Confining an Ag<sub>10</sub> Core in an Ag<sub>12</sub> Shell: A Four-Electron Superatom with Enhanced Photoluminescence upon Crystallization.
basic_science · Level V
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- Record sourced from PubMed, PMID 31017759.
- Also identified by DOI 10.1021/acsnano.9b01189.
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Abstract
We introduce a cluster coprotected by thiol and diphosphine ligands, [Ag<sub>22</sub>(dppe)<sub>4</sub>(2,5-DMBT)<sub>12</sub>Cl<sub>4</sub>]<sup>2+</sup> (dppe = 1,2-bis(diphenylphosphino)ethane; 2,5-DMBT= 2,5-dimethylbenzenethiol), which has an Ag<sub>10</sub> core encapsulated by an Ag<sub>12</sub>(dppe)<sub>4</sub>(2,5-DMBT)<sub>12</sub>Cl<sub>4</sub> shell. The Ag<sub>10</sub> core comprises two Ag<sub>5</sub> distorted trigonal bipyramidal units and is uncommon in Au and Ag nanoclusters. The electrospray ionization mass spectrum reveals that the cluster is divalent and contains four free electrons. An uncommon crystallization-induced enhancement of emission is observed in the cluster. The emission is weak in the solution and amorphous states. However, it is enhanced 12 times in the crystalline state compared to the amorphous state. A detailed investigation of the crystal structure suggests that well-arranged C-H···π and π···π interactions between the ligands are the major factors for this enhanced emission. Further, in-depth structural elucidation and density functional theory calculations suggest that the cluster is a superatom with four magic electrons.