化学
卤化物
结晶
钙钛矿(结构)
能量转换效率
单体
过程(计算)
化学工程
溶解过程
离子
分子
光伏系统
纳米技术
冷凝
无机化学
光化学
硅
调节器
光电子学
太阳能电池
作者
Jianfeng Qiu,Hongwei Zhu,Bingyao Shao,Yating Shi,Siyuan Xu,Mutalifu Abulikemu,Jiang Liu,Zhe Zheng,Aqil Jamal,Hamad Al-Saiari,Sarah Aqeel,Issam Gereige,Fei Zhang,Jun Yin,Chunju Li,Osman M. Bakr
摘要
Perovskite solar cells (PSCs) exhibit impressive power conversion efficiencies (PCEs), but their stability still falls short of industrial commercialization requirements, primarily due to inherent defects and halide ion migration within the perovskite materials. To address this shortcoming, we developed a novel electron-deficient biphen[n]arene macrocycle molecule, NBP[2], synthesized through the condensation of the monomer 2,2″,4,4″-tetramethoxy-4',6'-dinitro-1,1':3',1″-terphenyl (NP) with paraformaldehyde. When the macrocyclic molecule is introduced into the perovskite film via the antisolvent injection method, it functions as a regulator of the crystallization process of perovskite and an inhibitor of halide anion migration. In addition, NBP[2] can effectively bind with uncoordinated halide ions and Pb2+, reducing intrinsic defects through Lewis acid-base and cation-π interactions. As a result, NBP[2]-modified PSCs achieve a PCE of up to 25.38% (compared to 23.89% for the control) and retain 95.8% of their initial efficiency after 1000 h of maximum power point tracking under 1-sun illumination at room temperature in an N2 atmosphere.
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