Journal Article PUBDB-2024-00256

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Reactive Deposition Versus Strong Electrostatic Adsorption (SEA): A Key to Highly Active Single Atom Co‐Catalysts in Photocatalytic H$_2$ Generation

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2023
Wiley-VCH Weinheim

Advanced materials 35(32), 2211814 () [10.1002/adma.202211814]
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Abstract: In recent years, the use of single atoms (SAs) has become of a rapidly increasing significance in photocatalytic H$_2$ generation; here SA noble metals (mainly Pt SAs) can act as highly effective co-catalysts. The classic strategy to decorate oxide semiconductor surfaces with maximally dispersed SAs relies on “strong electrostatic adsorption” (SEA) of suitable noble metal complexes. In the case of TiO$_2$ – the classic benchmark photocatalyst – SEA calls for adsorption of cationic Pt complexes such as [(NH$_3$)$_4$Pt]$^{2+}$ which then are thermally reacted to surface-bound SAs. While SEA is widely used in literature, in the present work it is shown by a direct comparison that reactive attachment based on the reductive anchoring of SAs, e.g., from hexachloroplatinic(IV) acid (H$_2$PtCl$_6$) leads directly to SAs in a configuration with a significantly higher specific activity than SAs deposited with SEA – and this at a significantly lower Pt loading and without any thermal post-deposition treatments. Overall, the work demonstrates that the reactive deposition strategy is superior to the classic SEA concept as it provides a direct electronically well-connected SA-anchoring and thus leads to highly active single-atom sites in photocatalysis.

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Contributing Institute(s):
  1. DOOR-User (DOOR ; HAS-User)
Research Program(s):
  1. 6G3 - PETRA III (DESY) (POF4-6G3) (POF4-6G3)
Experiment(s):
  1. PETRA Beamline P65 (PETRA III)

Appears in the scientific report 2023
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Medline ; Creative Commons Attribution CC BY 4.0 ; OpenAccess ; Clarivate Analytics Master Journal List ; Current Contents - Engineering, Computing and Technology ; Current Contents - Physical, Chemical and Earth Sciences ; IF >= 25 ; JCR ; NationallizenzNationallizenz ; SCOPUS ; Web of Science Core Collection
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 Record created 2024-01-17, last modified 2025-07-24


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