4.7 Article

Dual co-catalysts decorated Zn-WO3 nanorod arrays with highly efficient photoelectrocatalytic performance

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 47, Issue 28, Pages 13641-13653

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.02.1220360-3199

Keywords

Co-catalyst; Photoelectrochemical water; splitting; WO3; Zn doping; Oxygen vacancies

Funding

  1. National Natural Science Foundation of China [21978200]
  2. Scientific Research Projects of the Ministry of Education of China [6141A02033522]

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In this study, a highly efficient and stable WO3 photoanode was constructed using a combination of transition metal doping and dual co-catalysts modification. The presence of abundant surface oxygen vacancies in Zn-WO3 was found, which, combined with the dual cocatalysts layer, improved carrier mobility, enhanced carrier separation and injection efficiency. The optimal 9-Zn-WO3-Fe/Co photoanode exhibited a photocurrent of 3.63 mA/cm2 at 1.23 V vs. RHE, equivalent to 90.7% of the theoretical value of WO3.
WO3 has been recognized as a promising photoanode for the conversion of solar energy to hydrogen energy through photoelectrochemical water splitting. Herein, Zn-WO3 nanorod arrays were synthesized by a two-step solvothermal method and then decorated with FeOOH and CoOOH dual co-catalysts layer through electrodeposition. Characterizations confirm the presence of abundant surface oxygen vacancies in Zn-WO3, leading to the increase of carriers with high mobility and thus improving the separation (from 63.7% to 92.0%) and injection (from 61.9% to 95.3%) efficiency of carriers. Meanwhile, the dual cocatalysts layer accelerates the transfer of the hole at the interface and inhibits the photocorrosion. Consequently, the optimal 9-Zn-WO3-Fe/Co exhibits the photocurrent of 3.63 mA/cm2 at 1.23 V vs. RHE, which is 90.7% of the theoretical value of WO3 (ca. 4.0 mA/cm2). This work constructs a highly efficient and stable WO3 photoanode by an integration strategy of transition metal doping and dual co-catalysts modification. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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