127
Views
2
CrossRef citations to date
0
Altmetric
Original Articles

C68: A non-IPR fullerene capable of binding extraordinary amounts of Cs atoms

ORCID Icon, , , ORCID Icon, ORCID Icon, & ORCID Icon show all
Pages 206-214 | Received 13 Sep 2018, Accepted 22 Oct 2018, Published online: 12 Jan 2019
 

Abstract

The non-IPR fulleride compound CsxC68 was investigated in analogy to previous experiments on CsxC58. While the vibrational properties as well as the electronic structure in the valence band range appear to be pretty similar to CsxC58, a striking difference could be observed by XPS and Photoemission Microscopy analysis: apparently, C68 forms different phases within a thick film including islands in which it is able to store more than 70 Cs atoms per fullerene cage and to keep these amounts even after annealing over 1100 K. This means that CsxC68 constitutes the highest alkali metal doping degree of any Fullerene species known so far. Spatially resolved photoemission analysis also revealed that the Cs-rich fulleride phases constitute a unique chemical state that has never been observed before.

Additional information

Funding

This work was funded by the DFG Center of Functional Nanostructures (CFN, subproject C4.6). The access to the ESCA Microscopy Beamline at Elettra Synchrotron Laboratory was granted under proposal 20130315. Deutsche Forschungsgemeinschaft.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 906.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.