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Alkali modified P25 with enhanced CO(2) adsorption for CO(2) photoreduction

To improve the CO(2) adsorption on the photocatalyst, which is an essential step for CO(2) photoreduction, solid solutions were fabricated using a facile calcination treatment at 900 °C. Using various alkalis, namely NaOH, Na(2)CO(3), KOH, K(2)CO(3), the resulted samples presented a much higher CO(2...

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Autores principales: Tan, Jeannie Z. Y., Gavrielides, Stelios, Xu, Hao R., Thompson, Warren A., Maroto-Valer, M. Mercedes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055653/
https://www.ncbi.nlm.nih.gov/pubmed/35519115
http://dx.doi.org/10.1039/d0ra05010e
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author Tan, Jeannie Z. Y.
Gavrielides, Stelios
Xu, Hao R.
Thompson, Warren A.
Maroto-Valer, M. Mercedes
author_facet Tan, Jeannie Z. Y.
Gavrielides, Stelios
Xu, Hao R.
Thompson, Warren A.
Maroto-Valer, M. Mercedes
author_sort Tan, Jeannie Z. Y.
collection PubMed
description To improve the CO(2) adsorption on the photocatalyst, which is an essential step for CO(2) photoreduction, solid solutions were fabricated using a facile calcination treatment at 900 °C. Using various alkalis, namely NaOH, Na(2)CO(3), KOH, K(2)CO(3), the resulted samples presented a much higher CO(2) adsorption capacity, which was measured with the pulse injection of CO(2) on the temperature programmed desorption workstation, compared to the pristine Evonik P25. As a result, all of the fabricated solid solutions produced higer yield of CO under UV light irradiation due to the increased basicity of the solid solutions even though they possessed only the rutile polymorph of TiO(2). The highest CO(2) adsorption capacity under UV irradiation was observed in the sample treated with NaOH, which contained the highest amount of isolated hydroxyls, as shown in the FTIR studies.
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spelling pubmed-90556532022-05-04 Alkali modified P25 with enhanced CO(2) adsorption for CO(2) photoreduction Tan, Jeannie Z. Y. Gavrielides, Stelios Xu, Hao R. Thompson, Warren A. Maroto-Valer, M. Mercedes RSC Adv Chemistry To improve the CO(2) adsorption on the photocatalyst, which is an essential step for CO(2) photoreduction, solid solutions were fabricated using a facile calcination treatment at 900 °C. Using various alkalis, namely NaOH, Na(2)CO(3), KOH, K(2)CO(3), the resulted samples presented a much higher CO(2) adsorption capacity, which was measured with the pulse injection of CO(2) on the temperature programmed desorption workstation, compared to the pristine Evonik P25. As a result, all of the fabricated solid solutions produced higer yield of CO under UV light irradiation due to the increased basicity of the solid solutions even though they possessed only the rutile polymorph of TiO(2). The highest CO(2) adsorption capacity under UV irradiation was observed in the sample treated with NaOH, which contained the highest amount of isolated hydroxyls, as shown in the FTIR studies. The Royal Society of Chemistry 2020-07-27 /pmc/articles/PMC9055653/ /pubmed/35519115 http://dx.doi.org/10.1039/d0ra05010e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Tan, Jeannie Z. Y.
Gavrielides, Stelios
Xu, Hao R.
Thompson, Warren A.
Maroto-Valer, M. Mercedes
Alkali modified P25 with enhanced CO(2) adsorption for CO(2) photoreduction
title Alkali modified P25 with enhanced CO(2) adsorption for CO(2) photoreduction
title_full Alkali modified P25 with enhanced CO(2) adsorption for CO(2) photoreduction
title_fullStr Alkali modified P25 with enhanced CO(2) adsorption for CO(2) photoreduction
title_full_unstemmed Alkali modified P25 with enhanced CO(2) adsorption for CO(2) photoreduction
title_short Alkali modified P25 with enhanced CO(2) adsorption for CO(2) photoreduction
title_sort alkali modified p25 with enhanced co(2) adsorption for co(2) photoreduction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055653/
https://www.ncbi.nlm.nih.gov/pubmed/35519115
http://dx.doi.org/10.1039/d0ra05010e
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