Abstract
Transition metal-based nanomaterials represent an emerging class of highly active and low-cost precatalysts for the oxygen evolution reaction (OER) in alkaline electrolyzers. However, most OER precatalysts undergo slow or incomplete self-reconstructions to generate real active sites, which is a time-consuming process for achieving high OER performance. Thus, we report a new class of OER precatalysts that can achieve highly active OER species by a rapid and deep self-reconstruction (denoted by SELF-RECON). The precatalysts with a core-shell structure comprising NiMoO4 (core) and NiFe/NiFeOx nanoparticles in N-doped amorphous carbons (shell) (denoted by NiMoFeO@NC), can realize rapid MoO42− dissolution and fast formation of NiOOH with Fe incorporation simultaneously. In situ Raman spectroscopy together with electron microscopy, X-ray photoelectron spectroscopy, and electrochemical tests indicate that the obtained NiFeOOH/NiFe-LDH after SELF-RECON behave as the real active species that outperform NiMoFeO@NC, with ultralow overpotentials and extraordinary long-term stability.
Original language | English |
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Pages (from-to) | 2124-2137 |
Number of pages | 14 |
Journal | Matter |
Volume | 3 |
Issue number | 6 |
DOIs | |
State | Published - 2 Dec 2020 |
Keywords
- MAP2: Benchmark
- Prussian blue analog (PBA)
- SELF-RECONCAT
- anion etching
- core-shell
- in situ Raman spectroscopy
- ion exchange
- nickel-iron oxyhydroxides
- oxygen evolution reaction (OER)