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The broken out and confinement phase separation structure evolution with the solution aggregation and relative crystallization degree in P3HT/N2200
Zhang, Rui1,2; Yan, Ye1,2; Yang, Hua3,4; Yu, Xinhong1; Liu, Jiangang1; Zhang, Jidong1; Han, Yanchun1
刊名POLYMER
2018-02-28
卷号138页码:49-56
关键词Polymer Blends Molecular Weight Solution Aggregation Relative Crystallization Degree Phase Separation
ISSN号0032-3861
DOI10.1016/j.polymer.2018.01.059
英文摘要The phase separation structure evolution process, i.e. confinement and broke out phenomenon in crystallization/crystallization poly (3-hexylthiophene) (P3HT) and poly [[N, N-bis(2-octyldodecyl)-napthalene- 1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5, 5'-(2,2'-bithiophene)] (N2200) blends were controlled by the polymer solution aggregation behavior and relative crystallization degree of each component. In this study, two different molecular weight of P3HT, M-w = 6 kDa and M-w = 55 kDa were selected and blend with N2200 as the model systems. Different molecular weight of P3HT had different crystalline ability in blend films. A similar phase separation of both two polymer blends could form in good solvent chloroform (CF). Marginal solvents and thermal annealing were employed to change the polymer solution aggregation behavior and relative crystallization degree of the two components. On one hand, when p-xylene (pX) was added as the co-solvent to increase the aggregation of P3HT molecules, for P3HT (Mw = 6 kDa)/N2200, the P3HT phase broke the restriction of N2200 phase while there was almost unchanged in P3HT (Mw = 55 kDa)/N2200. On the other hand, during thermal annealing, the P3HT molecule had a stronger molecular moving ability in P3HT (Mw = 6 kDa)/N2200 than that in P3HT (Mw = 55 kDa)/N2200 (the relative crystallization degree of these two polymers in P3HT (Mw = 6 kDa)/N2200 and P3HT (Mw = 55 kDa)/N2200 are 142 and 3, respectively). The pristine phase separation of P3HT (Mw = 6 kDa)/N2200 was destroyed effectively due to the unmatched crystallization degree of the two components and large sized fibrous phase separation was formed during thermal annealing. However, the pristine phase separation was almost unchanged in P3HT (Mw = 55 kDa)/N2200, and the P3HT molecule could partly ordered arrangement, which probably come from the almost matched crystallization degree of these two polymers. The results indicate that it is the Gibbs free energy that controls the phase separation in different relative crystallization degree. And different chain entanglements behavior was likely to be the main source of the morphological stability. (C) 2018 Elsevier Ltd. All rights reserved.
语种英语
出版者ELSEVIER SCI LTD
WOS记录号WOS:000426264300007
内容类型期刊论文
源URL[http://ir.iccas.ac.cn/handle/121111/45613]  
专题中国科学院化学研究所
通讯作者Liu, Jiangang; Zhang, Jidong; 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, Jilin, Peoples R China
2.Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
3.Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
4.Dongguan Neutron Sci Ctr, 1 Zhongziyuan Rd, Dalang 523803, Dongguan, Peoples R China
推荐引用方式
GB/T 7714
Zhang, Rui,Yan, Ye,Yang, Hua,et al. The broken out and confinement phase separation structure evolution with the solution aggregation and relative crystallization degree in P3HT/N2200[J]. POLYMER,2018,138:49-56.
APA Zhang, Rui.,Yan, Ye.,Yang, Hua.,Yu, Xinhong.,Liu, Jiangang.,...&Han, Yanchun.(2018).The broken out and confinement phase separation structure evolution with the solution aggregation and relative crystallization degree in P3HT/N2200.POLYMER,138,49-56.
MLA Zhang, Rui,et al."The broken out and confinement phase separation structure evolution with the solution aggregation and relative crystallization degree in P3HT/N2200".POLYMER 138(2018):49-56.
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