期刊
MACROMOLECULES
卷 54, 期 11, 页码 5278-5285出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.1c00744
关键词
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资金
- National Natural Science Foundation of China [21975115, 21733005, 51773087]
- Shenzhen Fundamental Research Programs [JCYJ20190809161413310, JCYJ20180302180238419, KQJSCX20180319114442157]
- Guangdong Provincial Key Laboratory of Catalysis [2020B121201002]
- Guangdong Basic and Applied Basic Research Foundation [2020A1515110845]
- Guangdong Innovative and Entrepreneurial Research Team Program [2016ZT06G587]
- Shenzhen Sci-Tech Fund [KYTDPT20181011104007]
By introducing chlorine into the poly(p-phenylenevinylene) (PPV) core, a series of 1D rod-like micelles with controlled sizes were produced, and the transformation from 1D rod-like micelles to 2D uniform diamond-like micelles was achieved through thermally induced nucleation SA. The sizes of the 2D diamond-like micelles could be tuned by the annealing temperature and the ratio of unimer to seed, and the morphology transformation was based on energetics including thermodynamic and kinetic points.
Precisely controlled organic one-dimensional (1D) and two-dimensional (2D) materials with unique optoelectronic properties have attracted wide interests. By the introduction of chlorine into the poly(p-phenylenevinylene) (PPV) core, we produced a series of 1D rod-like micelles, whose sizes were controlled by the concentrations of solutions, using self-assembly (SA) of conjugated copolymers (PPV-Cl-20%)(10)-b-P2VP(20). The transformation from ID rod-like micelles to 2D uniform diamond-like micelles was achieved by the thermally induced nucleation SA. The sizes of the 2D diamond-like micelles could be tuned by the annealing temperature and the ratio of unimer to seed. It is demonstrated that the morphology transformation from rod-like micelles to diamond-like micelles was based on energetics including thermodynamic and kinetic points.
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