For large-scale energy storage devices,all-solid-state sodium-ion batteries(SIBs)have been revered for the abundant resources,low cost,safety performance and a wide operating temperature range.Na-ion solid-state elect...For large-scale energy storage devices,all-solid-state sodium-ion batteries(SIBs)have been revered for the abundant resources,low cost,safety performance and a wide operating temperature range.Na-ion solid-state electrolytes(Na-ion SSEs)are the critical parts and mostly determine the electrochemical performance of SIBs.Among the studied ones,inorganic Na-ion SSEs stand out for their good safety performance and high ionic conductivity.In this review,we outline the research progress of inorganic SSEs in SIBs based on the perspectives of crystal structure,performance optimization,synthesis methods,allsolid-state SIBs,interface modification and related characterization techniques.We hope to provide some ideas for the design of future high-performance Na-ion SSEs.展开更多
Single ion gel polymer electrolyte has the advantages of high Li^(+)conductivity and dendrite mitigation.However,the addition of organic solvent makes the electrolyte flammable,posing serious safety hazards.Herein,we ...Single ion gel polymer electrolyte has the advantages of high Li^(+)conductivity and dendrite mitigation.However,the addition of organic solvent makes the electrolyte flammable,posing serious safety hazards.Herein,we report a flame-retard ant cross-linked sp^(3)boron-based single-ion gel polymer electrolyte(BSIPE).BSIPE was prepared by a simple one-step photoinitiated in situ thiol-ene click reaction.Due to the boron-based anions being immobilized in the cross-linking network,the developed BSIPE/PFN exhibits a high t_(Li^(+))(0.87),which can mitigate concentration polarization phenomenon and suppress the growth of lithium dendrites.BSIPE/PFN plasticized with triethyl phosphate(TEP),fluoroethylene carbonate(FEC)and LiNO_(3)exhibits enhanced ionic conductivity of 4.25×10^(-4)S cm^(-1)at 30℃ and flame retardancy.FEC and LiNO_(3) are conducive to form a stable solid electrolyte interphase(SEI)rich in Li_(3)N and LiF to improve interface stability.As expected,the dendrite-free Li‖BSIPE/PFN‖Li symmetric cell exhibits considerable cycling life over 1500 h.BSIPE/PFN significantly boosts the performance of LFP‖Li cell,which displays a capacity retention of 84.6%after 500 cycles.The BSIPE/PFN has promising applications in highsafety and high-performance lithium metal batteries.展开更多
Black phosphorus(BP)is recognized as a promising anode for sodium-ion batteries(SIBs)due to its high safety and theoretical capacity.However,traditional ball milling methodologies for fabricating BP composite anodes h...Black phosphorus(BP)is recognized as a promising anode for sodium-ion batteries(SIBs)due to its high safety and theoretical capacity.However,traditional ball milling methodologies for fabricating BP composite anodes have not satisfactorily addressed the challenges of poor rate performance and short cycle life.To fill this scientific gap,we herein pioneer incorporating the sodium fast ionic conductorβ"-Al_(2)O_(3)into ball-milled BP with carbon,which facilitates the formation of three-dimensional mass transfer channels in the resulting composite.To stabilize these channels,we develop a novel and environmentally friendly functional binder that outperforms traditional binders in thermal stability,wettability,and mechanical properties.The newly established binder is capable of remarkably mitigating volume expansion and interfacial side reactions in the BP/β"-Al_(2)O_(3)/C composite anode.Additionally,we identify synergistic effects of the binder interacting with the BP/β"-Al_(2)O_(3)/C composite during cycling,characterized by the in-situ formation of P-O-C bonds,which is the first instance of a strong,durable chemical bond between the binder and the active material to the best of our knowledge.These advancements allow the composite electrode to exhibit exceptional sodium storage,including high initial Coulombic efficiency and long-term cycling stability,which surpasses most previous phosphorus-based anodes fabricated via traditional approaches.Notably,when paired with a Na_(4)Fe_(3)(PO_(4))_(2)P_(2)O_7(NFPP)cathode,the full cell exhibits unexpectedly high energy and power densities,highlighting the BP potential in SIBs.The findings presented in the present work contribute to the promotion of economical and efficient applications of phosphorus-based anode materials.展开更多
