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In situ analysis of dynamic evolution of the additive-regulated cathode processes in quasi-solid-state lithium-metal batteries
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作者 jian-xin tian Hui-Juan Guo +3 位作者 Jing Wan Gui-Xian Liu Rui Wen Li-Jun Wan 《Science China Chemistry》 SCIE EI CAS CSCD 2023年第10期2921-2928,共8页
The implementation of high-energy-density storage devices can be facilitated by the built-in situ cathode electrolyte interphase(CEI)between Ni-rich cathodes and gel polymer electrolytes,as it improves interfacial com... The implementation of high-energy-density storage devices can be facilitated by the built-in situ cathode electrolyte interphase(CEI)between Ni-rich cathodes and gel polymer electrolytes,as it improves interfacial compatibility and enhances security.Understanding the interphase processes of cathode materials,including the structural evolution and the formation of cathode electrolyte interphase upon charging/discharging,is crucial for the design of solid-state lithium batteries.Here,we employed in situ atomic force microscopy(AFM)to investigate the effects of lithium difluoro(oxalato)borate(Li DFOB)on the dynamic evolution of the cathode interphase.In the presence of Li DFOB,the adhesion of nanoparticles and a thin amorphous film on the cathode surface resulted in the formation of a homogeneous CEI,inducing the production of LixPFyas byproducts.Furthermore,the stable CEI formed between the cathode and electrolyte helps maintain the integrity of the composition and structure,reduces interfacial resistance,and improves the cycle stability of the batteries.The visualization of in situ AFM in quasi-solid-state lithium-metal batteries provides valuable insights into the distinct nanostructures and growth dynamics of Li DFOB-mediated CEI on the LiNi_(6)Co_(2)Mn_(2)O_(2) cathode,thus offering a universal and convenient technique for interfacial analysis and a mechanistic understanding of solid-state batteries. 展开更多
关键词 atomic force microscopy ELECTROCHEMISTRY interfacial dynamics solid-state lithium batteries cathode electrolyte interphase
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