Owing to their exceptional properties,high-entropy alloys(HEAs)and high-entropy materials have emerged as promising research areas and shown diverse applications.Here,the recent advances in the field are comprehensive...Owing to their exceptional properties,high-entropy alloys(HEAs)and high-entropy materials have emerged as promising research areas and shown diverse applications.Here,the recent advances in the field are comprehensively reviewed,organized into five sections.The first section introduces the background of HEAs,covering their definition,significance,application prospects,basic properties,design principles,and microstructure.The subsequent section focuses on cutting-edge high-entropy structural materials,highlighting developments such as nanostructured alloys,grain boundary engineering,eutectic systems,cryogenic alloys,thin films,micro-nano-lattice structures,additive manufacturing,high entropy metallic glasses,nano-precipitate strengthened alloys,composition modulation,alloy fibers,and refractory systems.In the following section,the emphasis shifts to functional materials,exploring HEAs as catalysts,magneto-caloric materials,corrosion-resistant alloys,radiation-resistant alloys,hydrogen storage systems,and materials for biomedicine.Additionally,the review encompasses functional high-entropy materials outside the realm of alloys,including thermoelectric,quantum dots,nanooxide catalysts,energy storage materials,negative thermal expansion ceramics,and high-entropy wave absorption materials.The paper concludes with an outlook,discussing future directions and potential growth areas in the field.Through this comprehensive review,researchers,engineers,and scientists may gain valuable insights into the recent progress and opportunities for further exploration in the exciting domains of high-entropy alloys and functional materials.展开更多
The massive distribution of microplastics(MPs)and even nanoplastics(NPs),which resulted from the wide utilization and mismanagement of plastics,exerted serious risk and threat to ecosystem and human health due to thei...The massive distribution of microplastics(MPs)and even nanoplastics(NPs),which resulted from the wide utilization and mismanagement of plastics,exerted serious risk and threat to ecosystem and human health due to their physical damages and chemical toxicity.展开更多
Nonlinear optical/birefringent crystals as important optical functional materials have been widely applied in optical communication,laser information processing,and laser polarization technology.In recent decades,hydr...Nonlinear optical/birefringent crystals as important optical functional materials have been widely applied in optical communication,laser information processing,and laser polarization technology.In recent decades,hydroxyborates,fluorooxoborates and hydroxyfluorooxoborates have attracted significant interest as key branches of the borate family because of their outstanding(deep-)ultraviolet nonlinear optics or other optical functional performances.Negatively charged terminal groups OH^(-)and F^(-)can regulate the structure and the material characteristics.OH^(-)and F^(-)have the same valence and both appear in the terminal position of the anionic framework,which can be substituted by each other theoretically.However,it is found that the introduction of OH^(-)and F^(-)is apparently different in structure and properties.In this mini-review,a variety of theoretical and experimental characterization methods to identify OH^(-)and F^(-)was discussed.The different role of OH^(-)and F^(-)in involved systems'microstructures and macro-properties including nonlinear optics was comprehensively analyzed.We aim to provide guidance for designing and synthesizing novel materials with balanced properties used in deep-ultraviolet applications.展开更多
High entropy materials(HEMs)are the promising electrocatalysts for anion exchange membrane electrolyser(AEMs)and proton exchange membrane fuel cells(PEMFCs)due to the intriguing cocktail effect,wide design space,tailo...High entropy materials(HEMs)are the promising electrocatalysts for anion exchange membrane electrolyser(AEMs)and proton exchange membrane fuel cells(PEMFCs)due to the intriguing cocktail effect,wide design space,tailorable electronic structure,and entropy stabilization effect.The precise fabrication of HEMs with functional nanostructures provides a crucial avenue to optimize the adsorption strength and catalytic activity for electrocatalysis.This review comprehensively summarizes the development of HEMs,focusing on the principles and strategies of structural design,and the catalytic mechanism towards hydrogen evolution reaction,oxygen evolution reaction and oxygen reduction reaction for the development of high-performance electrocatalysts.The complexity inherent in the interactions between different elements,the changes in the d-band center and the Gibbs free energies during the catalytic progress,as well as the coordination environment of the active sites associated with the unique crystal structure to improve the catalytic performance are discussed.We also provide a perspective on the challenges and future development direction of HEMs in electrocatalysis.This review will contribute to the design and development of HEMs-based catalysts for the next generation of electrochemical applications.展开更多
Enhancing the photovoltaic performance of perovskite solar cells(PSCs)via the strategy of spectral conversion garners significant attention in recent years.However,developing a spectral conversion layer with excellent...Enhancing the photovoltaic performance of perovskite solar cells(PSCs)via the strategy of spectral conversion garners significant attention in recent years.However,developing a spectral conversion layer with excellent stability and low series resistance remains challenging.Here,we propose a spectral conversion material termed perylenetetracarboxylic diimide functionalized CsPbCl_(3):Mn^(2+)quantum dots(CMI),which is incorporated at the SnO_(2)/perovskite interface as a down-conversion layer.This innovation effectively resolves the trade-off between spectral conversion efficiency and electrical performance of the spectral conversion layer.CMI converts ultraviolet light into visible light that is more readily absorbed by the perovskite,thus enhancing the light utilization and reducing the ultraviolet-induced degradation of perovskites.The rough and hydrophobic surface of CMI can modulate nucleation site arrangement and enhance grain boundary mobility,resulting in perovskite films with larger and denser grains.Furthermore,the C=O groups in CMI simultaneously passivate the oxygen vacancies in SnO_(2)and the Pb^(2+)dangling bonds at the buried interface of the perovskite,reducing recombination losses and facilitating charge carrier transfer and extraction,and further enhancing power conversion efficiency(PCE).Consequently,the PSCs incorporating CMI as a down-conversion layer achieve an improved PCE,which rises from 21.26%to 23.61%,along with enhanced stability.展开更多
