Simultaneous Inside and Outside Functionalization of Single‐Walled Carbon Nanotubes

Author:

Kraus Jan1,Meingast Laura2,Hald Janina1,Beil Sebastian B.1,Biskupek Johannes3,Ritterhoff Christian L.4,Gsänger Sebastian4,Eisenkolb Jasmin5,Meyer Bernd4ORCID,Kaiser Ute3,Maultzsch Janina2ORCID,von Delius Max1ORCID

Affiliation:

1. Institute of Organic Chemistry Ulm University Albert-Einstein-Allee 11 89081 Ulm Germany

2. Department of Physics Friedrich-Alexander-Universität Erlangen-Nürnberg Staudtstraße 7 91058 Erlangen Germany

3. Central Facility of Electron Microscopy Electron Microscopy Group of Materials Science Ulm University Albert-Einstein-Allee 11 89081 Ulm Germany

4. Interdisciplinary Center for Molecular Materials (ICMM) and Computer Chemistry Center (CCC) Friedrich-Alexander-Universität Erlangen-Nürnberg Nägelsbachstraße 25 91052 Erlangen Germany

5. Department of Chemistry and Pharmacy and Center of Advanced Materials and Processes (ZMP) Friedrich-Alexander-Universität Erlangen-Nürnberg Dr.-Mack-Str. 81 90762 Fürth Germany

Abstract

AbstractFunctionalizing single‐walled carbon nanotubes (SWCNTs) in a robust way that does not affect the sp2 carbon framework is a considerable research challenge. Here we describe how triiodide salts of positively charged macrocycles can be used not only to functionalize SWCNTs from the outside, but simultaneously from the inside. We employed disulfide exchange in aqueous solvent to maximize the solvophobic effect and therefore achieve a high degree of macrocycle immobilization. Characterization by Raman spectroscopy, EDX‐STEM and HR‐TEM clearly showed that serendipitously this wet‐chemical functionalization procedure also led to the encapsulation of polyiodide chains inside the nanotubes. The resulting three‐shell composite materials are redox‐active and experience an intriguing interplay of electrostatic, solvophobic and mechanical effects that could be of interest for applications in energy storage.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

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