材料科学
兴奋剂
电极
氧化还原
阳离子聚合
共价键
过渡金属
离子
化学工程
盐(化学)
冶金
物理化学
催化作用
高分子化学
化学
光电子学
有机化学
工程类
作者
Yuji Mahara,Hideaki Oka,Takamasa Nonaka,Satoru Kosaka,Naoko Takahashi,Yasuhito Kondo,Yoshinari Makimura
标识
DOI:10.1002/aenm.202301843
摘要
Abstract Disordered rock‐salt (DRS) type active materials are highly significant because of their large reversible capacities, which are due to their unique Li + diffusion pathway and the redox capabilities of cationic transition metals (TMs) and anionic O ions. Loosely crystalline DRS materials have weak covalent bonds between TMs and O, increasing the O redox contribution and thereby enhancing their capacities. In this study, Mn‐based positive electrode materials with DRS structures are activated and stabilized by mechanochemical doping of nonmetallic elements P and B into interstitial sites. Synthesized Li 0.90 Mn 0.84 P 0.04 O 2 (LMPO5) exhibits an initial discharge capacity of 346 mAh g −1 (1050 Wh kg −1 ) during charging/discharging. Li 0.91 Mn 0.83 B 0.10 O 2 (LMBO5) has a moderately expanded lattice size, which facilitates high‐capacity retention during cycling (≈284 mAh g −1 at the 30th cycle). The structural properties of the synthesized active materials are extensively characterized. By introducing nonmetallic elements into the interstitial sites of Mn‐based materials, inexpensive, high‐capacity, and long‐cycling/calendar‐life Co/Ni‐free monometallic positive electrode materials may be further developed.
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