Among various architectures of polymers,end-group-free rings have attracted growing interests due to their distinct physicochemical performances over the linear counterparts which are exemplified by reduced hydrodynam...Among various architectures of polymers,end-group-free rings have attracted growing interests due to their distinct physicochemical performances over the linear counterparts which are exemplified by reduced hydrodynamic size and slower degradation.It is key to develop facile methods to large-scale synthesis of polymer rings with tunable compositions and microstructures.Recent progresses in large-scale synthesis of polymer rings against single-chain dynamic nanoparticles,and the example applications in synchronous enhancing toughness and strength of polymer nanocomposites are summarized.Once there is the breakthrough in rational design and effective large-scale synthesis of polymer rings and their functional derivatives,a family of cyclic functional hybrids would be available,thus providing a new paradigm in developing polymer science and engineering.展开更多
In the context of the global energy low-carbon transition,phase change energy storage technology becomes a key technology to solve the problem of intermittent renewable energy.Oriented phase change composites(OCPCMs)r...In the context of the global energy low-carbon transition,phase change energy storage technology becomes a key technology to solve the problem of intermittent renewable energy.Oriented phase change composites(OCPCMs)receive widespread attention in practical energy storage applications due to their unique oriented thermally conductive structure,which achieves significant thermal conductivity enhancement in specific directions while retaining the high energy storage capacity of the phase change components.This review systematically summarizes the overall analysis of OCPCMs from synthesis and preparation to application scenarios in recent years.Herein,we introduce the analysis of the heat transfer mechanism of the materials and explore the advantages of the oriented structure in OCPCMs in the heat transfer behavior from a bionic perspective.We then focus on summarizing and generalizing the methods for preparing OCPCMs,giving suggestions for suitable methods according to different scenarios.Besides,we discuss the application of finite element simulation methods to the monitoring of the thermal management behavior of OCPCMs,and look into the potential future application areas of such materials.Finally,it is hoped that this review will provide guidance for the academic community in developing high-performance OCPCMs.展开更多
NASICON-type Na_(3)V_(2)(PO_(4))_(3)(NVP)materials are seen as highly promising cathode materials in the field of sodium-ion batteries due to their low cost,a solid three-dimensional skeleton and good theoretical capa...NASICON-type Na_(3)V_(2)(PO_(4))_(3)(NVP)materials are seen as highly promising cathode materials in the field of sodium-ion batteries due to their low cost,a solid three-dimensional skeleton and good theoretical capacity,as well as high ionic conductivity.Nevertheless,the problem of low intrinsic electronic conductivity and energy density has limited the practical application of the materials.To address this issue,the relevant research team has successfully achieved remarkable research results through unremitting exploration and practical innovation.In this work,the crystal structure,ion migration mechanism and sodium storage mechanism of NVP cathode materials are systematically reviewed,with a focus on summarizing the latest progress of V-site doping modification research,classifying and exploring V-site doping from the perspectives of electronic structure,lattice strain and entropy,and briefly describing the optimization mechanism of V-site doping on electrochemical performance.In addition,the challenges and prospects for the future development of NVP cathode materials are presented,which are believed to provide new thinking for the design and development of high-performance NVP cathode materials and contribute to the large-scale application of sodium-ion batteries.展开更多
The preparation of a novel nanoscale imazalil(IMZ)-based coordination polymer[Zn(HBTC)(IMZ)_(2)]_(n)(PDCP1)(H_(3)BTC=1,3,5-benzenetricarboxylic acid),and its antifungal application within a sustainable delivery system...The preparation of a novel nanoscale imazalil(IMZ)-based coordination polymer[Zn(HBTC)(IMZ)_(2)]_(n)(PDCP1)(H_(3)BTC=1,3,5-benzenetricarboxylic acid),and its antifungal application within a sustainable delivery system was reported.The intermolecular interactions presented in the structure,and their contributions to crystal packing were studied by Hirshfeld,Fingerprint plot and Mayer bond order.The obtained PDCP1 had a relativelyhigh loadingrate of IMZ(68.5%).PDCP1 exhibitednotable antifungal activities againstColletotrichum gloeosporioides,Magnaporthe Oryzae,and Alternaria Nees strains,with EC_(50) values of 0.72,0.92,and 0.56μg/mL,respectively.The key benefits of the application of PDCP1 as a control release pesticide include high fungicide loading and offer nearly complete release,pH-responsive release,enhanced UV stability,exhibits favorable biosafety profiles.The remarkable inhibition of C.gloeosporioides growth by PDCP1 underscores a promising strategy for agrochemical material development,high loading of active ingredients and readily delivery fosters more efficient pesticides utilization in agricultural processes.展开更多
Achieving high-energy density remains a key objective for advanced energy storage systems.However,challenges,such as poor cathode conductivity,anode dendrite formation,polysulfide shuttling,and electrolyte degradation...Achieving high-energy density remains a key objective for advanced energy storage systems.However,challenges,such as poor cathode conductivity,anode dendrite formation,polysulfide shuttling,and electrolyte degradation,continue to limit performance and stability.Molecular and ionic dipole interactions have emerged as an effective strategy to address these issues by regulating ionic transport,modulating solvation structures,optimizing interfacial chemistry,and enhancing charge transfer kinetics.These interactions also stabilize electrode interfaces,suppress side reactions,and mitigate anode corrosion,collectively improving the durability of high-energy batteries.A deeper understanding of these mechanisms is essential to guide the design of next-generation battery materials.Herein,this review summarizes the development,classification,and advantages of dipole interactions in high-energy batteries.The roles of dipoles,including facilitating ion transport,controlling solvation dynamics,stabilizing the electric double layer,optimizing solid electrolyte interphase and cathode–electrolyte interface layers,and inhibiting parasitic reactions—are comprehensively discussed.Finally,perspectives on future research directions are proposed to advance dipole-enabled strategies for high-performance energy storage.This review aims to provide insights into the rational design of dipole-interactive systems and promote the progress of electrochemical energy storage technologies.展开更多
The development of high-performance bifunctional electrocatalysts is crucial for advancing zinc-air batteries.However,the fundamentally distinct mechanisms of the oxygen reduction and evolution reactions(ORR/OER)hinde...The development of high-performance bifunctional electrocatalysts is crucial for advancing zinc-air batteries.However,the fundamentally distinct mechanisms of the oxygen reduction and evolution reactions(ORR/OER)hinder the simultaneous realization of high activity within a single catalyst.Herein,we propose a spatial decoupling strategy to overcome this limitation by engineering isolated Fe singleatoms and Fe-Ir dual-atom pairs on a nitrogen-doped carbon matrix(Fe/FeIr-NC).In this architecture,Fe single atoms serve as ORR centers,while Fe-Ir pairs with tunable spacing are tailored for OER,enabling complete functional separation and independent optimization of the reactions.As a result,the catalyst delivers an ORR half-wave potential of 0.91 V and an OER overpotential of 250 mV at 10 mA cm^(-2),yielding a record-low bifunctional gap(ΔE=0.57 V)that outperforms all reported single-and dual-atom catalysts.A flexible fiber zincair battery was developed based on this catalyst,delivering a peak power density of 3920 W kg^(-1),along with a 1.4-fold increase in energy efficiency and a 2.6-fold extension in cycle life compared to the commercial Pt/C+IrO_(2)benchmark.This work not only breaks the traditional activity trade-off in bifunctional catalysis but also offers a promising route toward high-performance power sources for wearable electronics.展开更多
