In situ scanning tunneling microscopy imaging of electropolymerized poly(3,4-ethylenedioxythiophene) on an iodine-modified Au(111) single crystal electrode

被引:15
|
作者
Lapitan, Lorico D. S., Jr. [2 ,4 ]
Tongol, Bernard John V. [1 ,2 ,3 ]
Yau, Shueh-Lin [4 ]
机构
[1] Univ Santo Tomas, Dept Chem, Coll Sci, Manila 1015, Philippines
[2] Univ Santo Tomas, Grad Sch, Manila 1015, Philippines
[3] Univ Santo Tomas, Res Ctr Nat & Appl Sci, Manila 1015, Philippines
[4] Natl Cent Univ, Dept Chem, Chungli 320, Taoyuan County, Taiwan
关键词
Poly(3,4-ethylenedioxythiophene); Au(111) single crystal electrode; In situ scanning tunneling microscopy; Iodine-modified Au(111) electrode; PEDOT nanowires; 0.1 M HCLO4; CYCLIC VOLTAMMETRY; DIRECT VISUALIZATION; ELECTROCHEMICAL STM; SURFACES; POLYMERIZATION; NANOWIRES; 3,4-ETHYLENEDIOXYTHIOPHENE; NANOSTRUCTURES; SPECTROSCOPY;
D O I
10.1016/j.electacta.2011.12.053
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The electrochemical polymerization of 3,4-ethylenedioxythiophene (EDOT) on an iodine-modified Au(1 1 1) single crystal electrode in aqueous 0.10 M HClO4 was investigated by cyclic voltammetry (CV) and electrochemical scanning tunneling microscopy (EC-STM). The cyclic voltammetric and EC-STM data revealed the stability of the iodine adlayer provided a suitable potential range for EDOT electropolymerization was controlled at 1.20V (vs. the reversible hydrogen electrode). EC-STM was used to examine the formation of the PEDOT adlayer on the iodine-modified Au(1 1 1) electrode. In situ electropolymerization of EDOT was carried out by slowly increasing the electrode potential to 1.20V. This process resulted in the formation of single molecular chains of PEDOT with a diameter of 0.90 nm and lengths of 5-7 nm. Higher resolution STM images further revealed PEDOT nanostructures with bent polymer backbones at angles of 105 degrees, 144 degrees and 180 degrees. The growth of PEDOT multi-layers was observed when the potential was held for a longer time. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:433 / 440
页数:8
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