Insuasty Alberto, Atienza Carmen, López Juan Luis, Marco-Martínez Juan, Casado Santiago, Saha Avishek, Guldi Dirk M, Martín Nazario
Departamento de Química Orgánica I, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, E-28040 Madrid, Spain.
IMDEA- Nanoscience, Campus de Cantoblanco, E-28049 Madrid, Spain.
Sci Rep. 2015 Sep 15;5:14154. doi: 10.1038/srep14154.
Currently, there is a broad interest in the control over creating ordered electroactive nanostructures, in which electron donors and acceptors are organized at similar length scales. In this article, a simple and efficient procedure is reported en-route towards the construction of 1D arrays of crystalline pristine C60 and phenyl-C61-butyric acid methyl ester (PCBM) coated onto supramolecular fibers based on exTTF-pentapeptides. The resulting n/p-nanohybrids have been fully characterized by a variety of spectroscopic (FTIR, UV-Vis, circular dichroism, Raman and transient absorption), microscopic (AFM, TEM, and SEM), and powder diffraction (X-ray) techniques. Our experimental findings document the tendency of electroactive exTTF-fibers to induce the crystallization of C60 and PCBM, on one hand, and to afford 1D n/p-nanohybrids, on the other hand. Furthermore, photogenerated radical ion pairs, formed upon visible light irradiation of the n/p-nanohybrids, feature lifetimes on the range of 0.9-1.2 ns.
目前,人们对控制创建有序的电活性纳米结构有着广泛的兴趣,其中电子供体和受体以相似的长度尺度进行组织。在本文中,报道了一种简单有效的方法,用于构建基于exTTF-五肽的超分子纤维上包覆的结晶原始C60和苯基-C61-丁酸甲酯(PCBM)的一维阵列。所得的n/p-纳米杂化物已通过多种光谱(FTIR、UV-Vis、圆二色性、拉曼和瞬态吸收)、显微镜(AFM、TEM和SEM)以及粉末衍射(X射线)技术进行了全面表征。我们的实验结果表明,一方面,电活性exTTF-纤维有诱导C60和PCBM结晶的趋势,另一方面,能形成一维n/p-纳米杂化物。此外,n/p-纳米杂化物在可见光照射下形成的光生自由基离子对的寿命在0.9 - 1.2 ns范围内。