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Light-driven oxygen evolution from water oxidation with immobilised TiO2 engineered for high performance

Title
Light-driven oxygen evolution from water oxidation with immobilised TiO2 engineered for high performance
Type
Article in International Scientific Journal
Year
2021
Authors
Yu, ZP
(Author)
Other
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Lopes, JC
(Author)
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Tavares, PB
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Liu, LF
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Journal
Title: Scientific ReportsImported from Authenticus Search for Journal Publications
Vol. 11
ISSN: 2045-2322
Publisher: Springer Nature
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Publicação em ISI Web of Knowledge ISI Web of Knowledge - 0 Citations
Publicação em Scopus Scopus - 0 Citations
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Authenticus ID: P-00V-NFC
Abstract (EN): Calcination treatments in the range of 500-900 degrees C of TiO2 synthesised by the sol-gel resulted in materials with variable physicochemical (i.e., optical, specific surface area, crystallite size and crystalline phase) and morphological properties. The photocatalytic performance of the prepared materials was evaluated in the oxygen evolution reaction (OER) following UV-LED irradiation of aqueous solutions containing iron ions as sacrificial electron acceptors. The highest activity for water oxidation was obtained with the photocatalyst thermally treated at 700 degrees C (TiO2-700). Photocatalysts with larger anatase to rutile ratio of the crystalline phases and higher surface density of oxygen vacancies (defects) displayed the best performance in OER. The oxygen defects at the photocatalyst surface have proven to be responsible for the enhanced photoactivity, acting as important active adsorption sites for water oxidation. Seeking technological application, water oxidation was accomplished by immobilising the photocatalyst with the highest OER rate measured under the established batch conditions (TiO2-700). Experiments operating under continuous mode revealed a remarkable efficiency for oxygen production, exceeding 12% of the apparent quantum efficiency (AQE) at 384 nm (UV-LED system) compared to the batch operation mode.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 11
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