To resolve severe slag penetration and erosion in Al_(2)O_(3)-SiC-C refractories during high scrap ratio iron ladle operation,a novel strategy utilizing exogenous MgAl_(2)O_(4) spinel as a sacrificial FeO_(x) scavenge...To resolve severe slag penetration and erosion in Al_(2)O_(3)-SiC-C refractories during high scrap ratio iron ladle operation,a novel strategy utilizing exogenous MgAl_(2)O_(4) spinel as a sacrificial FeO_(x) scavenger was proposed.Al_(2)O_(3)-SiC-C refractories produced with plate-like corundum,silicon carbide,and flake graphite incorporating MgAl_(2)O_(4) additives were cured at 1400℃ in the condition of carbon embedding.The impacts of additives on phase composition,microscopic morphology,and performance of materials were studied.The results indicated that Al_(2)O_(3)-SiC-C refractories with the addition of 2 wt.%MgAl_(2)O_(4) exhibited a smaller oxidation area after oxidation tests compared to samples without MgAl_(2)O_(4),resulting in 28%improvement in oxidation resistance compared to blank samples.In the erosion test,the results informed that adding 4 wt.%MgAl_(2)O_(4) induced significant interfacial slag modification:MgAl_(2)O_(4) dynamically dissolved FeO_(x) to form protective Mg(Fe,Al)_(2)O_(4) solid solution on the slag-refractory interface.This sacrificial dissolution effectively immobilized FeO_(x),elevated local slag viscosity,and fundamentally inhibited slag penetration and matrix dissolution.The erosion index decreased from 50%in the blank group to 27.4%.展开更多
In this work,we report a fabrication of recyclable iron oxide decorated MoS_(2)nanosheets via a facile liq-uid exfoliation approach and solvothermal reaction for visible-light photodegradation of tetracycline.The prep...In this work,we report a fabrication of recyclable iron oxide decorated MoS_(2)nanosheets via a facile liq-uid exfoliation approach and solvothermal reaction for visible-light photodegradation of tetracycline.The prepared Fe_(3)O_(4)-MoS_(2)was characterized by X-ray diffraction,transmission electron microscopy,X-ray photoelectron spectros-copy,Raman spectroscopy,magnetic hysteresis,and nitrogen adsorption-desorption isotherms.Experimental results indicate that,successful attachment of Fe_(3)O_(4)nanoparticles to MoS_(2)sheets has been achieved.The enhanced surface area of Fe_(3)O_(4)-MoS_(2)induced high rates of adsorption and the adsorbed tetracycline was degraded to 90%after 150 min of visible exposure,which is better than that from pure MoS_(2).The introduction of Fe_(3)O_(4)not only enhances the photo-catalytic performance of Fe_(3)O_(4)-MoS_(2),but also enables its convenient recovery from water by an external magnetic field.Furthermore,both the photocatalytic activity and composite phase of Fe_(3)O_(4)-MoS_(2)were well-retained over cy-cles.Owing to its efficient photocatalytic activity,good stability and magnetic recyclability,the Fe_(3)O_(4)-MoS_(2)nano-composite is considered to be a promising photocatalyst for wastewater treatment.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
Na_(3)V_(2)(PO_(4))_(3)(NVP)is a promising electrode material that exhibits magnetic anisotropy;however,the potential of this magnetic anisotropy to optimize battery performance has been largely unexplored.This study ...Na_(3)V_(2)(PO_(4))_(3)(NVP)is a promising electrode material that exhibits magnetic anisotropy;however,the potential of this magnetic anisotropy to optimize battery performance has been largely unexplored.This study proposes a cost-effective and efficient method to induce the alignment of NVP along the(113)crystal plane by applying a vertical magnetic field during the slurry coating process,thereby enhancing its battery performance.Comprehensive structural characterizations and theoretical analysis elucidate the structure-activity relationship between the preferred crystal orientation and ion transport kinetics,facilitating the formation of more ordered Na+deintercalation pathways in NVP electrodes.This alignment reduces electrode tortuosity,enhances interfacial compatibility,and substantially improves battery performance,particularly in terms of high-rate cycling capability.As a result,the magnetic-field-modulated NVP(NVP-M⊥)electrode exhibits a high capacity retention of85.1%after 500 cycles at 5 C,significantly surpassing that of the pristine electrode.The NVP-M⊥electrode also demonstrates considerable reversible capacity at 40 C and maintains excellent stability under high temperature and prolonged cycling conditions.Furthermore,superior battery performance is observed in the assembled NVP-M⊥‖hard-carbon pouch cell and commercial NVP electrode following magnetic-field modulation,thereby validating the efficacy of this method.Consequently,this magnetic-field-induced crystal-orientation optimization strategy provides an innovative approach for low-cost and highthroughput preparation of high-performance sodium-ion batteries.展开更多
