Highly efficient water-splitting electrodes with stable operation at 3 A cm−2 in alkaline media through molecular linker assembly-induced all-in-one structured NiMo and NiFe electrocatalysts
- Authors
- Son, Youhyun; Mo, Jeongmin; Yong, Euiju; Ahn, Jeongyeon; Kim, Gyuchan; Lee, Wonyoung; Kwon, Cheong Hoon; Ju, Hyun; Lee, Seung Woo; Kim, Byung-Hyun; Kim, Myeongjin; Cho, Jinhan
- Issue Date
- Apr-2024
- Publisher
- Elsevier BV
- Keywords
- Binary nonnoble metal; Carbon nanotube; Water-splitting
- Citation
- Applied Catalysis B: Environmental, v.343, pp 1 - 16
- Pages
- 16
- Indexed
- SCIE
SCOPUS
- Journal Title
- Applied Catalysis B: Environmental
- Volume
- 343
- Start Page
- 1
- End Page
- 16
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/116215
- DOI
- 10.1016/j.apcatb.2023.123563
- ISSN
- 0926-3373
1873-3883
- Abstract
- Developing nonnoble electrocatalyst-based water-splitting electrodes with high operational stability and low overpotentials is one of the most critical challenges in commercially available water-splitting reactions. In this study, we present water-splitting textile electrodes enabling remarkably low overpotentials and high stable operation. We first assembled conductive multi-walled-carbon-nanotubes (MWCNTs) with amine molecule-based linkers onto cotton textiles and subsequently electrodeposited Ni onto the MWCNT-incorporated textile. For the preparation of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) electrodes, NiMo and NiFe were further electrodeposited onto the Ni-electrodeposited textile electrode, respectively. These electrodes exhibited considerably low overpotentials in alkaline media (8 mV at 10 mA cm−2 for HER and 189 mV at 50 mA cm−2 for OER). Furthermore, the full-cell electrodes preserved a low cell voltage of 2.01 V at an unprecedentedly high current density of 3000 mA cm−2 for a prolonged duration (> at least 1000 h). © 2023 The Authors
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Collections - COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING > 1. Journal Articles

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