including HF or LiF/HCl,while fluorine-free methods include electrochemical etching,chemical vapor deposition(CVD),alkaline etching,Lewis acid-based etching,etc.These techniques result in the emergence of functional groups such as-F,-O,-OH,-Cl,etc.on the MXenes surface,depending on the synthesis method used.Properties of MXenes,such as electrical conductivity,electronic properties,catalytic activity,magnetic properties,mechanical strength,and chemical and thermal stability,are examined,and the role of functional groups in determining these properties is explored.The review delves into the diverse applications of MXenes,encompassing supercapacitors,battery materials,hydrogen storage,fuel cells,electromagnetic interference(EMI) shielding,pollutant removal,water purification,flexible electronics,sensors,additive manufacturing,catalysis,biomedical and healthcare fields,etc.Finally,this article outlines the challenges and opportunities in the current and future development of MXenes research,addressing various aspects such as synthesis scalability,etching challenges,and multifunctionality,and exploring novel applications.The review concludes with future prospects and conclusions envisioning the impact of MXenes on future technologies and innovation.
基金financially supported by the National Research Foundation of Korea(NRF)from the Korea Government(MEST,No.NRF-2022R1F1A1070886MSIT,No.RS2023-00217581)the Commercialization Promotion Agency for R&D Outcomes(COMPA)from the Korea Government(MEST,No.1711175258)。
文摘Heteroatom-doped transition metal oxides have attracted great attention as advanced anode materials for lithium-ion batteries due to their high theoretical capacity and superior properties.However,the limited resource availability has led to a substantial rise in prices for valuable metals such as Ni and Co,posing a significant challenge for their application.To address this issue,recycling of these metals from waste materials have gained prominence,and particularly the recovery of Co has been mostly focused on its economic benefits.Herein,we introduced a novel recycling strategy for fabrication of heteroatomdoped CoO_(x)(comprising mainly Co_(3)O_(4)with a minor CoO phase)anode with a yolk–shell structure for lithium-ion batteries,by separating Co from cemented tungsten carbide waste.By employing a simple leaching process and subsequent spray pyrolysis,the yolk–shell structured microsphere comprising CoO_(x)was successfully synthesized.Moreover,the presence of other waste metals in the leachate facilitated multi-heteroatom doping during synthesis.Interestingly,the introduction of various dopants into CoO_(x)induced oxygen vacancy formation,thereby enhancing the electrochemical properties of the CoO_(x)anode.As a result,compared with the phase-pure(undoped)CoO_(x)yolk–shell,the heteroatom-doped CoO_(x)yolk–shell exhibited robust cycling stability(602 mAh·g^(-1)for 200 cycles at 1 A·g^(-1))and excellent rate capability(210 mAh·g^(-1)at 10 A·g^(-1)).
基金supported by the National Research Foundation of Korea(NRF)funded by the Korean government(MSIT)(No.2022R1A2C1006743).
文摘Advanced hybrid materials with unique properties are essential for addressing the demands of increasingly complex applications.Despite their importance,the self-assembly of layered double hydroxides(LDH)with metallic oxide nanoparticles and dicarboxylic acids is constrained by a limited understanding of the formation mechanisms and difficulties in evaluating their anticorrosive performance.In this study,we developed a novel anticorrosive system by intercalating CeNiLDH with a complex of vanadium pentoxide(V2O5)nanoparticles and(2E)-but-2-enedioic acid((2E)-BDA)on a MgO layer created through plasma-electrolysis of AZ31 Mg alloy.This system was compared with LDH films intercalated with either V2O5 or(2E)-BDA alone.The intercalation of LDH with V_(2)O_(5)and(2E)-BDA resulted in a flower-like structure,while modification with their complex led to a more compact,cloud-like formation.These cloud-like structures,driven by enhanced absorption and robust hydrogen bonding throughout the hierarchical network,effectively suppress corrosion by delaying the movement of corrosive anions.This was reflected in a polarization resistance of 1.51×10^(10)Ω·cm^(2),which is approximately two orders of magnitude times higher than the resistance of the unmodified LDH film(3.41×10^(8)Ω·cm^(2)).Additionally,the corrosion current density(icorr)of the VOBDA sample showed a decrease by four orders of magnitude compared to the unmodified LDH sample,emphasizing the superior anticorrosive performance of this hybrid coating.Density functional theory(DFT)was used to elucidate the bonding and formation mechanisms between LDH and the inorganic-organic complex.