The limited redox capability of photocatalysts often leads to harmful NO_(2) byproduct formation during photocatalytic NO oxidation.Herein,Bi_(4)Ti_(3)O_(12) nanosheets modified with plasmonic metallic bismuth and abu...The limited redox capability of photocatalysts often leads to harmful NO_(2) byproduct formation during photocatalytic NO oxidation.Herein,Bi_(4)Ti_(3)O_(12) nanosheets modified with plasmonic metallic bismuth and abundant oxygen vacancies were synthesized via an in-situ reduction method.The optimized catalyst(BTOR2,with a molar ratio of 40%NaBH_(4) to Bi_(4)Ti_(3)O_(12))achieved a maximum NO removal efficiency of 62.3%,significantly higher than pristine Bi_(4)Ti_(3)O_(12)(40.5%) while minimizing NO_(2) production.The results reveal that the synergistic effects of Bi’s plasmonic resonance and oxygen vacancies enhanced visible light absorption and charge separation.The density functional theory(DFT)analysis showed electrons can transfer from Bi_(4)Ti_(3)O_(12)to Bi,promoting O_(2)activation to·O_(2)^(-)radicals.In-situ diffuse reflectance infrared Fourier transform spectroscopy(DRIFTS)confirmed that light-induced H2O adsorption was strengthened,improving·OH radical generation.These radicals promoted the selective conversion of activated NO^(-) to NO_(3)^(-),rather than NO_(2).This work provides valuable insights for advancing research into efficient photocatalysts for air pollution control.展开更多
基金support from the project supported by the National Natural Science Foundation of China(Grant No.52402034)the Science and Technology Innovation Team Foundation of Hubei Province(Grant No.T2023001)+1 种基金the Natural Science Foundation of Hubei Province(Grant No.2023BAB106)the Natural Science Foundation of Wuhan(Grant No.2024040701010051).
文摘To resolve severe slag penetration and erosion in Al_(2)O_(3)-SiC-C refractories during high scrap ratio iron ladle operation,a novel strategy utilizing exogenous MgAl_(2)O_(4) spinel as a sacrificial FeO_(x) scavenger was proposed.Al_(2)O_(3)-SiC-C refractories produced with plate-like corundum,silicon carbide,and flake graphite incorporating MgAl_(2)O_(4) additives were cured at 1400℃ in the condition of carbon embedding.The impacts of additives on phase composition,microscopic morphology,and performance of materials were studied.The results indicated that Al_(2)O_(3)-SiC-C refractories with the addition of 2 wt.%MgAl_(2)O_(4) exhibited a smaller oxidation area after oxidation tests compared to samples without MgAl_(2)O_(4),resulting in 28%improvement in oxidation resistance compared to blank samples.In the erosion test,the results informed that adding 4 wt.%MgAl_(2)O_(4) induced significant interfacial slag modification:MgAl_(2)O_(4) dynamically dissolved FeO_(x) to form protective Mg(Fe,Al)_(2)O_(4) solid solution on the slag-refractory interface.This sacrificial dissolution effectively immobilized FeO_(x),elevated local slag viscosity,and fundamentally inhibited slag penetration and matrix dissolution.The erosion index decreased from 50%in the blank group to 27.4%.
文摘In this work,we report a fabrication of recyclable iron oxide decorated MoS_(2)nanosheets via a facile liq-uid exfoliation approach and solvothermal reaction for visible-light photodegradation of tetracycline.The prepared Fe_(3)O_(4)-MoS_(2)was characterized by X-ray diffraction,transmission electron microscopy,X-ray photoelectron spectros-copy,Raman spectroscopy,magnetic hysteresis,and nitrogen adsorption-desorption isotherms.Experimental results indicate that,successful attachment of Fe_(3)O_(4)nanoparticles to MoS_(2)sheets has been achieved.The enhanced surface area of Fe_(3)O_(4)-MoS_(2)induced high rates of adsorption and the adsorbed tetracycline was degraded to 90%after 150 min of visible exposure,which is better than that from pure MoS_(2).The introduction of Fe_(3)O_(4)not only enhances the photo-catalytic performance of Fe_(3)O_(4)-MoS_(2),but also enables its convenient recovery from water by an external magnetic field.Furthermore,both the photocatalytic activity and composite phase of Fe_(3)O_(4)-MoS_(2)were well-retained over cy-cles.Owing to its efficient photocatalytic activity,good stability and magnetic recyclability,the Fe_(3)O_(4)-MoS_(2)nano-composite is considered to be a promising photocatalyst for wastewater treatment.
