Abstract
The development of efficient and robust bifunctional electrocatalysts for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is crucial for cleaner hydrogen production. Herein, we report a sophisticated core-shell electrocatalyst by hydrothermal and calcination methods using metal-organic frameworks (MOFs) as precursors. The derivation of MOF features cobalt disulfide (CoS2) as cores seamlessly integrated with a nitrogen-doped carbon matrix, which further supports an outer shell of rhenium disulfide (ReS2) nanosheets (CoS2-NC@ReS2). Hollow core-shell architecture synergistically combines the high conductivity and stability of the N-doped carbon, the favorable catalytic activity of CoS2 and ReS2. Abundant heterointerfaces between CoS2 and ReS2 and tunable local charge distributions not only provide abundant surface active sites but also facilitate electrolyte penetration and release of generated H2/O2 bubbles. These synergistic effects significantly promote water dissociation and accelerate the electrocatalytic reaction kinetics. When evaluated for overall water splitting, the catalyst demonstrates exceptional bifunctional performance, requiring low overpotentials of 145 and 279 mV for both HER and OER to drive 10 mA cm−2with a total water-splitting voltage of 1.65 V. Furthermore, the robust core-shell structure endows the catalyst with remarkable long-term electrochemical stability and negligible performance decay. This work provides a viable MOF-derived strategy for constructing advanced heterostructured electrocatalysts for renewable energy applications.
| Original language | English |
|---|---|
| Article number | 119769 |
| Journal | Journal of Electroanalytical Chemistry |
| Volume | 1003 |
| DOIs | |
| State | Published - 15 Feb 2026 |
Keywords
- Heterostructure
- Hollow
- Hydrogen evolution
- Oxygen evolution
- Rhenium disulfide
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