文摘The high compacted density LiNi<sub>0.5-x</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub>Mg<sub>x</sub>O<sub>2</sub> cathode material for lithium-ion batteries was synthesized by high temperature solid-state method, taking the Mg element as a doping element and the spherical Ni<sub>0.5</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub> (OH)<sub>2</sub>, Li<sub>2</sub>CO<sub>3</sub> as raw materials. The effects of calcination temperature on the structure and properties of the products were investigated. The structure and morphology of cathode materials powder were analyzed by X-ray diffraction spectroscopy (XRD) and scanning electronmicroscopy (SEM). The electrochemical properties of the cathode materials were studied by charge-discharge test and cyclic properties test. The results show that LiNi<sub>0.4985</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub> Mg<sub>0.0015</sub>O<sub>2</sub> cathode material prepared at calcination temperature 930°C has a good layered structure, and the compacted density of the electrode sheet is above 3.68 g/cm<sup>3</sup>. The discharge capacity retention rate is more than 97.5% after 100 cycles at a charge-discharge rate of 1C, displaying a good cyclic performance.
文摘(2E,6E)-4-methyl-2,6-bis(pyridin-3-ylmethylene)cyclohexan-1-one(L_(1))and 4-methyl-2,6-bis[(E)-4-(pyridin-4-yl)benzylidene]cyclohexan-1-one(L_(2))were synthesized and combined with isophthalic acid(H_(2)IP),then under solvothermal conditions,to react with transition metals achieving four novel metal-organic frameworks(MOFs):[Zn(IP)(L_(1))]_(n)(1),{[Cd(IP)(L_(1))]·H_(2)O}_(n)(2),{[Co(IP)(L_(1))]·H_(2)O}_(n)(3),and[Zn(IP)(L_(2))(H_(2)O)]_(n)(4).MOFs 1-4 have been characterized by single-crystal X-ray diffraction,powder X-ray diffraction,thermogravimetry,and elemental analysis.Single-crystal X-ray diffraction shows that MOF 1 crystallizes in the monoclinic crystal system with space group P2_(1)/n,and MOFs 2-4 belong to the triclinic system with the P1 space group.1-3 are 2D sheet structures,2 and 3 have similar structural characters,whereas 4 is a 1D chain structure.Furthermore,1-3 exhibited certain photocatalytic capability in the degradation of rhodamine B(Rh B)and pararosaniline hydrochloride(PH).4could be used as a heterogeneous catalyst for the Knoevenagel reaction starting with benzaldehyde derivative and malononitrile.4 could promote the reaction to achieve corresponding products in moderate yields within 3 h.Moreover,the catalyst exhibited recyclability for up to three cycles without significantly dropping its activity.A mechanism for MOF 4 catalyzed Knoevenagel condensation reaction of aromatic aldehyde and malononitrile has been initially proposed.CCDC:2356488,1;2356497,2;2356499,3;2356498,4.
基金financially supported by the Materials/Parts Technology Development Program(No.RS-202400456324)funded by the Ministry of Trade,Industry&Energy(MOTIE,Korea)by the National Research Foundation(NRF)of Korea grant(No.RS-2024-00454367)funded by the Ministry of Science and ICT(MSIT,Korea)。
文摘K–Se batteries have been identified as promising energy storage systems owing to their high energy density and cost-effectiveness.However,challenges such as substantial volume changes and low Se utilization require further investigation.In this study,novel N-doped multichannel carbon nanofibers(h-NMCNFs)with hierarchical porous structures were successfully synthesized as efficient cathode hosts for K–Se batteries through the carbonization of two electrospun immiscible polymer nanofibers and subsequent chemical activation.Mesopores originated from the decomposition of the polymer embedded in the carbon nanofibers,and micropores were introduced via KOH activation.During the activation step,hierarchical porous carbon nanofibers with enhanced pore volumes were formed because of the micropores in the carbon nanofibers.Owing to the mesopores that enabled easy access to the electrolyte and the high utilization of chain-like Se within the micropores,the Se-loaded hierarchical porous carbon nanofibers(60 wt%Se)exhibited a high discharge capacity and excellent rate performance.The discharge capacity of the nanofibers at the 1,000th cycle was 210.8 mA.h.g^(-1)at a current density of 0.5C.The capacity retention after the initial activation was 64%.In addition,a discharge capacity of 165 mA.h.g^(-1)was obtained at an extremely high current density of 3.0C.
