Zhou Xing, Chang Chia-Yu, Yu Dongfang, Zhang Kai, Li Zhi, Jiang Shi-Kai, Zhu Yizhou, Xia Yongyao, Hwang Bing Joe, Wang Yonggang
Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Fudan University, Shanghai, China.
Contemporary Amperex Technology Ltd. (CATL), Ningde, China.
Nat Commun. 2025 Jan 2;16(1):112. doi: 10.1038/s41467-024-55695-9.
The application of high-voltage positive electrode materials in sulfide all-solid-state lithium batteries is hindered by the limited oxidation potential of sulfide-based solid-state electrolytes (SSEs). Consequently, surface coating on positive electrode materials is widely applied to alleviate detrimental interfacial reactions. However, most coating layers also react with sulfide-based SSEs, generating electronic conductors and causing gradual interface degradation and capacity fading. To address this, we propose a LiZrF coating layer on LiCoO, which exhibits minimal reaction with SSEs, and its decomposition products are electron-conductive-free. Furthermore, this coating layer also efficiently mitigates the layered-to-spinel/rock-salt surface structural transformation in LiCoO. As a result, the In-Li|LiPSCl | LiZrF-LiCoO all-solid-state cell demonstrates an initial areal capacity of 5.2 mAh cm and a capacity retention of 80.5% after 1500 cycles at 70 mA/g with high LiCoO areal mass loading (30.19 mg cm) and a cut-off voltage of 3.9 V (corresponding to potential of 4.5 V versus Li/Li), at 25 °C.
硫化物基固态电解质(SSE)有限的氧化电位阻碍了高压正极材料在硫化物全固态锂电池中的应用。因此,正极材料表面涂层被广泛应用以减轻有害的界面反应。然而,大多数涂层也会与硫化物基SSE发生反应,生成电子导体,导致界面逐渐退化和容量衰减。为了解决这个问题,我们提出在LiCoO上涂覆一层LiZrF涂层,该涂层与SSE的反应极小,且其分解产物无电子导电性。此外,该涂层还能有效减轻LiCoO中从层状到尖晶石/岩盐的表面结构转变。结果,In-Li|LiPSCl | LiZrF-LiCoO全固态电池在25℃下,以70 mA/g的电流密度、3.9 V的截止电压(对应相对于Li/Li的4.5 V电位)、高LiCoO面质量负载(30.19 mg cm)进行1500次循环后,初始面积容量为5.2 mAh cm,容量保持率为80.5%。