Abstract
Constructing hetero-structured catalyst is promising but still challenging to achieve overall water splitting for hydrogen production with high efficiency. Herein, we developed a sulfide-based MoS2/Co1−xS@C hetero-structure for highly efficient electrochemical hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The carbon derived from the filter paper acts as a conducting carrier to ensure adequate exposure of the active sites guaranteed with improved catalytic stability. The unique hierarchical nano-sheets facilitate the charge and ion transfer by shortening the diffusion path during electro-catalysis. Meanwhile, the robust hetero-interfaces in MoS2/Co1−xS@C can expose rich electrochemical active sites and facilitate the charge transfer, which further cooperates synergistically toward electro-catalytic reactions. Consequently, the optimal MoS2/Co1−xS@C hetero-structures present small over-potentials toward HER (135 mV @ 10 mA·cm−2) and OER (230 mV @ 10 mA·cm−2). The MoS2/Co1−xS@C electrolyzer requires an ultralow voltage of 1.6 V at the current density of 10 mA·cm−2 with excellent durability, outperforming the state-of-the-art electro-catalysts. This work sheds light on the design of the hetero-structured catalysts with interfacial engineering toward large-scale water splitting.
Original language | English |
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Pages (from-to) | 589-597 |
Number of pages | 9 |
Journal | Tungsten |
Volume | 5 |
Issue number | 4 |
DOIs | |
Publication status | Published - Dec 2023 |
Keywords
- Composite
- Interface regulation
- Molybdenum cobalt sulfides
- Overall water splitting
- Pyrolysis
ASJC Scopus subject areas
- Materials Science (miscellaneous)
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry