Chromium plays a vital role in stainless steel due to its ability to improve the corrosion resistance of the latter.However,the re-lease of chromium from stainless steel slag(SSS)during SSS stockpiling causes detrimen...Chromium plays a vital role in stainless steel due to its ability to improve the corrosion resistance of the latter.However,the re-lease of chromium from stainless steel slag(SSS)during SSS stockpiling causes detrimental environmental issues.To prevent chromium pollution,the effects of iron oxide on crystallization behavior and spatial distribution of spinel were investigated in this work.The results revealed that FeO was more conducive to the growth of spinels compared with Fe2O3 and Fe3O4.Spinels were found to be mainly distrib-uted at the top and bottom of slag.The amount of spinel phase at the bottom decreased with the increasing FeO content,while that at the top increased.The average particle size of spinel in the slag with 18wt%FeO content was 12.8μm.Meanwhile,no notable structural changes were observed with a further increase in FeO content.In other words,the spatial distribution of spinel changed when the content of iron oxide varied in the range of 8wt%to 18wt%.Finally,less spinel was found at the bottom of slag with a FeO content of 23wt%.展开更多
Urea holds promise as an alternative water-oxidation substrate in electrolytic cells.High-valence nickelbased spinel,especially after heteroatom doping,excels in urea oxidation reactions(UOR).However,traditional spine...Urea holds promise as an alternative water-oxidation substrate in electrolytic cells.High-valence nickelbased spinel,especially after heteroatom doping,excels in urea oxidation reactions(UOR).However,traditional spinel synthesis methods with prolonged high-temperature reactions lack kinetic precision,hindering the balance between controlled doping and highly active two-dimensional(2D)porous structures design.This significantly impedes the identification of electron configuration-dependent active sites in doped 2D nickel-based spinels.Herein,we present a microwave shock method for the preparation of 2D porous NiCo_(2)O_(4)spinel.Utilizing the transient on-off property of microwave pulses for precise heteroatom doping and 2D porous structural design,non-metal doping(boron,phosphorus,and sulfur)with distinct extranuclear electron disparities serves as straightforward examples for investigation.Precise tuning of lattice parameter reveals the impact of covalent bond strength on NiCo_(2)O_(4)structural stability.The introduced defect levels induce unpaired d-electrons in transition metals,enhancing the adsorption of electron-donating amino groups in urea molecules.Simultaneously,Bode plots confirm the impact mechanism of rapid electron migration caused by reduced band gaps on UOR activity.The prepared phosphorus-doped 2D porous NiCo_(2)O_(4),with optimal electron configuration control,outperforms most reported spinels.This controlled modification strategy advances understanding theoretical structure-activity mechanisms of high-performance 2D spinels in UOR.展开更多
Spinel metal oxides containing Mn,Co,or Fe(AB_(2)O_(4),A/B=Mn/Fe/Co)are one of the most promising nonPt electrocatalysts for oxygen reduction reaction(ORR)in alkaline conditions.However,the low conductivity of metal o...Spinel metal oxides containing Mn,Co,or Fe(AB_(2)O_(4),A/B=Mn/Fe/Co)are one of the most promising nonPt electrocatalysts for oxygen reduction reaction(ORR)in alkaline conditions.However,the low conductivity of metal oxides and the poor intrinsic activities of transition metal sites lead to unsatisfactory ORR performance.In this study,eutectic molten salt(EMS)treatment is employed to reconstruct the atomic arrangement of MnFe_(2)O_(4)electrocatalyst as a prototype for enhancing ORR performance.Comprehensive analyses by using XAFS,soft XAS,XPS,and electrochemical methods reveal that the EMS treatment reduces the oxygen vacancies and spinel inverse in MnFe_(2)O_(4)effectively,which improves the electric conductivity and increases the population of more catalytically active Mn^(2+)sites with tetrahedral coordination.Moreover,the enhanced Mn-O interaction after EMS treatment is conducive to the adsorption and activation of O_(2),which promotes the first electron transfer step(generally considered as the ratedetermining step)of the ORR process.As a result,the EMS treated MnFe_(2)O_(4)catalyst delivers a positive shift of 40 mV in the ORR half-wave potential and a two-fold enhanced mass/specific activity.This work provides a convenient approach to manipulate the atomic architecture and local electronic structure of spinel oxides as ORR electrocatalysts and a comprehensive understanding of the structureperformance relationship from the molecular/atomic scale.展开更多
