CdTe quantum dot-functionalized P25 titania composite with enhanced photocatalytic NO2 storage selectivity under UV and vis irradiation
Composite systems of P25 (titania) functionalized with thioglycolic acid (TGA)-capped CdTe colloidal quantum dots (QDs) were synthesized, structurally characterized, and photocatalytically tested in the photocatalytic NOx oxidation and storage during NO(g) + O2(g) reaction. Pure P25 yielded moderate...
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sg-ntu-dr.10356-1434412020-09-01T09:14:17Z CdTe quantum dot-functionalized P25 titania composite with enhanced photocatalytic NO2 storage selectivity under UV and vis irradiation Leinen, Merve Balci Dede, Didem Khan, Munir Ullah Çağlayan, Mustafa Koçak, Yusuf Demir, Hilmi Volkan Ozensoy, Emrah School of Electrical and Electronic Engineering School of Materials Science and Engineering School of Physical and Mathematical Sciences Engineering::Electrical and electronic engineering CdTe Colloidal Quantum Dots Titanium Dioxide Composite systems of P25 (titania) functionalized with thioglycolic acid (TGA)-capped CdTe colloidal quantum dots (QDs) were synthesized, structurally characterized, and photocatalytically tested in the photocatalytic NOx oxidation and storage during NO(g) + O2(g) reaction. Pure P25 yielded moderate-to-high NO conversion (31% in UV-A and 40% in visible (vis)) but exhibited extremely poor selectivity toward NOx storage in solid state (25% in UV-A and 35% in vis). Therefore, P25 could efficiently photooxidize NO(g) + O2(g) into NO2; however, it failed to store photogenerated NO2 and released toxic NO2(g) to the atmosphere. CdTe QD-functionalized P25 revealed a major boost in photocatalytic performance with respect to pure P25, where NO conversion reached 42% under UV-A and 43% under vis illumination, while the respective selectivity climbed up to 92 and 97%, rendering the CdTe/P25 composite system an efficient broad-band photocatalyst, which can harvest both UV-A and vis light efficiently and display a strong NOx abatement effect. Control experiments suggested that photocatalytic active sites responsible for the NO(g) + O2(g) photooxidation and formation of NO2 reside mostly on titania, while the main functions of the TGA capping agent and the CdTe QDs are associated with the photocatalytic conversion of the generated NO2 to the adsorbed NOx species, significantly boosting the selectivity toward solid-state NOx storage. Reuse experiments showed that photocatalytic performance of the CdTe/P25 system can be preserved to a reasonable extent with only a moderate decrease in the photocatalytic performance. Although some decrease in the photocatalytic activity was observed after aging, CdTe/P25 could still outperform P25 benchmark photocatalyst. Increasing CdTe QDs loading from the currently optimized minuscule concentrations could be a useful strategy to increase further the catalytic lifetime/stability of the CdTe/P25 system with only a minor penalty in catalytic activity. Accepted version E.O. acknowledges the scientific collaboration with TARLA project founded by the Ministry of Development of Turkey (project code: DPT2006K-120470). H.V.D. is grateful to the support from TUBA. The authors acknowledge SASOL Ltd. for providing Puralox SBA200 γ-Al2O3 materials. 2020-09-01T09:14:17Z 2020-09-01T09:14:17Z 2018 Journal Article Leinen, M. B., Dede, D., Khan, M. U., Çağlayan, M., Koçak, Y., Demir, H. V., & Ozensoy, E. (2019). CdTe quantum dot-functionalized P25 titania composite with enhanced photocatalytic NO2 storage selectivity under UV and vis irradiation. ACS Applied Materials & Interfaces, 11(1), 865-879. doi:10.1021/acsami.8b18036 1944-8244 https://hdl.handle.net/10356/143441 10.1021/acsami.8b18036 30525435 2-s2.0-85059425564 1 11 865 879 en ACS Applied Materials & Interfaces This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Materials & Interfaces, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsami.8b18036 application/pdf |
