4.8 Article

Surface Engineering to Reduce the Interfacial Resistance for Enhanced Photocatalytic Water Oxidation

Journal

ACS CATALYSIS
Volume 10, Issue 15, Pages 8742-8750

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.0c02063

Keywords

TiO2; water oxidation; hole-transfer; photocatalysis; IrOx; cocatalyst

Funding

  1. National Key Research Program of China [2017YFA0204800, 2016YFA0202403]
  2. Natural Science Foundation of China [21603136]
  3. Changjiang Scholar and Innovative Research Team [IRT_14R33]
  4. Fundamental Research Funds for the Central Universities [GK202003042]
  5. 111 Project [B14041]
  6. Chinese National 1000-Talent-Plan program

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Interfacial resistance of the charge carriers across TiO2 to cocatalysts is one of the main limiting factors for realizing high photocatalytic efficiency of water oxidation. Herein, an amorphous TiOx layer is introduced on the surface of crystalline TiO2 catalyst to form the core-shell structure (am@TiO2) via an oxidation corrosion method. Owing to the surface disordered TiO layer, the obtained ampTiO(2) exposes abundant -OH groups for the homogeneous loading of nanosized IrOx, while the charge carrier interfacial migration is substantially enhanced. The as-prepared IrOx-am@TiO2 exhibits photocatalytic water oxidation performance with an O-2 evolution rate of 143.6 mu mol/g.h, which is approximately 14 times higher than that of the bare ampTiO(2). Moreover, an apparent quantum yield (AQY) of 18.99% is obtained under LED-405 illumination. This work provides a direction for improving the photocatalytic performance and helps to gain a fundamental understanding of the water oxidation steps.

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