Developing stable and efficient nonprecious-metal-based oxygen evolution catalysts in the neutral electrolyte is a challenging but essential goal for various electrochemical systems.Particularly,cobalt-based spinels h...Developing stable and efficient nonprecious-metal-based oxygen evolution catalysts in the neutral electrolyte is a challenging but essential goal for various electrochemical systems.Particularly,cobalt-based spinels have drawn a considerable amount of attention but most of them operate in alkali solutions.However,the frequently studied Co-Fe spinel system never exhibits appreciable stability in nonbasic conditions,not to mention attract further investigation on its key structural motif and transition states for activity loss.Herein,we report exceptional stable Co-Fe spinel oxygen evolution catalysts(~30%Fe is optimal)in a neutral electrolyte,owing to its unique metal ion arrangements in the crystal lattice.The introduced iron content enters both the octahedral and tetrahedral sites of the spinel as Fe^(2+)and Fe^(3+)(with Co ions having mixed distribution as well).Combining density functional theory calculations,we find that the introduction of Fe to Co_(3)O_(4)lowers the covalency of metal-oxygen bonds and can help suppress the oxidation of Co^(2+/3+)and 0^(2-).It implies that the Co-Fe spinel will have minor surface reconstruction and less lattice oxygen loss during the oxygen evolution reaction process in comparison with Co_(3)O_(4)and hence show much better stability.These findings suggest that there is still much chance for the spinel structures,especially using reasonable sublattices engineering via multimetal doping to develop advanced oxygen evolution catalysts.展开更多
Spinel cobalt oxide(Co_(3)O_(4)),consisting of tetrahedral Co^(2+)(CoTd)and octahedral Co^(3+)(CoOh),is considered as promising earth-abundant electrocatalyst for chlorine evolution reaction(CER).Identifying the catal...Spinel cobalt oxide(Co_(3)O_(4)),consisting of tetrahedral Co^(2+)(CoTd)and octahedral Co^(3+)(CoOh),is considered as promising earth-abundant electrocatalyst for chlorine evolution reaction(CER).Identifying the catalytic contribution of geometric Co site in the electrocatalytic CER plays a pivotal role to precisely modulate electronic configuration of active Co sites to boost CER.Herein,combining density functional theory calculations and experiment results assisted with operando analysis,we found that the Co_(Oh) site acts as the main active site for CER in spinel Co_(3)O_(4),which shows better Cl^(-)adsorption and more moderate intermediate adsorption toward CER than CoTd site,and does not undergo redox transition under CER condition at applied potentials.Guided by above findings,the oxygen vacancies were further introduced into the Co_(3)O_(4) to precisely manipulate the electronic configuration of Co_(Oh) to boost Cl^(-)adsorption and optimize the reaction path of CER and thus to enhance the intrinsic CER activity significantly.Our work figures out the importance of geometric configuration dependent CER activity,shedding light on the rational design of advanced electrocatalysts from geometric configuration optimization at the atomic level.展开更多
In gemmology,the term“Alexandrite effect”is used to describe colour change phenomenon when a gemstone is observed under different light sources,usually between daylight and incandescent light.The definition of the A...In gemmology,the term“Alexandrite effect”is used to describe colour change phenomenon when a gemstone is observed under different light sources,usually between daylight and incandescent light.The definition of the Alexandrite effect is constantly being broadened with new discovery of gem resource.The traditional definition of the Alexandrite effect attributing the colour change phenomenon to the presence of two maximum transmission regions and a maximum absorption region in the absorption spectra.In this study,7 blue spinels and 5 blue gemstones(including tanzanite,kyanite,fluorite,and 2 sapphires)showing the Alexandrite effect were investigated.The goal is to explain the cause of blue-to-violet Alexandrite effect and the spectral features causing such colour change.In the UV-Vis spectra,all samples showed a maximum absorption peak in the range of 534-610 nm,within the green region to orange region.The traditional explanation of green to red Alexandrite effect required a transmission window in the red region;however,some of our samples did not show this transmission window and the blue-to-violet Alexandrite effect was still visible.Therefore,it is incomplete to explain the mechanism of the Alexandrite effect according to their characteristic absorption spectra,a systematic study based on modern colour science and colour perception in human vision is required to elucidate the blue-to-violet Alexandrite effect.展开更多
