DNA-guided lattice remodeling of carbon nanotubes

Author:

Lin Zhiwei1ORCID,Beltrán Leticia C.2,De los Santos Zeus A.1ORCID,Li Yinong3ORCID,Adel Tehseen4,Fagan Jeffrey A1ORCID,Hight Walker Angela R.4ORCID,Egelman Edward H.2ORCID,Zheng Ming1ORCID

Affiliation:

1. Materials Science and Engineering Division, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA.

2. Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, VA 22908, USA.

3. South China Advanced Institute for Soft Matter Science and Technology, School of Emergent Soft Matter, South China University of Technology, Guangzhou 510640, China.

4. Quantum Metrology Division, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA.

Abstract

Covalent modification of carbon nanotubes is a promising strategy for engineering their electronic structures. However, keeping modification sites in registration with a nanotube lattice is challenging. We report a solution using DNA-directed, guanine (G)-specific cross-linking chemistry. Through DNA screening we identify a sequence, C 3 GC 7 GC 3 , whose reaction with an (8,3) enantiomer yields minimum disorder-induced Raman mode intensities and photoluminescence Stokes shift, suggesting ordered defect array formation. Single-particle cryo–electron microscopy shows that the C 3 GC 7 GC 3 functionalized (8,3) has an ordered helical structure with a 6.5 angstroms periodicity. Reaction mechanism analysis suggests that the helical periodicity arises from an array of G-modified carbon-carbon bonds separated by a fixed distance along an armchair helical line. Our findings may be used to remodel nanotube lattices for novel electronic properties.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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