TiB_(2)coatings can significantly enhance the high-temperature oxidation resistance of molybdenum,which would broaden the application range of molybdenum and alloys thereof.However,traditional methods for preparing Ti...TiB_(2)coatings can significantly enhance the high-temperature oxidation resistance of molybdenum,which would broaden the application range of molybdenum and alloys thereof.However,traditional methods for preparing TiB_(2)coatings have disadvantages such as high equipment costs,complicated processes,and highly toxic gas emissions.This paper proposes an environmentally friendly method,which requires inexpensive equipment and simple processing,for preparing TiB_(2)coating on molybdenum via electrophoretic deposition within Na3AlF6-based molten salts.The produced TiB_(2)layer had an approximate thickness of 60μm and exhibited high density,outstanding hardness(38.2 GPa)and robust adhesion strength(51 N).Additionally,high-temperature oxidation experiments revealed that,at900℃,the TiB_(2)coating provided effective protection to the molybdenum substrate against oxidation for 3 h.This result indicates that the TiB_(2)coating prepared on molybdenum using molten salt electrophoretic deposition possesses good high-temperature oxidation resistance.展开更多
The rapid expansion of the photovoltaic industry has generated heavily oxidized waste silicon(wSi),which hinders efficient recycling owing to its small particle size and uncontrolled surface oxidation.This study intro...The rapid expansion of the photovoltaic industry has generated heavily oxidized waste silicon(wSi),which hinders efficient recycling owing to its small particle size and uncontrolled surface oxidation.This study introduces a molten salt electrochemical strategy for converting photovoltaic wSi into NiSi_(2)-silicon nanorods(NiSi_(2)-SiNRs)as high-performance anode materials for lithium-ion batteries.A stable oxidized passivation layer is formed on the wSi surface via controlled oxidation,and further in situ generated highly active NiSi_(2) droplets.The molten salt electric field modulates the surface energy of silicon,while particle integration drives localized directional growth,enabling the self-assembly of NiSi_(2)-SiNRs composites.These NiSi_(2)-SiNRs anodes exhibit rapid ion transport and effective strain buffering.The high aspect ratio of SiNRs and the presence of retained NiSi_(2) facilitate both longitudinal and transverse Li^(+) diffusion.Owing to their robust structural design,the NiSi_(2)-SiNRs anode achieves an excellent initial Coulombic efficiency of 91.61%and retains 72.99%of its capacity after 800 cycles at 2 A·g^(−1).This study establishes a model system for investigating silicide/silicon interfaces in molten salt electrochemical synthesis and provides an effective strategy for upcycling photovoltaic wSi into high-performance lithium-ion battery anodes.展开更多
The electrical conductivity of NaF-AlF3-CaF2-Al2O3-ZrO2 system was studied by a tube-type cell with fixed cell constant. The results show that the electrical conductivity of NaF-AlF3-3%Al2O3-3%CaF2-ZrO2 molten salt sy...The electrical conductivity of NaF-AlF3-CaF2-Al2O3-ZrO2 system was studied by a tube-type cell with fixed cell constant. The results show that the electrical conductivity of NaF-AlF3-3%Al2O3-3%CaF2-ZrO2 molten salt system decreases with increase of ZrO2 content in an interval of 0-5%. The increase of 1%ZrO2 results in a corresponding electrical conductivity decrease of 0.02 S/cm, and the equivalent conductivity increases with the increase of molar ratio of NaF to AlF3. When the temperature increases by 1 °C, the electrical conductivity increases by 0.004 S/cm. At last, the regression equations of electrical conductivity relative to temperature and ZrO2 are obtained by quadratic regression analysis.展开更多
The NaF-CaF_2 system has been studied by molecular dynamics simulation.The pair correlation functions between cations and anions and the bond angle distributions of cation and anion triplets have been obtained.The bri...The NaF-CaF_2 system has been studied by molecular dynamics simulation.The pair correlation functions between cations and anions and the bond angle distributions of cation and anion triplets have been obtained.The bridging and complexing in the system are discussed based on the pair correlation functions and bond angle distributions.The results simulated show that the F^- ions around a Ca^(2+)ion do not form tetrahedron coordination,so some of small complexing clusters such as CaF_4^(2-)are hardly found.A possible structure of F^- ions around Ca^(2+)ions is that three Ca^(2+)ions constitute an equilateral triangle through three Ca-F-Ca bridges and two F^- ions are located over and under the center of the right triangle,respectively.Meanwhile,on the outside of the triangle,every Ca^(2+)ion has other two F^- ions as its neighbors.展开更多
