中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Diketopyrrolopyrrole-Based Polymer Nanowires: Control of Chain Conformation and Nucleation

文献类型:期刊论文

作者Cao, Xinxiu1,2; Chen, Liang1,2; Zhao, Kefeng1,2; Liu, Jiangang1,2; Han, Yanchun1,2
刊名JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS
出版日期2018-06-01
卷号56期号:11页码:833-841
关键词Conformation Nanowires Nucleation Process Slow Evaporation Of The Main Solvent
ISSN号0887-6266
DOI10.1002/polb.24598
英文摘要Understanding the nucleation process is very important in growing polymer nanowires as it plays a decisive role in determining the crystal structure and size distribution. Polymer chain conformation determines whether the polymer chains could assemble to nuclei or not. Here, chain conformation and the nucleation process were controlled to grow 3,6-bis-(thiophen-2-yl)-N,N'-bis(2-decyl-1-tetradecyl)-1,4-dioxo-pyrrolo[3,4-c]pyrrole and thieno[3,2-b]thiophene (DT-PDBT-TT) nanowires. We changed the conformation of DT-PDBT-TT in solution and controlled the nucleation process by using a main solvent:cosolvent system. The main solvent was a low boiling point good solvent, and the cosolvent was consisted of two high boiling point solvents with different solubility. In fact, the chain conformation in the pristine solution was changed by choosing different main solvents (with H-bond, pi-pi or none interaction with the main chain) and temperatures. The absorption spectrum and TEM images showed that trichloro ethylene (TCE) was the best main solvent because it has H-bond interaction with the polymer main chain and DT-PDBT-TT conformation in it approaching unimer coil conformation, which is beneficial to grow nanowires. Mixed o-dichlorobenzene (ODCB) and anisole (AS) with different ratios were used to changing the solubility step by step to control nucleation process. Only when marginal cosolvent (ODCB:AS=1:1) was added, could it decrease the nuclei number and avoided the aggregates simultaneously. As the main solvent evaporated slowly, the nucleation and growth happened, leading to the nanowires formation. The resulting nanowires were about 63 nm in width and one to two microns in length. The width of the DT-PDBT-TT structures suggests that the polymer chains are oriented along the fibril axis. Our results indicated that there are two requirements for the nanowire formation, (1) the polymer chain conformation should approach unimer coil; (2) the nucleation density should be optimized, not too much and no aggregation happened. (C) 2018 Wiley Periodicals, Inc.
语种英语
WOS记录号WOS:000430394500002
出版者WILEY
源URL[http://ir.iccas.ac.cn/handle/121111/46075]  
专题中国科学院化学研究所
通讯作者Liu, Jiangang; Han, Yanchun
作者单位1.Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, 5625 Renmin St, Changchun 130022, Peoples R China
2.Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Cao, Xinxiu,Chen, Liang,Zhao, Kefeng,et al. Diketopyrrolopyrrole-Based Polymer Nanowires: Control of Chain Conformation and Nucleation[J]. JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS,2018,56(11):833-841.
APA Cao, Xinxiu,Chen, Liang,Zhao, Kefeng,Liu, Jiangang,&Han, Yanchun.(2018).Diketopyrrolopyrrole-Based Polymer Nanowires: Control of Chain Conformation and Nucleation.JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS,56(11),833-841.
MLA Cao, Xinxiu,et al."Diketopyrrolopyrrole-Based Polymer Nanowires: Control of Chain Conformation and Nucleation".JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS 56.11(2018):833-841.

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来源:化学研究所

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