SacrificialAgent-Controlled Photodeposition: RevealingPt-Photodeposition Key Features of Pt-Nanoparticle Co-catalysts forMaximized Photocatalytic H<sub>2</sub> Evolution

Photocatalytic H<sub>2</sub> production from TiO<sub>2</sub> substrates (and many other common semiconductors) relies on the use of a suitable co-catalyst. The most widely used co-catalyst is Pt that is typically photodeposited as metallic Pt<sup>0</sup> nanoparticles (NPs) on various titania structures. In this Pt photodeposition process, parameters such as the Pt concentration in the solution or the nature of the sacrificial agents strongly affect the NP deposition amount, the particle size, and its distribution. Despite considerable investigations, unifying concepts that connect Pt-deposit features with H<sub>2</sub> evolution efficiency focus mainly on a critical Pt loading amount but are often inconclusive. In the present work, we use thin-film sputter-deposited anatase layers as well-defined photoabsorbers for Pt deposition under a wide range of conditions, characterize the NPs, and measure photocatalytic H<sub>2</sub> evolution. From the results, we find that a unifying criterion for achieving a maximized co-catalytic efficiency of Pt deposits is to overcome a critical Pt particle density, independent of the detailed particle features of Pt deposition conditions.

Publication Details

Journal
Figshare
Published
2025-03-26
DOI
https://doi.org/10.1021/acselectrochem.5c00011.s001
Primary Topic
TiO2 Photocatalysis and Solar Cells
Type
article
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article

SacrificialAgent-Controlled Photodeposition: RevealingPt-Photodeposition Key Features of Pt-Nanoparticle Co-catalysts forMaximized Photocatalytic H2 Evolution

Figshare
TiO2 Photocatalysis and Solar Cells
article

SacrificialAgent-Controlled Photodeposition: RevealingPt-Photodeposition Key Features of Pt-Nanoparticle Co-catalysts forMaximized Photocatalytic H2 Evolution

article en

Abstract

Photocatalytic H<sub>2</sub> production from TiO<sub>2</sub> substrates (and many other common semiconductors) relies on the use of a suitable co-catalyst. The most widely used co-catalyst is Pt that is typically photodeposited as metallic Pt<sup>0</sup> nanoparticles (NPs) on various titania structures. In this Pt photodeposition process, parameters such as the Pt concentration in the solution or the nature of the sacrificial agents strongly affect the NP deposition amount, the particle size, and its distribution. Despite considerable investigations, unifying concepts that connect Pt-deposit features with H<sub>2</sub> evolution efficiency focus mainly on a critical Pt loading amount but are often inconclusive. In the present work, we use thin-film sputter-deposited anatase layers as well-defined photoabsorbers for Pt deposition under a wide range of conditions, characterize the NPs, and measure photocatalytic H<sub>2</sub> evolution. From the results, we find that a unifying criterion for achieving a maximized co-catalytic efficiency of Pt deposits is to overcome a critical Pt particle density, independent of the detailed particle features of Pt deposition conditions.

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Openalex Percentile: Top 69%
TiO2 Photocatalysis and Solar Cells
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