Charge Pair Separation Dynamics in Organic Bulk-Heterojunction Solar Cells

被引:10
|
作者
Albes, Tim [1 ]
Gagliardi, Alessio [1 ]
机构
[1] Tech Univ Munich, Dept Elect & Comp Engn, Arcisstr 21, D-80333 Munich, Germany
关键词
bulk-heterojunction; charge separation; kinetic Monte Carlo; organic solar cells; permittivity; INTERNAL QUANTUM EFFICIENCY; 25TH ANNIVERSARY ARTICLE; MONTE-CARLO-SIMULATION; BIMOLECULAR RECOMBINATION; DIELECTRIC-CONSTANT; PHOTOVOLTAIC DEVICES; CONJUGATED POLYMER; CARRIER MOBILITY; DISSOCIATION; ENERGY;
D O I
10.1002/adts.201800032
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Charge pair separation in organic bulk-heterojunction (BHJ) solar cells is a complex interplay between numerous factors, such as the spatial geometry of the blend, the distribution of energetic disorder, the electric field, thermal fluctuations, and the mutual electron-hole Coulomb attraction. Insufficient separation from the interface and concomitant charge pair recombination is a main limitation in improving the PCE of organic BHJ solar cells and requires an in-depth understanding of the timescales involved. Here, a 3D kinetic Monte Carlo model of a BHJ organic solar cell is set up and the time-dependent evolution of mutual electron-hole pair distances separating from the heterojunction interface is investigated. Large fluctuations in separation times are found, in particular in dependence of the energetic disorder and the permittivity of the organic materials. At commonly observed values of energetic disorder, slight modifications of the permittivity can drastically influence the charge separation time and even outweigh orders of magnitude of geminate recombination rates, hence help to suppress geminate recombination. Thus, the results strongly support the recent trend of developing high-permittivity organic materials for solar cell applications.
引用
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页数:12
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