基金supported by the National Research Foundation of Korea(NRF)funded by the Korean government(MSIT)(No.2022R1A2C1006743).
文摘This study presents a novel approach to improving the anticorrosive performance of AZ31 Mg alloy by exploiting the role of the hydration reaction to induce interactions between Quinolin-8-ol(8HQ)molecules and the porous MgO layer formed via plasma electrolytic oxidation(PEO).The AZ31 Mg alloy,initially coated with a PEO layer,underwent a dipping treatment in an ethanolic solution of 0.05 M 8HQ at 50℃ for 3 h.The results were compared with those from a different procedure where the PEO layer was subjected to a hydration reaction for 2 h at 90℃ before immersion in the 8HQ solution under the same conditions.The hydration treatment played a crucial role by converting MgO to Mg(OH)_(2),significantly enhancing the surface reactivity.This transformation introduced hydroxyl groups(−OH)on the surface,which facilitated donor-acceptor interactions with the electron-accepting sites on 8HQ molecules.The calculated binding energy(Ebinding)from DFT indicated that the interaction energy of 8HQ with Mg(OH)_(2) was lower compared to 8HQ with MgO,suggesting easier adsorption of 8HQ molecules on the hydrated surface.This,combined with the increased number of active sites and enhanced surface area,allowed for extensive surface coverage by 8HQ,leading to the formation of a stable,flake-like protective layer that sealed the majority of pores on the PEO layer.DFT calculations further suggested that the hydration treatment provided multiple active sites,enabling effective contact with 8HQ and rapid electron transfer,creating ideal conditions for charge-transfer-induced physical and chemical bonding.This study shows that hydration and 8HQ treatments significantly enhance the corrosion resistance of Mg alloys,highlighting their potential for advanced anticorrosive coatings.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korean government(MSIT)(No.2020R1C1C1003375)。
文摘Recently,hollow carbon nanospheres(HCSs)have garnered significant attention as potential Li metal hosts owing to their unique large voids and ease of fabrication.However,similar to other nanoscale hosts,their practical performance is limited by inhomogeneous agglomeration,increased binder requirements,and high tortuosity within the electrode.To overcome these problems and high tortuosity within the electrode,this study introduces a pomegranate-like carbon microcluster composed of primary HCSs(P-CMs)as a novel Li metal host.This unique nanostructure can be easily prepared using the spray-drying technique,enabling its mass production.Comprehensive analyses with various tools demonstrate that compared with HCS hosts,the P-CM host requires a smaller amount of binder to fabricate a sufficiently robust and even surface electrode.Furthermore,owing to reduced tortuosity,the well-designed P-CM electrode can provide continuous and shortened pathways for electron/ion transport,accelerating the Li-ion transfer kinetics and prohibiting preferential Li plating at the upper region of the electrode.Due to these characteristics,Li metal can be effectively encapsulated in the large inner voids of the primary HCSs constituting the P-CM,thereby enhancing the electrochemical performance of P-CM hosts in Li metal batteries.Specifically,the Coulombic efficiency of the P-CM host can be maintained at 97%over 100 cycles,with a high Li deposition areal capacity of 3 mAh·cm^(-2)and long cycle life(1000 h,1 mA·cm^(-2),and 1.0 mAh·cm^(-2)).Furthermore,a full cell incorporating a LiFePO4 cathode exhibits excellent cycle life.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korea government(MSIT)(No.NRF-2021M3H4A1A04091999).
文摘Microalloying addition plays a significant role in controlling the characteristics of precipitates in Al alloys.This study investigates the effects of Ag and Sc microalloying addition on the thermal stability of Al–Zn–Mg–Cu alloys,via differential scanning calorimetry,transmission electron microscopy,and atom-probe tomography.The results demonstrate that Ag and Sc additions increase the number density ofη-MgZn_(2) type nano-precipitates(formed during heat treatment)by forming direct(Mg–Ag phase,prototype of precipitate)or indirect precursors(Al_(2) Sc phase,constituent of precipitate)for the precipitate.In addition,the Ag and Sc elements can effectively prevent the coarsening ofηprecipitates and facilitate the high-density distribution of fineηprecipitates,during the over-aging period,improving the thermal stability of the Al–Zn–Mg–Cu alloys.The thermal stability is particularly improved by Ag addition because Ag atoms directly prevent the coarsening ofηprecipitates by hindering Zn diffusion into the precipitate.On the contrary,Sc addition indirectly prevents the coarsening ofηprecipitates by depleting the solute species from the Al matrix,enabling abundant precipitates limited growth.Thus Ag addition improves precipitation strengthening by preventing the coarsening of precipitates during over-aging.
