材料科学
热稳定性
无定形固体
聚合物
光伏
光伏系统
载流子
降级(电信)
有机太阳能电池
化学工程
玻璃化转变
热的
相(物质)
电子迁移率
光电子学
聚合物太阳能电池
电荷(物理)
热分析
作者
Xun Pan,Jinhui Zhao,Jessica M. de la Perrelle,Matthew J. Griffith,Mats R. Andersson
标识
DOI:10.1021/acs.macromol.5c03396
摘要
A completely amorphous donor polymer PIDT-T8BT recently showed enhanced photovoltaic performance when paired with Y6 using unconventional low donor:acceptor (D:A) ratios, while its analogue PIDT-T12BT achieved high PCEs at conventional 1:1.2 ratios. Two new polymers, PIDT-T6BT and PIDT-T10BT, were synthesized with varying side-chain lengths. All exhibited amorphous phase behavior with shorter side-chains yielding higher glass transition temperatures. Photovoltaic devices based on PIDT-TxBT (x = 6, 8, 10, 12):Y6 were investigated across broad D:A ratios, revealing different optimal ratios for each donor. Thermal stability testing at 85 °C showed that low donor content PIDT-T6BT:Y6 (1:10) devices had significantly enhanced stability. Notably, PIDT-T8BT:Y6 (1:10) devices demonstrated superior thermal stability compared to high-performing PM6:Y6 and D18:Y6 systems at both conventional and low D:A ratios. Dynamic mechanical thermal analysis revealed that blends with lower polymer content retained high storage modulus at elevated temperatures, indicating enhanced morphological stability, particularly for 1:10 blends. Charge carrier dynamics studies showed that stable 1:10 device performance results from enhanced carrier mobility offsetting decreased carrier lifetime after thermal aging, minimizing charge collection changes. Conversely, PM6:Y6, D18:Y6, and 1:1.2 PIDT-T6BT:Y6 devices exhibited additional performance degradation from poor charge generation due to undesirable phase-separated morphologies.
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