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Shin, Hyeon Suk
Lab for Carbon and 2D Materials
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Ultrahigh-current-density niobium disulfide catalysts for hydrogen evolution

Author(s)
Yang, JieunMohmad, Abdul RahmanWang, YanFullon, RaymondSong, XiujuZhao, FangBozkurt, IbrahimAugustin, MathiasSantos, Elton J. G.Shin, Hyeon SukZhang, WenjingVoiry, DamienJeong, Hu YoungChhowalla, Manish
Issued Date
2019-12
DOI
10.1038/s41563-019-0463-8
URI
https://scholarworks.unist.ac.kr/handle/201301/29071
Fulltext
https://www.nature.com/articles/s41563-019-0463-8
Citation
NATURE MATERIALS, v.18, no.12, pp.1309 - 1314
Abstract
Metallic transition metal dichalcogenides (TMDs)1–8 are good catalysts for the hydrogen evolution reaction (HER). The overpotential and Tafel slope values of metallic phases and edges9 of two-dimensional (2D) TMDs approach those of Pt. However, the overall current density of 2D TMD catalysts remains orders of magnitude lower (~10–100 mA cm−2) than industrial Pt and Ir electrolysers (>1,000 mA cm−2)10,11. Here, we report the synthesis of the metallic 2H phase of niobium disulfide with additional niobium (2H Nb1+xS2, where x is ~0.35)12 as a HER catalyst with current densities of >5,000 mA cm−2 at ~420 mV versus a reversible hydrogen electrode. We find the exchange current density at 0 V for 2H Nb1.35S2 to be ~0.8 mA cm−2, corresponding to a turnover frequency of ~0.2 s−1. We demonstrate an electrolyser based on a 2H Nb1+ xS2 cathode that can generate current densities of 1,000 mA cm−2. Our theoretical results reveal that 2H Nb1+ xS2 with Nb-terminated surface has free energy for hydrogen adsorption that is close to thermoneutral, facilitating HER. Therefore, 2H Nb1+ xS2 could be a viable catalyst for practical electrolysers.
Publisher
Nature Publishing Group
ISSN
1476-1122
Keyword
ACTIVE EDGE SITESINITIO MOLECULAR-DYNAMICSTOTAL-ENERGY CALCULATIONSMOS2 NANOSHEETSELECTROCATALYSISMOLYBDENUMTRANSITIONLAYER

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