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Co-catalytic Effects of CoS 2 on the Activity of the MoS 2 Catalyst for Electrochemical Hydrogen Evolution.

Authors :
Bose R
Jin Z
Shin S
Kim S
Lee S
Min YS
Source :
Langmuir : the ACS journal of surfaces and colloids [Langmuir] 2017 Jun 13; Vol. 33 (23), pp. 5628-5635. Date of Electronic Publication: 2017 Jun 02.
Publication Year :
2017

Abstract

MoS <subscript>2</subscript> is a promising material to replace the Pt catalyst in the electrochemical hydrogen evolution reaction (HER). It is well known that the activity of the MoS <subscript>2</subscript> catalyst in the HER is significantly promoted by doping cobalt atoms. Recently, the Co-Mo-S phase, in which cobalt atoms decorate the edge positions of the MoS <subscript>2</subscript> slabs, has been identified as a co-catalytic phase in the Co-doped MoS <subscript>2</subscript> (Co-MoS <subscript>x</subscript> ) with low Co content. Here, we report the effect of the incorporation of cobalt atoms in the chemical state of the Co-MoS <subscript>x</subscript> catalyst, which gives rise to the co-catalytic effect. Co-MoS <subscript>x</subscript> catalysts with various Co contents were prepared on carbon fiber paper by a simple hydrothermal process. On the Co-MoS <subscript>x</subscript> catalyst with high Co content (Co/Mo ≈ 2.3), a dramatically higher catalytic activity was observed compared to that for the catalyst with low Co content (Co/Mo ≈ 0.36). Furthermore, the co-catalytic phase in the Co-MoS <subscript>x</subscript> catalyst with the high Co content was found not to be the Co-Mo-S phase but was identified as CoS <subscript>2</subscript> by Raman spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, and transmission electron microscopy. It is believed that CoS <subscript>2</subscript> is an alternative choice to co-catalyze HER on MoS <subscript>2</subscript> -based catalysts.

Details

Language :
English
ISSN :
1520-5827
Volume :
33
Issue :
23
Database :
MEDLINE
Journal :
Langmuir : the ACS journal of surfaces and colloids
Publication Type :
Academic Journal
Accession number :
28544849
Full Text :
https://doi.org/10.1021/acs.langmuir.7b00580