Single‐atom Iron Catalyst with Biomimetic Active Center to Accelerate Proton Spillover for Medical‐level Electrosynthesis of H2O2Disinfectant

Author:

Li Yan12,Chen Junxiang3,Ji Yaxin3,Zhao Zilin1,Cui Wenjun4,Sang Xiahan4,Cheng Yi5,Yang Bin1,Li Zhongjian1,Zhang Qinghua1,Lei Lecheng16,Wen Zhenhai3,Dai Liming2,Hou Yang167ORCID

Affiliation:

1. Key Laboratory of Biomass Chemical Engineering of Ministry of Education College of Chemical and Biological Engineering Zhejiang University 310027 Hangzhou China

2. Center of Advanced Carbon Materials School of Chemical Engineering University of New South Wales 2052 Sydney NSW Australia

3. CAS Key Laboratory of Design and Assembly of Functional Nanostructures Fujian Provincial Key Laboratory of Nanomaterials Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences 350002 Fuzhou Fujian China

4. Research and Testing Centre of Material School of Materials Science and Engineering Wuhan University of Technology 430070 Wuhan China

5. Zhejiang Hengyi Petrochemical Research Institute Co., Ltd. 311200 Hangzhou China

6. Institute of Zhejiang University—Quzhou 324000 Quzhou China

7. Donghai Laboratory 316021 Zhoushan China

Abstract

AbstractElectrosynthesis of H2O2has great potential for directly converting O2into disinfectant, yet it is still a big challenge to develop effective electrocatalysts for medical‐level H2O2production. Herein, we report the design and fabrication of electrocatalysts with biomimetic active centers, consisting of single atomic iron asymmetrically coordinated with both nitrogen and sulfur, dispersed on hierarchically porous carbon (FeSA‐NS/C). The newly‐developed FeSA‐NS/C catalyst exhibited a high catalytic activity and selectivity for oxygen reduction to produce H2O2at a high current of 100 mA cm−2with a record high H2O2selectivity of 90 %. An accumulated H2O2concentration of 5.8 wt.% is obtained for the electrocatalysis process, which is sufficient for medical disinfection. Combined theoretical calculations and experimental characterizations verified the rationally‐designed catalytic active center with the atomic Fe site stabilized by three‐coordinated nitrogen atoms and one‐sulfur atom (Fe‐N3S‐C). It was further found that the replacement of one N atom with S atom in the classical Fe‐N4‐C active center could induce an asymmetric charge distribution over N atoms surrounding the Fe reactive center to accelerate proton spillover for a rapid formation of the OOH* intermediate, thus speeding up the whole reaction kinetics of oxygen reduction for H2O2electrosynthesis.

Funder

National Archives and Records Administration

Fundamental Research Funds for Central Universities of the Central South University

Australian Research Council

Publisher

Wiley

Subject

General Chemistry,Catalysis

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