Designing a heterogeneous interface to improve the kinetics of electrocatalysts represents an effective yet challenging approach for enhancing the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER).Herei...Designing a heterogeneous interface to improve the kinetics of electrocatalysts represents an effective yet challenging approach for enhancing the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER).Herein,a simple MOF-assisted etching-pyrolysis strategy is proposed to fabricate an advanced Mott-Schottky(M–S)electrocatalyst composed of Co/CeO_(2)hetero-nanoparticles embedded within N-doped hollow carbon nanoboxes(H-Co/CeO_(2)@NCBs).Notably,the interfacial Co–O–Ce bond bridging productively facilitates the electron transfer and modulates the charge distribution of the active center,thereby contributing to the ORR/OER kinetics.As expected,the optimal M–S H-Co/CeO_(2)@NCBs catalyst exhibits promising bifunctional electrocatalytic activity with a small potential discrepancy of 0.65 V.Theoretical calculations reveal that the built-in electric field in the M–S heterojunction promotes electron transfer in oxygen electrocatalysis and the interfacial bridge-induced electron redistribution optimizes the adsorption/desorption of the oxygen intermediates,leading to reduced activation energy for the bifunctional ORR/OER reactions.Importantly,H-Co/CeO_(2)@NCBs-assembled Zn-air battery(ZAB)delivers high power density(179.8 mW cm^(−2))and long-term stability(400 h).Furthermore,the assembled flexible solid-state ZAB with H-Co/CeO_(2)@NCBs cathode also exhibits excellent charge–discharge reversibility and flexibility at various bending angles.This work provides a novel perspective on developing efficient and stable M–S bifunctional oxygen electrocatalysts.展开更多
Sustainable development for our life is important task,which is driven by key materials and technologies.In this roadmap,we discuss three main aspects in addressing environmental questions,green chemical processes and...Sustainable development for our life is important task,which is driven by key materials and technologies.In this roadmap,we discuss three main aspects in addressing environmental questions,green chemical processes and energy challenges.They are included,such as gas treatment and separation,wastewater treatment,waste gas treatment,solid waste treatment,lithium extraction,hydrogen production,water splitting,CO_(2) reduction,photocatalytic clean technologies,plastic degradation,fuel cells,lithium batteries,sodium batteries,aqueous batteries,solid state batteries,metal air batteries and supercapacitors.Their status,challenges,progress and future perspectives are also discussed.We hope that this paper can give clear views on sustainable development in materials and technologies.展开更多
Issues like morphology control and further multifunctional applications are of significant importance for rare earth nano-oxides,e.g.,cerium dioxide(CeO_(2))nanostructures,however,relevant results in this respect are ...Issues like morphology control and further multifunctional applications are of significant importance for rare earth nano-oxides,e.g.,cerium dioxide(CeO_(2))nanostructures,however,relevant results in this respect are rather limited up to now.In the present work,ultrathin CeO_(2)nanosheets were synthesized through a facile lowtemperature hydrothermal method.The structure,morphology and specific surface area of these CeO_(2)nanosheets were characterized by X-ray diffraction(XRD),field emission scanning electron microscope(FESEM)and N2 adsorption-desorption.Significantly,CeO_(2)nanosheets have the potential as bifunctional sensing materials to detect both humidity and formaldehyde vapor.The CeO_(2)nanosheet humidity sensor exhibited excellent sensing characteristics in the relative humidity range of 11%-97%with the response value as high as 3.1×10^(4).Meanwhile,the CeO_(2)nanosheet gas sensor showed superior sensitivity and repeatability with fast response/recovery speed toward formaldehyde vapor at 300℃.Finally,the humidity and formaldehyde sensing mechanism were discussed as well.展开更多
Rechargeable zinc-air batteries(ZABs)have attracted much attention as the next-generation energy conversion and storage devices due to the abundance and environmental friendliness of zinc(Zn)for anode materials,as wel...Rechargeable zinc-air batteries(ZABs)have attracted much attention as the next-generation energy conversion and storage devices due to the abundance and environmental friendliness of zinc(Zn)for anode materials,as well as the safety and low cost of aqueous electrolytes.However,rational design of nonprecious and low-cost integrated air cathode materials with a desirable bifunctional oxygen electrocatalytic performance remains a great challenge for the commercialization of rechargeable ZABs.In previous research studies,various cost-effective carbon-supported electrocatalysts and light-weight carbon-based current collectors for air cathodes have been developed,showing vast potential in the application of carbon-based materials.To improve the bifunctional performance and integration of air cathodes,efforts with respect to the design of morphology,defects,and synergistic effects of carbon-based materials have been made.In this perspective,the general understanding of the air cathode construction and the battery working mechanism is discussed.The recent progress in the design of carbon-based materials for air cathodes in rechargeable ZABs is summarized.Several possible future research directions and the expected development trends are also discussed,aiming to facilitate the commercialization of advanced rechargeable ZABs in our life.展开更多
Overview Shenzhen Key Laboratory of Organic Optoelectromagnetic Functional Materials was established in 2014 and is located at the University Town of Shenzhen.The laboratory provides leading materials,technological pr...Overview Shenzhen Key Laboratory of Organic Optoelectromagnetic Functional Materials was established in 2014 and is located at the University Town of Shenzhen.The laboratory provides leading materials,technological process and equipment supports in organic electronics research,including the synthesis of functional organic small molecules and polymers,design and fabrication of organic electronic devices,and the application demonstration of organic electronics.展开更多
