Li‐Rich Li[Li1/6Fe1/6Ni1/6Mn1/2]O2 (LFNMO) Cathodes: Atomic Scale Insight on the Mechanisms of Cycling Decay and of the Improvement due to Cobalt Phosphate Surface Modification |
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| Authors: | Xing Li Kangjia Zhang David Mitlin Eunsu Paek Mingshan Wang Fei Jiang Yun Huang Zhenzhong Yang Yue Gong Lin Gu Wengao Zhao Yingge Du Jianming Zheng |
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| Affiliation: | 1. The Center of New Energy Materials and Technology, Southwest Petroleum University, Chengdu, Sichuan, China;2. Chemical & Biomolecular Engineering, Clarkson University, Potsdam, NY, USA;3. Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA;4. Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, China;5. Energy and Environment Directorate, Pacific Northwest National Laboratory, Richland, WA, USA;6. Research Institute (RI), NingDe Amperex Technology Limited, Ningde, Fujian, China |
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| Abstract: | Lithium‐rich Li[Li1/6Fe1/6Ni1/6Mn1/2]O2 (0.4Li2MnO3‐0.6LiFe1/3Ni1/3Mn1/3O2, LFNMO) is a new member of the xLi2MnO3·(1 ? x)LiMO2 family of high capacity–high voltage lithium‐ion battery (LIB) cathodes. Unfortunately, it suffers from the severe degradation during cycling both in terms of reversible capacity and operating voltage. Here, the corresponding degradation occurring in LFNMO at an atomic scale has been documented for the first time, using high‐angle annular dark‐field scanning transmission electron microscopy (HAADF‐STEM), as well as tracing the elemental crossover to the Li metal anode using X‐ray photoelectron spectroscopy (XPS). It is also demonstrated that a cobalt phosphate surface treatment significantly boosts LFNMO cycling stability and rate capability. Due to cycling, the unmodified LFNMO undergoes extensive elemental dissolution (especially Mn) and O loss, forming Kirkendall‐type voids. The associated structural degradation is from the as‐synthesized R‐3m layered structure to a disordered rock‐salt phase. Prior to cycling, the cobalt phosphate coating is epitaxial, sharing the crystallography of the parent material. During cycling, a 2–3 nm thick disordered Co‐rich rock‐salt structure is formed as the outer shell, while the bulk material retains R‐3m crystallography. These combined cathode–anode findings significantly advance the microstructural design principles for next‐generation Li‐rich cathode materials and coatings. |
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| Keywords: | capacity degradation mechanism crossover high‐voltage cathode Li‐ and Mn‐rich cathode phosphate coating |
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