Isolation Strategy towards Earth-Abundant Single-Site Co-Catalysts for Photocatalytic Hydrogen Evolution Reaction
Achieving efficient photocatalytic water splitting remains one of the most vital challenges in the photocatalysis field, as the performance of contemporary heterogeneous catalysts is still limited by their insufficient activity and low predictability. To address this challenge, this work takes inspi...
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doaj-69d8b21f40e64b3eb678d2f6e9fd5e242021-03-26T00:00:55ZengMDPI AGCatalysts2073-43442021-03-011141741710.3390/catal11040417Isolation Strategy towards Earth-Abundant Single-Site Co-Catalysts for Photocatalytic Hydrogen Evolution ReactionPablo Ayala0Ariane Giesriegl1Sreejith P. Nandan2Stephen Nagaraju Myakala3Peter Wobrauschek4Alexey Cherevan5Institute for Materials Chemistry, TU Wien, 1060 Vienna, AustriaInstitute for Materials Chemistry, TU Wien, 1060 Vienna, AustriaInstitute for Materials Chemistry, TU Wien, 1060 Vienna, AustriaInstitute for Materials Chemistry, TU Wien, 1060 Vienna, AustriaAtominstitute, TU Wien, 10640 Vienna, AustriaInstitute for Materials Chemistry, TU Wien, 1060 Vienna, AustriaAchieving efficient photocatalytic water splitting remains one of the most vital challenges in the photocatalysis field, as the performance of contemporary heterogeneous catalysts is still limited by their insufficient activity and low predictability. To address this challenge, this work takes inspiration from the concept of heterogeneous single-metal-site catalysts (HSMSCs) and follows the idea of site-isolation, aiming towards single-site co-catalyst species and a higher atom-utilization efficiency. We synthesized a set of photocatalysts through an adsorption-limited wet impregnation process using bare and phosphate-modified TiO<sub>2</sub> as model supports and earth-abundant metals (Cu and Ni) with various loadings (0.008–5 wt.%) as co-catalyst species. The catalysts are characterized by TXRF for the determination of the real co-catalyst loadings, UV-vis and FTIR spectroscopes for semi-quantitative analysis of the metal state and binding modes to the substrate, and HRTEM for resolving the morphology of the sample’s surface. All samples were then evaluated towards the photocatalytic hydrogen evolution reaction (HER). We show that much higher turnover frequencies (TOFs) are obtained for both Cu- and Ni-based systems when lower co-catalyst loadings are used, which indicates an improved atom-utilization efficiency that reaches performances comparable to the noble Au co-catalyst. We also introduce a structural model to explain the observed TOF trends, which confirms that both earth-abundant systems undergo a strong structural reconstruction upon site-isolation towards smaller, perhaps even single-site-like species.https://www.mdpi.com/2073-4344/11/4/417single-sitesingle-atomwater splittingheterogeneous single-metal-site catalystssingle-atom-catalysis (SAC)photocatalysis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Pablo Ayala Ariane Giesriegl Sreejith P. Nandan Stephen Nagaraju Myakala Peter Wobrauschek Alexey Cherevan |
spellingShingle |
Pablo Ayala Ariane Giesriegl Sreejith P. Nandan Stephen Nagaraju Myakala Peter Wobrauschek Alexey Cherevan Isolation Strategy towards Earth-Abundant Single-Site Co-Catalysts for Photocatalytic Hydrogen Evolution Reaction Catalysts single-site single-atom water splitting heterogeneous single-metal-site catalysts single-atom-catalysis (SAC) photocatalysis |
author_facet |
Pablo Ayala Ariane Giesriegl Sreejith P. Nandan Stephen Nagaraju Myakala Peter Wobrauschek Alexey Cherevan |
author_sort |
Pablo Ayala |
title |
Isolation Strategy towards Earth-Abundant Single-Site Co-Catalysts for Photocatalytic Hydrogen Evolution Reaction |
title_short |
Isolation Strategy towards Earth-Abundant Single-Site Co-Catalysts for Photocatalytic Hydrogen Evolution Reaction |
title_full |
Isolation Strategy towards Earth-Abundant Single-Site Co-Catalysts for Photocatalytic Hydrogen Evolution Reaction |
title_fullStr |
Isolation Strategy towards Earth-Abundant Single-Site Co-Catalysts for Photocatalytic Hydrogen Evolution Reaction |
title_full_unstemmed |
Isolation Strategy towards Earth-Abundant Single-Site Co-Catalysts for Photocatalytic Hydrogen Evolution Reaction |
title_sort |
isolation strategy towards earth-abundant single-site co-catalysts for photocatalytic hydrogen evolution reaction |
publisher |
MDPI AG |
series |
Catalysts |
issn |
2073-4344 |
publishDate |
2021-03-01 |
description |
Achieving efficient photocatalytic water splitting remains one of the most vital challenges in the photocatalysis field, as the performance of contemporary heterogeneous catalysts is still limited by their insufficient activity and low predictability. To address this challenge, this work takes inspiration from the concept of heterogeneous single-metal-site catalysts (HSMSCs) and follows the idea of site-isolation, aiming towards single-site co-catalyst species and a higher atom-utilization efficiency. We synthesized a set of photocatalysts through an adsorption-limited wet impregnation process using bare and phosphate-modified TiO<sub>2</sub> as model supports and earth-abundant metals (Cu and Ni) with various loadings (0.008–5 wt.%) as co-catalyst species. The catalysts are characterized by TXRF for the determination of the real co-catalyst loadings, UV-vis and FTIR spectroscopes for semi-quantitative analysis of the metal state and binding modes to the substrate, and HRTEM for resolving the morphology of the sample’s surface. All samples were then evaluated towards the photocatalytic hydrogen evolution reaction (HER). We show that much higher turnover frequencies (TOFs) are obtained for both Cu- and Ni-based systems when lower co-catalyst loadings are used, which indicates an improved atom-utilization efficiency that reaches performances comparable to the noble Au co-catalyst. We also introduce a structural model to explain the observed TOF trends, which confirms that both earth-abundant systems undergo a strong structural reconstruction upon site-isolation towards smaller, perhaps even single-site-like species. |
topic |
single-site single-atom water splitting heterogeneous single-metal-site catalysts single-atom-catalysis (SAC) photocatalysis |
url |
https://www.mdpi.com/2073-4344/11/4/417 |
work_keys_str_mv |
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