Supramolecular chemistry during the synthesis of carbon-nitrogen-based materials has recently experienced a renaissance in the arena of photocatalysis and electrocatalysis.In this review,we start with the discussion o...Supramolecular chemistry during the synthesis of carbon-nitrogen-based materials has recently experienced a renaissance in the arena of photocatalysis and electrocatalysis.In this review,we start with the discussion of supramolecular assemblies-derived carbon-nitrogen-based materials’regulation from the aspect of morphology,chemical composition,and micro/nanostructural control.Afterwards the recent advances of these materials in energy and environment related applications,including degradation of pollutants,water splitting,oxygen reduction reactions,CO_(2) reduction reactions along with organic synthesis are summarized.The correlations between the structural features and physicochemical properties of the carbonnitrogen-based materials and the specific catalytic activity are discussed in depth.By highlighting the opportunities and challenges of supramolecular assembly strategies,we attempt an outlook on possible future developments for highly efficient carbon-based photo/electrocatalysts.展开更多
In recent years,photochromic(PC)materials have garnered widespread interest due to their potential applications in next-generation optical storage devices and photocatalysis.These materials,which control luminescence ...In recent years,photochromic(PC)materials have garnered widespread interest due to their potential applications in next-generation optical storage devices and photocatalysis.These materials,which control luminescence intensity via PC reactions,are not only suitable for optical switches and information storage but also play a crucial role in enhancing catalytic efficiency in photocatalytic applications.However,quantifying the PC effect on performance in these applications is challenging,complicating the material design needed to meet performance specifications.This study reports on a multifunctional Na_(0.5)Bi_(4.5)Ti_(4)O_(15)(NBT)material that achieves adjustable photoluminescence(PL)and photocatalytic(PCA)performance through precise control of the PC reaction.Under alternating exposure to 405 nm light and thermal annealing,the Er/Yb co-doped NBT samples display remarkable photochromic(PC)behavior,capable of reversible color transitions between yellow and gray.After 30 s of 405 nm irradiation,strong energy transfer facilitates a high up-conversion(UC)luminescence contrast of 78.02%.Additionally,the PC reaction promotes the ideal separation of photoexcited carriers and significantly enhances the utilization of electron-hole pairs,nearly doubling the PCA efficiency of the NBT samples by 1.9 times.Furthermore,the luminescence contrast and PCA efficiency controlled by PC can be regulated through varying Er/Yb doping levels,maintaining consistent trends.This study provides theoretical and experimental foundations for the performance modulation of rare-earth-doped multifunctional photochromic materials.展开更多
The practical application of aqueous zinc-ion batteries(AZIBs)is primarily constrained by issues such as corrosion,zinc dendrite formation,and the hydrogen evolution reaction occurring at the zinc metal anode.To overc...The practical application of aqueous zinc-ion batteries(AZIBs)is primarily constrained by issues such as corrosion,zinc dendrite formation,and the hydrogen evolution reaction occurring at the zinc metal anode.To overcome these challenges,strategies for optimizing the electrolyte are crucial for enhancing the stability of the zinc anode.Inspired by the role of hemoglobin in blood cells,which facilitates oxygen transport during human respiration,an innovative inorganic colloidal electrolyte has been developed:calcium silicate-ZnSO_(4)(denoted as CS-ZSO).This electrolyte operates in weak acidic environment and releases calcium ions,which participate in homotopic substitution with zinc ions,while the solvation environment of hydrated zinc ions in the electrolyte is regulated.The reduced energy barrier for the transfer of zinc ions and the energy barrier for the desolvation of hydrated ions imply faster ion transfer kinetics and accelerated desolvation processes,thus favoring the mass transfer process.Furthermore,the silicate colloidal particles act as lubricants,improving the transfer of zinc ions.Together,these factors contribute to the more uniform concentration of zinc ions at the electrode/electrolyte interface,effectively inhibiting zinc dendrite formation and reducing by-product accumulation.The Zn//CS-ZSO//Zn symmetric cell demonstrates stable operation for over 5000 h at 1 mA cm^(-2),representing 29-fold improvement compared to the Zn//ZSO//Zn symmetric cell,which lasts only 170 h.Additionally,the Zn//CS-ZSO//Cu asymmetric cell shows stable average Coulombic efficiency(CE)exceeding 99.6%over2400 cycles,significantly surpassing the performance of the ZSO electrolyte.This modification strategy for electrolytes not only addresses key limitations associated with zinc anodes but also provides valuable insights into stabilizing anodes for the advancement of high-performance aqueous zinc-ion energy storage systems.展开更多
基金financially supported by the National Key R&D Program of China(No.2021YFB3802800)the National Natural Science Foundation of China(Nos.52222104,12261160364,51871120,51520105001,22275089,52071157,52231005,52201174,52171165,52261033,52371155,51801128,52171219,U20A20278,52371106,22071221,52122408,52201190,22075014,52272040,62222405,22125602,and 52301052)+11 种基金the Natural Science Foundation of Jiangsu Province(Nos.BK20200019,BK20220858 and BK20231458)support by the open research fund of Songshan Lake Materials Laboratory(No.2022SLABFN19)support by Guangdong Basic and Applied Basic Research Foundation(No2024B1515020010)support by Shanxi Province Youth Innovation Team Project(No.22JP042)support by the National Science Fund for Distinguished Young Scholars of China(No.52325102)support by the Large Scientific Facility Open Subject of Songshan Lake,Dongguan,Guangdongsupport by the research institute for Advanced Manufacturing Fund(No.P0046108)support by the Hong Kong RGC general research fund(No.11200623)and CRF project C7074-23Gfinancial support from the Australian Research CouncilHBIS-UQ Innovation Centre for Sustainable Steel projectthe QUT Capacity Building Professor Programsupport by the Fundamental Research Funds for the Central Universities(No.30923010211)。
文摘Owing to their exceptional properties,high-entropy alloys(HEAs)and high-entropy materials have emerged as promising research areas and shown diverse applications.Here,the recent advances in the field are comprehensively reviewed,organized into five sections.The first section introduces the background of HEAs,covering their definition,significance,application prospects,basic properties,design principles,and microstructure.The subsequent section focuses on cutting-edge high-entropy structural materials,highlighting developments such as nanostructured alloys,grain boundary engineering,eutectic systems,cryogenic alloys,thin films,micro-nano-lattice structures,additive manufacturing,high entropy metallic glasses,nano-precipitate strengthened alloys,composition modulation,alloy fibers,and refractory systems.In the following section,the emphasis shifts to functional materials,exploring HEAs as catalysts,magneto-caloric materials,corrosion-resistant alloys,radiation-resistant alloys,hydrogen storage systems,and materials for biomedicine.Additionally,the review encompasses functional high-entropy materials outside the realm of alloys,including thermoelectric,quantum dots,nanooxide catalysts,energy storage materials,negative thermal expansion ceramics,and high-entropy wave absorption materials.The paper concludes with an outlook,discussing future directions and potential growth areas in the field.Through this comprehensive review,researchers,engineers,and scientists may gain valuable insights into the recent progress and opportunities for further exploration in the exciting domains of high-entropy alloys and functional materials.