Direct utilization of co-existed ferrous oxide(FeO)dust in CO_(2)flue gas from the steel industry to product value-added materials is yet to be established.Inspired by the form of CaO-CaCO_(3)as natural carbon cycle a...Direct utilization of co-existed ferrous oxide(FeO)dust in CO_(2)flue gas from the steel industry to product value-added materials is yet to be established.Inspired by the form of CaO-CaCO_(3)as natural carbon cycle and the high oxide dissolution capacity of molten salts,CaO is herein introduced into the affordable molten NaCl-CaCl_(2)-FeO salt to generate CO_(3)^(2-)through an efficient capture of CO_(2).The subsequent coelectrolysis of FeO and CO_(3)^(2-)successfully produces cathodic Fe-encapsulated carbon nanotubes(Fe@CNT)with enhanced energy efficiency(current efficiency of 83.1%for CO_(2)reduction and energy consumption of 22.49 kWh kg^(1)for Fe@CNT generation).The in-situ capture of CO_(2)by O^(2)generated from the electro-deoxidation of FeO bridges the electrolysis of CO_(2)and FeO,rendering the enhanced current efficiency of the co-electrolysis and template-free generation of Fe@CNT.When evaluated as functional materials for electromagnetic wave absorption,the Fe@CNT integrates dielectric loss of CNT and electromagnetic loss from Fe.The Fe well-defined in CNT induces the synergistic loss and further improves the impedance matching,resulting in excellent electromagnetic wave absorption performance.The coelectrolysis establishes a promising strategy for converting CO_(2)into highly functional materials directly from CO_(2)-containing flue gas from steel industrial without dust removal.展开更多
Carbon-based materials have been widely applied for pollutant removal relying on their rich pore structure,functional groups,chemical stability,and expandability.However,the traditional manufacturing process of carbon...Carbon-based materials have been widely applied for pollutant removal relying on their rich pore structure,functional groups,chemical stability,and expandability.However,the traditional manufacturing process of carbon materials based on organic compounds pyrolysis is high energy-consuming and high-emission,which is not conducive to addressing the climate crisis and achieving the goal of carbon neutrality.Molten salt electrolysis technology enables the direct capture and reduction of CO_(2)to produce solid carbon,resulting in significant environmental benefits while achieving carbon emissions reduction.The molten salt also has a purification function,enabling the production of high-purity carbon materials.The kinetics of the electrochemical reduction process can be easily controlled,and the co-reduction of multiple elements provides convenience for the in-situ optimization of carbon material structure and the expansion of its applications.Therefore,this review focuses on the thermodynamics&kinetics processes of molten salt capture and electrochemical reduction of CO_(2)to prepare carbon materials.It further reviews the recent research progress on the preparation of carbon materials for pollutant removal based on molten salt electrochemical processes for the first time.Finally,we analyze the advantages and challenges of the current molten salt electrochemical processes and offers prospects for future research directions.展开更多
One-dimensional titanium dioxide(TiO_(2))whiskers with controllable aspect ratios were synthesized by molten salt method adopting anatase TiO_(2)nanoparticles as precursor,sodium chloride(NaCl)and dibasic sodium phosp...One-dimensional titanium dioxide(TiO_(2))whiskers with controllable aspect ratios were synthesized by molten salt method adopting anatase TiO_(2)nanoparticles as precursor,sodium chloride(NaCl)and dibasic sodium phosphate(Na_(2)HPO_(4))as medium.The particle size of TiO_(2)nanoparticles and ratio of precursor and medium that can help to generate high aspect ratio TiO_(2)whiskers were studied and selected.Light-colored antimony-doped tin oxide@titanium dioxide(ATO@TiO_(2))conductive whiskers were prepared by coating ATO on TiO_(2)whiskers through coprecipitation then.Finally,the ATO@TiO_(2)light-colored conductive whiskers were dispersed in polyacrylonitrile(PAN)to fabricate light-colored conductive fibers.The experimental results show that the ATO@TiO_(2)whiskers exhibits ideal whiteness and conductivity with 65.5 Wb and 106Ω·cm,respectively,and the resistivity of conductive fibers was 6.07×10^(6)Ω·cm with 15wt%whisker content.展开更多
