Synergistic Fe−Se Atom Pairs as Bifunctional Oxygen Electrocatalysts Boost Low‐Temperature Rechargeable Zn‐Air Battery

Author:

Wang Yao1,Wu Jiao2,Tang Shuaihao3,Yang Jiarui4,Ye Chenliang5,Chen Juan6,Lei Yongpeng2,Wang Dingsheng4ORCID

Affiliation:

1. School of Chemical and Material Engineering Jiangnan University 214122 Wuxi Jiangsu China

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

3. Energy Materials Computing Center School of Energy and Mechanical Engineering Jiangxi University of Science and Technology 330013 Nanchang China

4. Department of Chemistry Tsinghua University 100084 Beijing China

5. College of Materials Science and Engineering Shenzhen University 518060 Shenzhen China

6. State Key Laboratory of Heavy Oil Processing College of Chemical Engineering and environment China University of Petroleum 102249 Beijing China

Abstract

AbstractHerein, we successfully construct bifunctional electrocatalysts by synthesizing atomically dispersed Fe−Se atom pairs supported on N‐doped carbon (Fe−Se/NC). The obtained Fe−Se/NC shows a noteworthy bifunctional oxygen catalytic performance with a low potential difference of 0.698 V, far superior to that of reported Fe‐based single‐atom catalysts. The theoretical calculations reveal that p‐d orbital hybridization around the Fe−Se atom pairs leads to remarkably asymmetrical polarized charge distributions. Fe−Se/NC based solid‐state rechargeable Zn‐air batteries (ZABs−Fe−Se/NC) present stable charge/discharge of 200 h (1090 cycles) at 20 mA cm−2at 25 °C, which is 6.9 times of ZABs−Pt/C+Ir/C. At extremely low temperature of −40 °C, ZABs−Fe−Se/NC displays an ultra‐robust cycling performance of 741 h (4041 cycles) at 1 mA cm−2, which is about 11.7 times of ZABs−Pt/C+Ir/C. More importantly, ZABs−Fe−Se/NC could be operated for 133 h (725 cycles) even at 5 mA cm−2at −40 °C.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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