过电位
阳极
材料科学
电解质
阴极
成核
化学工程
降级(电信)
化学浴沉积
纳米技术
电极
光电子学
薄膜
电化学
化学
电气工程
有机化学
物理化学
工程类
作者
Dong‐Bum Seo,Dohun Kim,Mee Ree Kim,Jimin Kwon,Hyeong Jun Kook,Saewon Kang,Soonmin Yim,Sun Sook Lee,Dong Ok Shin,Ki‐Seok An,Sangbaek Park
标识
DOI:10.1007/s40820-025-01729-w
摘要
Abstract Anode-free all-solid-state batteries (AFASSBs) are potential candidates for next-generation electric mobility devices that offer superior energy density and stability by eliminating Li from the anode. However, despite its potential to stabilize the interface between sulfide solid electrolytes (SEs) and anode-free current collectors (CCs) efficiently, a controllable approach to incorporating MoS 2 into AFASSBs has not yet been found. Herein, we propose a strategy for stabilizing the interface of Li-free all-solid-state batteries using controllable MoS 2 sacrificial thin films. MoS 2 was controllably grown on CCs by metal–organic chemical vapor deposition, and the MoS 2 sacrificial layer in contact with the SEs formed an interlayer composed of Mo metal and Li 2 S through a conversion reaction. In the AFASSBs with MoS 2 , Mo significantly reduces the nucleation overpotential of Li, which results in uniform Li plating. In addition, MoS 2 -based Li 2 S facilitates the formation of a uniform and robust SE interface, thereby enhancing the stability of AFASSBs. Based on these advantages, cells fabricated with MoS 2 exhibited better performance as both asymmetrical and full cells with LiNi 0.6 Co 0.2 Mn 0.2 O 2 cathodes than did cells without MoS 2 . Moreover, the cell performance was affected by the MoS 2 size, and full cells having an optimal MoS 2 thickness demonstrated a 1.18-fold increase in the initial discharge capacity and a sevenfold improvement in capacity retention relative to SUS CCs. This study offers a promising path for exploiting the full potential of MoS 2 for interface stabilization and efficient AFASSB applications.
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