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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Main Authors: Pablo Ayala, Ariane Giesriegl, Sreejith P. Nandan, Stephen Nagaraju Myakala, Peter Wobrauschek, Alexey Cherevan
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:Catalysts
Subjects:
Online Access:https://www.mdpi.com/2073-4344/11/4/417
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spelling 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
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