Abstract
Metallic nickel nanoparticles well dispersed in graphitized carbon matrix (Ni@C) by pyrolysis of metal-organic frameworks and leaching treatment of hydrochloric acid could greatly enhance the photocatalytic activity of g-C3N4 under visible light irradiation. For 2.0 wt% Ni@C/g-C3N4, the average hydrogen evolution rate is 2.15 mmol h−1 g−1, which is around 88 times higher than that of pure g-C3N4, and even better than that of platinum-loaded g-C3N4. The remarkably improved photocatalytic activities through loading Ni@C can be attributed to the cooperative work of Ni nanoparticles and graphene layers, which facilitate the separation of photo-generated carriers and suppress the recombination of the electron-hole pairs. In addition, the hollow onion-like structure can restrain the formation of Ni-hydrogen bonds which modulates desorption of hydrogen. Our studies may open up a promising strategy to design economical noble-metal-free co-catalysts for efficient solar energy conversion.
| Original language | English |
|---|---|
| Pages (from-to) | 578-584 |
| Number of pages | 7 |
| Journal | Applied Catalysis B: Environmental |
| Volume | 200 |
| DOIs | |
| State | Published - 1 Jan 2017 |
| Externally published | Yes |
Keywords
- Co-catalyst
- Graphene layers
- Hydrogen
- Ni@C
- Photocatalysis