Origin of the Tunable Open-Circuit Voltage in Ternary Blend Bulk Heterojunction Organic Solar Cells

被引:308
作者
Street, Robert A. [1 ]
Davies, Daniel [1 ]
Khlyabich, Petr P. [2 ,3 ]
Burkhart, Beate [2 ,3 ]
Thompson, Barry C. [2 ,3 ]
机构
[1] Xerox Corp, Palo Alto Res Ctr, Palo Alto, CA 94304 USA
[2] Univ So Calif, Dept Chem, Los Angeles, CA 90089 USA
[3] Univ So Calif, Loker Hydrocarbon Res Inst, Los Angeles, CA 90089 USA
关键词
STATES; ENERGY; DONOR;
D O I
10.1021/ja3112143
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ternary blend bulk heterojunction organic solar cells comprising either a polythiophene donor and two fullerene acceptors or two polythiophene donors and a fullerene acceptor are shown to have unique electronic properties. Measurements of the photocurrent spectral response and the open-circuit voltage show that the HOMO and LUMO levels change continuously with composition in the respective two-component acceptor or donor pair, consistent with the formation of an organic alloy. However, optical absorption of the exciton states retains the individual molecular properties of the two materials across the blend composition. This difference is attributed to the highly localized molecular nature of the exciton and the more delocalized intermolecular nature of electrons and holes that reflect the average composition of the alloy. As established here, the combination of molecular excitations that can harvest a wide range of photon energies and electronic alloy states that can adjust the open-circuit voltage provides the underlying basis of ternary blends as a platform for highly efficient next-generation organic solar cells.
引用
收藏
页码:986 / 989
页数:4
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