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Ultrafine M-doped TiO2 (M = Fe, Ce, La) nanosphere photoanodes for photoelectrochemical water-splitting applications
In this study, Fe-, Ce-, and La-doped TiO2 ultrafine nanospheres were synthesized via low-temperature solvothermal method. The structural and morphological variations of bare and M (Fe, Ce, La)- doped TiO2 were confirmed by X-ray photoelectron spectroscopy and transmission electron microscopy images...
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Published in: | Materials characterization 2019-06, Vol.152, p.188-203 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | In this study, Fe-, Ce-, and La-doped TiO2 ultrafine nanospheres were synthesized via low-temperature solvothermal method. The structural and morphological variations of bare and M (Fe, Ce, La)- doped TiO2 were confirmed by X-ray photoelectron spectroscopy and transmission electron microscopy images. The fabricated photoanodes were tested using 1 M KOH electrolyte and demonstrated that they can be used for eco-friendly photoelectrochemical solar water-splitting application. Compared to bare TiO2 photoanodes, foreign cations (Fe, Ce, La)-doped TiO2-based photoanodes exhibited higher photocurrent response without bias. In nutshell, the rare-earth element La-doped TiO2 nanosphere photoanode showed good photocurrent response to approximately 0.48 mA/cm2 under illumination, with lower flat band potential shift of −0.83 V. The highest photostability of 96% was achieved over 2 h for 10% La-doped TiO2 nanosphere photoanode and was suitable for solar water-splitting applications.
•Highest photostability of 96% is achieved over 2 h for 10% La-doped TiO2.•10% La-doped TiO2 nanospheres showed highest photocurrent response of 0.48 mA/cm2.•Lowest flat band potential of around −0.83 V with the negative shift was obtained.•Highest photostability over 7200 s with 96% of retention under irradiation |
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ISSN: | 1044-5803 1873-4189 |
DOI: | 10.1016/j.matchar.2019.04.024 |