Lithium-carbon dioxide(Li-CO_(2))batteries using high ion-conductive inorganic molten salt electrolytes have recently attracted much attention due to the high energy density and potential application of carbon neutral...Lithium-carbon dioxide(Li-CO_(2))batteries using high ion-conductive inorganic molten salt electrolytes have recently attracted much attention due to the high energy density and potential application of carbon neutrality.However,the poor Li-ion conductivity of the molten-salt electrolytes at room temperature(RT)makes these batteries lose most of their capacity and power as the temperature falls below 80℃.Here,inspired by the greenhouse effect,we report an RT molten salt Li-CO_(2)battery where solar energy can be efficiently harvested and converted into heat that is further localized on the cathode consisting of plasmonic ruthenium(Ru)catalysts and Li_(2)CO_(3)-based products via a greenhouse-like phenomenon.As a result,the solar-driven molten salt Li-CO_(2)battery demonstrates a larger full discharge/charge capacity of 9.5 mA h/8.1 mA h,and a longer cycle lifespan of 250 cycles at 500 mA/g with a limited capacity of 500 mA h/g at RT than the molten salt Li-CO_(2)battery at 130℃.Notably,the average temperature of the cathode increases by 8℃ after discharge to 0.75 mA h,which indicates the infrared radiation from Ru catalysts can be effectively suppressed by discharged Li_(2)CO_(3)-based products.This battery technology paves the way for developing low-temperature molten salt energy storage devices.展开更多
The instantaneous desulfurization of CaO-Al_(2)O_(3)-SiO_(2)slag particles in the molten steel was in situ observed using a high-temperature confocal scanning laser microscope.The desulfurization effect of CaO-Al_(2)O...The instantaneous desulfurization of CaO-Al_(2)O_(3)-SiO_(2)slag particles in the molten steel was in situ observed using a high-temperature confocal scanning laser microscope.The desulfurization effect of CaO-Al_(2)O_(3)-SiO_(2)slags with different compositions was discussed.The influence of CaO/Al_(2)O_(3)and CaO/SiO_(2)on the desulfurization effect was analyzed.It was shown that in the liquid phase range,the higher CaO/SiO_(2)and CaO/Al_(2)O_(3)can significantly improve the desulfurization effect of the slag.A dimensionless desulfurization index Sindex was introduced to evaluate the desulfurization ability of CaO-Al_(2)O_(3)-SiO_(2)slags quantitatively.The Sindex values of CaO-Al_(2)O_(3)-SiO_(2)with different compositions at 1550°C were calculated.It was suggested to use(65%-75%)CaO-(0-20%)SiO_(2)-(20%-40%)Al_(2)O_(3)slags to improve the molten steel desulfurization.展开更多
A molten salt method was developed to prepare porous La1‐xSrxMn0.8Fe0.2O3 （0≤ x ≤ 0.6） micro‐spheres using hierarchical porous δ‐MnO2 microspheres as a template in eutectic NaNO3‐KNO3. X‐ray diffraction patt...A molten salt method was developed to prepare porous La1‐xSrxMn0.8Fe0.2O3 （0≤ x ≤ 0.6） micro‐spheres using hierarchical porous δ‐MnO2 microspheres as a template in eutectic NaNO3‐KNO3. X‐ray diffraction patterns showed that single phase LaMn0.8Fe0.2O3 with good crystallinity was syn‐thesized at 450℃ after 4 h. Transmission electron microscope images exhibited that the LaMn0.8Fe0.2O3 sample obtained at 450？？ after 4 h possessed a porous spherical morphology com‐posed of aggregated nanocrystallites. Field emission scanning electron microscope images indicated that the growth of the porous LaMn0.8Fe0.2O3 microspheres has two stages. SEM pictures showed that a higher calcination temperature than 450？？ had an adverse effect on the formation of a po‐rous spherical structure. The LaMn0.8Fe0.2O3 sample obtained at 450？？ after 4 h displayed a high BET surface area of 55.73 m2/g with a pore size of 9.38 nm. Fourier transform infrared spectra suggested that Sr2＋ions entered the A sites and induced a decrease of the binding energy between Mn and O. The CO conversion with the La1‐xSrxMn0.8Fe0.2O3 （0≤x≤0.6） samples indicated that the La0.4Sr0.6Mn0.8Fe0.2O3 sample had the best catalytic activity and stability. Further analysis by X‐ray photoelectron spectroscopy demonstrated that Sr2＋doping altered the content of Mn4＋ions, oxygen vacancies and adsorbed oxygen species on the surface, which affected the catalytic performance for CO oxidation.展开更多
基金supported by the Original Exploratory Program of the National Natural Science Foundation of China(No.52450012)。
文摘TiB_(2)coatings can significantly enhance the high-temperature oxidation resistance of molybdenum,which would broaden the application range of molybdenum and alloys thereof.However,traditional methods for preparing TiB_(2)coatings have disadvantages such as high equipment costs,complicated processes,and highly toxic gas emissions.This paper proposes an environmentally friendly method,which requires inexpensive equipment and simple processing,for preparing TiB_(2)coating on molybdenum via electrophoretic deposition within Na3AlF6-based molten salts.The produced TiB_(2)layer had an approximate thickness of 60μm and exhibited high density,outstanding hardness(38.2 GPa)and robust adhesion strength(51 N).Additionally,high-temperature oxidation experiments revealed that,at900℃,the TiB_(2)coating provided effective protection to the molybdenum substrate against oxidation for 3 h.This result indicates that the TiB_(2)coating prepared on molybdenum using molten salt electrophoretic deposition possesses good high-temperature oxidation resistance.