The densification and microstructure of different spinelized magnesium aluminate spinels（MAS） were studied adding Sc_2O_3 as additive. Sintered products were then characterized in terms of densification, phase analy...The densification and microstructure of different spinelized magnesium aluminate spinels（MAS） were studied adding Sc_2O_3 as additive. Sintered products were then characterized in terms of densification, phase analysis, quantitative elemental analysis and microstructure. The results show that Sc_2O_3 is found to be beneficial for the densification of MAS. Sc_2O_3 has a more significant effect on the densification of partially spinelized MAS batch than that of fully spinelized MAS batch. At the sintering temperature of 1650 °C, the bulk density of sintered products of partially spinelized powders increases by 0.243 g/cm3 as the Sc_2O_3 content increases from 0 to 4%（mass fraction） and that of fully spinelized powder increases by 0.14 g/cm3. Compared with the sintered samples prepared from the fully spinelized powder, the sintered samples using the partially spinelized powders as raw materials have more compact microstructures.展开更多
New types of refractory materials need to be developed for designing the man-made ledge of the Hall-Heroult cell for aluminum electrolysis, which are currently constructed by frozen ledge.Magnesium aluminate spinel （...New types of refractory materials need to be developed for designing the man-made ledge of the Hall-Heroult cell for aluminum electrolysis, which are currently constructed by frozen ledge.Magnesium aluminate spinel （MAS） as potential candidate materials was prepared by two-step sintering. The densification and grain growth of the MAS wereinvestigatedbytheArchimedes drainage method and scanning electron microscope （SEM）. All the specimens were corroded in aNa3AlF6-AlF3-CaF2-Al2O3bath to assess the corrosion resistance. The results show that a MAS material with a high relative density of 99.2% and ahomogeneous microstructure is achieved under two-step sintering conditions. The corrosion mechanisms of MAS inNa3AlF6-AlF3-CaF2-Al2O3 bathare mainly proposed by dissolution of MAS, formation of aluminum oxide, and diffusion of fluorides. The MAS prepared by two-step sintering exhibits good corrosion resistance to theNa3AlF6-AlF3-CaF2-Al2O3bath.展开更多
High-entropy design is attracting growing interest as it offers unique structures and unprecedented application potential for ma-terials.In this article,a novel high-entropy ferrite(CoNi)_(x/2)(CuZnAl)_((1-x)/3)Fe_(2)...High-entropy design is attracting growing interest as it offers unique structures and unprecedented application potential for ma-terials.In this article,a novel high-entropy ferrite(CoNi)_(x/2)(CuZnAl)_((1-x)/3)Fe_(2)O_(4)(x=0.25,0.34,0.40,0.50)with a single spinel phase of space group Fd3m was successfully developed by the solid-state reaction method.By tuning the Co-Ni content,the magnetic properties of the material,especially the coercivity,changed regularly,and the microwave absorption properties were improved.In particular,the ef-fective absorption bandwidth of the material increased from 4.8 to 7.2 GHz,and the matched thickness decreased from 3.9 to 2.3 mm,while the minimum reflection loss remained below-20 dB.This study provides a practical method for modifying the properties of fer-rites used to absorb electromagnetic waves.展开更多
Nanocrystalline Ni-Fe FCC alloy coatings with Fe content of 1.3%-39%（mass fraction） were fabricated on the nickel substrates using a DC electrodeposition technique. The crystal structure, lattice strain, grain size ...Nanocrystalline Ni-Fe FCC alloy coatings with Fe content of 1.3%-39%（mass fraction） were fabricated on the nickel substrates using a DC electrodeposition technique. The crystal structure, lattice strain, grain size and lattice constant of the Ni-Fe alloy coatings were studied by X-ray diffraction technique. The chemical composition and surface morphology of the FCC Ni-Fe alloy coatings were investigated with the energy dispersive X-ray spectroscopy（EDS） and atomic force microscopy（AFM）. The