基金supported by the National Research Foundation of Korea(NRF)funded by the Korean government(MSIT)(No.2022R1A2C1006743).
文摘This study presents a novel photocatalytic system exploiting the unique properties of ZrO_(2) and its integration with layered double hydroxide(LDH)films on porous coatings produced via plasma electrolytic oxidation(PEO).Herein,CoFe-LDHfilms were created on the porous surface of PEO-coated AZ31 Mg alloy using a hydrothermal treatment in cobalt and iron nitrate solutions,followed by a secondary hydrothermal process in a ZrO_(2) solution for 10 h at 70℃.The impact of ZrO_(2) on the morphological,compositional,and photocatalytic performance was then compared to the case where ZrO_(2) nanoparticles were electrophoretically incorporated into the porous PEO coating.Characterization results revealed that the ZrO_(2)-modified LDH coatings exhibited a dispersedflake-like structure with an increased surface area,a reduced band gap energy of 3.14 eV,and enhanced electron-hole separation.Experimental results demonstrated an outstanding 99.8%degradation of indigo carmine within 15 mins,with remarkable multi-cycle stability overfive consecutive cycles without significant performance decline.This system demonstrates faster degradation rates and greater durability compared to previously reported catalysts,underscoring its potential for effective and sustainable environmental remediation.The synergistic integration of ZrO_(2),LDH,and PEO highlights a promising strategy for wastewater treatment,particularly for the removal of persistent organic dyes like indigo carmine.
基金supported by the Nano&Material Technology Development Program through the National Research Foundation of Korea(NRF)funded by the Ministry of Science and ICT(RS-2024-00436563)supported by Brain Pool program funded by the Ministry of Science and ICT through the National Research Foundation of Korea(Grant No.RS-2023-00284361).
文摘Seawater is the most abundant source of molecular hydrogen.Utilizing the hydrogen reserves present in the seawater may inaugurate innovative strategies aimed at advancing sustainable energy and environmental preservation endeavors in the future.Recently,there has been a surge in study in the field addressing the production of hydrogen through the electrochemical seawater splitting.However,the performance and durability of the electrode have limitations due to the fact that there are a few challenges that need to be addressed in order to make the technology suitable for the industrial purpose.The active site blockage caused by chloride ions that are prevalent in seawater and chloride corrosion is the most significant issue;it has a negative impact on both the activity and the durability of the anode component.Addressing this particular issue is of upmost importance in the seawater splitting area.This review concentrates on the newly developed materials and techniques for inhibiting chloride ions by blocking the active sites,simultaneously preventing the chloride corrosion.It is anticipated that the concept will be advantageous for a large audience and will inspire researchers to study on this particular area of concern.
基金supported by the National Research Foundation of Korea(NRF)funded by the Korean government(MSIT)(No.2022R1A2C1006743).
文摘This study explores the development of an organic-inorganic hybrid coating to enhance the corrosion resistance and photocatalytic properties of AZ31 Mg alloy modified by plasma electrolytic oxidation(PEO).The PEO process typically generates a porous oxide layer,which can reduce corrosion protection by allowing corrosive agents to penetrate the substrate.To address this limitation,phenopyridine(PHEN)and 2-methylimidazole(2-IMD)were incorporated into the PEO surface to form a robust organic layer on the Mg alloy.Potassium hydroxide(KOH)was used to adjust the pH,improving the interaction and solubility between the organic molecules and the PEO coating.The hybrid coating exhibited unique twig-like surface structures that contributed to forming a multifunctional coating with high corrosion resistance and superior photocatalytic activity.The PEO-PHEN-2IMD sample on the Mg alloy demonstrated exceptional corrosion resistance,with the lowest corrosion current density(I_(corr))of 1.92×10^(-10) A/cm^(2),a high corrosion potential(E_(corr)),and the highest top layer resistance(R_(top))of 2.57×10^(6)Ω·cm^(2),indicating excellent barrier properties.Additionally,the coating achieved complete(100%)degradation of methylene blue(MB)within 30 min under visible light.Density Functional Theory(DFT)calculations provide deeper insights into the bonding mechanisms and interaction stability between PHEN,2-IMD,and the PEO layer on the Mg alloy and MB dye.These findings confirmed the enhanced performance of the hybrid coating in both corrosion resistance and photocatalytic applications.
