Abstract
Carbon-based nanomaterials have been widely studied as promising electrocatalysts for energy conversion and storage. Understanding the oxygen evolution and reduction reactions on carbon-based nanomaterials is of critical importance for development of highly active metal-free electrocatalysts. Here, the adsorption of oxygenated intermediates during oxygen evolution reaction (OER) on carbon nanotubes (CNTs) was examined by ex-situ X-ray photoelectron spectroscopy and in situ electrochemical impedance spectroscopy. The results demonstrate that the carbon atoms on CNTs near the C-O functional groups are active for OER. On the basis of this result, we further revealed the origin of the enhanced intermediate adsorption on surface-oxidized CNTs and the relationship between surface groups and apparent activation energy. Our study gained new understanding of OER on oxygen-doped carbon nanomaterials and provided an effective approach for investigating electrocatalysis on heteroatom-doped carbon electrocatalysts.
| Original language | English |
|---|---|
| Pages (from-to) | 294-300 |
| Number of pages | 7 |
| Journal | ACS Energy Letters |
| Volume | 2 |
| Issue number | 2 |
| DOIs | |
| State | Published - 10 Feb 2017 |
| 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
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