基金supported by the Yunnan Province Basic Research General Program,China(No.202201BE070001-002)the Major Science and Technology Projects in Yunnan Province,China(No.202402AF 080005).
文摘The rapid expansion of the photovoltaic industry has generated heavily oxidized waste silicon(wSi),which hinders efficient recycling owing to its small particle size and uncontrolled surface oxidation.This study introduces a molten salt electrochemical strategy for converting photovoltaic wSi into NiSi_(2)-silicon nanorods(NiSi_(2)-SiNRs)as high-performance anode materials for lithium-ion batteries.A stable oxidized passivation layer is formed on the wSi surface via controlled oxidation,and further in situ generated highly active NiSi_(2) droplets.The molten salt electric field modulates the surface energy of silicon,while particle integration drives localized directional growth,enabling the self-assembly of NiSi_(2)-SiNRs composites.These NiSi_(2)-SiNRs anodes exhibit rapid ion transport and effective strain buffering.The high aspect ratio of SiNRs and the presence of retained NiSi_(2) facilitate both longitudinal and transverse Li^(+) diffusion.Owing to their robust structural design,the NiSi_(2)-SiNRs anode achieves an excellent initial Coulombic efficiency of 91.61%and retains 72.99%of its capacity after 800 cycles at 2 A·g^(−1).This study establishes a model system for investigating silicide/silicon interfaces in molten salt electrochemical synthesis and provides an effective strategy for upcycling photovoltaic wSi into high-performance lithium-ion battery anodes.
基金Project (2007CB210305) supported by the National Basic Research Program of ChinaProject (51074045) supported by the National Natural Science Foundation of China
文摘The electrical conductivity of NaF-AlF3-CaF2-Al2O3-ZrO2 system was studied by a tube-type cell with fixed cell constant. The results show that the electrical conductivity of NaF-AlF3-3%Al2O3-3%CaF2-ZrO2 molten salt system decreases with increase of ZrO2 content in an interval of 0-5%. The increase of 1%ZrO2 results in a corresponding electrical conductivity decrease of 0.02 S/cm, and the equivalent conductivity increases with the increase of molar ratio of NaF to AlF3. When the temperature increases by 1 °C, the electrical conductivity increases by 0.004 S/cm. At last, the regression equations of electrical conductivity relative to temperature and ZrO2 are obtained by quadratic regression analysis.
文摘The NaF-CaF_2 system has been studied by molecular dynamics simulation.The pair correlation functions between cations and anions and the bond angle distributions of cation and anion triplets have been obtained.The bridging and complexing in the system are discussed based on the pair correlation functions and bond angle distributions.The results simulated show that the F^- ions around a Ca^(2+)ion do not form tetrahedron coordination,so some of small complexing clusters such as CaF_4^(2-)are hardly found.A possible structure of F^- ions around Ca^(2+)ions is that three Ca^(2+)ions constitute an equilateral triangle through three Ca-F-Ca bridges and two F^- ions are located over and under the center of the right triangle,respectively.Meanwhile,on the outside of the triangle,every Ca^(2+)ion has other two F^- ions as its neighbors.
