材料科学
锰
阴极
电化学
中子衍射
锂(药物)
化学工程
溶胶凝胶
电极
衍射
纳米技术
冶金
物理化学
物理
工程类
内分泌学
化学
光学
医学
作者
Shripad Patil,Devendrasinh Darbar,Ethan C. Self,Thomas F. Malkowski,Vincent C. Wu,Raynald Giovine,Nathan J. Szymanski,Rebecca D. McAuliffe,Bo Jiang,Jong K. Keum,Krishna Prasad Koirala,Bin Ouyang,Katharine Page,Chongmin Wang,Gerbrand Ceder,Raphaële J. Clément,Jagjit Nanda
标识
DOI:10.1002/aenm.202203207
摘要
Abstract Cation‐disordered rocksalt (DRX) cathodes have recently emerged as a promising class of cobalt‐free, high‐capacity cathodes for lithium‐ion batteries. To facilitate their commercialization, the development of scalable synthesis techniques providing control over composition and morphology is critical. To this end, a sol‐gel synthesis route to prepare Mn‐rich DRX cathodes with high capacities is presented here. Several compositions with varied Mn content and nominal F doping are successfully prepared using this technique. In‐situ X‐ray diffraction measurements demonstrate that DRX formation proceeds at moderate temperature (800 °C) through the sol‐gel route, which enables intimate mixing among reactive intermediate phases that form at lower temperatures. All synthesized compositions possess cation short‐range order, as evidenced by neutron pair distribution function and electron diffraction analysis. These DRX materials demonstrate promising electrochemical performance with reversible capacities up to 275 mAh g. Compared to the baseline oxide (Li 1.2 Mn 0.4 Ti 0.4 O 2 ), the Mn‐rich compositions exhibit improved cycling stability, with some showing an increase in capacity upon cycling. Overall, this study demonstrates the feasibility of preparing high‐capacity DRX cathodes through a sol‐gel based synthesis route, which may be further optimized to provide better control over the product morphology compared to traditional synthesis methods.
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