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Abstract Herein, we report on the synthesis of ultrasmall Pd nanoclusters (∼2 nm) protected by L‐cysteine [HOCOCH(NH2)CH2SH] ligands (Pdn(L‐Cys)m) and supported on the surfaces of CeO2, TiO2, Fe3O4, and ZnO nanoparticles for CO catalytic oxidation. The Pdn(L‐Cys)mnanoclusters supported on the reducible metal oxides CeO2, TiO2and Fe3O4exhibit a remarkable catalytic activity towards CO oxidation, significantly higher than the reported Pd nanoparticle catalysts. The high catalytic activity of the ligand‐protected clusters Pdn(L‐Cys)mis observed on the three reducible oxides where 100 % CO conversion occurs at 93–110 °C. The high activity is attributed to the ligand‐protected Pd nanoclusters where the L‐cysteine ligands aid in achieving monodispersity of the Pd clusters by limiting the cluster size to the active sub‐2‐nm region and decreasing the tendency of the clusters for agglomeration. In the case of the ceria support, a complete removal of the L‐cysteine ligands results in connected agglomerated Pd clusters which are less reactive than the ligand‐protected clusters. However, for the TiO2and Fe3O4supports, complete removal of the ligands from the Pdn(L‐Cys)mclusters leads to a slight decrease in activity where the T100%CO conversion occurs at 99 °C and 107 °C, respectively. The high porosity of the TiO2and Fe3O4supports appears to aid in efficient encapsulation of the bare Pdnnanoclusters within the mesoporous pores of the support.
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This content will become publicly available on May 16, 2026
Atomically Precise Nanoclusters as Co‐Catalysts for Light‐Activated Microswimmer Motility
Abstract Microswimmers are self‐propelled particles that navigate fluid environments, offering significant potential for applications in environmental pollutant decomposition, biosensing, and targeted drug delivery. Their performance relies on engineered catalytic surfaces. Gold nanoclusters (AuNCs), with atomically precise structures, tunable optical properties, and high surface area‐to‐volume ratio, provide a new optimal catalyst for enhancing microswimmer propulsion. Unlike bulk gold or nanoparticles, AuNCs may deliver tunable photocatalytic activity and increased catalytic specificity, making them ideal co‐catalysts for hybrid microswimmers. For the first time, this study combines AuNCs with TiO2/Cr2O3Janus microswimmers, combining the unique properties of both materials. This hybrid system capitalizes on the tuned optical properties of AuNCs and their role as co‐catalysts with TiO2, driving enhanced photocatalytic performance under ultraviolet (UV) excitation. Using motion analysis, it is shown that the AuNC‐microswimmers exhibit significantly greater propulsion and mean squared displacement (MSD) as compared to controls. These findings suggest that the integration of nanoclusters with semiconductor materials enables state of the art, light‐switchable microswimmers. These AuNC‐microswimmer systems may thus offer new opportunities for environmental catalysis and other applications, providing precise control over catalytic and motile behaviors at the microscale.
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- Award ID(s):
- 2425226
- PAR ID:
- 10609210
- Publisher / Repository:
- Wiley
- Date Published:
- Journal Name:
- Small
- ISSN:
- 1613-6810
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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