Assembly of Poly(3-hexylthiophene)/CdSe Hybrid Nanowires by Cocrystallization

被引:39
作者
Bokel, Felicia A. [1 ]
Sudeep, Pallikkara K. [1 ]
Pentzer, Emily [1 ]
Emrick, Todd [1 ]
Hayward, Ryan C. [1 ]
机构
[1] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
基金
美国国家科学基金会;
关键词
POLYMER SOLAR-CELLS; REGIOREGULAR POLY(3-HEXYLTHIOPHENE); CONJUGATED POLYMER; CDSE NANORODS; MORPHOLOGY; SOLIDIFICATION; POLYTHIOPHENE; PHOTOVOLTAICS; PERFORMANCE;
D O I
10.1021/ma2003807
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A new approach to simultaneously organize crystalline n- and p-type materials into hybrid inorganic/organic nanowires was described. Solution crystallization of poly-(3-hexylthiophene) (P3HT) to form nanowires was induced by adding a poor solvent, CH2Cl2, to a solution of P3HT in CHCl3 to yield a final polymer concentration of 0.75 or 1.1 mg/mL. The graft density of P3HT ligands on the nanorods, estimated thermogravimetrically, is found to be substantially below the density of chains within a crystalline fibril, providing a viable mechanism for interpenetration of grafted chains into the P3HT fibrils. The orientations between rod and fibril axes are not consistent with a single Gaussian distribution about 0°, instead suggesting a secondary preferred orientation near 35°. The nanowires grow into stable structures over a 1-2 day period and remain suspended with no significant structural changes for at least many months.
引用
收藏
页码:1768 / 1770
页数:3
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