Structurally directed thienylenevinylene self-assembly for improved charge carrier mobility: 2D sheets vs. 1D fibers

被引:9
|
作者
Ghosh, Samrat [1 ,5 ]
Prasanthkumar, Seelam [1 ,2 ,6 ]
Das, Satyajit [1 ,2 ]
Saeki, Akinori [3 ]
Seki, Shu [4 ]
Ajayaghosh, Ayyappanpillai [1 ,2 ]
机构
[1] CSIR Natl Inst Interdisciplinary Sci & Technol CS, Chem Sci & Technol Div, Photosci & Photon Sect, Thiruvananthapuram 695019, Kerala, India
[2] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, Uttar Pradesh, India
[3] Osaka Univ, Grad Sch Engn, Dept Appl Chem, Suita, Osaka 5650871, Japan
[4] Kyoto Univ, Grad Sch Engn, Dept Mol Engn, Nishikyo Ku, Kyoto 6158510, Japan
[5] CSIR Cent Leather Res Inst CSIR CLRI, Inorgan & Phys Chem Lab, Chennai 600020, Tamil Nadu, India
[6] CSIR Indian Inst Chem Technol CSIR IICT, Polymer & Funct Mat Div, Hyderabad 500007, Telangana, India
关键词
PERFORMANCE; MORPHOLOGY; HETEROJUNCTIONS; NANOFIBERS; CHAIN;
D O I
10.1039/d2cc02111k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
High charge carrier mobility is a prerequisite for organic electronics for which molecular arrangement and morphology play a vital role. Herein, we report how the self-assembly of thienylenevinylenes T1 and T2 can achieve morphologically distinct nanostructures with improved charge carrier mobility. Morphological analysis revealed that T1 forms 2D nanosheets that further extend to an array of hierarchical pseudo-1D assemblies, whereas T2 results in 1D nanofibers. Flash photolysis - time resolved microwave conductivity and transient absorption spectroscopy (FP-TRMC and TAS) revealed that 1D fibers of T2 show 1.75 fold higher charge carrier mobility (9.2 x 10(-2) cm(2) V-1 s(-1)) when compared to the array of 2D sheets obtained from T1 (5.0 x 10(-2) cm(2) V-1 s(-1)). This simple approach can be extended to design self-assembled organic photoconducting materials for optoelectronic applications.
引用
收藏
页码:6837 / 6840
页数:4
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