Lithium halide solid-state electrolytes,with the general formula of Li_(3±m)M_(n)X_(6),are regarded as the promising families of electrolyte material for all solid-state lithium-ion batteries because of the relat...Lithium halide solid-state electrolytes,with the general formula of Li_(3±m)M_(n)X_(6),are regarded as the promising families of electrolyte material for all solid-state lithium-ion batteries because of the relatively good ionic conductivity,high oxidative stability against high-voltage oxide cathodes,and broad electrochemical stability window[1].Here,M stands for one or multiple metal elements and X for one or multiple halogen elements.展开更多
Increasing the charging cut-off voltage can significantly enhance the energy density of LiCoO_(2).However,the continuous deterioration of interface structure and transport kinetics under high voltage poses challenges ...Increasing the charging cut-off voltage can significantly enhance the energy density of LiCoO_(2).However,the continuous deterioration of interface structure and transport kinetics under high voltage poses challenges to electrochemical stability.This work proposes to in-situ construct a uniform element gradient modification structure on the surface and subsurface of LiCoO_(2).The modification structure contains an Sb_(2)O_(3)&SbF_(x)composite coating layer and an Sb-F doped spinel-like transition layer,simultaneously.The modified sample maintains an initial discharge specific capacity of 221.2 mA h g^(-1)and a capacity retention of 86%after 200 cycles at 3–4.6 V and 0.5 C.Moreover,it has a discharge specific capacity of163.3 mA h g^(-1)at a high rate of 5 C.Meanwhile,combining highly electronegative Sb^(3+)&F^(-)that widen the Li^(+)transport channel with the amorphous coating of F^(-)doped Sb_(2)O_(3)with higher conductivity improves the interface transport kinetics.This breaks the stereotypical view in traditional concepts that fluorinated coatings or inert metal oxide coatings inhibit Li^(+)transport.Moreover,the inert composite coating combined with Sb–O–F with high bond energy stabilizes the surface structure.A series of characterizations confirm that the joint improvement of interface structure stability and transport kinetics significantly enhances the electrochemical performance of LiCoO_(2).展开更多
The mechanical,thermodynamic properties and electrical conductivities of L1_(2)-Al_(3)X(X=Zr,Sc,Er,Yb,Hf)structural phases in aluminum conductors were investigated through a first-principles study.The results demonstr...The mechanical,thermodynamic properties and electrical conductivities of L1_(2)-Al_(3)X(X=Zr,Sc,Er,Yb,Hf)structural phases in aluminum conductors were investigated through a first-principles study.The results demonstrate that all structural phases have good alloy-forming ability and structural stability,where Al_(3)Zr is the most superior.Al_(3)Zr,Al_(3)Hf and Al_(3)Sc have enhanced shear and deformation resistance in comparison to other phases.Within the temperature range of 200−600 K,Al_(3)Er and Al_(3)Yb possess the greatest thermodynamic stability,followed by Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.Al_(3)Er and Al_(3)Yb have higher thermodynamic stability than Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.All structural phases exhibit substantial metallic properties,indicating their good electrical conductivity.The electrical conductivities of Al_(3)Hf and Al_(3)Zr are higher than those of Al_(3)Er,Al_(3)Yb and Al_(3)Sc.The covalent bond properties in Al_(3)Sc,Al_(3)Er and Al_(3)Yb enhance the hardness,brittleness and thermodynamic stability of the structural phase.The thermodynamic stability of Al_(3)Sc is significantly reduced by ionic bonds.展开更多
Single-ion conductors based on covalent organic frameworks(COFs)have garnered attention as a potential alternative to currently prevalent inorganic ion conductors owing to their structural uniqueness and chemical vers...Single-ion conductors based on covalent organic frameworks(COFs)have garnered attention as a potential alternative to currently prevalent inorganic ion conductors owing to their structural uniqueness and chemical versatility.However,the sluggish Li+conduction has hindered their practical applications.Here,we present a class of solvent-free COF single-ion conductors(Li-COF@P)based on weak ion-dipole interaction as opposed to traditional strong ion-ion interaction.The ion(Li+from the COF)-dipole(oxygen from poly(ethylene glycol)diacrylate embedded in the COF pores)interaction in the Li-COF@P promotes ion dissociation and Li+migration via directional ionic channels.Driven by this single-ion transport behavior,the Li-COF@P enables reversible Li plating/stripping on Li-metal electrodes and stable cycling performance(88.3%after 2000 cycles)in organic batteries(Li metal anode||5,5’-dimethyl-2,2’-bis-p-benzoquinone(Me2BBQ)cathode)under ambient operating conditions,highlighting the electrochemical viability of the Li-COF@P for all-solid-state organic batteries.展开更多
