4.8 Article

Efficient Photocatalytic Water Splitting Using Al-Doped SrTiO3 Coloaded with Molybdenum Oxide and Rhodium-Chromium Oxide

Journal

ACS CATALYSIS
Volume 8, Issue 4, Pages 2782-2788

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.7b04264

Keywords

cocatalyst; coloading; molybdenum oxide; quantum yield; water splitting; hydrogen evolution

Funding

  1. Taiwan Ministry of Science and Technology from Taiwan [MST 105-2918-1-239-001]
  2. Japan Society for the Promotion of Science (JSPS) [16H02417, 15H05494]
  3. Artificial Photosynthesis Project of the New Energy and Industrial Technology Development Organization (NEDO)
  4. Nanotechnology Platform of the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan
  5. Grants-in-Aid for Scientific Research [16K06862, 17H01216, 15H05494] Funding Source: KAKEN

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Al-doped SrTiO3 loaded with a rhodium chromium mixed oxide (RECrOx/STO:A1) efficiently promotes photocatalytic overall water splitting with an apparent quantum yield (AQY) of 56% under 365 nm ultraviolet (UV) light. Further increasing this AQY is of vital importance, because this value determines the maximum solar to hydrogen energy conversion efficiency that can be achieved. Herein, we demonstrate that the AQY during overall water splitting by RhCrOx/STO:Al is improved by 20% (to 69% at 365 nm) by coloading of molybdenum oxide (MoOy, 0.03 wt % as Mo) followed by calcination. Reductively photodeposited MoOy modifies the chemical state of the RhCrOx cocatalyst and likely promotes photocatalytic H-2 evolution, whereas MoOy loaded onto STO:Al does not catalyze either photocatalytic H-2 or O-2 evolution. The present study indicates a means of further enhancing the water-splitting activity of highly efficient cocatalyst/photocatalyst composites by loading small amounts of promoters in a facile manner.

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