钙钛矿(结构)
卤化物
磺酸盐
光伏
材料科学
分子
工作职能
能量转换效率
化学工程
水溶液
无机化学
氟化物
纳米技术
金属
电解质
离子
氟
离子键合
氢键
光化学
钙钛矿太阳能电池
化学
氢
脱质子化
成核
半导体
作者
Jun‐Xing Zhong,M Chen,Ying Tan,Ying‐Tong Xiao,Guo Yang,Huanyu Chen,Shi‐Wen Fan,Jie‐Yi Yang,Wen Zou,Junlei Tao,Yecheng Zhou,Ruliang Liu,Weiqin Xu,Xueqing Chang,Dai‐Bin Kuang,Wu‐Qiang Wu
标识
DOI:10.1002/ange.202518552
摘要
Abstract Hole transport layer‐free carbon‐based perovskite solar cells (HTL‐free C‐PSCs) hold promise for low‐cost, stable photovoltaics but suffer from poor interfacial charge extraction, inferior defect passivation, and unresolved environmental risk. Here, we reported a multifunctional interfacial engineering strategy using fluorinated lead‐chelating (FLC) molecules containing sulfonate groups, fluoride atoms, and metal ions. Sulfonate groups coordinated with undercoordinated Pb 2+ ions, fluoride atoms formed hydrogen bonds with organic cations, and K + ions stabilized halide anions, synergistically passivating deep‐level defects and enhancing thermal stability. FLC modification also reduced the perovskite work function (from −4.14 to −4.39 eV), improving energy level alignment and facilitating hole extraction at the perovskite/carbon interface. As a result, the optimized devices achieved a champion power conversion efficiency of 20.7%, among the highest for fully solution‐processed planar HTL‐free C‐PSCs. Unencapsulated devices retained over 93% of initial efficiency after 2000 h in ambient air or after 500 h at 60 °C. Importantly, strong FLC‐Pb 2+ chelation significantly reduced lead leakage from severely damaged devices under acidic aqueous environment (334.7 to 53.7 mg m −2 h −1 ), achieving ∼84% sequestration efficiency. This work presents a unified strategy to enhance efficiency, stability, and environmental safety of simplified perovskite photovoltaics.
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