Abstract
To accomplish mass hydrogen production by electrochemical water-splitting, it is a necessary to develop robust, highly active, stable, and cost-effective hydrogen evolution reaction (HER) electrocatalysts that perform comparably to Pt in the universal pH range. In this work, cobalt phosphide hybrid nanosheets supported on carbon felt (CoP HNS/CF) are presented, which exhibit the superior electrocatalytic hydrogen production under a universal-pH. In these nanosheets, a single CoP HNS is composed of polycrystalline CoP and oxygen-enriched amorphous Co-O-P phase. Benefiting from its unique nanoarchitecture, as-fabricated CoP HNS/CF exhibits a tremendous electrocatalytic HER activity and outperforms Pt/C as well as state-of-the-art CoP electrocatalysts in universal-pH. In acidic and neutral media, the CoP HNS/CF shows superior electrocatalytic activity while maintaining its original hybrid crystalline-amorphous phase and morphology. In alkaline medium, the unexpected phase and morphological reorganization of CoP HNS/CF results in outstanding electrocatalytic operation. CoP HNS/CF not only achieves high electrocatalytic activity and kinetics, but also a stable and long operating lifetime even under a high current density of 500 mA·cm−2. Furthermore, the fabrication of CoP HNS/CF can be scaled up easily, and the large CoP HNS/CF electrode also exhibits similar electrocatalytic activity and stability. [Figure not available: see fulltext.].
Original language | English |
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Pages (from-to) | 2469-2477 |
Number of pages | 9 |
Journal | Nano Research |
Volume | 13 |
Issue number | 9 |
DOIs | |
Publication status | Published - 2020 |
Keywords
- cobalt phosphide
- electrocatalyst
- hydrogen evolution reaction
- large-scale
- self-supporting
- universal-pH
ASJC Scopus subject areas
- Materials Science(all)
- Electrical and Electronic Engineering