Cha G, Hwang I, Hejazi S, Dobrota AS, Pašti IA, Osuagwu B, Kim H, Will J, Yokosawa T, Badura Z, Kment Š, Mohajernia S, Mazare AV, Skorodumova NV, Spiecker E, Schmuki P (2021)
Publication Type: Journal article
Publication year: 2021
Book Volume: 24
Article Number: 102938
Journal Issue: 8
DOI: 10.1016/j.isci.2021.102938
Here, we evaluate three different noble metal co-catalysts (Pd, Pt, and Au) that are present as single atoms (SAs) on the classic benchmark photocatalyst, TiO2. To trap the single atoms on the surface, we introduced controlled surface vacancies (Ti3+-Ov) on anatase TiO2 nanosheets by a thermal reduction treatment. After anchoring identical loadings of single atoms of Pd, Pt, and Au, we measure the photocatalytic H2 generation rate and compare it to the classic nanoparticle co-catalysts on the nanosheets. While nanoparticles yield the well-established the hydrogen evolution reaction activity sequence (Pt > Pd > Au), for the single atom form, Pd radically outperforms Pt and Au. Based on density functional theory (DFT), we ascribe this unusual photocatalytic co-catalyst sequence to the nature of the charge localization on the noble metal SAs embedded in the TiO2 surface.
APA:
Cha, G., Hwang, I., Hejazi, S., Dobrota, A.S., Pašti, I.A., Osuagwu, B.,... Schmuki, P. (2021). As a single atom Pd outperforms Pt as the most active co-catalyst for photocatalytic H2 evolution. iScience, 24(8). https://doi.org/10.1016/j.isci.2021.102938
MLA:
Cha, Gi, et al. "As a single atom Pd outperforms Pt as the most active co-catalyst for photocatalytic H2 evolution." iScience 24.8 (2021).
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