材料科学
光伏
串联
钙钛矿(结构)
终端(电信)
光电子学
纳米技术
分析化学(期刊)
光伏系统
化学工程
电气工程
电信
复合材料
环境化学
计算机科学
工程类
化学
作者
Chi Li,Şifa Doğan,Yuheng Li,Huifeng Zhang,Shicheng Tang,Zhen Yuan,Lusheng Liang,Zilong Zhang,Li Wang,Chunming Liu,Ye Yang,Mine Ince,Peng Gao
标识
DOI:10.1002/aenm.202402856
摘要
Abstract The performance of perovskite solar cells (PSCs) is often constrained by significant open‐circuit voltage ( V OC ) losses attributed to non‐radiative recombination processes induced by detrimental trap states. Surface treatments using passivating ligands typically involve single active binding sites on perovskite, posing challenges for effective passivation. Here, an aromatic donor‐acceptor (D‐A) configured phthalocyanine treatment is proposed to aim at dual‐site passivation of uncoordinated lead ions and effective mitigation of shallow and deep‐level defects on the perovskite surface. The resulting benign p‐type surface facilitates a more favorable energy level alignment and reduces energetic mismatches at the perovskite/Spiro‐OMeTAD interface. Pc‐BTBC, with its aromatic D‐A configuration, demonstrated compatibility with various perovskite compositions. Optimized PSCs achieves a power conversion efficiency (PCE) of 25.15% and reduces the V OC deficit to 0.379 V. Furthermore, encapsulated devices exhibited enhanced stability under damp‐heat conditions (ISOS‐D‐2, 50% RH, 65°C) with a T 92 of 1000 h and maintained maximum power point tracking under continuous light in ambient air at 65°C (ISOS‐L‐2). Notably, fabricated wide‐bandgap semitransparent PSCs (ST‐PSCs) achieved a PCE of 20.29%, while four‐terminal perovskite/silicon tandem solar cells (4T‐P/STSCs) demonstrated an efficiency of 29.38%. This study provides insights into minimizing V OC losses and represents significant progress toward commercializing perovskite photovoltaics.
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