文摘The massive distribution of microplastics(MPs)and even nanoplastics(NPs),which resulted from the wide utilization and mismanagement of plastics,exerted serious risk and threat to ecosystem and human health due to their physical damages and chemical toxicity.
基金supported by the CAS Project for Young Scientists in Basic Research(YSBR-024)the National Key Research and Development Program of China(2021YFB3601502)+4 种基金the Key Research Program of Frontier Sciences,Chinese Academy of Sciences(ZDBS-LY-SLH035)the National Natural Science Foundation of China(22193044,22361132544)the Strategic Priority Research Program of the Chinese Academy of Sciences(XDB0880000)the Tianshan Basic Research Talents(2022TSYCJU0001)the Xinjiang Major Science and Technology Project(2021A01001)。
文摘Nonlinear optical/birefringent crystals as important optical functional materials have been widely applied in optical communication,laser information processing,and laser polarization technology.In recent decades,hydroxyborates,fluorooxoborates and hydroxyfluorooxoborates have attracted significant interest as key branches of the borate family because of their outstanding(deep-)ultraviolet nonlinear optics or other optical functional performances.Negatively charged terminal groups OH^(-)and F^(-)can regulate the structure and the material characteristics.OH^(-)and F^(-)have the same valence and both appear in the terminal position of the anionic framework,which can be substituted by each other theoretically.However,it is found that the introduction of OH^(-)and F^(-)is apparently different in structure and properties.In this mini-review,a variety of theoretical and experimental characterization methods to identify OH^(-)and F^(-)was discussed.The different role of OH^(-)and F^(-)in involved systems'microstructures and macro-properties including nonlinear optics was comprehensively analyzed.We aim to provide guidance for designing and synthesizing novel materials with balanced properties used in deep-ultraviolet applications.
基金supported by the Guangdong Basic and Applied Basic Research Fund Project(2022A1515140061,No.11000-2344014)Startup Foundation for Postdoctor by Dongguan University of Technology(No.11000-221110149)the High-level Talents Program(contract number 2023JC10L014)of the Department of Science and Technology of Guangdong Province。
文摘High entropy materials(HEMs)are the promising electrocatalysts for anion exchange membrane electrolyser(AEMs)and proton exchange membrane fuel cells(PEMFCs)due to the intriguing cocktail effect,wide design space,tailorable electronic structure,and entropy stabilization effect.The precise fabrication of HEMs with functional nanostructures provides a crucial avenue to optimize the adsorption strength and catalytic activity for electrocatalysis.This review comprehensively summarizes the development of HEMs,focusing on the principles and strategies of structural design,and the catalytic mechanism towards hydrogen evolution reaction,oxygen evolution reaction and oxygen reduction reaction for the development of high-performance electrocatalysts.The complexity inherent in the interactions between different elements,the changes in the d-band center and the Gibbs free energies during the catalytic progress,as well as the coordination environment of the active sites associated with the unique crystal structure to improve the catalytic performance are discussed.We also provide a perspective on the challenges and future development direction of HEMs in electrocatalysis.This review will contribute to the design and development of HEMs-based catalysts for the next generation of electrochemical applications.
基金supported by the National Natural Science Foundation of China(Nos.62275101 and 22075101)the Program for the Development of Science and Technology of Jilin Province(No.YDZJ202201ZYTS300).
文摘Enhancing the photovoltaic performance of perovskite solar cells(PSCs)via the strategy of spectral conversion garners significant attention in recent years.However,developing a spectral conversion layer with excellent stability and low series resistance remains challenging.Here,we propose a spectral conversion material termed perylenetetracarboxylic diimide functionalized CsPbCl_(3):Mn^(2+)quantum dots(CMI),which is incorporated at the SnO_(2)/perovskite interface as a down-conversion layer.This innovation effectively resolves the trade-off between spectral conversion efficiency and electrical performance of the spectral conversion layer.CMI converts ultraviolet light into visible light that is more readily absorbed by the perovskite,thus enhancing the light utilization and reducing the ultraviolet-induced degradation of perovskites.The rough and hydrophobic surface of CMI can modulate nucleation site arrangement and enhance grain boundary mobility,resulting in perovskite films with larger and denser grains.Furthermore,the C=O groups in CMI simultaneously passivate the oxygen vacancies in SnO_(2)and the Pb^(2+)dangling bonds at the buried interface of the perovskite,reducing recombination losses and facilitating charge carrier transfer and extraction,and further enhancing power conversion efficiency(PCE).Consequently,the PSCs incorporating CMI as a down-conversion layer achieve an improved PCE,which rises from 21.26%to 23.61%,along with enhanced stability.
基金Supported by the National Natural Science Foundation of China(Nos.52293472,22473096 and 22471164)。
文摘Among various architectures of polymers,end-group-free rings have attracted growing interests due to their distinct physicochemical performances over the linear counterparts which are exemplified by reduced hydrodynamic size and slower degradation.It is key to develop facile methods to large-scale synthesis of polymer rings with tunable compositions and microstructures.Recent progresses in large-scale synthesis of polymer rings against single-chain dynamic nanoparticles,and the example applications in synchronous enhancing toughness and strength of polymer nanocomposites are summarized.Once there is the breakthrough in rational design and effective large-scale synthesis of polymer rings and their functional derivatives,a family of cyclic functional hybrids would be available,thus providing a new paradigm in developing polymer science and engineering.
