Low-concentration coal mine methane(LC-CMM),which is predominantly composed of methane,serves as a clean and low-carbon energy resource with significant potential for utilization.Utilizing LC-CMM as fuel for solid oxi...Low-concentration coal mine methane(LC-CMM),which is predominantly composed of methane,serves as a clean and low-carbon energy resource with significant potential for utilization.Utilizing LC-CMM as fuel for solid oxide fuel cells(SOFCs)represents an efficient and promising strategy for its effective utilization.However,direct application in Ni-based anodes induces carbon deposition,which severely degrades cell performance.Herein,a medium-entropy oxide Sr_(2)FeNi_(0.1)Cr_(0.3)Mn_(0.3)Mo_(0.3)O_(6−δ)(SFNCMM)was developed as an anode internal reforming catalyst.Following reduction treatment,FeNi_(3) nano-alloy particles precipitate on the surface of the material,thereby significantly enhancing its catalytic activity for LC-CMM reforming process.The catalyst achieved a methane conversion rate of 53.3%,demonstrating excellent catalytic performance.Electrochemical evaluations revealed that SFNCMM-Gd_(0.1)Ce_(0.9)O_(2−δ)(GDC)with a weight ratio of 7:3 exhibited superior electrochemical performance when employed as the anodic catalytic layer.With H_(2) and LC-CMM as fuels,the single cell achieved maximum power densities of 1467.32 and 1116.97 mW·cm^(−2) at 800℃,respectively,with corresponding polarization impedances of 0.17 and 1.35Ω·cm^(2).Furthermore,the single cell maintained stable operation for over 100 h under LC-CMM fueling without significant carbon deposition,confirming its robust resistance to carbon formation.These results underscore the potential of medium-entropy oxides as highly effective catalytic layers for mitigating carbon deposition in SOFCs.展开更多
Developing highly active and stable air electrodes remains challenging for reversible solid oxide cells(R-SOCs).Herein,we re-port an A-site high-entropy engineered perovskite oxide,La_(0.2)Pr_(0.2)Nd_(0.2)Ba_(0.2)Sr_(...Developing highly active and stable air electrodes remains challenging for reversible solid oxide cells(R-SOCs).Herein,we re-port an A-site high-entropy engineered perovskite oxide,La_(0.2)Pr_(0.2)Nd_(0.2)Ba_(0.2)Sr_(0.2)Co_(0.8)Fe_(0.2)O_(3−δ)(HE-LSCF),and its electrocatalytic activity and stability property are systematically probed for tubular R-SOCs.The HE-LSCF air electrode exhibits excellent oxygen reduction reac-tion(ORR)activity with a low polarization resistance of 0.042Ω·cm^(2)at 700℃,which is much lower than that of La0.6Sr0.4Co_(0.8)Fe_(0.2)O_(3−δ)(LSCF),indicating the excellent catalytic activity of HE-LSCF.Meanwhile,the tubular R-SOCs with HE-LSCF shows a high peak power density of 1.18 W·cm^(−2)in the fuel cell mode and a promising electrolysis current density of−0.52 A·cm^(−2)at 1.5 V in the electrolysis mode with H_(2)(~10%H_(2)O)atmosphere at 700℃.More importantly,the tubular R-SOCs with HE-LSCF shows favorable stability under 180 h reversible cycling test.Our results show the high-entropy design can significantly enhance the activity and robustness of LSCF electrode for tubular R-SOCs.展开更多
Foreword It is our great privilege,as vip Editors of the International Journal of Minerals,Metallurgy and Materials(IJMMM),to present this special issue on“High-Entropy and Multicomponent-Doped Materials for Energy...Foreword It is our great privilege,as vip Editors of the International Journal of Minerals,Metallurgy and Materials(IJMMM),to present this special issue on“High-Entropy and Multicomponent-Doped Materials for Energy Applications:Innovations in Energy Conversion and Storage.”This collection highlights the latest research developments in the preparation,optimizing properties,and exploring potential applications of high-entropy materials(HEMs)and other com-pounds with increased configurational entropy.展开更多
