Arc plasma‐deposited Co single‐atom catalysts supported on an aligned carbon nanofiber for hydrogen peroxide electrosynthesis and an electro‐Fenton process

Author:

Hwang Chang‐Kyu12,Kim Sooyeon3,Yoon Ki Ro4,Le Thao Thi5,Hoang Chinh V.5,Choi Jae Won1,Zhang Wenjun16,Paek Sae Yane1,Lee Chung Hyeon1,Lee Ji Hyun4,Chae Keun Hwa7,Jeong Sohee1,Lee Seung Yong1,Ju Byeong‐Kwon28,Kim Sang Hoon569,Han Sang Soo3,Kim Jong Min169ORCID

Affiliation:

1. Materials Architecturing Research Center Korea Institute of Science and Technology (KIST) Seoul Seongbuk‐gu Republic of Korea

2. Department of Micro/Nano Systems Korea University Seoul Seongbuk‐gu Republic of Korea

3. Computational Science Research Center Korea Institute of Science and Technology (KIST) Seoul Seongbuk‐gu Republic of Korea

4. Advanced Textile R&D Department Korea Institute of Industrial Technology (KITECH) Ansan Gyeonggi‐do Republic of Korea

5. Extreme Materials Research Center Korea Institute of Science and Technology (KIST) Seoul Seongbuk‐gu Republic of Korea

6. Nanoscience and Technology, KIST School University of Science and Technology Seoul Republic of Korea

7. Advanced Analysis and Data Center Korea Institute of Science and Technology Seoul Seongbuk‐gu Republic of Korea

8. Display and Nanosensor Laboratory, School of Electrical Engineering Korea University Seoul Seongbuk‐gu Republic of Korea

9. KHU‐KIST Department of Converging Science and Technology Kyung Hee University Seoul Seongbuk‐gu Republic of Korea

Abstract

AbstractAtomically dispersed single‐atom catalysts (SACs) on carbon supports show great promise for H2O2 electrosynthesis, but conventional wet chemistry methods using particulate carbon blacks in powder form have limited their potential as two‐electron (2e) oxygen reduction reaction (ORR) catalysts. Here, we demonstrate high‐performance Co SACs supported on a free‐standing aligned carbon nanofiber (CNF) using electrospinning and arc plasma deposition (APD). Based on the surface oxidation treatment of aligned CNF and precise control of the deposition amount in a dry‐based APD process, we successfully form densely populated Co SACs on aligned CNF. Through experimental analyses and density functional theory calculations, we reveal that Co SAC has a Co–N2–O2 moiety with one epoxy group, leading to excellent 2e ORR activity. Furthermore, the aligned CNF significantly improves mass transfer in flow cells compared to randomly oriented CNF, showing an overpotential reduction of 30 mV and a 1.3‐fold improvement (84.5%) in Faradaic efficiency, and finally achieves an outstanding production rate of 15.75 mol gcat−1 h−1 at 300 mA cm−2. The high‐performance Co SAC supported on well‐aligned CNF is also applied in an electro‐Fenton process, demonstrating rapid removal of methylene blue and bisphenol F due to its exceptional 2e ORR activity.

Publisher

Wiley

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