Qu Yunpeng, Su Qing, Li Sijun, Lu Guanghao, Zhou Xun, Zhang Jidong, Chen Zhaobin, Yang Xiaoniu
University of Chinese Academy of Sciences, Beijing 100049, P. R. China.
ACS Macro Lett. 2012 Nov 20;1(11):1274-1278. doi: 10.1021/mz300430h. Epub 2012 Oct 17.
New large-size poly(3-butylthiophene) (P3BT) spherulites are obtained by solution aging. These P3BT spherulites are composed of nanoribbons, and the P3BT molecules arrange into Form II structure with a backbone π-stacking distance of 0.47 nm. P3BT lamellae adopt "flat-on" orientation at the edge of the spherulite, and the spherulite preferentially grows along the π-π stacking direction. These spherulites could be obtained in bulk solution or at the top or bottom of the solution, depending on the competition of gravity and Brownian motion. Temperature-dependent photoluminescence spectra demonstrate that the polymer chains are arranged in H-aggregation model. The 0-0 transition in UV-visible absorption spectra blue shifts from 2.03 eV (610 nm, Form I) to 2.11 eV (589 nm, Form II). These results provide a further understanding of the crystallization and photophysical properties of poly(3-alkylthiophene) (P3AT), and the preparation method of large size and pure P3AT spherulites shows potential in applications of organic electronics.
通过溶液老化获得了新型大尺寸聚(3-丁基噻吩)(P3BT)球晶。这些P3BT球晶由纳米带组成,且P3BT分子排列成II型结构,主链π-堆积距离为0.47nm。P3BT片晶在球晶边缘呈“平躺”取向,并且球晶优先沿π-π堆积方向生长。根据重力和布朗运动的竞争情况,这些球晶可以在本体溶液中或溶液的顶部或底部获得。变温光致发光光谱表明聚合物链以H-聚集模型排列。紫外可见吸收光谱中的0-0跃迁从2.03eV(610nm,I型)蓝移至2.11eV(589nm,II型)。这些结果进一步加深了对聚(3-烷基噻吩)(P3AT)结晶和光物理性质的理解,并且大尺寸和纯P3AT球晶的制备方法在有机电子学应用中显示出潜力。