Chirality-dependent reactivity of individual single-walled carbon nanotubes

Bilu Liu, Hua Jiang, Arkady V. Krasheninnikov, Albert G. Nasibulin, Wencai Ren, Chang Liu, Esko I. Kauppinen, Hui Ming Cheng

Research output: Contribution to journalArticlepeer-review

36 Citations (Scopus)


Electronic characteristics of a single-walled carbon nanotube (SWCNT) strongly depend on minor variations in its atomic arrangement, specifically chirality. Therefore, precise control over nanotube chirality is highly desired for their application. Theoretically, SWCNTs with different structures have different chemical reactivities, which can be further used for their chirality selection. Here, an approach is developed to examine the relationship between the chirality of SWCNTs and their intrinsic chemical reactivity. By oxidizing individual, high-quality, suspended SWCNTs and using the nanobeam electron diffraction technique, it is shown that the reactivity of SWCNTs to O 2 is intricately related to their diameters, metallicity, and chiral angles. In particular, even minor differences in chiral angles lead to big differences in their reactivity, which concords with first-principles calculations. Based on the experimental observations, a chirality-dependent reactivity sequence is constructed for SWCNTs. These findings shed light on effective chiral separation of SWCNTs for their practical application in many fields. The intrinsic chemical reactivity of individual and suspended single-walled carbon nanotubes is investigated using electron diffraction. The results reveal that the reactivity of nanotubes is not only related to their diameters and electronic properties, but also to their chiral angles. Simple air treatment at medium temperatures may selectively enrich large-diameter and high-chiral-angle semiconducting carbon nanotubes.

Original languageEnglish
Pages (from-to)1379-1386
Number of pages8
Issue number8
Publication statusPublished - 22 Apr 2013
Externally publishedYes


  • carbon nanotubes
  • chemical reactivity
  • chirality
  • electron diffraction
  • first-principles calculations


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