results show that the Fe content of the Ni-Fe alloy coatings has a great influence on the preferred orientation, grain size, lattice constant and lattice strain. FCC Ni-Fe alloy coatings exhibit preferred orientations of（200） or（200）（111）. With an increase of Fe content, the preferred growth orientation of（200） plane is weakened gradually, while the preferred growth orientation of（111） increases. An increase of the Fe content in the range of 1.3%-25%（mass fraction） results in a significant grain refinement of the coatings. Increasing the Fe content beyond 25% does not decrease the grain size of FCC Ni-Fe alloys further. The lattice strain increases with increasing the Fe content in the FCC Ni-Fe alloys. Since the alloys with Fe content not less than 25% has similar grain size（~11 nm）, the increase in the lattice strain with the increase of Fe content cannot be attributed to the change in the grain size.展开更多
基金the National Natural Science Foundation of China(Nos.52074078 and 52374327)the Applied Fundamental Research Program of Liaoning Province(No.2023JH2/101600002)+2 种基金the Shenyang Young Middle-Aged Scientific and Technological Innovation Talent Support Program(No.RC220491)the Liaoning Province Steel Industry-University-Research Innovation Alliance Cooperation Project of Bensteel Group(No.KJBLM202202)the Fundamental Research Funds for the Central Universities(Nos.N2201023 and N2325009).
文摘Chromium plays a vital role in stainless steel due to its ability to improve the corrosion resistance of the latter.However,the re-lease of chromium from stainless steel slag(SSS)during SSS stockpiling causes detrimental environmental issues.To prevent chromium pollution,the effects of iron oxide on crystallization behavior and spatial distribution of spinel were investigated in this work.The results revealed that FeO was more conducive to the growth of spinels compared with Fe2O3 and Fe3O4.Spinels were found to be mainly distrib-uted at the top and bottom of slag.The amount of spinel phase at the bottom decreased with the increasing FeO content,while that at the top increased.The average particle size of spinel in the slag with 18wt%FeO content was 12.8μm.Meanwhile,no notable structural changes were observed with a further increase in FeO content.In other words,the spatial distribution of spinel changed when the content of iron oxide varied in the range of 8wt%to 18wt%.Finally,less spinel was found at the bottom of slag with a FeO content of 23wt%.
基金financial support from the National Natural Science Foundation of China(52203070)the Open Fund of State Key Laboratory of New Textile Materials and Advanced Processing Technologies(FZ2022005)+2 种基金the Open Fund of Hubei Key Laboratory of Biomass Fiber and Ecological Dyeing and Finishing(STRZ202203)the financial support provided by the China Scholarship Council(CSC)Visiting Scholar Programfinancial support from Institute for Sustainability,Energy and Resources,The University of Adelaide,Future Making Fellowship。
文摘Urea holds promise as an alternative water-oxidation substrate in electrolytic cells.High-valence nickelbased spinel,especially after heteroatom doping,excels in urea oxidation reactions(UOR).However,traditional spinel synthesis methods with prolonged high-temperature reactions lack kinetic precision,hindering the balance between controlled doping and highly active two-dimensional(2D)porous structures design.This significantly impedes the identification of electron configuration-dependent active sites in doped 2D nickel-based spinels.Herein,we present a microwave shock method for the preparation of 2D porous NiCo_(2)O_(4)spinel.Utilizing the transient on-off property of microwave pulses for precise heteroatom doping and 2D porous structural design,non-metal doping(boron,phosphorus,and sulfur)with distinct extranuclear electron disparities serves as straightforward examples for investigation.Precise tuning of lattice parameter reveals the impact of covalent bond strength on NiCo_(2)O_(4)structural stability.The introduced defect levels induce unpaired d-electrons in transition metals,enhancing the adsorption of electron-donating amino groups in urea molecules.Simultaneously,Bode plots confirm the impact mechanism of rapid electron migration caused by reduced band gaps on UOR activity.The prepared phosphorus-doped 2D porous NiCo_(2)O_(4),with optimal electron configuration control,outperforms most reported spinels.This controlled modification strategy advances understanding theoretical structure-activity mechanisms of high-performance 2D spinels in UOR.
