跟踪(心理语言学)
图层(电子)
过程(计算)
溶剂
活动层
有机太阳能电池
化学
有机溶剂
环境科学
化学工程
环境化学
材料科学
工艺工程
纳米技术
计算机科学
有机化学
工程类
聚合物
操作系统
哲学
薄膜晶体管
语言学
作者
Fang Yang,Er-ming Feng,Yunfei Han,Chujun Zhang,Jianhui Chang,Hengyue Li,Jiayan Shi,Qun Luo,Chang‐Qi Ma,Junliang Yang
标识
DOI:10.1021/acs.jpclett.5c02365
摘要
Organic solar cells (OSCs) are attracting widespread attention as a promising renewable energy technology. The solvent purity exhibits a great impact on the photovoltaic performance of OSCs, but how trace water in solvent influences the formation process of the active layer and the device performance remains unclear. Here, we systematically investigate the impact of trace water in chloroform (CF) on film formation and performance of PM6:L8-BO OSCs. It demonstrates that lower trace water content significantly accelerates the liquid-to-solid transition and nucleation time during film formation, facilitating ordered molecular aggregation and crystallization. Thus, it results in producing efficient exciton dissociation, charge transport and collection, and suppressing charge recombination. By precisely controlling the water content in CF (200, 70, and 30 ppm), devices fabricated with CF-30 (30 ppm) exhibit a remarkable power conversion efficiency (PCE) of 18.49%, surpassing efficiencies of 16.12% and 13.15% from CF-70 and CF-200, respectively. Using 2PACz and Ph-4PACz as hole transport layers further raises PCEs to 19.57% and 19.92%. Furthermore, the strategy is validated across other binary systems, underscoring its general applicability. This work highlights the critical role of solvent purity in enhancing the efficiency and reproducibility of OSCs, offering valuable insights to guide future device optimization strategies.
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