4.7 Article

CuO/Pd composite photocathodes for photoelectrochemical hydrogen evolution reaction

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 39, Issue 15, Pages 7686-7696

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2014.03.084

Keywords

Photoelectrochemical cell; Solar water splitting; Hydrogen evolution reaction; Copper oxide; Palladium nanoparticles

Funding

  1. National Natural Science Foundation of China [NSFC 21173016, 20973020]
  2. Beijing Natural Science Foundation [2142020]
  3. Doctoral Fund of Ministry of Education of China [20101102110002]

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CuO has been considered as a promising photocathodic material for photoelectrochemical (PEC) hydrogen evolution reaction (HER). In this work, CuO films were prepared by a facile and cost-effective method that involves solution synthesis, spin-coating and thermal treatment processes. The resulting CuO films had a monoclinic crystal structure with bandgap energy of 1.56 eV and a conduction band position of 3.73 eV below the vacuum level in borate buffer solution. The CuO films exhibited good PEC activity toward HER and the preparation conditions had great effect on the activity. The photoactivity of the CuO film decayed to approximately 19% of its original value after reaction for 10 h under illumination. The reduction of CuO to Cu2O has been confirmed to be a parallel competitive reaction against HER. The mismatched band structure of the resulting CuO/Cu2O hetero-junction was believed to be the main cause of the decay of photoactivity. The photo-assisted electrodeposition method was developed to prepare CuO/Pd composite photocathode. The presence of Pd on CuO greatly increased the photocurrent especially at low overpotentials. In addition, the CuO/Pd composite exhibited significantly improved photostability compared to CuO. This work demonstrates the feasibility of increasing PEG activity and stability of CuO-based photocathodes by combining CuO with noble metal nanoparticles. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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