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Actinide elements encaged in a superatomic cluster can exhibit unique properties due to their hyperactive valence electrons. Herein, the electronic and spectroscopic properties of Th@Au14 are predicted and compared with that of the isoelectronic entities [Ac@Au14]- and [Pa@Au14]+ using density functional theory. The calculation results indicate that these clusters all adopt a closedshell superatomic 18-electron configuration of the 1S21P61D10 Jellium state. The absorption spectrum of Th@Au14 can be interpreted by the Jelliumatic orbital model. In addition, calculated spectra of pyridine-Th@Au14 complexes in the blue laser band exhibit strong peaks attributable to charge transfer (CT) from the metal to the pyridine molecule. These charge-transfer bands lead to a resonant surface-enhanced Raman scattering (SERS) enhancement of ~104. This work suggests a basis for designing and synthesizing SERS substrate materials based on actinide-embedded gold superatom models.

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nr-9-3-622_ESM.pdf (1.2 MB)
Publication history
Copyright

Publication history

Received: 28 September 2015
Revised: 06 November 2015
Accepted: 10 November 2015
Published: 22 January 2016
Issue date: March 2016

Copyright

© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2015
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