基金supported by the National Key R&D Program of China(2023YFA1508001)the National Natural Science Foundation of China(22272120 and U2202251)+2 种基金the Fundamental Research Funds for the Central Universities(2042022kf1174)the Hainan Province Science and Technology Special Fund(ZDYF2023SHFZ120 and ZDYF2021SHFZ058)the Research Foundation of Marine Science and Technology Collaborative Innovation Center of Hainan University(XTCX2022HYB01)。
文摘Direct utilization of co-existed ferrous oxide(FeO)dust in CO_(2)flue gas from the steel industry to product value-added materials is yet to be established.Inspired by the form of CaO-CaCO_(3)as natural carbon cycle and the high oxide dissolution capacity of molten salts,CaO is herein introduced into the affordable molten NaCl-CaCl_(2)-FeO salt to generate CO_(3)^(2-)through an efficient capture of CO_(2).The subsequent coelectrolysis of FeO and CO_(3)^(2-)successfully produces cathodic Fe-encapsulated carbon nanotubes(Fe@CNT)with enhanced energy efficiency(current efficiency of 83.1%for CO_(2)reduction and energy consumption of 22.49 kWh kg^(1)for Fe@CNT generation).The in-situ capture of CO_(2)by O^(2)generated from the electro-deoxidation of FeO bridges the electrolysis of CO_(2)and FeO,rendering the enhanced current efficiency of the co-electrolysis and template-free generation of Fe@CNT.When evaluated as functional materials for electromagnetic wave absorption,the Fe@CNT integrates dielectric loss of CNT and electromagnetic loss from Fe.The Fe well-defined in CNT induces the synergistic loss and further improves the impedance matching,resulting in excellent electromagnetic wave absorption performance.The coelectrolysis establishes a promising strategy for converting CO_(2)into highly functional materials directly from CO_(2)-containing flue gas from steel industrial without dust removal.
基金supported by the National Natural Science Foundation of China(Nos.52200143,51979011 and 52276208)the Natural Science Foundation of Hubei Province(No.2024AFB546)the Fundamental Research Funds for Central Public Welfare Research Institutes(Nos.CKSF2023302/CL and CKSF2023314/CL).
文摘Carbon-based materials have been widely applied for pollutant removal relying on their rich pore structure,functional groups,chemical stability,and expandability.However,the traditional manufacturing process of carbon materials based on organic compounds pyrolysis is high energy-consuming and high-emission,which is not conducive to addressing the climate crisis and achieving the goal of carbon neutrality.Molten salt electrolysis technology enables the direct capture and reduction of CO_(2)to produce solid carbon,resulting in significant environmental benefits while achieving carbon emissions reduction.The molten salt also has a purification function,enabling the production of high-purity carbon materials.The kinetics of the electrochemical reduction process can be easily controlled,and the co-reduction of multiple elements provides convenience for the in-situ optimization of carbon material structure and the expansion of its applications.Therefore,this review focuses on the thermodynamics&kinetics processes of molten salt capture and electrochemical reduction of CO_(2)to prepare carbon materials.It further reviews the recent research progress on the preparation of carbon materials for pollutant removal based on molten salt electrochemical processes for the first time.Finally,we analyze the advantages and challenges of the current molten salt electrochemical processes and offers prospects for future research directions.
基金Funded by the National Natural Science Foundation of China(No.51803076)the Natural Science Foundation of Jiangsu Province of China(No.BK20180629)+1 种基金the China Postdoctoral Science Foundation(No.2018M632231)the Key Laboratory of Special Protective Textiles of Ministry of Education(Jiangnan University)(No.TZFH-24-006)。
文摘One-dimensional titanium dioxide(TiO_(2))whiskers with controllable aspect ratios were synthesized by molten salt method adopting anatase TiO_(2)nanoparticles as precursor,sodium chloride(NaCl)and dibasic sodium phosphate(Na_(2)HPO_(4))as medium.The particle size of TiO_(2)nanoparticles and ratio of precursor and medium that can help to generate high aspect ratio TiO_(2)whiskers were studied and selected.Light-colored antimony-doped tin oxide@titanium dioxide(ATO@TiO_(2))conductive whiskers were prepared by coating ATO on TiO_(2)whiskers through coprecipitation then.Finally,the ATO@TiO_(2)light-colored conductive whiskers were dispersed in polyacrylonitrile(PAN)to fabricate light-colored conductive fibers.The experimental results show that the ATO@TiO_(2)whiskers exhibits ideal whiteness and conductivity with 65.5 Wb and 106Ω·cm,respectively,and the resistivity of conductive fibers was 6.07×10^(6)Ω·cm with 15wt%whisker content.