基金financially supported by the Fundamental Research Funds for the Central Universities(No.FRF-KST-25-001)the Beijing Natural Science Foundation(No.L253029)。
文摘In the context of the global energy low-carbon transition,phase change energy storage technology becomes a key technology to solve the problem of intermittent renewable energy.Oriented phase change composites(OCPCMs)receive widespread attention in practical energy storage applications due to their unique oriented thermally conductive structure,which achieves significant thermal conductivity enhancement in specific directions while retaining the high energy storage capacity of the phase change components.This review systematically summarizes the overall analysis of OCPCMs from synthesis and preparation to application scenarios in recent years.Herein,we introduce the analysis of the heat transfer mechanism of the materials and explore the advantages of the oriented structure in OCPCMs in the heat transfer behavior from a bionic perspective.We then focus on summarizing and generalizing the methods for preparing OCPCMs,giving suggestions for suitable methods according to different scenarios.Besides,we discuss the application of finite element simulation methods to the monitoring of the thermal management behavior of OCPCMs,and look into the potential future application areas of such materials.Finally,it is hoped that this review will provide guidance for the academic community in developing high-performance OCPCMs.
基金supported by the National Natural Science Foundation of China(no.52574348)the Natural Science Foundation of Hebei Province(no.B2024501004)+2 种基金the Fundamental Research Funds for the Central Universities(no.N2423013)the Shijiazhuang Basic Research Project(no.241790667A)the Performance Subsidy Fund for Key Laboratory of Dielectric and Electrolyte Functional Material Hebei Province(no.22567627H).
文摘NASICON-type Na_(3)V_(2)(PO_(4))_(3)(NVP)materials are seen as highly promising cathode materials in the field of sodium-ion batteries due to their low cost,a solid three-dimensional skeleton and good theoretical capacity,as well as high ionic conductivity.Nevertheless,the problem of low intrinsic electronic conductivity and energy density has limited the practical application of the materials.To address this issue,the relevant research team has successfully achieved remarkable research results through unremitting exploration and practical innovation.In this work,the crystal structure,ion migration mechanism and sodium storage mechanism of NVP cathode materials are systematically reviewed,with a focus on summarizing the latest progress of V-site doping modification research,classifying and exploring V-site doping from the perspectives of electronic structure,lattice strain and entropy,and briefly describing the optimization mechanism of V-site doping on electrochemical performance.In addition,the challenges and prospects for the future development of NVP cathode materials are presented,which are believed to provide new thinking for the design and development of high-performance NVP cathode materials and contribute to the large-scale application of sodium-ion batteries.
基金supported by Beijing Innovation Consortium of Agriculture Research System(No.BAIC01).
文摘The preparation of a novel nanoscale imazalil(IMZ)-based coordination polymer[Zn(HBTC)(IMZ)_(2)]_(n)(PDCP1)(H_(3)BTC=1,3,5-benzenetricarboxylic acid),and its antifungal application within a sustainable delivery system was reported.The intermolecular interactions presented in the structure,and their contributions to crystal packing were studied by Hirshfeld,Fingerprint plot and Mayer bond order.The obtained PDCP1 had a relativelyhigh loadingrate of IMZ(68.5%).PDCP1 exhibitednotable antifungal activities againstColletotrichum gloeosporioides,Magnaporthe Oryzae,and Alternaria Nees strains,with EC_(50) values of 0.72,0.92,and 0.56μg/mL,respectively.The key benefits of the application of PDCP1 as a control release pesticide include high fungicide loading and offer nearly complete release,pH-responsive release,enhanced UV stability,exhibits favorable biosafety profiles.The remarkable inhibition of C.gloeosporioides growth by PDCP1 underscores a promising strategy for agrochemical material development,high loading of active ingredients and readily delivery fosters more efficient pesticides utilization in agricultural processes.
基金supported by the introduction of Talent Research Fund in Nanjing Institute of Technology(YKJ202204)the National Natural Science Foundation of China(52401282 and 52300206)the Natural Science Foundation of Jiangsu Province(BK20230701 and BK20230705).
文摘Achieving high-energy density remains a key objective for advanced energy storage systems.However,challenges,such as poor cathode conductivity,anode dendrite formation,polysulfide shuttling,and electrolyte degradation,continue to limit performance and stability.Molecular and ionic dipole interactions have emerged as an effective strategy to address these issues by regulating ionic transport,modulating solvation structures,optimizing interfacial chemistry,and enhancing charge transfer kinetics.These interactions also stabilize electrode interfaces,suppress side reactions,and mitigate anode corrosion,collectively improving the durability of high-energy batteries.A deeper understanding of these mechanisms is essential to guide the design of next-generation battery materials.Herein,this review summarizes the development,classification,and advantages of dipole interactions in high-energy batteries.The roles of dipoles,including facilitating ion transport,controlling solvation dynamics,stabilizing the electric double layer,optimizing solid electrolyte interphase and cathode–electrolyte interface layers,and inhibiting parasitic reactions—are comprehensively discussed.Finally,perspectives on future research directions are proposed to advance dipole-enabled strategies for high-performance energy storage.This review aims to provide insights into the rational design of dipole-interactive systems and promote the progress of electrochemical energy storage technologies.
