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Phys. Rev. B 80, 205427 (2009) [5 pages]

Disentanglement of the electronic properties of metallicity-selected single-walled carbon nanotubes

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P. Ayala1, Y. Miyata2,3, K. De Blauwe1, H. Shiozawa4, Y. Feng5, K. Yanagi5, C. Kramberger1, S. R. P. Silva4, R. Follath6, H. Kataura5,7, and T. Pichler1
1Faculty of Physics, University of Vienna, 1090 Wien, Austria
2Nanotechnology Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba 305-8562, Japan
3Department of Chemistry, Nagoya University, Nagoya 464-8602, Japan
4Advanced Technology Institute, University of Surrey, Guildford GU2 7XH, United Kingdom
5Nanotechnology Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba 305-8562, Japan
6BESSY II, D-12489 Berlin, Germany
7JST, CREST, Kawaguchi, Saitama 330–0012, Japan

Received 26 October 2009; published 30 November 2009

The inherent structure of single-walled carbon nanotubes (SWCNTs) provides them tremendous value as archetypical one-dimensional (1D) solids, which exhibit van Hove singularities in their local density of states, Tomonaga-Luttinger liquid behavior, ballistic transport properties, and in many other aspects, features of 1D quantum systems, which allow the study of fundamental problems. Therefore, unraveling the signature of their peculiar electronic structure as pristine material is a prerequisite for tracing any modification. Here, we show the disentanglement of the unique 1D features and bonding environments in clean metallicity sorted nanotube films. The photoemission and x-ray absorption responses unambiguously reveal how the fine structure in the C1s edge and photoemission valence band separately discerns the SWCNT metallic and semiconducting nature. This has crucial implications for applications allowing for instance finding the limit of maximum conductivity in transparent electrodes or the uniformity of power transistors, among others.

© 2009 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevB.80.205427
DOI:
10.1103/PhysRevB.80.205427
PACS:
71.20.Tx, 71.10.Hf, 73.63.Fg