分离器(采油)
阳极
材料科学
锂(药物)
化学工程
化学
电极
热力学
物理
工程类
物理化学
医学
内分泌学
作者
Ahu Shao,Helin Wang,Min Zhang,Jiacheng Liu,Cheng Lü,Yunsong Li,Yuxiang Guo,Zhiqiao Wang,Qiurong Jia,Xin Wang,Xiaoyu Tang,Xiaodong Zhao,Yue Ma
标识
DOI:10.1038/s41467-025-59521-8
摘要
Anode-free lithium batteries represent a promising avenue for high-energy-density storage, yet their practical application is hindered by lithium inventory loss from parasitic interfacial reactions, cathode degradation, and limited Li+ reversibility. Herein, we propose a polyolefin separator integrated with a Li2S@C sacrificial layer, achieving multiscale interfacial stabilization in Ah-class anode-free pouch cells. This approach simultaneously replenishes the customized Li+ inventory during the formation cycle and establishes the lithium polysulfide-containing cathode interface with high-voltage tolerance (till 4.5 V). Real-time tracking via in-situ electrochemical impedance spectroscopy and transmission-mode operando X-ray diffraction reveals accelerated Li+ diffusion kinetics and stabilized phase evolution in LiNi0.8Co0.1Mn0.1O2 cathode interfaced with Li2S@C|PE prelithiation separator. Consequently, a 1.22 Ah pouch cell with an Ag-modified Cu foil and LiNi0.8Co0.1Mn0.1O2 cathode is assembled with Li2S@C|PE separator and exhibits gravimetric and volumetric energy densities of 450 Wh kg-1 and 1355 Wh L-1, respectively. This prelithiation protocol demonstrates upscaling potential and generic applicability to secure the interfacial chemistries for anode free/less lithium metal batteries.
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