材料科学
八面体
过渡金属
结晶学
堆积
扫描透射电子显微镜
相变
插层(化学)
相(物质)
化学物理
透射电子显微镜
无机化学
晶体结构
纳米技术
化学
热力学
物理
催化作用
有机化学
生物化学
作者
Jae Chul Kim,Deok‐Hwang Kwon,Julia H. Yang,Hyunchul Kim,Shou‐Hang Bo,Lijun Wu,Haegyeom Kim,Dong‐Hwa Seo,Tan Shi,Jingyang Wang,Yimei Zhu,Gerbrand Ceder
标识
DOI:10.1002/aenm.202001151
摘要
Abstract The oxygen stacking of O3‐type layered sodium transition metal oxides (O3‐NaTMO 2 ) changes dynamically upon topotactic Na extraction and reinsertion. While the phase transition from octahedral to prismatic Na coordination that occurs at intermediate desodiation by transition metal slab gliding is well understood, the structural evolution at high desodiation, crucial to achieve high reversible capacity, remains mostly uncharted. In this work, the phase transitions of O3‐type layered NaTMO 2 at high voltage are investigated by combining experimental and computational approaches. An OP2‐type phase that consists of alternating octahedral and prismatic Na layers is directly observed by in situ X‐ray diffraction and high‐resolution scanning transmission electron microscopy. The origin of this peculiar phase is explained by atomic interactions involving Jahn–Teller active Fe 4+ and distortion tolerant Ti 4+ that stabilize the local Na environment. The path‐dependent desodiation and resodiation pathways are also rationalized in this material through the different kinetics of the prismatic and octahedral layers, presenting a comprehensive picture about the structural stability of the layered materials upon Na intercalation.
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