Activating and Stabilizing a Reversible four Electron Redox Reaction of I/I+ for Aqueous Zn‐Iodine Battery

Author:

Wang Chenggang1ORCID,Ji Xiaoxing1,Liang Jianing2,Zhao Shunshun3,Zhang Xixi1,Qu Guangmeng4,Shao Wenfeng1,Li Chuanlin1,Zhao Gang1,Xu Xijin1ORCID,Li Huiqiao2ORCID

Affiliation:

1. School of Physics and Technology University of Jinan Jinan 250022 China

2. State Key Laboratory of Materials Processing and Die & Mould Technology School of Materials Science and Engineering Huazhong University of Science and Technology (HUST) Wuhan 430074 P. R. China

3. State Key Laboratory of Chemical Resource Engineering Beijing Key Laboratory of Electrochemical Process and Technology of Materials Beijing University of Chemical Technology Beijing 100029 China

4. School of Chemistry and Chemical Engineering Shandong University Jinan 250100 China

Abstract

AbstractLow capacity and poor cycle stability greatly inhibit the development of zinc‐iodine batteries. Herein, a high‐performance Zn‐iodine battery has been reached by designing and optimizing both electrode and electrolyte. The Br is introduced as the activator to trigger I+, and coupled with I+ forming interhalogen to stabilize I+ to achieve a four‐electron reaction, which greatly promotes the capacity. And the Ni−Fe−I LDH nanoflowers serve as the confinement host to enable the reactions of I/I+ occurring in the layer due to the spacious and stable interlayer spacing of Ni−Fe−I LDH, which effectively suppresses the iodine‐species shuttle ensuring high cycling stability. As a result, the electrochemical performance is greatly enhanced, especially in specific capacity (as high as 350 mAh g−1 at 1 A g−1 far higher than two‐electron transfer Zn‐iodine batteries) and cycling performance (94.6 % capacity retention after 10000 cycles). This strategy provides a new way to realize high capacity and long‐term stability of Zn‐iodine batteries.

Publisher

Wiley

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