Solid oxide cells(SOCs)have attracted great attention in the past decades because of their high conversion efficiency,low environmental pollution and diversified fuel options.Nickel-based catalysts are the most widely...Solid oxide cells(SOCs)have attracted great attention in the past decades because of their high conversion efficiency,low environmental pollution and diversified fuel options.Nickel-based catalysts are the most widely used fuel electrode materials for SOCs due to the low price and high activity.However,when hydrocarbon fuels are employed,nickel-based electrodes face serious carbon deposition challenges,leading to a rapid decline of cell performance.Great efforts have been devoted to understanding the occurrence of the coking reaction,and to improving the stability of the electrodes in hydrocarbon fuels.In this review,we summarize recent research progress of utilizing surface modification to improve the stability and activity of Ni-based electrodes for SOCs by preventing carbon coking.The review starts with a briefly introduction about the reaction mechanism of carbon deposition,followed by listing several surface modification technologies and their working principles.Then we introduce representative works using surface modification strategies to prevent carbon coking on Ni-based electrodes.Finally,we highlight future direction of improving electrode catalytic activity and anti-coking performance through surface engineering.展开更多
Protonic ceramic energy devices represent a promising frontier for sustainable energy conversion and storage,operating efficiently at intermediate temperatures(350-650℃)and facilitating integration with renewable ene...Protonic ceramic energy devices represent a promising frontier for sustainable energy conversion and storage,operating efficiently at intermediate temperatures(350-650℃)and facilitating integration with renewable energy sources.Among protonic ceramic materials,yttrium-doped barium zirconate(BaZr_(1-x)Y_(x)O_(3-δ),BZY)stands out for its competitive proton conductivity,chemical resilience,and compatibility with diverse fuels and environments.This review critically examines the fundamentals and multiscale design strategies for BZY-based ceramic cells.We discuss atomic-level composition-structure relationships,innovative synthesis routes,and advanced processing methods to overcome manufacturing and scalability challenges.We then highlight microstructure engineering and interface design approaches that minimize resistance and elevate device performance,supported by state-of-the-art characterization and predictive modeling techniques,including density functional theory and machine learning.Recent advances,such as hybrid architectures and AI-driven defect optimization,demonstrate significant improvements in conductivity,stability,and Faradaic efficiency,confirming BZY's pivotal role in green hydrogen production and power-to-chemicals applications.By integrating insights across materials chemistry,electrochemistry,and engineering,this review provides a comprehensive roadmap for researchers aiming to translate laboratory breakthroughs into robust,scalable protonic ceramic technologies for decarbonized energy systems.展开更多
Hydrocarbon fuels have the advantages of being low-cost,easy to store and transport,and can be converted into biomass gas through oxidation and reforming processes,further increasing their potential applications.Howev...Hydrocarbon fuels have the advantages of being low-cost,easy to store and transport,and can be converted into biomass gas through oxidation and reforming processes,further increasing their potential applications.However,incomplete reforming and carbon deposition under practical conditions hinder the utilization of hydrocarbon fuels.In this work,Ni_(0.1)Fe_(0.1)Ce_(0.8)O_(2−δ)(NFCO)is employed as the anode reforming catalyst for tubular solid oxide fuel cells(T-SOFCs)with low-concentration ethanol-carbon dioxide fuel.With the in situ-formed NiFe alloy,the T-SOFC with NFCO achieves peak power densities of 538,614,and 608 mW·cm^(−2)in 5%,10%,and 15%ethanol,respectively,which are higher than those of the cell without NFCO.More importantly,no significant degradation is observed during long-term operation.As confirmed by density functional theory(DFT)calculations,the introduction of a NiFe alloy on the basis of CeO_(2)significantly improved the adsorption energy of H2O,thereby increasing the adsorption capacity of water molecules and promoting the adsorption and conversion of ethanol fuel.The results indicate that the heterostructure between the NiFe alloy and high-oxygen-vacancy CeO_(2)enhances the anode catalytic activity and inhibits the carbon deposition of T-SOFCs under low-concentration ethanol-carbon dioxide fuel,providing important insights for the development of high-performance,carbon-tolerant T-SOFCs under direct hydrocarbon fuel.展开更多
