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Substitutional Vanadium Sulfide Nanodispersed in MoS2 Film for Pt-Scalable Catalyst

Authors
Agyapong-Fordjour, Frederick Osei-TutuYun, Seok JoonKim, Hyung-JinChoi, WooseonKirubasankar, BalakrishnanChoi, Soo HoAdofo, Laud AnimBoandoh, StephenKim, Yong InKim, Soo MinKim, Young-MinLee, Young HeeHan, Young-KyuKim, Ki Kang
Issue Date
Aug-2021
Publisher
WILEY
Keywords
first-principles calculations; hydrogen evolution; molybdenum disulfide; transition metal dichalcogenides; vanadium disulfide
Citation
ADVANCED SCIENCE, v.8, no.16, pp 1 - 8
Pages
8
Journal Title
ADVANCED SCIENCE
Volume
8
Number
16
Start Page
1
End Page
8
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/146496
DOI
10.1002/advs.202003709
ISSN
2198-3844
2198-3844
Abstract
Among transition metal dichalcogenides (TMdCs) as alternatives for Pt-based catalysts, metallic-TMdCs catalysts have highly reactive basal-plane but are unstable. Meanwhile, chemically stable semiconducting-TMdCs show limiting catalytic activity due to their inactive basal-plane. Here, metallic vanadium sulfide (VSn) nanodispersed in a semiconducting MoS2 film (V-MoS2) is proposed as an efficient catalyst. During synthesis, vanadium atoms are substituted into hexagonal monolayer MoS2 to form randomly distributed VSn units. The V-MoS2 film on a Cu electrode exhibits Pt-scalable catalytic performance; current density of 1000 mA cm(-2) at 0.6 V and overpotential of -0.08 V at a current density of 10 mA cm(-2) with excellent cycle stability for hydrogen-evolution-reaction (HER). The high intrinsic HER performance of V-MoS2 is explained by the efficient electron transfer from the Cu electrode to chalcogen vacancies near vanadium sites with optimal Gibbs free energy (-0.02 eV). This study provides insight into ways to engineer TMdCs at the atomic-level to boost intrinsic catalytic activity for hydrogen evolution.
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