High-temperature superconducting(HTS)rare-earth Ba_(2)Cu_(3)O_(7-x)(REBCO)coated conductors(CCs)have significant potential in high-current and high-field applications.However,owing to the weak interface strength of th...High-temperature superconducting(HTS)rare-earth Ba_(2)Cu_(3)O_(7-x)(REBCO)coated conductors(CCs)have significant potential in high-current and high-field applications.However,owing to the weak interface strength of the laminated composite REBCO CCs,the damage induced by the thermal mismatch stress under a combination of epoxy impregnation,cooling,and quenching can cause premature degradation of the critical current.In this study,a three-dimensional(3D)electromagnetic-thermal-mechanical model based on the H-formulation and cohesive zone model(CZM)is developed to study the critical current degradation characteristics in an epoxy-impregnated REBCO CC caused by the damage during a quench.The temperature variation,critical current degradation of the REBCO CC,and its degradation onset temperature calculated by the numerical model are in agreement with the experimental data taken from the literature.The delamination of the REBCO CC predicted by the numerical model is consistent with the experimental result.The numerical results also indicate that the shear stress is the main contributor to the damage propagation inside the REBCO CC.The premature degradation of the critical current during a quench is closely related to the interface shear strength inside the REBCO CC.Finally,the effects of the coefficient of thermal expansion(CTE)of the epoxy resin,thickness of the substrate,and substrate material on the critical current degradation characteristics of the epoxy-impregnated REBCO CC during a quench are also discussed.These results help us understand the relationship between the current-carrying degradation and damage in the HTS applications.展开更多
提出一种基于人工磁导体(Artificial Magnetic Conductor, AMC)的高增益宽带天线,该天线由一个AMC超表面和一个微带贴片天线组成。利用AMC的同相反射特性,将天线的后向辐射反射与前向辐射叠加,从而提升了天线的增益。天线的整体尺寸为0....提出一种基于人工磁导体(Artificial Magnetic Conductor, AMC)的高增益宽带天线,该天线由一个AMC超表面和一个微带贴片天线组成。利用AMC的同相反射特性,将天线的后向辐射反射与前向辐射叠加,从而提升了天线的增益。天线的整体尺寸为0.6λ_(0)×0.6λ_(0)×0.12λ_(0) (λ_(0)为天线谐振频率对应的波长)。测试结果表明,在4.55~6.1 GHz (27.7%)的工作频段内,天线的峰值增益达到8.4 dB。与利用理想电导体(Perfect Electric Conductor, PEC)提升增益的方法相比,其剖面从0.37λ_(0)降低到0.12λ_(0)。该天线剖面低、尺寸小、增益高、成本低廉,可以应用于WLAN波段通信。展开更多
基金supported by the National Natural Science Foundation of China(Nos.22175070,22293041)supported by the National Key Research and Development Program(Nos.2021YFB2500200,2021YFB2400300)+1 种基金the National Natural Science Foundation of China(No.52177214)China Fujian Energy Devices Science and Technology Innovation Laboratory Open Fund(No.21C-OP202211)。
文摘For large-scale energy storage devices,all-solid-state sodium-ion batteries(SIBs)have been revered for the abundant resources,low cost,safety performance and a wide operating temperature range.Na-ion solid-state electrolytes(Na-ion SSEs)are the critical parts and mostly determine the electrochemical performance of SIBs.Among the studied ones,inorganic Na-ion SSEs stand out for their good safety performance and high ionic conductivity.In this review,we outline the research progress of inorganic SSEs in SIBs based on the perspectives of crystal structure,performance optimization,synthesis methods,allsolid-state SIBs,interface modification and related characterization techniques.We hope to provide some ideas for the design of future high-performance Na-ion SSEs.
基金supported by the National Natural Science Foundation of China(22179149,22075329,51573215,and 21978332)Research and Development Project of Henan Academy Sciences China(232018002)。
文摘Single ion gel polymer electrolyte has the advantages of high Li^(+)conductivity and dendrite mitigation.However,the addition of organic solvent makes the electrolyte flammable,posing serious safety hazards.Herein,we report a flame-retard ant cross-linked sp^(3)boron-based single-ion gel polymer electrolyte(BSIPE).BSIPE was prepared by a simple one-step photoinitiated in situ thiol-ene click reaction.Due to the boron-based anions being immobilized in the cross-linking network,the developed BSIPE/PFN exhibits a high t_(Li^(+))(0.87),which can mitigate concentration polarization phenomenon and suppress the growth of lithium dendrites.BSIPE/PFN plasticized with triethyl phosphate(TEP),fluoroethylene carbonate(FEC)and LiNO_(3)exhibits enhanced ionic conductivity of 4.25×10^(-4)S cm^(-1)at 30℃ and flame retardancy.FEC and LiNO_(3) are conducive to form a stable solid electrolyte interphase(SEI)rich in Li_(3)N and LiF to improve interface stability.As expected,the dendrite-free Li‖BSIPE/PFN‖Li symmetric cell exhibits considerable cycling life over 1500 h.BSIPE/PFN significantly boosts the performance of LFP‖Li cell,which displays a capacity retention of 84.6%after 500 cycles.The BSIPE/PFN has promising applications in highsafety and high-performance lithium metal batteries.