基金financially supported by the Zhejiang Provincial Natural Science Foundation of China(LMS25E030001)the Fundamental Research Funds of Zhejiang Sci-Tech University(25212142-Y and 23212200-Y)。
文摘The development of high-performance bifunctional electrocatalysts is crucial for advancing zinc-air batteries.However,the fundamentally distinct mechanisms of the oxygen reduction and evolution reactions(ORR/OER)hinder the simultaneous realization of high activity within a single catalyst.Herein,we propose a spatial decoupling strategy to overcome this limitation by engineering isolated Fe singleatoms and Fe-Ir dual-atom pairs on a nitrogen-doped carbon matrix(Fe/FeIr-NC).In this architecture,Fe single atoms serve as ORR centers,while Fe-Ir pairs with tunable spacing are tailored for OER,enabling complete functional separation and independent optimization of the reactions.As a result,the catalyst delivers an ORR half-wave potential of 0.91 V and an OER overpotential of 250 mV at 10 mA cm^(-2),yielding a record-low bifunctional gap(ΔE=0.57 V)that outperforms all reported single-and dual-atom catalysts.A flexible fiber zincair battery was developed based on this catalyst,delivering a peak power density of 3920 W kg^(-1),along with a 1.4-fold increase in energy efficiency and a 2.6-fold extension in cycle life compared to the commercial Pt/C+IrO_(2)benchmark.This work not only breaks the traditional activity trade-off in bifunctional catalysis but also offers a promising route toward high-performance power sources for wearable electronics.
基金supported by the National Natural Science Foundation of China(U24A20550,52273264 and 52470073)the Key Project of the Heilongjiang Provincial Natural Science Foundation(ZD2024B001)Outstanding Youth Fund of Heilongjiang Province(JQ2022E005).
文摘Designing a heterogeneous interface to improve the kinetics of electrocatalysts represents an effective yet challenging approach for enhancing the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER).Herein,a simple MOF-assisted etching-pyrolysis strategy is proposed to fabricate an advanced Mott-Schottky(M–S)electrocatalyst composed of Co/CeO_(2)hetero-nanoparticles embedded within N-doped hollow carbon nanoboxes(H-Co/CeO_(2)@NCBs).Notably,the interfacial Co–O–Ce bond bridging productively facilitates the electron transfer and modulates the charge distribution of the active center,thereby contributing to the ORR/OER kinetics.As expected,the optimal M–S H-Co/CeO_(2)@NCBs catalyst exhibits promising bifunctional electrocatalytic activity with a small potential discrepancy of 0.65 V.Theoretical calculations reveal that the built-in electric field in the M–S heterojunction promotes electron transfer in oxygen electrocatalysis and the interfacial bridge-induced electron redistribution optimizes the adsorption/desorption of the oxygen intermediates,leading to reduced activation energy for the bifunctional ORR/OER reactions.Importantly,H-Co/CeO_(2)@NCBs-assembled Zn-air battery(ZAB)delivers high power density(179.8 mW cm^(−2))and long-term stability(400 h).Furthermore,the assembled flexible solid-state ZAB with H-Co/CeO_(2)@NCBs cathode also exhibits excellent charge–discharge reversibility and flexibility at various bending angles.This work provides a novel perspective on developing efficient and stable M–S bifunctional oxygen electrocatalysts.
基金supported by the Russian Science Foundation(No.22-13-00035)the National Outstanding Young Scientists Fund(No.52125002)+14 种基金the National Key Research and Development Program of China(Nos.2023YFC3904800 and 2022YFB4002501)the National Natural Science Foundation of China(Nos.52400228,52300139,22308063,52103340,U22A20418,22578302,52202208,52400163,52205054,22075171,52177214,22405201,52371072,52171078,52377218)the Key Research and Development Project of Science and Technology Department of Zhejiang Province(No.2024C03284(SD2))the Research Development Fund of Zhejiang A&F University(No.2024LFR042)the President Research Funds from Xiamen University(No.ZK1111)Nanqiang Youth Scholar program of Xiamen University,the Young Elite Scientists Sponsorship Program by CAST(No.2023QNRC001)Natural Science Foundation of Xiamen(No.3502z202471037)Open Fund of the State Environmental Protection Key Laboratory of Urban Air Particulate Matter Pollution Prevention and Control,College of Environmental Science and Engineering,Nankai University(No.NKPMLF202409)the Key Project of Research and Development Plan of Jiangxi Province(No.20243BBI91001)Natural Science Foundation of Shanghai(No.23ZR1423400)the Postdoctoral Science Research Program of Shaanxi(No.2023BSHEDzZ159)Xidian University Specially Funded Project for Interdisciplinary Exploration(No.TZJH2024062)the Open Project of Yunnan Precious Metals Laboratory Co.,Ltd.(No.YPML-20240502058)the Fundamental Research Program of Shanxi Province(No.202303021212159)the Natural Science Foundation of Shanxi Normal University(No.JCYJ2024017).
文摘Sustainable development for our life is important task,which is driven by key materials and technologies.In this roadmap,we discuss three main aspects in addressing environmental questions,green chemical processes and energy challenges.They are included,such as gas treatment and separation,wastewater treatment,waste gas treatment,solid waste treatment,lithium extraction,hydrogen production,water splitting,CO_(2) reduction,photocatalytic clean technologies,plastic degradation,fuel cells,lithium batteries,sodium batteries,aqueous batteries,solid state batteries,metal air batteries and supercapacitors.Their status,challenges,progress and future perspectives are also discussed.We hope that this paper can give clear views on sustainable development in materials and technologies.
基金financially supported by the National Natural Science Foundation of China(Nos.21601094 and 21401139)the Natural Science Foundation of Tianjin City(Nos.15JCQNJC02900 and 18JCQNJC73900)Tianjin Municipal Education Commission(No.2018KJ130)。
文摘Issues like morphology control and further multifunctional applications are of significant importance for rare earth nano-oxides,e.g.,cerium dioxide(CeO_(2))nanostructures,however,relevant results in this respect are rather limited up to now.In the present work,ultrathin CeO_(2)nanosheets were synthesized through a facile lowtemperature hydrothermal method.The structure,morphology and specific surface area of these CeO_(2)nanosheets were characterized by X-ray diffraction(XRD),field emission scanning electron microscope(FESEM)and N2 adsorption-desorption.Significantly,CeO_(2)nanosheets have the potential as bifunctional sensing materials to detect both humidity and formaldehyde vapor.The CeO_(2)nanosheet humidity sensor exhibited excellent sensing characteristics in the relative humidity range of 11%-97%with the response value as high as 3.1×10^(4).Meanwhile,the CeO_(2)nanosheet gas sensor showed superior sensitivity and repeatability with fast response/recovery speed toward formaldehyde vapor at 300℃.Finally,the humidity and formaldehyde sensing mechanism were discussed as well.
