期刊
ACS ENERGY LETTERS
卷 6, 期 2, 页码 459-467出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.0c02575
关键词
-
类别
资金
- U.S. NSF CAREER Award [CBET-1551693]
- National Natural Science Foundation of China [51772154, 51972174]
- Natural Science Foundation of Jiangsu Province [BK20170036]
- China Scholarship Council (CSC) [201806840082]
This study introduces a novel aqueous deep eutectic solvent gel electrolyte that enables reversible chloride storage in a graphite cathode through the formation of iodine-chloride interhalogens. The results demonstrate three reversible steps in the process, including iodine plating, oxidation to form I-Cl interhalides, and intercalation into graphite.
Anion storage in cathode of dual-ion batteries provides leeway for chemistries. For high energy density and better safety, it is desirable but challenging to reversibly intercalate chloride in a graphite cathode because either the oxygen or chlorine evolution reaction can prevail over chloride insertion. The primary barrier is the lack of suitable aqueous electrolytes that suppress these parasitic reactions. Herein, we report an aqueous deep eutectic solvent gel electrolyte that allows reversible chloride storage for graphite based on a chloride-based electrolyte via the formation of iodine-chloride interhalogens. The results suggest three reversible steps: iodine plating on the host surface, oxidation to form I-Cl interhalides, and then intercalation into graphite. As a result, the graphite cathode delivers a high reversible capacity of 291 mAh g(-1) with stable cycling performance. Facilitated by the same mechanism, a porous graphenic carbon delivered a record-high capacity of over 1100 mAh g(-1).
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据