4.6 Article

Cathodic shift of a photo-potential on a Ta3N5 photoanode by post-heating a TiO2 passivation layer

Journal

RSC ADVANCES
Volume 7, Issue 49, Pages 30650-30656

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ra04647b

Keywords

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Funding

  1. National Basic Research Program of China (973 Program) [2015CB932200, 2014CB239303, 2013CB632404]
  2. Natural Science Foundation of Jiangsu Province of China [15KJB150010, BK20150955]
  3. Synergetic Innovation Center for Organic Electronics and Information Displays
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  5. Newton Research Collaboration Programme Type 2 Award [NRCP/1415/264]

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Ta3N5 is a promising photoanode material for solar water splitting due to its suitable band gap and high theoretical solar energy conversion. A high onset potential of Ta3N5 limits its photoelectrochemical performance due to serious surface charge recombination. In a previous study, a TiO2 passivation layer was usually coated on the surface of Ta3N5 to reduce the surface recombination and improve the performance of a sample. However, to date, there are no studies on the effect of conductivity of the TiO2 passivation layer on the photoelectrochemical properties of a Ta3N5 photoanode. In this work, for the first time, the conductivity of TiO2 is increased by post-heating of a TiO2 passivation layer, leading to a 90 mV cathodic shift of the photo-potential of Ta3N5. After further loading with a Ni(OH)(x)/FeOOH bilayer electrocatalyst, the Ta3N5 photoanode achieves a current density of 6.4 mA cm(-2) at 1.23 VRHE and a HC-STH (half-cell solar to hydrogen efficiency) of 0.72% under a sunlight simulator (100 mW cm(-2)), which are the highest values among the Ta3N5 photoanodes prepared by thermal oxidation and nitridation of Ta foil.

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