Conformation and Interactions of Polystyrene and Fullerenes in Dilute to Semidilute Solutions

被引:10
作者
Dattani, Rajeev [1 ,2 ]
Michels, Rolf [4 ]
Nedoma, Alisyn J. [1 ,2 ]
Schweins, Ralf [5 ]
Westacott, Paul [1 ,3 ]
Huber, Klaus [4 ]
Cabral, Joao T. [1 ,2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Ctr Plast Elect, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Chem Engn, London SW7 2AZ, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Mat, London SW7 2AZ, England
[4] Univ Paderborn, D-33098 Paderborn, Germany
[5] Inst Max Von Laue Paul Langevin, DS LSS, F-38042 Grenoble, France
基金
英国工程与自然科学研究理事会;
关键词
COLLOID-POLYMER MIXTURES; DIMENSIONS; SCATTERING; BEHAVIOR; TOLUENE; CHAINS; SANS; C-60;
D O I
10.1021/ma501015s
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report the polymer conformation and fullerene aggregation in a ternary system containing polystyrene, C-60, and toluene measured by small angle neutron, static, and dynamic light scattering. We investigate polymer concentrations across the dilute and semidilute regime for five polymer molecular weights (M-w = 20 kg/mol to 1 Mg/mol), and fullerene concentrations below and above its miscibility threshold in toluene. We find that the polymer radius of gyration (R-g(poly)), hydrodynamic radius (R-h), and the mixture correlation length (xi) remain unchanged upon addition of C-60. The miscibility of C-60 in toluene, however, decreases upon addition of polystyrene forming aggregates with a time-dependent radius on the order of 100 nm, and this effect is amplified with increasing polymer M-w. Our findings are relevant to the solution processing of organic photovoltaics, which generally require the effective solubilization of fullerene derivatives and polymer pairs in this concentration range.
引用
收藏
页码:6113 / 6120
页数:8
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