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Department of Electrical Engineering and Computer Science
Advanced Electronic Devices Research Group(AEDRG) - Jang Lab.
1. Journal Articles
Highly Sustainable h-BN Encapsulated MoS2 Hydrogen Evolution Catalysts
Lim, Jungmoon
;
Heo, Su Jin
;
Jung, Min
;
Kim, Taehun
;
Byeon, Junsung
;
Park, Hongju
;
Jang, Jae Eun
;
Hong, John
;
Moon, Janghyuk
;
Pak, Sangyeon
;
Cha, Seungnam
Department of Electrical Engineering and Computer Science
Advanced Electronic Devices Research Group(AEDRG) - Jang Lab.
1. Journal Articles
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Title
Highly Sustainable h-BN Encapsulated MoS2 Hydrogen Evolution Catalysts
Issued Date
2024-12
Citation
Lim, Jungmoon. (2024-12). Highly Sustainable h-BN Encapsulated MoS2 Hydrogen Evolution Catalysts. Small, 20(49). doi: 10.1002/smll.202402272
Type
Article
Author Keywords
2D MoS 2
;
hexagonal boron nitride (h-BN)
;
high current operation
;
high-durability catalysts
;
hydrogen evolution reaction (HER)
;
long-term stability
Keywords
GRAPHENE
;
METALS
;
SITES
;
MONOLAYER MOS2
;
NANOSHEETS
;
SUBSTRATE
;
TRANSPORT
;
OXIDATION
;
EFFICIENT
;
MEMBRANE
ISSN
1613-6810
Abstract
Despite the importance of the stability of the 2D catalysts in harsh electrolyte solutions, most studies have focused on improving the catalytic performance of molybdenum disulfide (MoS2) catalysts rather than the sustainability of hydrogen evolution. In previous studies, the vulnerability of MoS2 crystals is reported that the moisture and oxygen molecules can cause the oxidation of MoS2 crystals, accelerating the degradation of crystal structure. Therefore, optimization of catalytic stability is crucial for approaching practical applications in 2D catalysts. Here, it is proposed that monolayered MoS2 catalysts passivated with an atomically thin hexagonal boron nitride (h-BN) layer can effectively sustain hydrogen evolution reaction (HER) and demonstrate the ultra-high current density (500 mA cm⁻2 over 11 h) and super stable (64 h at 150 mA cm⁻2) catalytic performance. It is further confirmed with density functional theory (DFT) calculations that the atomically thin h-BN layer effectively prevents direct adsorption of water/acid molecules while allowing the protons to be adsorbed/penetrated. The selective penetration of protons and prevention of crystal structure degradation lead to maintained catalytic activity and maximized catalytic stability in the h-BN covered MoS2 catalysts. These findings propose a promising opportunity for approaching the practical application of 2D MoS2 catalysts having long-term stability at high-current operation. © 2024 Wiley-VCH GmbH.
URI
http://hdl.handle.net/20.500.11750/57397
DOI
10.1002/smll.202402272
Publisher
Wiley
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