New two-layer Ruddlesden-Popper(RP)oxide La_(0.25)Sr_(2.75)FeNiO_(7-δ)(LSFN)in the combination of Sr_(3)Fe_(2)O_(7-δ) and La_(3)Ni_(2)O_(7-δ) was successfully synthesized and studied as the potential active single-...New two-layer Ruddlesden-Popper(RP)oxide La_(0.25)Sr_(2.75)FeNiO_(7-δ)(LSFN)in the combination of Sr_(3)Fe_(2)O_(7-δ) and La_(3)Ni_(2)O_(7-δ) was successfully synthesized and studied as the potential active single-phase and composite cathode for protonic ceramics fuel cells(PCFCs).LSFN with the tetragonal symmetrical structure(IMmmm)is confinned,and the co-existence of Fe^(3+)/Fe^(4+) and Ni^(3+)/Ni^(2+) couples is demonstrated by X-ray photoelectron spectrometer(XPS)analysis.The LSFN conductivity is apparently enhanced after Ni doping in Fe-site,and nearly three times those of Sr_(3)Fe_(2)O_(7-δ),which is directly related to the carrier concentration and conductor mechanism.Importantly,anode supported PCFCs using LSFN-BaZr_(0.1)Ce_(0.7)Y_(0.2)O_(3-δ)(LSFN-BZCY)composite cathode achieved high power density(426 mW·cm^(-2) at 650℃)and low electrode interface polarization resistance(0.26Ω·cm^(2)).Besides,distribution of relaxation time(DRT)function technology was further used to analyse the electrode polarization processes.The observed three peaks(Pl,P2,and P3)separated by DRT shifted to the high frequency region with the decreasing temperature,suggesting that the charge transfer at the electrode-electrolyte interfaces becomes more difficult at reduced temperatures.Preliminary results demonstrate that new two-layer RP phase LSFN can be a promising cathode candidate for PCFCs.展开更多
探索具有优异导电性和稳定性的非贵金属电催化剂对氢经济至关重要.本研究将杂原子掺杂和石墨烯包覆相结合,以控制NiCo_(2)S_(4)(NCS)蛋黄壳微球的电子性能,并抵抗酸性介质中H_(2)O和O_(2)的腐蚀.密度泛函理论(DFT)模拟结合综合表征和实...探索具有优异导电性和稳定性的非贵金属电催化剂对氢经济至关重要.本研究将杂原子掺杂和石墨烯包覆相结合,以控制NiCo_(2)S_(4)(NCS)蛋黄壳微球的电子性能,并抵抗酸性介质中H_(2)O和O_(2)的腐蚀.密度泛函理论(DFT)模拟结合综合表征和实验首次揭示了在NCS中引入P杂原子不仅加速了电子从体相向表面的转移动力学,而且降低了掺杂P原子附近活性S位上的析氢反应势垒.利用DFT计算的穿透能垒预测了rGO覆盖层在P掺杂NCS(P-NCS)表面对质子的渗透性和对H_(2)O和O_(2)分子的抵抗性等重要功能,并用X射线光电子能谱对新催化剂和回收催化剂进行了验证.利用P掺杂剂和rGO覆盖层分别辅助电荷传递和质子传递,通过二者的协同作用获得了催化活性和耐久性之间的平衡.因此,优化后的P-NCS/rGO在70 mV的低过电位下实现了10 mA cm^(-2)的电流密度,并具有令人满意的80小时耐用性.本工作阐明了石墨烯覆盖硫化物催化剂可通过调控电子结构和质子/分子穿透提高电催化性能.展开更多
Joule-heating reactors have the higher energy efficiency and product selectivity compared with the reactors based on radiative heating.Current Joule-heating reactors are constructed with electrically-conductive metals...Joule-heating reactors have the higher energy efficiency and product selectivity compared with the reactors based on radiative heating.Current Joule-heating reactors are constructed with electrically-conductive metals or carbon materials,and therefore suffer from stability issue due to the presence of corrosive or oxidizing gases during high-temperature reactions.In this study,chemicallystable and electrically-conductive(La_(0.80)Sr_(0.20))_(0.95)FeO_(3)(LSF)/Gd_(0.1)Ce_(0.9)O_(2)(GDC)ceramics have been used to construct Joule-heating reactors for the first time.Taking the advantage of the resistance decrease of the ceramic reactors with temperature increase,the ceramic reactors heated under current control mode achieved the automatic adjustment of heating to stabilize reactor temperatures.In addition,the electrical resistance of LSF/GDC reactors can be tuned by the content of the highconductive LSF in composite ceramics and ceramic density via sintering temperature,which offers flexibility to control reactor temperatures.The ceramic reactors with dendritic channels(less than 100μm in diameter)showed the catalytic activity for CO oxidation,which was further improved by coating efficient MnO_(2)nanocatalyst on reactor channel wall.The Joule-heating ceramic reactors achieved complete CO oxidation at a low temperature of 165℃.Therefore,robust ceramic reactors have successfully demonstrated effective Joule heating for CO oxidation,which are potentially applied in other high-temperature catalytic reactions.展开更多
基金supported by the National Key R&D Program of China(No.2024YFB4007501)the Natural Science Foundation of Jiangsu Province(No.BK20240109)the project of Jiangsu Key Laboratory for Clean Utilization of Carbon Resources(No.BM2024007).
