Hierarchical Nanomorphologies Promote Exciton Dissociation in Polymer/Fullerene Bulk Heterojunction Solar Cells

Wei Chen(Argonne National Laboratory), Tao Xu(University of Chicago), Feng He(University of Chicago), Wei Wang(University of Chicago), Cheng Wang(Lawrence Berkeley National Laboratory), Joseph Strzalka(Argonne National Laboratory), Yun Liu(NIST Center for Neutron Research), Jianguo Wen(Argonne National Laboratory), Dean J. Miller(Argonne National Laboratory), Jihua Chen(Oak Ridge National Laboratory), Kunlun Hong(Oak Ridge National Laboratory), Luping Yu(University of Chicago), Seth B. Darling(Argonne National Laboratory)
Nano Letters
August 8, 2011
Cited by 423

Abstract

PTB7 semiconducting copolymer comprising thieno[3,4-b]thiophene and benzodithiophene alternating repeat units set a historic record of solar energy conversion efficiency (7.4%) in polymer/fullerene bulk heterojunction solar cells. To further improve solar cell performance, a thorough understanding of structure-property relationships associated with PTB7/fullerene and related organic photovoltaic (OPV) devices is crucial. Traditionally, OPV active layers are viewed as an interpenetrating network of pure polymers and fullerenes with discrete interfaces. Here we show that the active layer of PTB7/fullerene OPV devices in fact involves hierarchical nanomorphologies ranging from several nanometers of crystallites to tens of nanometers of nanocrystallite aggregates in PTB7-rich and fullerene-rich domains, themselves hundreds of nanometers in size. These hierarchical nanomorphologies are coupled to significantly enhanced exciton dissociation, which consequently contribute to photocurrent, indicating that the nanostructural characteristics at multiple length scales is one of the key factors determining the performance of PTB7 copolymer, and likely most polymer/fullerene systems, in OPV devices.


Related Papers

No related papers found

Powered by citation graph analysis