阳极
材料科学
活动层
接受者
有机太阳能电池
化学物理
分子
聚合物
聚合物太阳能电池
图层(电子)
偏移量(计算机科学)
电极
纳米技术
复合材料
物理化学
化学
有机化学
凝聚态物理
物理
程序设计语言
薄膜晶体管
计算机科学
作者
Aaron Kramer,Waldemar Kaiser,Boya Zhang,Lakshmi N.S. Murthy,Alessio Gagliardi,Julia W. P. Hsu,William G. Vandenberghe
出处
期刊:Nano Energy
[Elsevier BV]
日期:2022-09-09
卷期号:103: 107793-107793
被引量:6
标识
DOI:10.1016/j.nanoen.2022.107793
摘要
Experimental results of organic solar cells with low donor concentrations using small molecule donors have displayed significantly lower fill factors (FFs) compared to dilute-donor solar cells (DDSCs) with polymer donors. We perform experiments and kinetic Monte Carlo simulations, to understand the observed FF discrepancy and how FF can be improved. Our results reveal that small molecule DDSCs collect holes from the region of the active layer near the anode whereas polymer DDSCs collect holes from a deeper volume inside the active layer. This enlarged collection region is facilitated by the morphology of polymer chains extending from the anode into the active layer. The chains permit holes to hop along the donor sites to the anode with no barrier. Small molecule DDSCs, in contrast, require a large electric field to transfer holes from isolated donor sites back to the acceptor matrix to reach the anode. Collections in small molecule DDSCs are thus constrained to photogenerated holes on donors near the anode. We propose strategies to increase DDSC FF to levels comparable to bulk-heterojunction organic solar cells by decreasing the donor-acceptor highest occupied molecular orbital energy offset, or by engineering the active layer morphology so that a higher density of donors are in proximity/contact with the anode.
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