Al<sub>13</sub><sup>-</sup> and B@Al<sub>12</sub><sup>-</sup> superatoms on a molecularly decorated substrate.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 35288553.
- Also identified by DOI 10.1038/s41467-022-29034-9 and PMC identifier 8921336.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Aluminum nanoclusters (Al<sub>n</sub> NCs), particularly Al<sub>13</sub><sup>-</sup> (n = 13), exhibit superatomic behavior with interplay between electron shell closure and geometrical packing in an anionic state. To fabricate superatom (SA) assemblies, substrates decorated with organic molecules can facilitate the optimization of cluster-surface interactions, because the molecularly local interactions for SAs govern the electronic properties via molecular complexation. In this study, Al<sub>n</sub> NCs are soft-landed on organic substrates pre-deposited with n-type fullerene (C<sub>60</sub>) and p-type hexa-tert-butyl-hexa-peri-hexabenzocoronene (HB-HBC, C<sub>66</sub>H<sub>66</sub>), and the electronic states of Al<sub>n</sub> are characterized by X-ray photoelectron spectroscopy and chemical oxidative measurements. On the C<sub>60</sub> substrate, Al<sub>n</sub> is fixed to be cationic but highly oxidative; however, on the HB-HBC substrate, they are stably fixed as anionic Al<sub>n</sub><sup>-</sup> without any oxidations. The results reveal that the careful selection of organic molecules controls the design of assembled materials containing both Al<sub>13</sub><sup>-</sup> and boron-doped B@Al<sub>12</sub><sup>-</sup> SAs through optimizing the cluster-surface interactions.