基金supported by the National Natural Science Foundation of China (12241502,52002367)the Fundamental Research Funds for the Central Universities (20720220010)the National Key Research and Development Program of China (2019YFA0405602)。
文摘Spinel metal oxides containing Mn,Co,or Fe(AB_(2)O_(4),A/B=Mn/Fe/Co)are one of the most promising nonPt electrocatalysts for oxygen reduction reaction(ORR)in alkaline conditions.However,the low conductivity of metal oxides and the poor intrinsic activities of transition metal sites lead to unsatisfactory ORR performance.In this study,eutectic molten salt(EMS)treatment is employed to reconstruct the atomic arrangement of MnFe_(2)O_(4)electrocatalyst as a prototype for enhancing ORR performance.Comprehensive analyses by using XAFS,soft XAS,XPS,and electrochemical methods reveal that the EMS treatment reduces the oxygen vacancies and spinel inverse in MnFe_(2)O_(4)effectively,which improves the electric conductivity and increases the population of more catalytically active Mn^(2+)sites with tetrahedral coordination.Moreover,the enhanced Mn-O interaction after EMS treatment is conducive to the adsorption and activation of O_(2),which promotes the first electron transfer step(generally considered as the ratedetermining step)of the ORR process.As a result,the EMS treated MnFe_(2)O_(4)catalyst delivers a positive shift of 40 mV in the ORR half-wave potential and a two-fold enhanced mass/specific activity.This work provides a convenient approach to manipulate the atomic architecture and local electronic structure of spinel oxides as ORR electrocatalysts and a comprehensive understanding of the structureperformance relationship from the molecular/atomic scale.
基金the financial support by the National Natural Science Foundation of China(NSFC,grant nos.21905288 and 51904288)Zhejiang Provincial Natural Science Foundation(LZ21B030001)+3 种基金K.C.Wong Education Foundation(GJTD-2019-13)Ningbo major special projects of the Plan“Science and Technology Innovation 2025”(grant nos.2018B10056 and 2019B10046)Ningbo 3315 ProgramYongjiang Talent Introduction Program(no.2021A-115-G)
文摘Developing stable and efficient nonprecious-metal-based oxygen evolution catalysts in the neutral electrolyte is a challenging but essential goal for various electrochemical systems.Particularly,cobalt-based spinels have drawn a considerable amount of attention but most of them operate in alkali solutions.However,the frequently studied Co-Fe spinel system never exhibits appreciable stability in nonbasic conditions,not to mention attract further investigation on its key structural motif and transition states for activity loss.Herein,we report exceptional stable Co-Fe spinel oxygen evolution catalysts(~30%Fe is optimal)in a neutral electrolyte,owing to its unique metal ion arrangements in the crystal lattice.The introduced iron content enters both the octahedral and tetrahedral sites of the spinel as Fe^(2+)and Fe^(3+)(with Co ions having mixed distribution as well).Combining density functional theory calculations,we find that the introduction of Fe to Co_(3)O_(4)lowers the covalency of metal-oxygen bonds and can help suppress the oxidation of Co^(2+/3+)and 0^(2-).It implies that the Co-Fe spinel will have minor surface reconstruction and less lattice oxygen loss during the oxygen evolution reaction process in comparison with Co_(3)O_(4)and hence show much better stability.These findings suggest that there is still much chance for the spinel structures,especially using reasonable sublattices engineering via multimetal doping to develop advanced oxygen evolution catalysts.