基金This study was supported by the National Science Foundation for Excellent Young Scholar(51722403)National Natural Science Foundation of China(51771134)+2 种基金Tianjin Natural Science Foundation for Distinguished Young Scholar(18JCJQJC46500)National Natural Science Foundation of China and Guangdong Province(U1601216)the National Youth Talent Support Program.
文摘Rechargeable zinc-air batteries(ZABs)have attracted much attention as the next-generation energy conversion and storage devices due to the abundance and environmental friendliness of zinc(Zn)for anode materials,as well as the safety and low cost of aqueous electrolytes.However,rational design of nonprecious and low-cost integrated air cathode materials with a desirable bifunctional oxygen electrocatalytic performance remains a great challenge for the commercialization of rechargeable ZABs.In previous research studies,various cost-effective carbon-supported electrocatalysts and light-weight carbon-based current collectors for air cathodes have been developed,showing vast potential in the application of carbon-based materials.To improve the bifunctional performance and integration of air cathodes,efforts with respect to the design of morphology,defects,and synergistic effects of carbon-based materials have been made.In this perspective,the general understanding of the air cathode construction and the battery working mechanism is discussed.The recent progress in the design of carbon-based materials for air cathodes in rechargeable ZABs is summarized.Several possible future research directions and the expected development trends are also discussed,aiming to facilitate the commercialization of advanced rechargeable ZABs in our life.
文摘Overview Shenzhen Key Laboratory of Organic Optoelectromagnetic Functional Materials was established in 2014 and is located at the University Town of Shenzhen.The laboratory provides leading materials,technological process and equipment supports in organic electronics research,including the synthesis of functional organic small molecules and polymers,design and fabrication of organic electronic devices,and the application demonstration of organic electronics.
基金This work was supported by the National Natural Science Foundation of China(52125202,21908110,U2004209)the Natural Science Foundation of Jiangsu Province(BK20190479)the Fundamental Research Funds for the Central Universities(30922010707).
文摘Supramolecular chemistry during the synthesis of carbon-nitrogen-based materials has recently experienced a renaissance in the arena of photocatalysis and electrocatalysis.In this review,we start with the discussion of supramolecular assemblies-derived carbon-nitrogen-based materials’regulation from the aspect of morphology,chemical composition,and micro/nanostructural control.Afterwards the recent advances of these materials in energy and environment related applications,including degradation of pollutants,water splitting,oxygen reduction reactions,CO_(2) reduction reactions along with organic synthesis are summarized.The correlations between the structural features and physicochemical properties of the carbonnitrogen-based materials and the specific catalytic activity are discussed in depth.By highlighting the opportunities and challenges of supramolecular assembly strategies,we attempt an outlook on possible future developments for highly efficient carbon-based photo/electrocatalysts.
基金Project supported by the Jiangsu Province Graduate Research and Innovation Program(KYCX24_0329)。
文摘In recent years,photochromic(PC)materials have garnered widespread interest due to their potential applications in next-generation optical storage devices and photocatalysis.These materials,which control luminescence intensity via PC reactions,are not only suitable for optical switches and information storage but also play a crucial role in enhancing catalytic efficiency in photocatalytic applications.However,quantifying the PC effect on performance in these applications is challenging,complicating the material design needed to meet performance specifications.This study reports on a multifunctional Na_(0.5)Bi_(4.5)Ti_(4)O_(15)(NBT)material that achieves adjustable photoluminescence(PL)and photocatalytic(PCA)performance through precise control of the PC reaction.Under alternating exposure to 405 nm light and thermal annealing,the Er/Yb co-doped NBT samples display remarkable photochromic(PC)behavior,capable of reversible color transitions between yellow and gray.After 30 s of 405 nm irradiation,strong energy transfer facilitates a high up-conversion(UC)luminescence contrast of 78.02%.Additionally,the PC reaction promotes the ideal separation of photoexcited carriers and significantly enhances the utilization of electron-hole pairs,nearly doubling the PCA efficiency of the NBT samples by 1.9 times.Furthermore,the luminescence contrast and PCA efficiency controlled by PC can be regulated through varying Er/Yb doping levels,maintaining consistent trends.This study provides theoretical and experimental foundations for the performance modulation of rare-earth-doped multifunctional photochromic materials.
基金the Doctoral Research Start-up Fund of Hubei University of Science and Technology(BK202504)the Natural Science Foundation of Liaoning Province(2023-MS-115)。
文摘The practical application of aqueous zinc-ion batteries(AZIBs)is primarily constrained by issues such as corrosion,zinc dendrite formation,and the hydrogen evolution reaction occurring at the zinc metal anode.To overcome these challenges,strategies for optimizing the electrolyte are crucial for enhancing the stability of the zinc anode.Inspired by the role of hemoglobin in blood cells,which facilitates oxygen transport during human respiration,an innovative inorganic colloidal electrolyte has been developed:calcium silicate-ZnSO_(4)(denoted as CS-ZSO).This electrolyte operates in weak acidic environment and releases calcium ions,which participate in homotopic substitution with zinc ions,while the solvation environment of hydrated zinc ions in the electrolyte is regulated.The reduced energy barrier for the transfer of zinc ions and the energy barrier for the desolvation of hydrated ions imply faster ion transfer kinetics and accelerated desolvation processes,thus favoring the mass transfer process.Furthermore,the silicate colloidal particles act as lubricants,improving the transfer of zinc ions.Together,these factors contribute to the more uniform concentration of zinc ions at the electrode/electrolyte interface,effectively inhibiting zinc dendrite formation and reducing by-product accumulation.The Zn//CS-ZSO//Zn symmetric cell demonstrates stable operation for over 5000 h at 1 mA cm^(-2),representing 29-fold improvement compared to the Zn//ZSO//Zn symmetric cell,which lasts only 170 h.Additionally,the Zn//CS-ZSO//Cu asymmetric cell shows stable average Coulombic efficiency(CE)exceeding 99.6%over2400 cycles,significantly surpassing the performance of the ZSO electrolyte.This modification strategy for electrolytes not only addresses key limitations associated with zinc anodes but also provides valuable insights into stabilizing anodes for the advancement of high-performance aqueous zinc-ion energy storage systems.
