Abstract
Undoped and boron-doped ZnO nanorods (NRs) were grown on ITO glass substrates by using hydrothermal techniques. The as grown nanorods were investigated by using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), UV–visible spectroscopy, and photoelectrochemical study. XRD spectra reveal the confirmations regarding the hexagonal wurtzite structure along with preferential orientation (002). The observation of (002) peak shows a red shift. The average size distribution of NRs in doped and undoped sample ranges from 169 to 191 nm. The absorption spectra clearly revealed the band gap tunability feature of the samples with a change in doping percentage. Photoluminescence spectra clearly indicate the presence of oxygen defects. Photocurrent density as high as ∼0.622 and 2.6 mA/cm2 were obtained for undoped and 6% B-doped ZnO NRs arrays respectively, at +0.44 V vs. Ag/AgCl electrode under visible light AM 1.5 G (100 mW/cm2) in 0.1 M electrolyte solutions of NaOH. More enhancement in photoconversion efficiency (PCE) from 0.491 to 2.054% was observed for undoped ZnO NRs and optimum 6% B-doped ZnO in 0.1 M NaOH electrolyte solution.
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Acknowledgements
The authors acknowledge the Department of Science and Technology (DST) for the project with grant number SR/FTP/PS-184/2012, SERB vide Dy. No. SERB/F/5439/2013-14 dated 25.11.2013 and Faculty Research Scheme-FRS (54)/2103-2014/APH. The authors would like to thank Indian Institute of Technology (Indian School of Mines), Dhanbad, India for providing research fellowship and Central Research Facility (CRF) respectively. One of the authors M.C. would like to acknowledge Indo-US Science and Technology Forum (IUSSTF) for providing international Bhaskara Advanced Solar Energy (BASE-2016) fellowship.
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Sharma, A., Chakraborty, M., Thangavel, R. et al. Hydrothermal growth of undoped and boron doped ZnO nanorods as a photoelectrode for solar water splitting applications. J Sol-Gel Sci Technol 85, 1–11 (2018). https://doi.org/10.1007/s10971-017-4536-3
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DOI: https://doi.org/10.1007/s10971-017-4536-3