Abstract
Precisely modulating the electronic structure of catalytic sites represents a promising strategy to design highly efficient electrocatalysts toward oxygen evolution reaction (OER). Here, the non-noble metal Co is successfully doped into the surface layer of ZnO and the doping concentration can be controllably adjusted by a partial cation exchange method. Our experimental and theoretical results demonstrate that the surface-doped Co can not only activate the inherently inert Zn sites by modifying their electronic structure and thereby promoting the OH∗ adsorption but also serve as active sites themselves for the adsorption of O∗ and OOH*, ultimately realizing the bimetallic synergetic effect in Co/ZnO for OER catalysis. Besides, the surface Co doping also benefits the obvious enhancement of electrical conductivity of the ZnO host. Therefore, relative to the inactive ZnO, the as-prepared Co/ZnO exhibits a much smaller overpotential and Tafel slope toward OER. This strategy provides a rational design of low-cost and efficient OER electrocatalysts.
| Original language | English |
|---|---|
| Pages (from-to) | 18055-18060 |
| Number of pages | 6 |
| Journal | ACS Sustainable Chemistry and Engineering |
| Volume | 7 |
| Issue number | 21 |
| DOIs | |
| Publication status | Published - Nov 4 2019 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- bimetallic synergetic effect
- electrocatalysts
- electronic structure
- oxygen evolution reaction
- surface doping
ASJC Scopus subject areas
- General Chemistry
- Environmental Chemistry
- General Chemical Engineering
- Renewable Energy, Sustainability and the Environment
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