Exciton dynamics reveal aggregates with intermolecular order at hidden interfaces in solution-cast organic semiconducting films

被引:67
作者
Wong, Cathy Y. [1 ]
Cotts, Benjamin L. [1 ]
Wu, Hao [1 ]
Ginsberg, Naomi S. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Berkeley, Dept Chem, D64 Hildebrand Hall, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Phys, Berkeley, CA 94720 USA
[3] Lawrence Livermore Natl Lab, Phys Biosci & Mat Sci Div, Berkeley, CA 94720 USA
[4] Kavli Energy NanoSci Inst, Berkeley, CA 94720 USA
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
FIELD-EFFECT TRANSISTORS; TRANSIENT ABSORPTION MICROSCOPY; THIN-FILMS; MOLECULAR PACKING; GRAIN-BOUNDARY; CARRIER TRANSPORT; SINGLE-CRYSTALS; TIPS-PENTACENE; FISSION; TEMPERATURE;
D O I
10.1038/ncomms6946
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Large-scale organic electronics manufacturing requires solution processing. For small-molecule organic semiconductors, solution processing results in crystalline domains with high charge mobility, but the interfaces between these domains impede charge transport, degrading device performance. Although understanding these interfaces is essential to improve device performance, their intermolecular and electronic structure is unknown: they are smaller than the diffraction limit, are hidden from surface probe techniques, and their nanoscale heterogeneity is not typically resolved using X-ray methods. Here we use transient absorption microscopy to isolate a unique signature of a hidden interface in a TIPS-pentacene thin film, exposing its exciton dynamics and intermolecular structure. Surprisingly, instead of finding an abrupt grain boundary, we reveal that the interface can be composed of nanoscale crystallites interleaved by a web of interfaces that compound decreases in charge mobility. Our novel approach provides critical missing information on interface morphology necessary to correlate solution-processing methods to optimal device performance.
引用
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页数:7
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