Martín-Gomis Luis, Rotas Georgios, Ohkubo Kei, Fernández-Lázaro Fernando, Fukuzumi Shunichi, Tagmatarchis Nikos, Sastre-Santos Ángela
Área de Química Orgánica Instituto de Bioingeniería, Universidad Miguel Hernández, Elche, Spain.
Nanoscale. 2015 Apr 28;7(16):7437-44. doi: 10.1039/c5nr00308c.
The first perylenediimide (PDI) covalently linked to an azafullerene (C59N) is described. PDI-C59N and PDI-C60 dyads where PDI acts as an electron-donor moiety have been synthesized by connection of the balls to the PDI 1-bay position. Photoexcitation of the PDI unit in both systems results in formation of the charge-separated state by photoinduced electron transfer from the singlet excited state of the PDI moiety to the C59N or to the C60 moiety. The charge-separated state has a lifetime of 400 ps in the case of PDI-C59N and 120 ps for the PDI-C60 dyad in benzonitrile at 298 K. This result has significant implications for the design of organic solar cells based on covalent donor-acceptor systems using C59N as an electron acceptor, indicating that longer-lived charge-separated states can be attained using C59N systems instead of C60 systems.
本文描述了首个与氮杂富勒烯(C59N)共价连接的苝二亚胺(PDI)。通过将球状物连接到PDI的1-位,合成了以PDI作为电子供体部分的PDI-C59N和PDI-C60二元体系。在这两个体系中,PDI单元的光激发通过光致电子从PDI部分的单重激发态转移到C59N或C60部分,导致电荷分离态的形成。在298K的苯甲腈中,PDI-C59N的电荷分离态寿命为400ps,PDI-C60二元体系的电荷分离态寿命为120ps。该结果对于基于使用C59N作为电子受体的共价供体-受体体系的有机太阳能电池设计具有重要意义,表明使用C59N体系而非C60体系可以获得寿命更长的电荷分离态。