基金supported by the Taishan Scholar Program of Shandong Province,China(tsqn202211162)National Natural Science Foundation of China(22372088 and 22102079)+1 种基金Natural Science Foundation of Shandong Province of China(ZR2021YQ10)the Materials/Parts Technology Development Program(RS-2024-00432627)funded by the Ministry of Trade,Industry and Energy,Korea.
文摘Reducing the Ir loading while preserving catalytic performance and mechanical robustness in anodic catalyst layers remains a critical challenge for the large-scale implementation of proton exchange membrane water electrolysis(PEMWE).Herein,we present a structural engineering strategy involving neodymium-doped Ir/IrO_(2)(Nd-Ir/IrO_(2))hollow nanospheres with precisely adjustable shell thickness and cavity dimensions.The optimized catalyst demonstrates excellent oxygen evolution reaction(OER)performance in acidic media,achieving a remarkably low overpotential of 259 mV at a benchmark current density of 10 mA cm^(-2) while exhibiting substantially enhanced durability compared to commercial IrO_(2) and Ir/IrO_(2) counterparts.Notably,the Nd-Ir/IrO_(2) catalyst delivers a mass activity of 541.6 A gIr^(-1) at 1.50 V vs RHE,representing a 74.5-fold enhancement over conventional IrO_(2).Through comprehensive electrochemical analysis and advanced characterization techniques reveal that,the hierarchical hollow architecture simultaneously addresses multiple critical requirements:(i)abundant exposed active sites enabled by an enhanced electrochemical surface area,(ii)optimized mass transport pathways through engineered porosity,and(iii)preserved structural integrity via a continuous conductive framework,collectively enabling significant Ir loading reduction without compromising catalytic layer performance.Fundamental mechanistic investigations further disclose that Nd doping induces critical interfacial Nd-O-Ir configurations that stabilize lattice oxygen,together with intensified electron effect among mixed valent Ir that inhibits the overoxidation of Ir active sites during the OER process,synergistically ensuring enhanced catalytic durability.Our work establishes a dual-modulation paradigm integrating nanoscale architectural engineering with atomic-level heteroatom doping,providing a viable pathway toward high-performance PEMWE systems with drastically reduced noble metal requirements.
基金supported by Korea Institute of Energy Technology Evaluation and Planning(KETEP)grant funded by the Korea government(MOTIE)(No.RS-2024-00398346,ESS BigData-Based O&M and Asset Management Technical Manpower Training)the National Research Foundation of Korea(NRF)grant funded by the Korea government(MSIT)(No.RS-2024-00350658).
文摘Pyrochlore oxide(Y_(2)Ru_(2)O_(7))has been identified as a promising catalyst for the oxygen evolution reaction(OER)in advanced green energy strategies.However,its electrochemical inertness necessitates the exploration of an effective strategy to facilitate electronic modulation.This study proposes a surface modification approach involving the integration of defective NiFe(D-NiFe)nanoparticles onto a Y_(2)Ru_(2)O_(7)(YRO)support(YRO@D-NiFeP/Ru)using a Prussian blue analog(PBA).Numerous cyanide(CN)vacancies are generated through the oxidation treatment of the NiFe PBA grown on the YRO support,yielding a defective PBA precursor(YRO@D-PBA).Subsequent annealing facilitates the transformation to the D-NiFe nanoparticles on the YRO support(YRO@D-NiFeP/Ru),which augments the exposure of Ni3+active sites beneficial for the OER.Moreover,the reduction of Ru cations from YRO results in the exsolution of Ru nanoparticles,which promotes synergistic charge transfer from the nanoparticles to the interior of Y_(2)Ru_(2)O_(7).Consequently,YRO@D-NiFeP/Ru exhibits a remarkable voltage of 1.49 V at 10 mA·cm^(−2) and the lowest Tafel slope of 42.4 mV·dec^(−1).In addition,a Zn–air battery constructed with YRO@D-NiFeP/Ru exhibits an outstanding power density of 136.2 mW·cm^(−2) and high charge–discharge stability,confirming the applicability of YRO@D-NiFeP/Ru in metal-air batteries.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korean Government(MSIT)(Nos.RS-2023-00217581 and RS-2023-00304768)the National Research Council of Science&Technology(NST)grant by the Korean Government(MSIT)(No.CAP 22073-000).
