Green Additive Limits Runaway Crystallinity in PM6:Y6 Organic Solar Cells but Causes Field-Independent Geminate Recombination

被引:1
|
作者
Alqahtani, Obaid [1 ,2 ]
Alotaibi, Awwad [1 ]
Burnes, Michael [1 ]
Collins, Brian A. [1 ]
机构
[1] Washington State Univ, Dept Phys & Astron, Pullman, WA 99164 USA
[2] Prince Sattam bin Abdulaziz Univ, Dept Phys, Alkharj 11942, Saudi Arabia
基金
美国国家科学基金会;
关键词
ORIENTATION; GENERATION; SEPARATION;
D O I
10.1021/acsenergylett.3c01604
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
Solvent additives are well-established for improving device performance of organic solar cells by enhancing nanodomain phase separation and crystallization. However, optimum additive concentrations are typically at trace amounts with slight fluctuations causing runaway crystallinity that short the device and limit scale-up potential. Here we show that a nonhalogenated solvent additive 1-phenylnaphthalene (PN) can be used to optimize high-performance PM6:Y6 devices, but without runaway crystallinity even at concentrations 10x above the optimum. Our holistic analysis of device losses shows that PN increases photoabsorption while decreasing bimolecular recombination. However, above the optimum, charge generation is reduced due to field-independent geminate recombination of charge transfer states that overcomes the other benefits. Rotated Y6 crystallite orientation is a likely culprit, where the device electric field is ineffective at separating the charges. Despite this, device performance remains higher than that of traditional additives, indicating a route to avoiding the high sensitivity of performance to processing conditions.
引用
收藏
页码:4643 / 4649
页数:7
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