As a single atom Pd outperforms Pt as the most active co-catalyst for photocatalytic H 2 evolution.

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, TiO ₂ . To trap the single atoms on the surface, we introduced controlled surface vacancies (Ti ³⁺ -O _v ) on anatase TiO ₂ nanosheets by a thermal reduction treatment. After anchoring identical loadings of single atoms of Pd, Pt, and Au, we measure the photocatalytic H ₂ 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 TiO ₂ surface.
Competing Interests: The authors declare no competing interests.
(© 2021 The Authors.)