文摘Aqueous zinc-ion batteries(AZIBs)have emerged as promising,practical energy storage devices based on their non-toxic nature,environmental friendliness,and high energy density.However,excellent rate characteristics and stable long-term cycling performance are essential.These essential aspects create a need for superior cathode materials,which represents a substantial challenge.In this study,we used MXenes as a framework for NH_(4)V_(4)O_(10)(NVO)construction and developed electrodes that combined the high capacity of NVO with the excellent conductivity of MXene/carbon nanofibers(MCNFs).We explored the electrochemical characteristics of electrodes with varying NVO contents.Considering the distinctive layered structure of NVO,the outstanding conductivity of MCNFs,and the strong synergies between the two components.NVO-MCNFs exhibited better charge transfer compared with earlier materials,as well as more ion storage sites,excellent conductivity,and short ion diffusion pathways.A composite electrode with optimized NVO content exhibited an excellent specific capacitance of 360.6mAh g^(-1) at 0.5 A g^(-1) and an outstanding rate performance.In particular,even at a high current density of 10 A g^(-1),the 32NVO-MCNF exhibited impressive cycling stability:88.6%over 2500 cycles.The mechanism involved was discovered via comprehensive characterization.We expect that the fabricated nanofibers will be useful in energy storage and conversion systems.
基金supported by the Fundamental Research Program(PNKA130)of the Korea Institute of Materials Science,Republic of Korea。
文摘This study investigates zinc’s(Zn)key role in enhancing the precipitation kinetics and refinement of Mg_(17)Al_(12)and Mg_(2)Sn phases in magnesium alloys through trace sodium(Na)additions.Magnesium alloys with varying compositions of aluminum(Al),tin(Sn),Zn,and Na were prepared and aged at 453 K.Microstructural analyses were conducted using transmission electron microscopy(TEM),scanning transmission electron microscopy(STEM),and atom probe tomography(APT).Trace additions of Na significantly enhanced the precipitation responses of both Mg_(17)Al_(12)and Mg_(2)Sn phases.When Zn was co-added with Na,as in the ATZ641N3 alloy(Mg–6Al–4Sn–1Zn–0.3Na),there was a pronounced refinement in precipitate morphology and acceleration of precipitation kinetics.The ATZ641N3 alloy achieved a peak hardness of 103 Hv at 36 hours,compared to 91 Hv at 72 hours for the ATZ641 alloy without Na.The simultaneous addition of Zn and Na led to the formation of Sn–Na–Zn particles that acted as effective nucleation sites for Mg_(2)Sn,promoting aluminum partitioning and accelerating the precipitation of Mg_(17)Al_(12)through Al-rich regions.Additionally,Zn and Na co-segregated within the Mg_(17)Al_(12)phase,reducing misfit strain caused by Zn substitution and improving precipitate stability and refinement.These findings highlight Zn’s critical role,alongside trace Na additions,in refining and accelerating the precipitation of Mg_(17)Al_(12)and Mg_(2)Sn phases,thereby enhancing the age-hardening response of magnesium alloys.
基金supported by National Research Foundation of Korea(2022M3D1A2054488)Technology Innovation Program(20025736,Development of MICS SoC and platform for in-vivo implantable electroceutical device)funded by the Ministry of Trade,Industry&Energy(MOTIE,Korea)。
文摘Piezoelectric and triboelectric effects are of growing interest for facilitating high-sensitivity and self-powered tactile sensor applications.The working principles of piezoelectric and triboelectric nanogenerators provide strategies for enhancing output voltage signals to achieve high sensitivity.Increasing the piezoelectric constant and surface triboelectric charge density are key factors in this enhancement.Methods such as annealing processes,doping techniques,grain orientation controls,crystallinity controls,and composite structures can effectively enhance the piezoelectric constant.For increasing triboelectric output,surface plasma treatment,charge injection,microstructuring,control of dielectric constant,and structural modification are effective methods.The fabrication methods present significant opportunities in tactile sensor applications.This review article summarizes the overall piezoelectric and triboelectric fabrication processes from materials to device aspects.It highlights applications in pressure,touch,bending,texture,distance,and material recognition sensors.The conclusion section addresses challenges and research opportunities,such as limited flexibility,stretchability,decoupling from multi-stimuli,multifunctional sensors,and data processing.
