有机太阳能电池
材料科学
电子
工程物理
化学工程
纳米技术
光电子学
化学
物理
复合材料
工程类
量子力学
聚合物
作者
Wisnu Tantyo Hadmojo,Furkan H. Isikgor,Yuanbao Lin,Zhaoheng Ling,Qiao He,Hendrik Faber,Emre Yengel,Roshan Ali,Abdus Samad,Ryanda Enggar Anugrah Ardhi,Sang Young Jeong,Han Young Woo,Udo Schwingenschlögl,Martin Heeney,Thomas D. Anthopoulos
出处
期刊:Energy & environmental materials
日期:2024-05-11
摘要
The development of high‐performance organic solar cells (OSCs) with high operational stability is essential to accelerate their commercialization. Unfortunately, our understanding of the origin of instabilities in state‐of‐the‐art OSCs based on bulk heterojunction (BHJ) featuring non‐fullerene acceptors (NFAs) remains limited. Herein, we developed NFA‐based OSCs using different charge extraction interlayer materials and studied their storage, thermal, and operational stabilities. Despite the high power conversion efficiency (PCE) of the OSCs (17.54%), we found that cells featuring self‐assembled monolayers (SAMs) as hole‐extraction interlayers exhibited poor stability. The time required for these OSCs to reach 80% of their initial performance (T 80 ) was only 6 h under continuous thermal stress at 85 °C in a nitrogen atmosphere and 1 h under maximum power point tracking (MPPT) in a vacuum. Inserting MoO x between ITO and SAM enhanced the T 80 to 50 and ~15 h after the thermal and operational stability tests, respectively, while maintaining a PCE of 16.9%. Replacing the organic PDINN electron transport layer with ZnO NPs further enhances the cells' thermal and operational stability, boosting the T 80 to 1000 and 170 h, respectively. Our work reveals the synergistic roles of charge‐selective interlayers and device architecture in developing efficient and stable OSCs.
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