Abstract
Designing active, stable, yet low cost electrocatalysts for the oxygen evolution reaction (OER) is pivotal to the next generation energy storage technology. However, conventional OER catalysts are of low electrochemical efficiency while the state-of-the-art nanoparticle-based catalysts require mechanical supports, thereby limiting their wide deployment. Here, it is demonstrated that, due to the excellent corrosion resistance of the Fe-Co-Ni-Cr-Nb high entropy intermetallic Laves phase, fabricating a high entropy bulk porous nanostructure is possible by dealloying the corresponding eutectic alloy precursor. As a result, a core-shell nanostructure with amorphous high entropy oxide ultrathin films wrapped around the nanosized intermetallic ligaments is obtained, which together, exhibits an extraordinarily large active surface area, fast dynamics, and superb long-term durability, outperforming the existing alloy- and ceramic-based OER electrocatalysts. The outcome of the research suggests that the paradigm of "high entropy" design can be used to develop high performance catalytic materials.
| Original language | English |
|---|---|
| Article number | 1900105 |
| Journal | Advanced Sustainable Systems |
| Volume | 4 |
| Issue number | 5 |
| Online published | 24 Feb 2020 |
| DOIs | |
| Publication status | Published - May 2020 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Research Keywords
- dealloying
- electrochemical catalysts
- high entropy alloys
- high entropy oxides
- oxygen evolution reaction
- BIFUNCTIONAL ELECTROCATALYST
- EFFICIENT
- REDUCTION
- COBALT
- ALLOYS
- ELECTRODE
- NITROGEN
- DESIGN
- FE
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