Volume 20, Issue 31 2400695
Research Article

Electrosynthesis of H2O2 Promoted by π–π Interaction on a Metal-Free Carbon Catalyst

Jiating Qu

Jiating Qu

State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian National Laboratory for Clean Energy, Dalian, Liaoning, 116023 China

University of Chinese Academy of Sciences, Beijing, 100049 China

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Guifa Long

Guifa Long

Guangxi Key Laboratory of Chemistry and Engineering of Forest Products, School of Chemistry and Chemical Engineering, Guangxi Minzu University, Nanning, 530008 China

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Lin Luo

Lin Luo

State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian National Laboratory for Clean Energy, Dalian, Liaoning, 116023 China

University of Chinese Academy of Sciences, Beijing, 100049 China

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Yang Yang

Yang Yang

State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian National Laboratory for Clean Energy, Dalian, Liaoning, 116023 China

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Wenjun Fan

Corresponding Author

Wenjun Fan

State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian National Laboratory for Clean Energy, Dalian, Liaoning, 116023 China

E-mail: [email protected]; [email protected]

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Fuxiang Zhang

Corresponding Author

Fuxiang Zhang

State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian National Laboratory for Clean Energy, Dalian, Liaoning, 116023 China

E-mail: [email protected]; [email protected]

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First published: 08 March 2024
Citations: 9

Abstract

The synthesis of hydrogen peroxide (H2O2) through electrocatalytic oxygen reduction reaction is an ideal alternative to the current energy-intensive anthraquinone process, but developing cost-effective and high-efficiency electrocatalysts is still challenging. Herein, a metal-free graphitic carbon nitride/carbon nanotube (g-C3N4/CNT) hybrid catalyst can enhance H2O2 production via π–π interaction is reported, achieving almost unity (97%) H2O2 production at 0.57 V with high selectivity of over 92% across the wide potential range from 0.6 to 0 V. Other carbon materials with weak interaction with g-C3N4, such as acetylene black and super P, show markedly weakened H2O2 production, indicating the importance of π–π interaction. Electron transfer kinetic analysis combined with density functional theory calculations indicates that the synergistic effect between g-C3N4 and CNT enhances electron transfer and O2 activation between g-C3N4 and CNT, leading to enhanced H2O2 production performance. This work provides a complementary approach for H2O2 production from oxygen reduction besides introducing oxygenated groups or heteroatom doping into carbon materials.

Conflict of Interest

The authors declare no conflict of interest.

Data Availability Statement

The data that support the findings of this study are available in the supplementary material of this article.

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