Atomic-level engineering of single Ag<sup>1+</sup> site distribution on titanium-oxo cluster surfaces to boost CO<sub>2</sub> electroreduction.
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ABSTRACT: Precise control over the distribution of active metal sites on catalyst surfaces is essential for maximizing catalytic efficiency. Addressing the limitations of traditional cluster catalysts with core-embedded catalytic sites, this work presents a strategy to position catalytic sites on the surfaces of oxide clusters. We utilize a calixarene-stabilized titanium-oxo cluster (Ti12L6) as a scaffold to anchor Ag1+ in situ, forming the unique nanocluster Ti12Ag4.5 with six surface-exposed Ag1+ sites. The in situ transformation from Ti12L6 into Ti12Ag4.5 clusters was traced through mass spectrometry, revealing a solvent-mediated dynamic process of disintegration and reassem
SUBMITTER: Meng RX
PROVIDER: S-EPMC11917444 | biostudies-literature | 2025 Apr
REPOSITORIES: biostudies-literature
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