兴奋剂
自行车
涂层
可扩展性
材料科学
电池(电)
纳米技术
化学工程
光电子学
计算机科学
工程类
物理
热力学
功率(物理)
考古
数据库
历史
作者
Jia Yao,Yuyu Li,Tiantian Xiong,Yameng Fan,Lingfei Zhao,Xiangxin Cheng,Yunan Tian,Lele Li,Yan Li,Wen Zhang,Peng Yu,Pingmei Guo,Zehui Yang,Jian Peng,Lixing Xue,Jiazhao Wang,Zhaohuai Li,Ming Xie,Huan Liu,Shi Xue Dou
标识
DOI:10.1002/anie.202407898
摘要
Abstract The quest for smart electronics with higher energy densities has intensified the development of high‐voltage LiCoO 2 (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 LiAlO 2 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.
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