Pathways to a New Efficiency Regime for Organic Solar Cells

被引:353
作者
Koster, L. Jan Anton [1 ]
Shaheen, Sean E. [2 ]
Hummelen, Jan C. [1 ,3 ]
机构
[1] Zernike Inst Adv Mat, NL-9747 AG Groningen, Netherlands
[2] Univ Denver, Dept Phys & Astron, Denver, CO 80208 USA
[3] Univ Groningen, Stratingh Inst Chem, NL-9747 AG Groningen, Netherlands
基金
美国国家科学基金会;
关键词
conjugated polymers; fullerenes; organic electronics; photovoltaic devices; solar cells; OPEN-CIRCUIT VOLTAGE; CHARGE-TRANSFER EXCITONS; PHOTOVOLTAIC DEVICES; ULTIMATE EFFICIENCY; CONJUGATED POLYMERS; ELECTRON-TRANSFER; TRANSFER STATES; HETEROJUNCTION; RECOMBINATION; DONOR;
D O I
10.1002/aenm.201200103
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
Three different theoretical approaches are presented to identify pathways to organic solar cells with power conversion efficiencies in excess of 20%. A radiation limit for organic solar cells is introduced that elucidates the role of charge-transfer (CT) state absorption. Provided this CT action is sufficiently weak, organic solar cells can be as efficient as their inorganic counterparts. Next, a model based on Marcus theory of electronic transfer that also considers exciton generation in both the electron donor and electron acceptor is used to show how reduction of the reorganization energies can lead to substantial efficiency gains. Finally, the dielectric constant is introduced as a central parameter for efficient solar cells. By using a driftdiffusion model, it is found that efficiencies of more than 20% are within reach.
引用
收藏
页码:1246 / 1253
页数:8
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