Abstract
Surface modification with uniform nanostructures is a promising way to fabricate functionalized surface, and the synthetic electrode functionalization can be performed by depositing atomically precise nanoclusters with a specific number of atoms and compositions. During atomic nucleation and growth in gas phase, atomic aggregates exhibit novel electronic properties, mimicking atoms at a specific number of atoms and composition, which is called superatom (SA). Tantalum-encapsulating Si16 cage nanoclusters (Ta@Si16) and aluminum 13-mer (Al13) are promising SAs for designing their assembled materials with tunable properties, where one-electron-excessive Ta@Si16 and one-electron-deficient Al13 exhibit alkali- and halogen-like characteristics, respectively, owing to the electron shell closing. In this study, with an intense nanocluster ion source, Ta@Si16
+ and Al13
− were generated during the formation of TaSi
n
+ cations and Al
n
− anions, where Ta@Si16
+ was remarkably generated compared with the neighboring species. SA deposition provided uniformly decorated surfaces exhibiting nanofunctional properties superior to those obtained by conventional atom deposition. With mass spectrometry, Ta@Si16
+ and Al13
− SAs were size-selectively soft-landed on the substrate surfaces predeposited with n-type fullerene (C60) and p-type hexa-tert-butyl-hexa-peri-hexabenzocoronene (HB-HBC, C66H66). The electronic states of Ta@Si16 and Al13 SAs immobilized on the organic substrates were characterized by X-ray photoelectron spectroscopy and oxidative reactivities under O2 exposure.
Funder
Japan Society for the Promotion of Science
Publisher
The Electrochemical Society
Subject
Materials Chemistry,Electrochemistry,Surfaces, Coatings and Films,Condensed Matter Physics,Renewable Energy, Sustainability and the Environment,Electronic, Optical and Magnetic Materials
Cited by
3 articles.
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