基金supported by the National Key R&D Program of China(2022YFB3807700)the National Natural Science Foundation of China(52072217,22179071,51772169,and 52104313)+3 种基金the Hubei Provincial Natural Science Foundation of China(2023AFB618 and 2024AFB993)the Hubei Natural Science Foundation Innovation Group Project(2022CFA020)the Joint Funds of the Hubei Natural Science Foundation Innovation and Development(2022CFD034)the Major Technological Innovation Project of Hubei Science and Technology Department(2019AAA164)。
文摘Black phosphorus(BP)is recognized as a promising anode for sodium-ion batteries(SIBs)due to its high safety and theoretical capacity.However,traditional ball milling methodologies for fabricating BP composite anodes have not satisfactorily addressed the challenges of poor rate performance and short cycle life.To fill this scientific gap,we herein pioneer incorporating the sodium fast ionic conductorβ"-Al_(2)O_(3)into ball-milled BP with carbon,which facilitates the formation of three-dimensional mass transfer channels in the resulting composite.To stabilize these channels,we develop a novel and environmentally friendly functional binder that outperforms traditional binders in thermal stability,wettability,and mechanical properties.The newly established binder is capable of remarkably mitigating volume expansion and interfacial side reactions in the BP/β"-Al_(2)O_(3)/C composite anode.Additionally,we identify synergistic effects of the binder interacting with the BP/β"-Al_(2)O_(3)/C composite during cycling,characterized by the in-situ formation of P-O-C bonds,which is the first instance of a strong,durable chemical bond between the binder and the active material to the best of our knowledge.These advancements allow the composite electrode to exhibit exceptional sodium storage,including high initial Coulombic efficiency and long-term cycling stability,which surpasses most previous phosphorus-based anodes fabricated via traditional approaches.Notably,when paired with a Na_(4)Fe_(3)(PO_(4))_(2)P_(2)O_7(NFPP)cathode,the full cell exhibits unexpectedly high energy and power densities,highlighting the BP potential in SIBs.The findings presented in the present work contribute to the promotion of economical and efficient applications of phosphorus-based anode materials.
文摘Lithium halide solid-state electrolytes,with the general formula of Li_(3±m)M_(n)X_(6),are regarded as the promising families of electrolyte material for all solid-state lithium-ion batteries because of the relatively good ionic conductivity,high oxidative stability against high-voltage oxide cathodes,and broad electrochemical stability window[1].Here,M stands for one or multiple metal elements and X for one or multiple halogen elements.
基金supported by the National Natural Science Foundation of China(22075170)employed resources from the BL11B station of the Shanghai Synchrotron Radiation Facility(SSRF,under contract number:2023-SSRF-PT-502681)。
文摘Increasing the charging cut-off voltage can significantly enhance the energy density of LiCoO_(2).However,the continuous deterioration of interface structure and transport kinetics under high voltage poses challenges to electrochemical stability.This work proposes to in-situ construct a uniform element gradient modification structure on the surface and subsurface of LiCoO_(2).The modification structure contains an Sb_(2)O_(3)&SbF_(x)composite coating layer and an Sb-F doped spinel-like transition layer,simultaneously.The modified sample maintains an initial discharge specific capacity of 221.2 mA h g^(-1)and a capacity retention of 86%after 200 cycles at 3–4.6 V and 0.5 C.Moreover,it has a discharge specific capacity of163.3 mA h g^(-1)at a high rate of 5 C.Meanwhile,combining highly electronegative Sb^(3+)&F^(-)that widen the Li^(+)transport channel with the amorphous coating of F^(-)doped Sb_(2)O_(3)with higher conductivity improves the interface transport kinetics.This breaks the stereotypical view in traditional concepts that fluorinated coatings or inert metal oxide coatings inhibit Li^(+)transport.Moreover,the inert composite coating combined with Sb–O–F with high bond energy stabilizes the surface structure.A series of characterizations confirm that the joint improvement of interface structure stability and transport kinetics significantly enhances the electrochemical performance of LiCoO_(2).
