4.8 Article

[Pt2Cu34(PET)22Cl4]2-: An Atomically Precise, 10-Electron PtCu Bimetal Nanocluster with a Direct Pt-Pt Bond

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 143, 期 31, 页码 12100-12107

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c04002

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资金

  1. Research Center Program of the IBS in Korea [IBS-R006-D1]
  2. NNSF of China [21890752, 21731005, 21721001]
  3. 111 Project [B08027]
  4. Academy of Finland [294217, 319208, 315549]
  5. Academy of Finland (AKA) [315549] Funding Source: Academy of Finland (AKA)

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Heteroatom-doped metal nanoclusters are synthesized by a metal-exchange strategy, leading to the discovery that Pt doping can significantly enhance the catalytic activity of Cu nanoclusters by around 300-fold. This synthetic approach has the potential to produce Ni-, Pd-, and Au-doped Cu nanoclusters, opening new avenues for studying their molecular structures and catalytic properties.
Heteroatom-doped metal nanoclusters (NCs) are highly desirable to gain fundamental insights into the effect of doping on the electronic structure and catalytic properties. Unfortunately, their controlled synthesis is highly challenging when the metal atomic sizes are largely different (e.g., Cu and Pt). Here, we design a metal-exchange strategy that enables simultaneous doping and resizing of NCs. Specifically, [Pt2Cu34(PET)(22)Cl-4](2-) NC, the first example of a Pt-doped Cu NC, is synthesized by utilizing the unique reactivity of [Cu-32(PET)(24)Cl2H8](2-) NC with Pt4+ ions. The single-crystal X-ray structure reveals that two directly bonded Pt atoms occupy the two centers of an unusually interpenetrating, incomplete biicosahedron core (Pt2Cu18), which is stabilized by a Cu-16(PET)(22)Cl-4 shell. The molecular structure and composition of the NC are validated by combined experimental and theoretical results. Electronic structure calculations, using the density functional theory, show that the Pt2Cu34 NC is a 10-electron superatom. The computed absorption spectrum matches well with the measured data and allows for assignment of the absorption peaks. The calculations also rationalize energetics for ligand exchange observed in the mass spectrometry data. The synergistic effects induced by Pt doping are found to enhance the catalytic activity of Cu NCs by similar to 300-fold in silane to silanol conversion under mild conditions. Furthermore, our synthetic strategy has potential to produce Ni-, Pd-, and Au-doped Cu NCs, which will open new avenues to uncover their molecular structures and catalytic properties.

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