Affiliation:
1. Frontiers Science Center for Transformative Molecules School of Chemistry and Chemical Engineering Zhangjiang Institute for Advanced Study Shanghai Jiao Tong University Shanghai 200240 China
2. State Key Laboratory of Molecular Engineering of Polymers Department of Macromolecular Science Laboratory of Advanced Materials Fudan University Shanghai 200438 China
Abstract
AbstractChlorine (Cl)‐based batteries such as Li/Cl2 batteries are recognized as promising candidates for energy storage with low cost and high performance. However, the current use of Li metal anodes in Cl‐based batteries has raised serious concerns regarding safety, cost, and production complexity. More importantly, the well‐documented parasitic reactions between Li metal and Cl‐based electrolytes require a large excess of Li metal, which inevitably sacrifices the electrochemical performance of the full cell. Therefore, it is crucial but challenging to establish new anode chemistry, particularly with electrochemical reversibility, for Cl‐based batteries. Here we show, for the first time, reversible Si redox in Cl‐based batteries through efficient electrolyte dilution and anode/electrolyte interface passivation using 1,2‐dichloroethane and cyclized polyacrylonitrile as key mediators. Our Si anode chemistry enables significantly increased cycling stability and shelf lives compared with conventional Li metal anodes. It also avoids the use of a large excess of anode materials, thus enabling the first rechargeable Cl2 full battery with remarkable energy and power densities of 809 Wh kg−1 and 4,277 W kg−1, respectively. The Si anode chemistry affords fast kinetics with remarkable rate capability and low‐temperature electrochemical performance, indicating its great potential in practical applications.
Funder
National Natural Science Foundation of China
Science and Technology Commission of Shanghai Municipality
Shanghai Municipal Education Commission
Subject
General Chemistry,Catalysis
Cited by
12 articles.
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