基金the National Natural Science Foundation of China(U21A20286,22206054 and 21805069)Natural Science Foundation of Hubei(2021CFB094)the Fundamental Research Funds for the Central China Normal University(CCNU)for financial support。
文摘Spinel cobalt oxide(Co_(3)O_(4)),consisting of tetrahedral Co^(2+)(CoTd)and octahedral Co^(3+)(CoOh),is considered as promising earth-abundant electrocatalyst for chlorine evolution reaction(CER).Identifying the catalytic contribution of geometric Co site in the electrocatalytic CER plays a pivotal role to precisely modulate electronic configuration of active Co sites to boost CER.Herein,combining density functional theory calculations and experiment results assisted with operando analysis,we found that the Co_(Oh) site acts as the main active site for CER in spinel Co_(3)O_(4),which shows better Cl^(-)adsorption and more moderate intermediate adsorption toward CER than CoTd site,and does not undergo redox transition under CER condition at applied potentials.Guided by above findings,the oxygen vacancies were further introduced into the Co_(3)O_(4) to precisely manipulate the electronic configuration of Co_(Oh) to boost Cl^(-)adsorption and optimize the reaction path of CER and thus to enhance the intrinsic CER activity significantly.Our work figures out the importance of geometric configuration dependent CER activity,shedding light on the rational design of advanced electrocatalysts from geometric configuration optimization at the atomic level.
基金This research was funded by the Youth Foundation Project,Basic and Applied Research Foundation of Guangdong Province of China(2022A1515110780)China Postdoctoral Science Foundation(2023M743293)China Univerisity of Geosciences(Wuhan)Gemmological Institute research project(GICTXM-04-S202103).
文摘In gemmology,the term“Alexandrite effect”is used to describe colour change phenomenon when a gemstone is observed under different light sources,usually between daylight and incandescent light.The definition of the Alexandrite effect is constantly being broadened with new discovery of gem resource.The traditional definition of the Alexandrite effect attributing the colour change phenomenon to the presence of two maximum transmission regions and a maximum absorption region in the absorption spectra.In this study,7 blue spinels and 5 blue gemstones(including tanzanite,kyanite,fluorite,and 2 sapphires)showing the Alexandrite effect were investigated.The goal is to explain the cause of blue-to-violet Alexandrite effect and the spectral features causing such colour change.In the UV-Vis spectra,all samples showed a maximum absorption peak in the range of 534-610 nm,within the green region to orange region.The traditional explanation of green to red Alexandrite effect required a transmission window in the red region;however,some of our samples did not show this transmission window and the blue-to-violet Alexandrite effect was still visible.Therefore,it is incomplete to explain the mechanism of the Alexandrite effect according to their characteristic absorption spectra,a systematic study based on modern colour science and colour perception in human vision is required to elucidate the blue-to-violet Alexandrite effect.
基金Project(51374240) supported by the National Natural Science Foundation of ChinaProject(2012BAE08B02) supported by the National Science and Technology Pillar Program of China
文摘The densification and microstructure of different spinelized magnesium aluminate spinels（MAS） were studied adding Sc_2O_3 as additive. Sintered products were then characterized in terms of densification, phase analysis, quantitative elemental analysis and microstructure. The results show that Sc_2O_3 is found to be beneficial for the densification of MAS. Sc_2O_3 has a more significant effect on the densification of partially spinelized MAS batch than that of fully spinelized MAS batch. At the sintering temperature of 1650 °C, the bulk density of sintered products of partially spinelized powders increases by 0.243 g/cm3 as the Sc_2O_3 content increases from 0 to 4%（mass fraction） and that of fully spinelized powder increases by 0.14 g/cm3. Compared with the sintered samples prepared from the fully spinelized powder, the sintered samples using the partially spinelized powders as raw materials have more compact microstructures.
