Realizing the potential of hydrophobic crystalline carbon as a support for oxygen evolution electrocatalystsopen access
- Authors
- Kim, Myeong-Geun; Lee, Tae Kyung; Lee, Eungjun; Park, Subin; Lee, Hyun Ju; Jin, Haneul; Lee, Dong Wook; Jeong, Min-Gi; Jung, Hun-Gi; Im, Kyungmin; Hu, Chuan; Ham, Hyung Chul; Song, Kwang Ho; Sung, Yung-Eun; Lee, Young Moo; Yoo, Sung Jong
- Issue Date
- Nov-2023
- Publisher
- Royal Society of Chemistry
- Keywords
- Carbon; Cobalt Alloys; Cobalt Compounds; Corrosion Resistance; Electrodes; Electrolysis; Hydrogen Production; Hydrophobicity; Ion Exchange Membranes; Iron Alloys; Iron Compounds; Nickel Compounds; Oxygen; Ternary Alloys; Anion Exchange; Carbon Emissions; Electrode Structure; Exchange Membranes; Hydrophobics; Oxygen Evolution; Performance; Sustainable Solution; Water Electrolysis; Zero Carbons; Electrocatalysts; Carbon; Catalyst; Diffusion; Durability; Electrode; Electrokinesis; Hydroxide; Mass Transport; Membrane
- Citation
- Energy & Environmental Science, v.16, no.11, pp 5019 - 5028
- Pages
- 10
- Indexed
- SCIE
SCOPUS
- Journal Title
- Energy & Environmental Science
- Volume
- 16
- Number
- 11
- Start Page
- 5019
- End Page
- 5028
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/25881
- DOI
- 10.1039/d3ee00987d
- ISSN
- 1754-5692
1754-5706
- Abstract
- Anion exchange membrane water electrolysis (AEMWE) is a sustainable solution for achieving net-zero carbon emissions and meeting growing energy demands through green H-2 production. However, its commercialization has not been realized thus far owing to inefficient catalyst use and unsatisfactory performance, which are correlated to the inadequacy of current electrode structures. In this study, we developed an efficient electrode structure based on a corrosion-resistant hydrophobic crystalline carbon support, which was incorporated as a support for Fe-Ni-Co layered double hydroxide electrocatalysts. We observed an AEMWE performance greater than that reported in previous studies in terms of activity [mass-specific power (24.1 kW g(metal)(-1))] and durability (-0.06 mV h(-1) for 520 h at 1.0 A cm(-2)). This could be attributed to the improved mass transport because of rapid water diffusion around the hydrophobic carbon and strong metal-carbon interactions. We believe that this study will promote the development of more carbon-supported oxygen evolution reaction electrocatalysts.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - College of Engineering > Department of Energy and Materials Engineering > 1. Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.