材料科学
成核
阴极
纳米尺度
电化学
氧化物
聚结(物理)
原子单位
纳米颗粒
纳米技术
化学工程
冶金
物理化学
电极
化学
物理
有机化学
量子力学
天体生物学
工程类
作者
Seok Hyun Song,Hwa Soo Kim,Kyoung Sun Kim,Seokjae Hong,Hyungkwon Jeon,Jun Lim,Young Hwa Jung,Hyungju Ahn,Jong Dae Jang,Man‐Ho Kim,Jong Hyeok Seo,Ji‐Hwan Kwon,Dokyung Kim,Young Joo Lee,Young‐Soo Han,Kyu‐Young Park,Chunjoong Kim,Seung‐Ho Yu,Hyeokjun Park,Hyeong Min Jin,Hyungsub Kim
标识
DOI:10.1002/adfm.202306654
摘要
Abstract Ni‐rich layered oxides are envisioned as the most promising cathode materials for next‐generation lithium‐ion batteries; however, their practical adoption is plagued by fast capacity decay originating from chemo‐mechanical degradation. The intrinsic chemical–mechanical instability, inherited from atomic‐ and nanoscale defects generated during synthesis, is not yet resolved. Here, atomic‐ and nanoscale structural evolution during solid‐state synthesis of Ni‐rich layered cathode, Li[Ni 0.92 Co 0.03 Mn 0.05 ]O 2 , is investigated using combined X‐ray/neutron scattering and electron/X‐ray microscopy. The multiscale analyses demonstrate the intertwined correlation between phase transition and microstructural evolution, with atomic‐scale defects derived from the decomposition of precursors leading to the creation of intra/inter‐granular pores. The nucleation and coalescence mechanism of pore defects during the synthesis of Ni‐rich layered cathodes are quantitatively revealed. Furthermore, a modified synthetic route is proposed to effectively circumvent the formation of nanoscale defects in Ni‐rich layered cathodes by facilitating uniform synthetic reactions, resulting in superior electrochemical and microstructural stability.
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