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 the Natural Science Foundation of China(Nos.22179020,12174057)Foreign Science and Technology Cooperation Project of Fuzhou Science and Technology Bureau(No.2024-Y-006)+3 种基金Natural Science Foundations of Fujian Province(No.2025J01659)Fujian province's“Young Eagle Program”Youth Top Talents ProgramNatural Science Foundation of Guangdong Province(2024A1515012077)Major Talent Programs of Guangdong Province(2023QN10C405)。
文摘Na_(3)V_(2)(PO_(4))_(3)(NVP)is a promising electrode material that exhibits magnetic anisotropy;however,the potential of this magnetic anisotropy to optimize battery performance has been largely unexplored.This study proposes a cost-effective and efficient method to induce the alignment of NVP along the(113)crystal plane by applying a vertical magnetic field during the slurry coating process,thereby enhancing its battery performance.Comprehensive structural characterizations and theoretical analysis elucidate the structure-activity relationship between the preferred crystal orientation and ion transport kinetics,facilitating the formation of more ordered Na+deintercalation pathways in NVP electrodes.This alignment reduces electrode tortuosity,enhances interfacial compatibility,and substantially improves battery performance,particularly in terms of high-rate cycling capability.As a result,the magnetic-field-modulated NVP(NVP-M⊥)electrode exhibits a high capacity retention of85.1%after 500 cycles at 5 C,significantly surpassing that of the pristine electrode.The NVP-M⊥electrode also demonstrates considerable reversible capacity at 40 C and maintains excellent stability under high temperature and prolonged cycling conditions.Furthermore,superior battery performance is observed in the assembled NVP-M⊥‖hard-carbon pouch cell and commercial NVP electrode following magnetic-field modulation,thereby validating the efficacy of this method.Consequently,this magnetic-field-induced crystal-orientation optimization strategy provides an innovative approach for low-cost and highthroughput preparation of high-performance sodium-ion batteries.
基金supported by the Natural Science Foundation of Chongqing(Nos.CSTB2024NSCQ-MSX1278,CSTB2023NSCQ-MSX0006)Technology Innovation Project of Shapingba District,Chongqing(No.2024004)+2 种基金Science and Technology Research Program of Chongqing Municipal Education Commission(Nos.KJZD-K202403102,KJQN202103110,KJQN202400512,KJQN202403107)National Natural Science Foundation of China(No.22406014)China Postdoctoral Science Foundation(No.2023MD744137).
文摘The limited redox capability of photocatalysts often leads to harmful NO_(2) byproduct formation during photocatalytic NO oxidation.Herein,Bi_(4)Ti_(3)O_(12) nanosheets modified with plasmonic metallic bismuth and abundant oxygen vacancies were synthesized via an in-situ reduction method.The optimized catalyst(BTOR2,with a molar ratio of 40%NaBH_(4) to Bi_(4)Ti_(3)O_(12))achieved a maximum NO removal efficiency of 62.3%,significantly higher than pristine Bi_(4)Ti_(3)O_(12)(40.5%) while minimizing NO_(2) production.The results reveal that the synergistic effects of Bi’s plasmonic resonance and oxygen vacancies enhanced visible light absorption and charge separation.The density functional theory(DFT)analysis showed electrons can transfer from Bi_(4)Ti_(3)O_(12)to Bi,promoting O_(2)activation to·O_(2)^(-)radicals.In-situ diffuse reflectance infrared Fourier transform spectroscopy(DRIFTS)confirmed that light-induced H2O adsorption was strengthened,improving·OH radical generation.These radicals promoted the selective conversion of activated NO^(-) to NO_(3)^(-),rather than NO_(2).This work provides valuable insights for advancing research into efficient photocatalysts for air pollution control.
