Abstract
Pursuing efficient and low-cost electrocatalysts is crucial for the performance of water-alkali electrolyzers toward water splitting. Earth-abundant transition-metal oxides, in spite of their alluring performances in the oxygen evolution reaction, are thought to be inactive in the hydrogen evolution reaction in alkaline media. Here, we demonstrate that pure TiO2 single crystals, a typical transition-metal oxide, can be activated toward electrocatalytic hydrogen evolution reaction in alkaline media through engineering interfacial oxygen vacancies. Experimental and theoretical results indicate that subsurface oxygen vacancies and low-coordinated Ti ions (Ti3+) can enhance the electrical conductivity and promote electron transfer and hydrogen desorption, which activate reduced TiO2 single crystals in the hydrogen evolution reaction in alkaline media. This study offers a rational route for developing reduced transition-metal oxides for low-cost and highly active hydrogen evolution reaction catalysts, to realize overall water splitting in alkaline media.
| Original language | English |
|---|---|
| Pages (from-to) | 4288-4293 |
| Number of pages | 6 |
| Journal | ACS Catalysis |
| Volume | 8 |
| Issue number | 5 |
| DOIs | |
| State | Published - 4 May 2018 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Ti ions
- alkaline media
- hydrogen evolution reaction
- in situ STM observation
- oxygen vacancy
- titania
- water splitting
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