Internal Electron Donor Accelerated Sulfur Redox for Aqueous Zn─S Batteries

Author:

Zhang Hui12,Yang Min123,Xiao Jin4,Wu Zhibin5,Xin Wenli12,Xiao Xilin12,Niu Mengfan12,Yan Zichao12,Zhu Zhiqiang12ORCID

Affiliation:

1. State Key Laboratory of Chemo/Biosensing and Chemometrics College of Chemistry and Chemical Engineering Hunan University Changsha 410082 China

2. Greater Bay Area Institute for Innovation Hunan University Guangzhou 511300 China

3. School of Chemistry Xiangtan University Xiangtan Hunan MD 411105 China

4. School of Science Hunan University of Technology Zhuzhou 412007 China

5. State Key Laboratory of Powder Metallurgy Central South University Changsha Hunan 410083 China

Abstract

AbstractImproving the electrical conductivity of sulfur cathode while ensuring its high affinity to catalyst holds the key to facilitate the reaction kinetics of aqueous zinc–sulfur batteries. Herein, the sulfur redox in aqueous electrolyte is accelerated by introducing selenium–sulfur bonds into the sulfur structure to build an internal electron transport path. The Se with less electronegativity can act as an electron donor to accelerate the binding between S and Zn2+. Meanwhile, the bonded Se in the electron‐poor state endows the modified sulfur cathode with a strong affinity to the I3 catalyst, which further facilitates the conversion efficiency. Thus, the internal electron donor assisted sulfur cathode delivers excellent electrochemical performance in terms of high reversible capacity (1490 mAh g−1 at 0.5 A g−1), competitive rate performance (1010 mAh g−1 at 4 A g−1), as well as outstanding cycle stability (735 mAh g−1 at 4 A g−1 after 500 cycles).

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hunan Province

Scientific Research Foundation of Hunan Provincial Education Department

Publisher

Wiley

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