Please use this identifier to cite or link to this item:
Full metadata record
DC FieldValueLanguage
dc.contributor.authorTran, Phong D.en
dc.contributor.authorPramana, Stevin S.en
dc.contributor.authorField, Martin J.en
dc.contributor.authorNguyen, Maien
dc.contributor.authorBhattacharjee, Anirbanen
dc.contributor.authorChiam, Sing Yangen
dc.contributor.authorFize, Jenniferen
dc.contributor.authorArtero, Vincenten
dc.contributor.authorWong, Lydia Helenaen
dc.contributor.authorLoo, Say Chye Joachimen
dc.contributor.authorBarber, Jamesen
dc.identifier.citationTran, P. D., Nguyen, M., Pramana, S. S., Bhattacharjee, A., Chiam, S. Y., Fize, J., Field, M. J., Artero, V., Wong, L. H., Loo, S. C. J., & Barber, J. (2012). Copper molybdenum sulfide: a new efficient electrocatalyst for hydrogen production from water. Energy & environmental science, 5(10), 8912-8916.en
dc.description.abstractA new inorganic solid state electrocatalyst for the hydrogen evolution reaction (HER) is reported. Highly crystalline layered ternary sulfide copper-molybdenum-sulfide (Cu2MoS4) was prepared by a simple precipitation method from CuI and [MoS4]2− precursors. In aqueous solution and over a wide pH range (pH 0 to 7), this Cu2MoS4 showed very good catalytic activity for HER with an overvoltage requirement of only ca. 135 mV and an apparent exchange current density of 0.040 mA cm−2 (Tafel slope of ca. 95 mV per decade was found irrespective of the pH value). This Cu2MoS4 catalyst was found to be stable during electrocatalytic hydrogen generation. Therefore, it represents an attractive alternative to platinum.en
dc.relation.ispartofseriesEnergy & environmental scienceen
dc.titleCopper molybdenum sulfide : a new efficient electrocatalyst for hydrogen production from wateren
dc.typeJournal Articleen
dc.contributor.schoolSchool of Materials Science & Engineeringen
dc.contributor.researchEnergy Research Institute @ NTU (ERI@N)en
dc.contributor.researchFacility for Analysis, Characterisation, Testing and Simulationen
item.fulltextNo Fulltext-
Appears in Collections:ERI@N Journal Articles
MSE Journal Articles

Google ScholarTM




Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.