基金National Natural Science Foundation of China (No. 52274403)。
文摘The mechanical,thermodynamic properties and electrical conductivities of L1_(2)-Al_(3)X(X=Zr,Sc,Er,Yb,Hf)structural phases in aluminum conductors were investigated through a first-principles study.The results demonstrate that all structural phases have good alloy-forming ability and structural stability,where Al_(3)Zr is the most superior.Al_(3)Zr,Al_(3)Hf and Al_(3)Sc have enhanced shear and deformation resistance in comparison to other phases.Within the temperature range of 200−600 K,Al_(3)Er and Al_(3)Yb possess the greatest thermodynamic stability,followed by Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.Al_(3)Er and Al_(3)Yb have higher thermodynamic stability than Al_(3)Hf,Al_(3)Zr and Al_(3)Sc.All structural phases exhibit substantial metallic properties,indicating their good electrical conductivity.The electrical conductivities of Al_(3)Hf and Al_(3)Zr are higher than those of Al_(3)Er,Al_(3)Yb and Al_(3)Sc.The covalent bond properties in Al_(3)Sc,Al_(3)Er and Al_(3)Yb enhance the hardness,brittleness and thermodynamic stability of the structural phase.The thermodynamic stability of Al_(3)Sc is significantly reduced by ionic bonds.
基金supported by the Basic Science Research Program (No.RS-2024-00344021) through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and future Planningthe financial support from the National Natural Science Foundation of China (52103277)+2 种基金the Program for Science & Technology Innovation Talents in Universities of Henan Province (23HASTIT015)Natural Science Foundation of Henan Province (242300421073)supported by the Technology Innovation Program (20010960) funded by the Ministry of Trade, Industry & Energy (MOTIE, Korea)
文摘Single-ion conductors based on covalent organic frameworks(COFs)have garnered attention as a potential alternative to currently prevalent inorganic ion conductors owing to their structural uniqueness and chemical versatility.However,the sluggish Li+conduction has hindered their practical applications.Here,we present a class of solvent-free COF single-ion conductors(Li-COF@P)based on weak ion-dipole interaction as opposed to traditional strong ion-ion interaction.The ion(Li+from the COF)-dipole(oxygen from poly(ethylene glycol)diacrylate embedded in the COF pores)interaction in the Li-COF@P promotes ion dissociation and Li+migration via directional ionic channels.Driven by this single-ion transport behavior,the Li-COF@P enables reversible Li plating/stripping on Li-metal electrodes and stable cycling performance(88.3%after 2000 cycles)in organic batteries(Li metal anode||5,5’-dimethyl-2,2’-bis-p-benzoquinone(Me2BBQ)cathode)under ambient operating conditions,highlighting the electrochemical viability of the Li-COF@P for all-solid-state organic batteries.
基金Project supported by the National Natural Science Foundation of China(Nos.12302278,U2241267,12172155,and 11932008)the Fundamental Research Funds for the Central Universities of China(No.lzujbky-2022-48)the Natural Science Foundation of Gansu Province of China(No.24JRRA473)。
文摘High-temperature superconducting(HTS)rare-earth Ba_(2)Cu_(3)O_(7-x)(REBCO)coated conductors(CCs)have significant potential in high-current and high-field applications.However,owing to the weak interface strength of the laminated composite REBCO CCs,the damage induced by the thermal mismatch stress under a combination of epoxy impregnation,cooling,and quenching can cause premature degradation of the critical current.In this study,a three-dimensional(3D)electromagnetic-thermal-mechanical model based on the H-formulation and cohesive zone model(CZM)is developed to study the critical current degradation characteristics in an epoxy-impregnated REBCO CC caused by the damage during a quench.The temperature variation,critical current degradation of the REBCO CC,and its degradation onset temperature calculated by the numerical model are in agreement with the experimental data taken from the literature.The delamination of the REBCO CC predicted by the numerical model is consistent with the experimental result.The numerical results also indicate that the shear stress is the main contributor to the damage propagation inside the REBCO CC.The premature degradation of the critical current during a quench is closely related to the interface shear strength inside the REBCO CC.Finally,the effects of the coefficient of thermal expansion(CTE)of the epoxy resin,thickness of the substrate,and substrate material on the critical current degradation characteristics of the epoxy-impregnated REBCO CC during a quench are also discussed.These results help us understand the relationship between the current-carrying degradation and damage in the HTS applications.
