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Activating MoS2 by interface engineering for efficient hydrogen evolution catalysis.
- Source :
-
Materials Research Bulletin . Apr2019, Vol. 112, p46-52. 7p. - Publication Year :
- 2019
-
Abstract
- Graphical abstract Herein, we proposed a facile strategy for the design of Au-MoS 2 nanoparticles with abundant edge sites and regular core-shell structure through the interface engineering. Highlights • Activating the pristine MoS 2 by introducing MoS 2 into core shell heterostructures through the interface engineering. • CNFs served as reactor and support to control the heterostructures of Au and MoS 2. • The Au-MoS 2 /CNFs exhibits the overpotential of 92 mV (10 mA cm−2) and a Tafel slope of 126 mV dec−1. Abstract Transition metal sulfides have been widely investigated and used as efficient catalysts for hydrogen evolution reactions (HER). However, the trade-off between catalytic activity and long-term stability represents a formidable challenge and has not been extensively addressed. Herein, we proposed a facile strategy for the design of Au-MoS 2 nanoparticles with abundant edge sites and regular core-shell structure through the interface engineering. The electrospun carbon nanofibers (CNFs) served as reactors and supports to control the preparation of core-shell heterostructures. Core-shell heterostructure exhibits more excellent catalytic than single component resulting from the synergistic effects at nano-interface. The obtained Au-MoS 2 /CNFs catalyst yield a current density of 10 mA cm−2 at the overpotential of 92 mV and a Tafel slope of 126 mV dec−1. Particularly, the durability of catalyst is relatively stable at the 50 h. The successful synthesis of core-shell nanocrystals provides a new path for designing advanced electrocatalysts. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00255408
- Volume :
- 112
- Database :
- Academic Search Index
- Journal :
- Materials Research Bulletin
- Publication Type :
- Academic Journal
- Accession number :
- 134323026
- Full Text :
- https://doi.org/10.1016/j.materresbull.2018.12.002