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Engineering::Electrical and electronic engineering CdTe Colloidal Quantum Dots Titanium Dioxide Leinen, Merve Balci Dede, Didem Khan, Munir Ullah Çağlayan, Mustafa Koçak, Yusuf Demir, Hilmi Volkan Ozensoy, Emrah CdTe quantum dot-functionalized P25 titania composite with enhanced photocatalytic NO2 storage selectivity under UV and vis irradiation |
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Composite systems of P25 (titania) functionalized with thioglycolic acid (TGA)-capped CdTe colloidal quantum dots (QDs) were synthesized, structurally characterized, and photocatalytically tested in the photocatalytic NOx oxidation and storage during NO(g) + O2(g) reaction. Pure P25 yielded moderate-to-high NO conversion (31% in UV-A and 40% in visible (vis)) but exhibited extremely poor selectivity toward NOx storage in solid state (25% in UV-A and 35% in vis). Therefore, P25 could efficiently photooxidize NO(g) + O2(g) into NO2; however, it failed to store photogenerated NO2 and released toxic NO2(g) to the atmosphere. CdTe QD-functionalized P25 revealed a major boost in photocatalytic performance with respect to pure P25, where NO conversion reached 42% under UV-A and 43% under vis illumination, while the respective selectivity climbed up to 92 and 97%, rendering the CdTe/P25 composite system an efficient broad-band photocatalyst, which can harvest both UV-A and vis light efficiently and display a strong NOx abatement effect. Control experiments suggested that photocatalytic active sites responsible for the NO(g) + O2(g) photooxidation and formation of NO2 reside mostly on titania, while the main functions of the TGA capping agent and the CdTe QDs are associated with the photocatalytic conversion of the generated NO2 to the adsorbed NOx species, significantly boosting the selectivity toward solid-state NOx storage. Reuse experiments showed that photocatalytic performance of the CdTe/P25 system can be preserved to a reasonable extent with only a moderate decrease in the photocatalytic performance. Although some decrease in the photocatalytic activity was observed after aging, CdTe/P25 could still outperform P25 benchmark photocatalyst. Increasing CdTe QDs loading from the currently optimized minuscule concentrations could be a useful strategy to increase further the catalytic lifetime/stability of the CdTe/P25 system with only a minor penalty in catalytic activity. |
author2 |
School of Electrical and Electronic Engineering |
author_facet |
School of Electrical and Electronic Engineering Leinen, Merve Balci Dede, Didem Khan, Munir Ullah Çağlayan, Mustafa Koçak, Yusuf Demir, Hilmi Volkan Ozensoy, Emrah |
format |
Article |
author |
Leinen, Merve Balci Dede, Didem Khan, Munir Ullah Çağlayan, Mustafa Koçak, Yusuf Demir, Hilmi Volkan Ozensoy, Emrah |
author_sort |
Leinen, Merve Balci |
title |
CdTe quantum dot-functionalized P25 titania composite with enhanced photocatalytic NO2 storage selectivity under UV and vis irradiation |
title_short |
CdTe quantum dot-functionalized P25 titania composite with enhanced photocatalytic NO2 storage selectivity under UV and vis irradiation |
title_full |
CdTe quantum dot-functionalized P25 titania composite with enhanced photocatalytic NO2 storage selectivity under UV and vis irradiation |
title_fullStr |
CdTe quantum dot-functionalized P25 titania composite with enhanced photocatalytic NO2 storage selectivity under UV and vis irradiation |
title_full_unstemmed |
CdTe quantum dot-functionalized P25 titania composite with enhanced photocatalytic NO2 storage selectivity under UV and vis irradiation |
title_sort |
cdte quantum dot-functionalized p25 titania composite with enhanced photocatalytic no2 storage selectivity under uv and vis irradiation |
publishDate |
2020 |
url |
https://hdl.handle.net/10356/143441 |
_version_ |
1681056911984689152 |