Scalable Precise Nanofilm Coating and Gradient Al Doping Enable Stable Battery Cycling of LiCoO2 at 4.7 V

Author:

Yao Jia12,Li Yuyu12,Xiong Tiantian3,Fan Yameng4,Zhao Lingfei4,Cheng Xiangxin12,Tian Yunan12,Li Lele12,Li Yan12,Zhang Wen5,Yu Peng5,Guo Pingmei12,Yang Zehui3,Peng Jian36ORCID,Xue Lixing7,Wang Jiazhao4,Li Zhaohuai12,Xie Ming1,Liu Huakun48,Dou Shixue8

Affiliation:

1. State Key Laboratory of Precision Blasting Jianghan University 430056 Wuhan China

2. Hubei Provincial Engineering Research Center of Surface and Interface Regulation Technology and Equipment for Renewable Energy Materials Jianghan University 430056 Wuhan China

3. Sustainable Energy Laboratory Faculty of Materials Science and Chemistry China University of Geosciences Wuhan 430074 Wuhan China

4. Institute for Superconducting and Electronic Materials, Australian Institute for Innovative Materials University of Wollongong Squires Way 2522 North Wollongong NSW,, Australia

5. State Key Laboratory of Material Processing and Die & Mold Technology School of Materials Science and Engineering Huazhong University of Science and Technology 430074 Wuhan China

6. Department of Mechanical and Materials Engineering Western University N6 A 5B9 London ON Canada

7. Cornex New Energy Co., Ltd. 432099 Wuhan China

8. Institute of Energy Materials Science University of Shanghai for Science and Technology 200093 Shanghai People's Republic of China

Abstract

AbstractThe quest for smart electronics with higher energy densities has intensified the development of high‐voltage LiCoO2 (LCO). Despite their potential, LCO materials operating at 4.7 V faces critical challenges, including interface degradation and structural collapse. Herein, we propose a collective surface architecture through precise nanofilm coating and doping that combines an ultra‐thin LiAlO2 coating layer and gradient doping of Al. This architecture not only mitigates side reactions, but also improves the Li+ migration kinetics on the LCO surface. Meanwhile, gradient doping of Al inhibited the severe lattice distortion caused by the irreversible phase transition of O3−H1−3−O1, thereby enhanced the electrochemical stability of LCO during 4.7 V cycling. DFT calculations further revealed that our approach significantly boosts the electronic conductivity. As a result, the modified LCO exhibited an outstanding reversible capacity of 230 mAh g−1 at 4.7 V, which is approximately 28 % higher than the conventional capacity at 4.5 V. To demonstrate their practical application, our cathode structure shows improved stability in full pouch cell configuration under high operating voltage. LCO exhibited an excellent cycling stability, retaining 82.33 % after 1000 cycles at 4.5 V. This multifunctional surface modification strategy offers a viable pathway for the practical application of LCO materials, setting a new standard for the development of high‐energy‐density and long‐lasting electrode materials.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Publisher

Wiley

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