Journal
FLATCHEM
Volume 4, Issue -, Pages 54-60Publisher
ELSEVIER
DOI: 10.1016/j.flatc.2017.06.005
Keywords
Transition metal dichalcogenides; Phase; Reduced graphene oxide; Photoelectrochemistry; Hydrogen evolution
Funding
- 2016 Research Fund of UNIST (Ulsan National Institute of Science Technology) [1.160075]
- KEIT - MOTIE [1005059]
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Transition metal dichalcogenides (TMDs) and their hybrids with reduced graphene oxide (rGO) have attracted great attention for use as electrocatalysts to replace Pt. However, their applications for photoelectrochemical (PEC) cells are not widely known. Herein, we report the fabrication of highly efficient photo-cathodes for PEC cells using only two-dimensional (2D) materials, MoS2, WS2 (with 1T and 2H phases) and rGO sheets. Two types of hybrid films were prepared based on various combinations of the components and optimization of the thickness; multi-layered (1T MoS2/2H MoS2/2H WS2/rGO/ITO) and multi-component (1T MoS2/(2H MoS2 + 2H WS2 + rGO)/ITO) films. The hybrid films with the same component materials but different structures showed high efficiency when used as cathodes in PEC cells in terms of the current density under illumination: the increase by 60 and 67%, respectively, for the multi-layered and the multi-component films. Furthermore, the roles of each component were identified. The 1T MoS2 layer contributes to catalytic activity for hydrogen evolution reaction. The hybrid of 2H MoS2 and 2H WS2 with different band structures facilitates more efficient carrier transport through proper band alignment than the individual MoS2 or WS2 sheets. The rGO sheets act as conductive interconnecting components to prevent the recombination of electrons and holes. Finally, the optimized hybrid film (1T MoS2/(2H MoS2 + 2H WS2 + rGO)/rGO/ITO), based on above roles of each component, showed highly efficient PEC performance. This study points out that the performance of PECs consisting of 2D materials is affected by the combination of 2D materials and the structure of the photoelectrode. (C) 2017 Published by Elsevier B.V.
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