Abstract
In the present work, the photoelectochemical (PEC) water oxidation property of the Zr-doped α-Fe2O3 (Zr-α-Fe2O3) nanostructure-based photoanode was improved by Co(OH)2 surface fictionalization. The surface functionalized Zr-α-Fe2O3 photoanode exhibits an improved water oxidation capability with photocurrent density of 1.9 mAcm−2 at 1.23 V vs. RHE while comparing with pure α-Fe2O3 (0.42 mAcm−2) and Zr-α-Fe2O3 (0.96 mAcm−2) photoanodes. Moreover, the Applied bias photon-to-current efficiency (ABPE) was calculated for all prepared photoanodes and it was found that Zr-α-Fe2O3/Co(OH)2 photoanode showed a higher value (0.22%) than pure α-Fe2O3 (0.04%) and Zr-α-Fe2O3 (0.08%) photoanodes. In addition, the charge transfer resistance (Rct) of Zr-α-Fe2O3/Co(OH)2 photoanode is only 21.6 Ω/cm2, which is lower than that of pure α-Fe2O3 (990 Ω/cm2) and Zr-α-Fe2O3 (32.8 Ω/cm2) photoanodes. The enhancement in the PEC water oxidation performance of the Zr-α-Fe2O3/Co(OH)2 photoanode is attributed by improvement of charge transfer process by surface-attached Co-based co-catalyst and thus improved overall PEC water oxidation efficiency.
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Acknowledgements
The authors extend their appreciation to the Deanship of Scientific Research at King Khalid University for funding this work through large group Research Project under grant number (R.G.P. 2/149/44).
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This work was funded by Deanship of Scientific Research, King Khalid University (Grant no.: R.G.P. 2/149/44).
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All authors contributed to the study conception and design. Material preparation, data collection, and analysis were performed by KR. The first draft of the manuscript was written by KR, MS, and RR. Experimental program planning and experimental guidance were performed by RR. All authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
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Ramachandran, K., Stanleydhinakar, M., Navaneethan, M. et al. Photoelectrochemical water oxidation of surface functionalized Zr-doped α-Fe2O3 photoanode. J Mater Sci: Mater Electron 35, 687 (2024). https://doi.org/10.1007/s10854-024-12443-5
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DOI: https://doi.org/10.1007/s10854-024-12443-5