Abstract

The main aim of this study was to investigate the effect of deposition time on the physicochemical and photoelectrochemical properties of cupric oxide (CuO) thin films synthesized via electrodeposition method. Firstly, the electrodeposition of amorphous CuO films on fluorine-doped tin oxide (FTO) working electrodes with varying deposition time between 5 and 30 min was carried out, followed by annealing treatment at 500 °C. Resultant nanocrystalline CuO thin films were characterised using field emission-scanning electron microscopy (FE-SEM), photocurrent density, and photoluminescence measurements. Through FE-SEM analysis, it was observed that the surface of thin films was composed of irregular-sized CuO nanocrystals. A smaller CuO nanocrystals size will lead to a higher photoactivity due to the increase in overall catalytic surface area. In addition, the smaller CuO nanocrystals size will prolongs the electron-hole recombination rate due to the increase in copious amount of surface defects. From this study, it was revealed that the relationship between deposition time and CuO film thickness was non-linear. This could be due to the detachment of CuO thin films from the FTO surface at an increasing amount of CuO mass being deposited. It was observed that the amount of light absorbed by CuO thin films increased with film thickness until a certain extent whereby, any further increase in the film thickness will result in a reduction of light photon penetration. Therefore, the CuO nanocrystals size and film thickness have to be compromised in order to yield a higher catalytic surface area and a lower rate of surface charge recombination. Finally, it was found that the deposition time of 15 min resulted in an average CuO nanocrystals size of 73.7 nm, optimum film thickness of 0.73 μm, and corresponding photocurrent density of 0.23 mA/cm 2 at the potential bias of - 0.3 V (versus Ag/AgCl). The PL spectra for the deposition time of 15 min has the lowest rate of recombination of photogenerated electron-hole pairs by referring to its lowest PL intensity.

Highlights

  • Photoelectrochemical (PEC) water splitting is a photodriven conversion process of water molecules into hydrogen and oxygen molecules through the use of semiconductor metal oxides photocatalysts [1]

  • The main aim of this study was to systematically investigate the effect of deposition time on the physicochemical and PEC properties of Cupric oxide (CuO) thin films synthesized via electrodeposition method

  • The CuO film thickness was found to increase with increasing deposition time due to that more Cu2+ ions being diffused to the fluorine-doped tin oxide (FTO) surface, underwent reduction reaction, and subsequently deposited on it as shown in Eq (1)

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Summary

Introduction

Photoelectrochemical (PEC) water splitting is a photodriven conversion process of water molecules into hydrogen and oxygen molecules through the use of semiconductor metal oxides photocatalysts [1]. The type of semiconductor photocatalysts used in the PEC water splitting process will affect the efficiency of waterto-hydrogen conversion process due to their inherent bandgap characteristics. The synthesis of nanostructured semiconductor metal oxides photocatalysts have attracted much attention due to their promising properties in different fields of application ranging from sensors, optoelectronics, and electronics to catalysis. Cupric oxide (CuO) is one of the p-type binary copper semiconductors with a narrow bandgap of 1.3 to 1.9 eV, and a corresponding theoretical photocurrent density of 35 mA/cm2 [3, 4]

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