Abstract
Herein, we report the anodic growth of nanostructured Cu(OH) 2 thin films on the copper surface by potentiostatic and potentiodynamic methods. The phase formation, crystalline feature, morphology and the progressive growth of Cu(OH) 2 thin films were controlled by the applied potential and concentrations of alkali utilized in anodization process. Electrochemical investigations suggest the rapid growth of Cu(OH) 2 and passivation at higher anodization potentials. In contrast, the lower anodization potentials favours the progressive growth of Cu(OH) 2 nanorod like features. The thermal treatment of Cu/Cu(OH) 2 reveals the formation of crystalline mixed copper oxide film with predominantly Cu 2 O phase at 673 K and 773 K. Photoelectrochemical investigations of these copper oxide thin films exhibit the p-type behavior with repeatable photovoltage (55 mV) and stable photocurrent responses (20–60 μA cm −2 ). The hydrogen evolution studies show better activity with nanostructured Cu(OH) 2 and copper oxides than with aggregated thin films and bare substrate.
Original language | English |
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Pages (from-to) | 7181-7193 |
Number of pages | 13 |
Journal | International Journal of Hydrogen Energy |
Volume | 44 |
Issue number | 14 |
DOIs | |
State | Published - 15 Mar 2019 |
Externally published | Yes |
Keywords
- Copper oxides
- Cu(OH) nanostructures
- Hydrogen evolution reaction
- Photocathode
- Potentiostatic electrodeposition
ASJC Scopus subject areas
- Renewable Energy, Sustainability and the Environment
- Fuel Technology
- Condensed Matter Physics
- Energy Engineering and Power Technology