4.5 Article

Effect of Hydrogen and Oxygen Evolution Cocatalysts on Photocatalytic Activity of GaN:ZnO

期刊

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
卷 -, 期 4, 页码 767-772

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.201300439

关键词

Photochemistry; Photocatalysis; Sustainable chemistry; Nanoparticles; Oxidation; Water splitting; Gallium

资金

  1. Japan Society for the Promotion of Science (JSPS) [23000009]
  2. Japan Science and Technology Agency (JST) through the Advanced Low Carbon Technology Research and Development Program (ALCA)
  3. Cabinet Office of Japan through the Funding Program for World-Leading Innovative R&D in Science and Technology (FIRST)
  4. Japan Chemical Industry Association
  5. Nippon Sheet Glass Foundation for Materials Science and Engineering
  6. Japan Society for the Promotion of Science KAKENHI [23245028]
  7. Japan Society for the Promotion of Science, Research Fellowship for Young Scientists [24.2251]
  8. Grants-in-Aid for Scientific Research [23245028] Funding Source: KAKEN

向作者/读者索取更多资源

The coloading effect of H-2 and O-2 evolution cocatalysts on the overall water splitting reaction was investigated using a solid solution of GaN and ZnO (hereafter termed GaN: ZnO) as a photocatalyst. GaN: ZnO was modified with nanoparticulate Mn3O4, RuO2, and IrO2 as O-2 evolution cocatalysts and with core/shell-type Rh/Cr2O3 composites as H-2 evolution cocatalysts. The photocatalytic activity of the coloaded samples for overall water splitting was higher than that of the samples modified with either of the O-2 or H-2 evolution cocatalysts alone. The activity enhancement induced by coloading was comparable for the three O-2 evolution cocatalysts investigated at the optimized loading amounts. Loading of a more efficient Rh/Cr2O3 cocatalyst prepared by adsorption of Rh nanoparticles further improved the photocatalytic activity. It was concluded that a simultaneous improvement in both oxidation and reduction reactions was effective at enhancing the photocatalytic activity of GaN:ZnO, whereas the reduction reactions limited the overall reaction rate of the coloaded system more significantly.

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