基金Project(51374240)supported by the National Natural Science Foundation of ChinaProject(2012BAE08B02)supported by the National Science and Technology Pillar Program of China
文摘New types of refractory materials need to be developed for designing the man-made ledge of the Hall-Heroult cell for aluminum electrolysis, which are currently constructed by frozen ledge.Magnesium aluminate spinel （MAS） as potential candidate materials was prepared by two-step sintering. The densification and grain growth of the MAS wereinvestigatedbytheArchimedes drainage method and scanning electron microscope （SEM）. All the specimens were corroded in aNa3AlF6-AlF3-CaF2-Al2O3bath to assess the corrosion resistance. The results show that a MAS material with a high relative density of 99.2% and ahomogeneous microstructure is achieved under two-step sintering conditions. The corrosion mechanisms of MAS inNa3AlF6-AlF3-CaF2-Al2O3 bathare mainly proposed by dissolution of MAS, formation of aluminum oxide, and diffusion of fluorides. The MAS prepared by two-step sintering exhibits good corrosion resistance to theNa3AlF6-AlF3-CaF2-Al2O3bath.
基金supported by the National Natural Science Foundation of China(No.52371231)the Key Research and Development Program of Shanxi Province,China(No.202102030201006)+1 种基金the Central Government Guides Local Science and Technology Development Special Fund Project(No.YDZJSX2022B003),the Natural Science Foundation of Shanxi Province,China(No.202203021212205)the Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi,China(No.2022L074).
文摘High-entropy design is attracting growing interest as it offers unique structures and unprecedented application potential for ma-terials.In this article,a novel high-entropy ferrite(CoNi)_(x/2)(CuZnAl)_((1-x)/3)Fe_(2)O_(4)(x=0.25,0.34,0.40,0.50)with a single spinel phase of space group Fd3m was successfully developed by the solid-state reaction method.By tuning the Co-Ni content,the magnetic properties of the material,especially the coercivity,changed regularly,and the microwave absorption properties were improved.In particular,the ef-fective absorption bandwidth of the material increased from 4.8 to 7.2 GHz,and the matched thickness decreased from 3.9 to 2.3 mm,while the minimum reflection loss remained below-20 dB.This study provides a practical method for modifying the properties of fer-rites used to absorb electromagnetic waves.
基金Project(51021063)supported by the National Natural Science Fund for Innovation Group of ChinaProject(2012M521540)supported by China Post Doctoral Science Foundation+1 种基金Project(2013RS4027)supported by the Post Doctoral Scientific Foundation of Hunan Province,ChinaProject(CSUZC2013023)supported by the Precious Apparatus Open Share Foundation of Central South University,China
文摘Nanocrystalline Ni-Fe FCC alloy coatings with Fe content of 1.3%-39%（mass fraction） were fabricated on the nickel substrates using a DC electrodeposition technique. The crystal structure, lattice strain, grain size and lattice constant of the Ni-Fe alloy coatings were studied by X-ray diffraction technique. The chemical composition and surface morphology of the FCC Ni-Fe alloy coatings were investigated with the energy dispersive X-ray spectroscopy（EDS） and atomic force microscopy（AFM）. The results show that the Fe content of the Ni-Fe alloy coatings has a great influence on the preferred orientation, grain size, lattice constant and lattice strain. FCC Ni-Fe alloy coatings exhibit preferred orientations of（200） or（200）（111）. With an increase of Fe content, the preferred growth orientation of（200） plane is weakened gradually, while the preferred growth orientation of（111） increases. An increase of the Fe content in the range of 1.3%-25%（mass fraction） results in a significant grain refinement of the coatings. Increasing the Fe content beyond 25% does not decrease the grain size of FCC Ni-Fe alloys further. The lattice strain increases with increasing the Fe content in the FCC Ni-Fe alloys. Since the alloys with Fe content not less than 25% has similar grain size（~11 nm）, the increase in the lattice strain with the increase of Fe content cannot be attributed to the change in the grain size.
