<div class="csl-bib-body">
<div class="csl-entry">Pollitt, S., Haunold, T., Hossain, S., Behrendt, G., Stöger-Pollach, M., Kawawaki, T., Barrabés, N., Behrens, M., Negishi, Y., & Rupprechter, G. (2025). Engineering Catalytic Efficiency by Thiolate-Protected Trimetallic (Cu, Pd, Au) Nanoclusters: Single-Atom Alloy Catalysts for Water–Gas Shift. <i>ACS Catalysis</i>, <i>15</i>(17), 15459–15474. https://doi.org/10.1021/acscatal.5c04165</div>
</div>
-
dc.identifier.issn
2155-5435
-
dc.identifier.uri
http://hdl.handle.net/20.500.12708/221702
-
dc.description.abstract
The "crude oil exodus" and energy transition will finally hinge on the availability of hydrogen. Catalytic processes like the water-gas shift (WGS) reaction may significantly contribute to its production and become crucial for utilizing alternative feedstocks. This work demonstrates how thiolate-protected gold nanoclusters can be employed as precursors for single-atom alloy (SAA) catalysts. The clusters serve as carriers of heteroatom dopants (Cu, Pd) while precisely maintaining 25 metal atoms per cluster (<1 nm). Using the 2PET ligand during synthesis led to high yield and cluster stability, but ligand exchange was required to link clusters to a ZnO support efficiently. Introducing pMBA as a ligand enabled a homogeneous cluster distribution on the ZnO surface, creating a well-defined catalyst with dual functionality. This SAA catalyst, outperforming a Cu/ZnO/Al2O3 benchmark in WGS, may get industrial relevance when upscaled while still serving as a well-defined model system in catalysis. Thereby, it bridges the gap between practical applications and fundamental research. Pre- and postreaction analysis by XPS proved the presence of the dopants in the catalysts in the expected stoichiometry, showed changes in the electronic structures, but also revealed sulfur migration from the clusters/ligands to the support, forming ZnS. Furthermore, XPS unveiled a pretreatment-induced SMSI decoration effect, stabilizing the small particles during catalysis. (S)-TEM indicated a homogeneous cluster distribution on ZnO after synthesis and proved small particle sizes throughout the experiments. In situ DRIFTS confirmed the accessibility of the dopant atoms by the reactant CO and also detected adsorbed byproducts. The precise size and doping control of thiolate-protected SAA nanoclusters, together with their catalytic performance, demonstrate the potential for targeted future investigations in a wide range of industrial applications.
en
dc.description.sponsorship
FWF - Österr. Wissenschaftsfonds
-
dc.description.sponsorship
FWF - Österr. Wissenschaftsfonds
-
dc.description.sponsorship
FWF - Österr. Wissenschaftsfonds
-
dc.description.sponsorship
FWF - Österr. Wissenschaftsfonds
-
dc.language.iso
en
-
dc.publisher
AMER CHEMICAL SOC
-
dc.relation.ispartof
ACS Catalysis
-
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
-
dc.subject
SMSI
en
dc.subject
single-atom alloy catalysts
en
dc.subject
thiolate-protected nanoclusters
en
dc.subject
trimetallic nanoclusters
en
dc.subject
water−gas shift reaction
en
dc.title
Engineering Catalytic Efficiency by Thiolate-Protected Trimetallic (Cu, Pd, Au) Nanoclusters: Single-Atom Alloy Catalysts for Water–Gas Shift