Nonequilibrium Thermodynamics of Charge Separation in Organic Solar Cells

被引:4
作者
Kaiser, Waldemar [1 ]
Jankovi, Veljko [2 ]
Vukmirovi, Nenad [2 ]
Gagliardi, Alessio [1 ]
机构
[1] Tech Univ Munich, Dept Elect & Comp Engn, D-80333 Munich, Germany
[2] Univ Belgrade, Inst Phys Belgrade, Belgrade 11080, Serbia
关键词
DONOR-ACCEPTOR INTERFACE; TRANSFER STATES; EXCITON DISSOCIATION; DISORDER; DELOCALIZATION; HOT; ENTROPY; GENERATION; EFFICIENCY; ENERGY;
D O I
10.1021/acs.jpclett.1c01817
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This work presents a novel theoretical description of the nonequilibrium thermodynamics of charge separation in organic solar cells (OSCs). Using stochastic thermodynamics, we take realistic state populations derived from the phonon-assisted dynamics of electron-hole pairs within photoexcited organic bilayers to connect the kinetics with the free energy profile of charge separation. Hereby, we quantify for the first time the difference between nonequilibrium and equilibrium free energy profile. We analyze the impact of energetic disorder and delocalization on free energy, average energy, and entropy. For a high disorder, the free energy profile is well-described as equilibrated. We observe significant deviations from equilibrium for delocalized electron-hole pairs at a small disorder, implying that charge separation in efficient OSCs proceeds via a cold but nonequilibrated pathway. Both a large Gibbs entropy and large initial electron-hole distance provide an efficient charge separation, while a decrease in the free energy barrier does not necessarily enhance charge separation.
引用
收藏
页码:6389 / 6397
页数:9
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