| Literature DB >> 25871327 |
Shun-Wei Liu1, Chih-Chien Lee2, Wei-Cheng Su2, Chih-Hsien Yuan2, Yi-Sheng Shu1, Wen-Chang Chang2, Jhih-Yan Guo1, Chien-Feng Chiu1, Ya-Ze Li1, Tsung-Hao Su1, Kuan-Ting Chen2, Po-Chien Chang1, Tzu-Hung Yeh1, Yu-Hsuan Liu2.
Abstract
In this study, we compared the use of neat bathocuproine (BCP) and BCP:C60 mixed buffer layers in chloroboron subphthalocyanine (SubPc)/C60 bilayer organic photovoltaic (OPV) devices and analyzed their influence on device performance. Replacing the conventional BCP with BCP:C60 enabled manipulating the optical field distribution for optimizing the optical properties of the devices. Estimation of the interfacial barrier indicated that the insertion of the BCP:C60 between the C60 and electrode can effectively reduce the barrier for electrons and enhance electron collection at the electrode. Temperature-dependent measurements of the OPV devices performed to calculate the barrier height at the SubPc/C60 interface suggested that band bending was larger when the BCP:C60 buffer layer was used, reflecting increased exciton dissociation efficiency. In addition, the device lifetime was considerably improved when the BCP:C60 buffer layer was used. The device performance was stabilized after the photodegradation of the active layers, thereby increasing the device lifetime compared with the use of the neat BCP buffer layer. Atomic force microscopy images showed that the neat BCP was easily crystallized and could degrade the cathodic interface, whereas the blend of C60 and BCP suppressed the crystallization of BCP. Therefore, the optimal buffer layer improved both the device performance and the device lifetime.Entities:
Keywords: cathodic buffer layer; lifetime; morphology; optical manipulation; power conversion efficiency; small-molecule organic photovoltaic
Year: 2015 PMID: 25871327 DOI: 10.1021/acsami.5b01888
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229