In Situ STM Imaging of Fused Thienothiopene Molecules Adsorbed on Au(111) Electrode

NCU Institutional Repository > 理學院 > 化學學系 > 期刊論文 > Item 987654321/50733

jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.lib.ncu.edu.tw/handle/987654321/50733

题名:	In Situ STM Imaging of Fused Thienothiopene Molecules Adsorbed on Au(111) Electrode
作者:	Hsu,YH;Yau,SL;Lin,YJ;Huang,PY;Chen,MC;Lo,PY
贡献者:	化學學系
关键词:	SCANNING-TUNNELING-MICROSCOPY;THIN-FILM TRANSISTORS;FIELD-EFFECT TRANSISTOR;SINGLE-CRYSTAL SURFACES;X-RAY-DIFFRACTION;PENTACENE MONOLAYER;CYCLIC VOLTAMMETRY;HIGH-PERFORMANCE;ORGANIC SEMICONDUCTOR;PT(111) ELECTRODES
日期:	2010
上传时间:	2012-03-27 18:08:57 (UTC+8)
出版者:	國立中央大學
摘要:	In situ scanning tunneling microscopy (STM) was used to reveal the structures of dithieno[2,3-b:3,2-d]hiophene diphenyl (DTT) molecules deposited onto Au(111) electrode from a dosing solution made of dichlorobenzene and 50 mu M DTT. Potential control was proven to be of prime importance in guiding the arrangement of DTT admolecules on Au(111) in 0.1 M HClO(4), as disorder DTT adlayer seen at E > 0.3 V (vs reversible hydrogen electrode) was transformed into a highly ordered (2 x 7 root 3)rect -2DTT structure when the potential was made to 0.05 to 0.2 V. The ordered structure was stable for hours between 0.05 and 0.2 V. However, switching the potential further negative to 0 V resulted in slow melting of the ordered structure. The (2 x 7 root 3)rect-DTT ordered adlattices recuperated when the potential was made positive to 0.2 V. Internal molecular functionalities of the thienothiophene and benzene in DTT admolecules were clearly discerned, from which the lateral structure for the (2 x 7 root 3)rect-2DTT structure and registries of admolecules were deduced. The dynamics of the Dry adlattices on the Au(111) electrode surface was examined by real-time STM imaging, showing reorientation of as many as 150 DTT admolecules to join a neighboring ordered array within minutes.
關聯:	LANGMUIR
显示于类别:	[化學學系] 期刊論文

文件中的档案:

档案	描述	大小	格式	浏览次数
index.html		0Kb	HTML	460	检视/开启

在NCUIR中所有的数据项都受到原著作权保护.

社群 sharing

数据加载中.....