理论(学习稳定性)
物理
能量密度
能量(信号处理)
统计物理学
热力学
材料科学
工作(物理)
理论物理学
总能量
经典力学
作者
Mozaffar Abdollahifar,Andrea Paolella
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-12-12
卷期号:11 (2): 1323-1348
被引量:12
标识
DOI:10.1021/acsenergylett.5c03401
摘要
High Resolution Image Download MS PowerPoint Slide The anode-free architecture represents the theoretical end point for battery energy density, a prize now being realized in practical pouch cells exceeding 500 Wh kg –1 . This design, however, causes a profound stability paradox: the very act of hostless metal plating induces complex electro-chemo-mechanical failure modes that severely degrade cycle life. This review critically analyzes this central conflict from the perspective of industrially relevant pouch cells. We elucidate a decisive paradigm shift in mitigation strategies, moving away from passive, monolithic materials toward the design of dynamic, multifunctional systems. The most successful approaches engineer a synergistic interplay between advanced electrolytes, architected current collectors, and precise operational protocols. These solutions function not as static barriers but as programmable, process-controlling systems that actively manage the anode interface. Securing the anode-free prize depends on mastering this new methodology of synergistic design.
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