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Cited 25 time in webofscience Cited 26 time in scopus
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Realizing the potential of hydrophobic crystalline carbon as a support for oxygen evolution electrocatalystsopen access

Authors
Kim, Myeong-GeunLee, Tae KyungLee, EungjunPark, SubinLee, Hyun JuJin, HaneulLee, Dong WookJeong, Min-GiJung, Hun-GiIm, KyungminHu, ChuanHam, Hyung ChulSong, Kwang HoSung, Yung-EunLee, Young MooYoo, 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.
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