文摘Low-concentration coal mine methane(LC-CMM),which is predominantly composed of methane,serves as a clean and low-carbon energy resource with significant potential for utilization.Utilizing LC-CMM as fuel for solid oxide fuel cells(SOFCs)represents an efficient and promising strategy for its effective utilization.However,direct application in Ni-based anodes induces carbon deposition,which severely degrades cell performance.Herein,a medium-entropy oxide Sr_(2)FeNi_(0.1)Cr_(0.3)Mn_(0.3)Mo_(0.3)O_(6−δ)(SFNCMM)was developed as an anode internal reforming catalyst.Following reduction treatment,FeNi_(3) nano-alloy particles precipitate on the surface of the material,thereby significantly enhancing its catalytic activity for LC-CMM reforming process.The catalyst achieved a methane conversion rate of 53.3%,demonstrating excellent catalytic performance.Electrochemical evaluations revealed that SFNCMM-Gd_(0.1)Ce_(0.9)O_(2−δ)(GDC)with a weight ratio of 7:3 exhibited superior electrochemical performance when employed as the anodic catalytic layer.With H_(2) and LC-CMM as fuels,the single cell achieved maximum power densities of 1467.32 and 1116.97 mW·cm^(−2) at 800℃,respectively,with corresponding polarization impedances of 0.17 and 1.35Ω·cm^(2).Furthermore,the single cell maintained stable operation for over 100 h under LC-CMM fueling without significant carbon deposition,confirming its robust resistance to carbon formation.These results underscore the potential of medium-entropy oxides as highly effective catalytic layers for mitigating carbon deposition in SOFCs.
基金support provided by the National Key R&D Program of China(No.2024YFE0101500)the National Natural Science Foundation of China(No.52272257)the Natural Science Foundation of Jiangsu Province(No.BK20240109).
文摘Developing highly active and stable air electrodes remains challenging for reversible solid oxide cells(R-SOCs).Herein,we re-port an A-site high-entropy engineered perovskite oxide,La_(0.2)Pr_(0.2)Nd_(0.2)Ba_(0.2)Sr_(0.2)Co_(0.8)Fe_(0.2)O_(3−δ)(HE-LSCF),and its electrocatalytic activity and stability property are systematically probed for tubular R-SOCs.The HE-LSCF air electrode exhibits excellent oxygen reduction reac-tion(ORR)activity with a low polarization resistance of 0.042Ω·cm^(2)at 700℃,which is much lower than that of La0.6Sr0.4Co_(0.8)Fe_(0.2)O_(3−δ)(LSCF),indicating the excellent catalytic activity of HE-LSCF.Meanwhile,the tubular R-SOCs with HE-LSCF shows a high peak power density of 1.18 W·cm^(−2)in the fuel cell mode and a promising electrolysis current density of−0.52 A·cm^(−2)at 1.5 V in the electrolysis mode with H_(2)(~10%H_(2)O)atmosphere at 700℃.More importantly,the tubular R-SOCs with HE-LSCF shows favorable stability under 180 h reversible cycling test.Our results show the high-entropy design can significantly enhance the activity and robustness of LSCF electrode for tubular R-SOCs.
文摘Foreword It is our great privilege,as vip Editors of the International Journal of Minerals,Metallurgy and Materials(IJMMM),to present this special issue on“High-Entropy and Multicomponent-Doped Materials for Energy Applications:Innovations in Energy Conversion and Storage.”This collection highlights the latest research developments in the preparation,optimizing properties,and exploring potential applications of high-entropy materials(HEMs)and other com-pounds with increased configurational entropy.
基金This work was supported by the National Natural Science Foundation of China(91745203)the State Key Laboratory of Pulp and Paper Engineering(2020C01)the Guangdong Pearl River Talent Program(2017GC010281).
文摘Solid oxide cells(SOCs)have attracted great attention in the past decades because of their high conversion efficiency,low environmental pollution and diversified fuel options.Nickel-based catalysts are the most widely used fuel electrode materials for SOCs due to the low price and high activity.However,when hydrocarbon fuels are employed,nickel-based electrodes face serious carbon deposition challenges,leading to a rapid decline of cell performance.Great efforts have been devoted to understanding the occurrence of the coking reaction,and to improving the stability of the electrodes in hydrocarbon fuels.In this review,we summarize recent research progress of utilizing surface modification to improve the stability and activity of Ni-based electrodes for SOCs by preventing carbon coking.The review starts with a briefly introduction about the reaction mechanism of carbon deposition,followed by listing several surface modification technologies and their working principles.Then we introduce representative works using surface modification strategies to prevent carbon coking on Ni-based electrodes.Finally,we highlight future direction of improving electrode catalytic activity and anti-coking performance through surface engineering.
