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dc.contributor.authorHsu, Chang-Lungen_US
dc.contributor.authorChang, Yung-Huangen_US
dc.contributor.authorChen, Tzu-Yinen_US
dc.contributor.authorTseng, Chien-Chihen_US
dc.contributor.authorWei, Kung-Hwaen_US
dc.contributor.authorLi, Lain-Jongen_US
dc.date.accessioned2014-12-08T15:35:54Z-
dc.date.available2014-12-08T15:35:54Z-
dc.date.issued2014-03-26en_US
dc.identifier.issn0360-3199en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.ijhydene.2014.01.090en_US
dc.identifier.urihttp://hdl.handle.net/11536/24279-
dc.description.abstractAmorphous molybdenum sulfide (MoSx) materials have been considered as cheap and promising catalysts for hydrogen evolution reaction (HER). In this contribution, we report that the amorphous MoSx catalysts prepared by the low temperature thermolysis of the (NH4)(2)MoS4 precursors on carbon clothes (catalyst loading: 3.2 mg/cm(2)) exhibit a Tefal slope of 50.5 mV/dec and a high exchange current density of 1.5 x 10(-3) mA/cm(2) in 0.5 M H2SO4 solutions. Spectroscopic studies of the amorphous MoSx catalysts show that the increase of HER efficiency is positively correlated to the concentration of S-2(2-) species, providing strong evidence to support the argument that S-2(2-) is an active species for electrocatalytic HER. Additionally, the method for preparing catalysts is simple, scalable and applicable for large-scale production. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectHydrogen evolution reactionen_US
dc.subjectElectrocatalytic reactionen_US
dc.subjectMolybdenum disulfideen_US
dc.subjectNiobium chlorideen_US
dc.titleEnhancing the electrocatalytic water splitting efficiency for amorphous MoSxen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ijhydene.2014.01.090en_US
dc.identifier.journalINTERNATIONAL JOURNAL OF HYDROGEN ENERGYen_US
dc.citation.volume39en_US
dc.citation.issue10en_US
dc.citation.spage4788en_US
dc.citation.epage4793en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000334130800003-
dc.citation.woscount3-
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