Selective oxidation on metallic carbon nanotubes by halogen oxoanions

被引:37
作者
Yoon, Seon-Mi [1 ,2 ]
Kim, Sung Jin [3 ,4 ]
Shin, Hyeon-Jin [1 ,2 ]
Benayad, Anass [1 ,2 ]
Choi, Seong Jae [1 ,2 ]
Kim, Ki Kang [3 ,4 ]
Kim, Soo Min [3 ,4 ]
Park, Yong Jin [3 ,4 ]
Kim, Gunn [3 ,4 ]
Choi, Jae-Young [1 ,2 ]
Lee, Young Hee [3 ,4 ]
机构
[1] Samsung Adv Inst Technol, Display Device & Proc Lab, Suwon 440600, South Korea
[2] Samsung Adv Inst Technol, Analyt Engn Ctr, Suwon 440600, South Korea
[3] Sungkyunkwan Univ, Dept Phys, Dept Nanosci & Nanotechnl, Sungkyunkwan Adv Inst Nanotechnol, Suwon 440746, South Korea
[4] Sungkyunkwan Univ, Sungkyunkwan Adv Inst Nanotechnol, Ctr Nanotubes & Nanostructured Composites, Suwon 440746, South Korea
关键词
D O I
10.1021/ja077449d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chlorine oxoanions with the chlorine atom at different oxidation states were introduced in an attempt to systematically tailor the electronic structures of single-walled carbon nanotubes (SWCNTs). The degree of selective oxidation was controlled systematically by the different oxidation state of the chlorine oxoanion. Selective suppression of the metallic SWCNTs with a minimal effect on the semiconducting SWCNTs was observed at a high oxidation state. The adsorption behavior and charge transfer at a low oxidation state were in contrast to that observed at a high oxidation state. Density functional calculations demonstrated the chemisorption of chloro oxoanions at the low oxidation state and their physisorption at high oxidation states. These results concurred with the experimental observations from X-ray photoelectron spectroscopy. The sheet resistance of the SWCNT film decreased significantly at high oxidation states, which was explained in terms of a p-doping phenomenon that is controlled by the oxidation state.
引用
收藏
页码:2610 / 2616
页数:7
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