基金supported by the U.S.Department of Energy(USDOE),Office of Energy Efficiency and Renewable Energy(EERE),Hydrogen and Fuel Cell Technologies Office(FCTO)under contract DEEE0011336H.D.would like to thank the startup research grant from the University of OklahomaW.B.thanks the support from the INL Laboratory Directed Research and Development(LDRD)Program 24A1081-098FP under DOE Idaho Operations Office Contract DE-AC07-05ID14517.
文摘Protonic ceramic energy devices represent a promising frontier for sustainable energy conversion and storage,operating efficiently at intermediate temperatures(350-650℃)and facilitating integration with renewable energy sources.Among protonic ceramic materials,yttrium-doped barium zirconate(BaZr_(1-x)Y_(x)O_(3-δ),BZY)stands out for its competitive proton conductivity,chemical resilience,and compatibility with diverse fuels and environments.This review critically examines the fundamentals and multiscale design strategies for BZY-based ceramic cells.We discuss atomic-level composition-structure relationships,innovative synthesis routes,and advanced processing methods to overcome manufacturing and scalability challenges.We then highlight microstructure engineering and interface design approaches that minimize resistance and elevate device performance,supported by state-of-the-art characterization and predictive modeling techniques,including density functional theory and machine learning.Recent advances,such as hybrid architectures and AI-driven defect optimization,demonstrate significant improvements in conductivity,stability,and Faradaic efficiency,confirming BZY's pivotal role in green hydrogen production and power-to-chemicals applications.By integrating insights across materials chemistry,electrochemistry,and engineering,this review provides a comprehensive roadmap for researchers aiming to translate laboratory breakthroughs into robust,scalable protonic ceramic technologies for decarbonized energy systems.
基金the financial support provided by the National Key R&D Program of China(No.2024YFB4007501)the Natural Science Foundation of Jiangsu Province(No.BK20240109)+1 种基金the Fundamental Research Funds for the Central Universities(No.2024QN11045)the China Postdoctoral Science Foundation(No.2024M753513).
文摘Hydrocarbon fuels have the advantages of being low-cost,easy to store and transport,and can be converted into biomass gas through oxidation and reforming processes,further increasing their potential applications.However,incomplete reforming and carbon deposition under practical conditions hinder the utilization of hydrocarbon fuels.In this work,Ni_(0.1)Fe_(0.1)Ce_(0.8)O_(2−δ)(NFCO)is employed as the anode reforming catalyst for tubular solid oxide fuel cells(T-SOFCs)with low-concentration ethanol-carbon dioxide fuel.With the in situ-formed NiFe alloy,the T-SOFC with NFCO achieves peak power densities of 538,614,and 608 mW·cm^(−2)in 5%,10%,and 15%ethanol,respectively,which are higher than those of the cell without NFCO.More importantly,no significant degradation is observed during long-term operation.As confirmed by density functional theory(DFT)calculations,the introduction of a NiFe alloy on the basis of CeO_(2)significantly improved the adsorption energy of H2O,thereby increasing the adsorption capacity of water molecules and promoting the adsorption and conversion of ethanol fuel.The results indicate that the heterostructure between the NiFe alloy and high-oxygen-vacancy CeO_(2)enhances the anode catalytic activity and inhibits the carbon deposition of T-SOFCs under low-concentration ethanol-carbon dioxide fuel,providing important insights for the development of high-performance,carbon-tolerant T-SOFCs under direct hydrocarbon fuel.
基金financially supported by the Fundamental Research Funds for the Central Universities(No.2019GF10).