基金supported by the National Natural Science Foundation of China(NSFC,62104099,61921005,62105048,62204117 and 62073299)the Science and Technology Research Program of Chongqing Education Commission(KJQN202100633)+5 种基金the Postdoctoral Science Foundation of China(2021M693768 and 2021M701057)the Key Scientific Research Project in Colleges and Universities of Henan Province,China(21A416001)the Key Laboratory for Special Functional Materials(KEKT2022-06)the Natural Science Foundation of Jiangsu Province(BK20210275 and BK20230498)the support from Jiangsu Province Science Foundation for Youths(BK20210275)National Natural Science Foundation of China(NSFC,62204117)。
文摘Lithium-carbon dioxide(Li-CO_(2))batteries using high ion-conductive inorganic molten salt electrolytes have recently attracted much attention due to the high energy density and potential application of carbon neutrality.However,the poor Li-ion conductivity of the molten-salt electrolytes at room temperature(RT)makes these batteries lose most of their capacity and power as the temperature falls below 80℃.Here,inspired by the greenhouse effect,we report an RT molten salt Li-CO_(2)battery where solar energy can be efficiently harvested and converted into heat that is further localized on the cathode consisting of plasmonic ruthenium(Ru)catalysts and Li_(2)CO_(3)-based products via a greenhouse-like phenomenon.As a result,the solar-driven molten salt Li-CO_(2)battery demonstrates a larger full discharge/charge capacity of 9.5 mA h/8.1 mA h,and a longer cycle lifespan of 250 cycles at 500 mA/g with a limited capacity of 500 mA h/g at RT than the molten salt Li-CO_(2)battery at 130℃.Notably,the average temperature of the cathode increases by 8℃ after discharge to 0.75 mA h,which indicates the infrared radiation from Ru catalysts can be effectively suppressed by discharged Li_(2)CO_(3)-based products.This battery technology paves the way for developing low-temperature molten salt energy storage devices.
基金support from the National Key R&D Program(No.2023YFB3709901)the National Natural Science Foundation of China(Grant No.U22A20171)China Baowu Low Carbon Metallurgy Innovation Foundation(BWLCF202315).
文摘The instantaneous desulfurization of CaO-Al_(2)O_(3)-SiO_(2)slag particles in the molten steel was in situ observed using a high-temperature confocal scanning laser microscope.The desulfurization effect of CaO-Al_(2)O_(3)-SiO_(2)slags with different compositions was discussed.The influence of CaO/Al_(2)O_(3)and CaO/SiO_(2)on the desulfurization effect was analyzed.It was shown that in the liquid phase range,the higher CaO/SiO_(2)and CaO/Al_(2)O_(3)can significantly improve the desulfurization effect of the slag.A dimensionless desulfurization index Sindex was introduced to evaluate the desulfurization ability of CaO-Al_(2)O_(3)-SiO_(2)slags quantitatively.The Sindex values of CaO-Al_(2)O_(3)-SiO_(2)with different compositions at 1550°C were calculated.It was suggested to use(65%-75%)CaO-(0-20%)SiO_(2)-(20%-40%)Al_(2)O_(3)slags to improve the molten steel desulfurization.
基金supported by the National Science Foundation for Young Scientists of China (51202171)~~
文摘A molten salt method was developed to prepare porous La1‐xSrxMn0.8Fe0.2O3 （0≤ x ≤ 0.6） micro‐spheres using hierarchical porous δ‐MnO2 microspheres as a template in eutectic NaNO3‐KNO3. X‐ray diffraction patterns showed that single phase LaMn0.8Fe0.2O3 with good crystallinity was syn‐thesized at 450℃ after 4 h. Transmission electron microscope images exhibited that the LaMn0.8Fe0.2O3 sample obtained at 450？？ after 4 h possessed a porous spherical morphology com‐posed of aggregated nanocrystallites. Field emission scanning electron microscope images indicated that the growth of the porous LaMn0.8Fe0.2O3 microspheres has two stages. SEM pictures showed that a higher calcination temperature than 450？？ had an adverse effect on the formation of a po‐rous spherical structure. The LaMn0.8Fe0.2O3 sample obtained at 450？？ after 4 h displayed a high BET surface area of 55.73 m2/g with a pore size of 9.38 nm. Fourier transform infrared spectra suggested that Sr2＋ions entered the A sites and induced a decrease of the binding energy between Mn and O. The CO conversion with the La1‐xSrxMn0.8Fe0.2O3 （0≤x≤0.6） samples indicated that the La0.4Sr0.6Mn0.8Fe0.2O3 sample had the best catalytic activity and stability. Further analysis by X‐ray photoelectron spectroscopy demonstrated that Sr2＋doping altered the content of Mn4＋ions, oxygen vacancies and adsorbed oxygen species on the surface, which affected the catalytic performance for CO oxidation.
