Reversible, band-gap-selective protonation of single-walled carbon nanotubes in solution

被引:317
作者
Strano, MS
Huffman, CB
Moore, VC
O'Connell, MJ
Haroz, EH
Hubbard, J
Miller, M
Rialon, K
Kittrell, C
Ramesh, S
Hauge, RH
Smalley, RE
机构
[1] Rice Univ, Dept Chem, Ctr Nanoscale Sci & Technol, Houston, TX 77005 USA
[2] Rice Univ, Ctr Biol & Environm Nanotechnol, Houston, TX 77005 USA
[3] Rice Univ, Dept Phys, Houston, TX 77005 USA
关键词
D O I
10.1021/jp027664a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In acidic solution between pH 6 and 2.5, protons react reversibly and selectively in the presence of preadsorbed oxygen at the sidewall of aqueous dispersed single-walled carbon nanotubes suspended in sodium dodecyl sulfate. This reactive complex, which protonates the nanotube sidewall, reversibly diminishes absorption intensity, fluorescent emission, and resonant Raman scattering intensity. The results document the first evidence of electronic selectivity with metallic nanotubes reacting initially near neutral pH, followed by successive protonation of nanotubes with increasing band gap as the solution is increasingly acidified. Preadsorption of molecular oxygen is shown to play a critical role in the interaction, and its desorption kinetics is followed using UV irradiation. The role of the charged electric double layer of the surfactant is discussed. This chemistry, which proceeds under relatively mild conditions, holds promise for separating nanotubes by metal and semiconducting types.
引用
收藏
页码:6979 / 6985
页数:7
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