High-voltage nickel(Ni)-rich layered oxide-based lithium metal batteries(LMBs)exhibit a great potential in advanced batteries due to the ultra-high energy density.However,it is still necessary to deal with the challen...High-voltage nickel(Ni)-rich layered oxide-based lithium metal batteries(LMBs)exhibit a great potential in advanced batteries due to the ultra-high energy density.However,it is still necessary to deal with the challenges in poor cyclic and thermal stability before realizing practical application where cycling life is considered.Among many improved strategies,mechanical and chemical stability for the electrode electrolyte interface plays a key role in addressing these challenges.Therefore,extensive effort has been made to address the challenges of electrode-electrolyte interface.In this progress,the failure mechanism of Ni-rich cathode,lithium metal anode and electrolytes are reviewed,and the latest breakthrough in stabilizing electrode-electrolyte interface is also summarized.Finally,the challenges and future research directions of Ni-rich LMBs are put forward.展开更多
Rechargeable lithium metal batteries(LMBs)meet the demands of high-energy applications in electric vehicles and truck transportation[1-4].Yet,the low coulombic efficiency(CE)hinders the widespread application of Li an...Rechargeable lithium metal batteries(LMBs)meet the demands of high-energy applications in electric vehicles and truck transportation[1-4].Yet,the low coulombic efficiency(CE)hinders the widespread application of Li anode,which is closely related to the electrolytes[5-7].The CE of traditional electrolytes for Li anodes is closely related to the speciation of the plated Li during cycling,where fluorinated solvents with weakly solvated Li+usually exhibit larger Li deposition particles with higher CE[8,9].But the relationship between the morphological difference and CE in different electrolytes is less studied[10,11].There are three relationships between the deposition kinetics of interface Li and the cycling of the battery,no correlation,positive correlation[12,13],and negative correlation[14,15]have been reported on active Li anodes,which neglects the reactivity of Li metal in kinetics.Solid electrolyte interphase(SEl)was formed by the electrolytes reacting with Li,and Li deposition can occur on the Li/SEl interface or the fresh Li/electrolyte interface[16,17].Each pathway has different deposition kinetics.Therefore,in order to understand the relationship between electrolyte kinetics and lithium deposition morphology,it is important to solve the kinetics of the two ways in the electrolyte.展开更多
基金National Natural Science Foundation of China,Grant/Award Numbers:U21A20311,51971090。
文摘High-voltage nickel(Ni)-rich layered oxide-based lithium metal batteries(LMBs)exhibit a great potential in advanced batteries due to the ultra-high energy density.However,it is still necessary to deal with the challenges in poor cyclic and thermal stability before realizing practical application where cycling life is considered.Among many improved strategies,mechanical and chemical stability for the electrode electrolyte interface plays a key role in addressing these challenges.Therefore,extensive effort has been made to address the challenges of electrode-electrolyte interface.In this progress,the failure mechanism of Ni-rich cathode,lithium metal anode and electrolytes are reviewed,and the latest breakthrough in stabilizing electrode-electrolyte interface is also summarized.Finally,the challenges and future research directions of Ni-rich LMBs are put forward.
文摘Rechargeable lithium metal batteries(LMBs)meet the demands of high-energy applications in electric vehicles and truck transportation[1-4].Yet,the low coulombic efficiency(CE)hinders the widespread application of Li anode,which is closely related to the electrolytes[5-7].The CE of traditional electrolytes for Li anodes is closely related to the speciation of the plated Li during cycling,where fluorinated solvents with weakly solvated Li+usually exhibit larger Li deposition particles with higher CE[8,9].But the relationship between the morphological difference and CE in different electrolytes is less studied[10,11].There are three relationships between the deposition kinetics of interface Li and the cycling of the battery,no correlation,positive correlation[12,13],and negative correlation[14,15]have been reported on active Li anodes,which neglects the reactivity of Li metal in kinetics.Solid electrolyte interphase(SEl)was formed by the electrolytes reacting with Li,and Li deposition can occur on the Li/SEl interface or the fresh Li/electrolyte interface[16,17].Each pathway has different deposition kinetics.Therefore,in order to understand the relationship between electrolyte kinetics and lithium deposition morphology,it is important to solve the kinetics of the two ways in the electrolyte.