文摘New two-layer Ruddlesden-Popper(RP)oxide La_(0.25)Sr_(2.75)FeNiO_(7-δ)(LSFN)in the combination of Sr_(3)Fe_(2)O_(7-δ) and La_(3)Ni_(2)O_(7-δ) was successfully synthesized and studied as the potential active single-phase and composite cathode for protonic ceramics fuel cells(PCFCs).LSFN with the tetragonal symmetrical structure(IMmmm)is confinned,and the co-existence of Fe^(3+)/Fe^(4+) and Ni^(3+)/Ni^(2+) couples is demonstrated by X-ray photoelectron spectrometer(XPS)analysis.The LSFN conductivity is apparently enhanced after Ni doping in Fe-site,and nearly three times those of Sr_(3)Fe_(2)O_(7-δ),which is directly related to the carrier concentration and conductor mechanism.Importantly,anode supported PCFCs using LSFN-BaZr_(0.1)Ce_(0.7)Y_(0.2)O_(3-δ)(LSFN-BZCY)composite cathode achieved high power density(426 mW·cm^(-2) at 650℃)and low electrode interface polarization resistance(0.26Ω·cm^(2)).Besides,distribution of relaxation time(DRT)function technology was further used to analyse the electrode polarization processes.The observed three peaks(Pl,P2,and P3)separated by DRT shifted to the high frequency region with the decreasing temperature,suggesting that the charge transfer at the electrode-electrolyte interfaces becomes more difficult at reduced temperatures.Preliminary results demonstrate that new two-layer RP phase LSFN can be a promising cathode candidate for PCFCs.
基金supported by the National Key R&D Program of China(2021YFA1501900)the National Natural Science Foundation of China-Yunnan Joint Fund(U2102215)+4 种基金the National Natural Science Foundation of China(22209203)China Postdoctoral Science Foundation(2021M693419)Jiangsu Key Laboratory of Coal-based Greenhouse Gas Control and Utilization(PCSX202202)the Material Science and Engineering Discipline Guidance Fund of China University of Mining and Technology(CUMTMS202202 and CUMTMS202207)the Open Sharing Fund for the Large-scale Instruments and Equipment of China University of Mining and Technology。
文摘探索具有优异导电性和稳定性的非贵金属电催化剂对氢经济至关重要.本研究将杂原子掺杂和石墨烯包覆相结合,以控制NiCo_(2)S_(4)(NCS)蛋黄壳微球的电子性能,并抵抗酸性介质中H_(2)O和O_(2)的腐蚀.密度泛函理论(DFT)模拟结合综合表征和实验首次揭示了在NCS中引入P杂原子不仅加速了电子从体相向表面的转移动力学,而且降低了掺杂P原子附近活性S位上的析氢反应势垒.利用DFT计算的穿透能垒预测了rGO覆盖层在P掺杂NCS(P-NCS)表面对质子的渗透性和对H_(2)O和O_(2)分子的抵抗性等重要功能,并用X射线光电子能谱对新催化剂和回收催化剂进行了验证.利用P掺杂剂和rGO覆盖层分别辅助电荷传递和质子传递,通过二者的协同作用获得了催化活性和耐久性之间的平衡.因此,优化后的P-NCS/rGO在70 mV的低过电位下实现了10 mA cm^(-2)的电流密度,并具有令人满意的80小时耐用性.本工作阐明了石墨烯覆盖硫化物催化剂可通过调控电子结构和质子/分子穿透提高电催化性能.
基金Prof.Dehua DONG acknowledges the financial support by the National Natural Science Foundation of China(51872123)Jinan Science and Technology Bureau(2020GXRC033).
文摘Joule-heating reactors have the higher energy efficiency and product selectivity compared with the reactors based on radiative heating.Current Joule-heating reactors are constructed with electrically-conductive metals or carbon materials,and therefore suffer from stability issue due to the presence of corrosive or oxidizing gases during high-temperature reactions.In this study,chemicallystable and electrically-conductive(La_(0.80)Sr_(0.20))_(0.95)FeO_(3)(LSF)/Gd_(0.1)Ce_(0.9)O_(2)(GDC)ceramics have been used to construct Joule-heating reactors for the first time.Taking the advantage of the resistance decrease of the ceramic reactors with temperature increase,the ceramic reactors heated under current control mode achieved the automatic adjustment of heating to stabilize reactor temperatures.In addition,the electrical resistance of LSF/GDC reactors can be tuned by the content of the highconductive LSF in composite ceramics and ceramic density via sintering temperature,which offers flexibility to control reactor temperatures.The ceramic reactors with dendritic channels(less than 100μm in diameter)showed the catalytic activity for CO oxidation,which was further improved by coating efficient MnO_(2)nanocatalyst on reactor channel wall.The Joule-heating ceramic reactors achieved complete CO oxidation at a low temperature of 165℃.Therefore,robust ceramic reactors have successfully demonstrated effective Joule heating for CO oxidation,which are potentially applied in other high-temperature catalytic reactions.
