材料科学
钝化
钙钛矿(结构)
能量转换效率
异质结
再分配(选举)
化学工程
胺气处理
共轭体系
纳米技术
反应性(心理学)
离子
光电子学
甲脒
光伏系统
钙钛矿太阳能电池
铵
无机化学
阳极
色素敏化染料
作者
Xiaoyuan Liu,Zhenhuang Su,可馨 吴,Hong Lin,Zeyi Zhang,Qinghe Wu,Qixiang Gao,鲁渝慈,Xia Gao,Yifan Lv,X X Xu,Yu Wang,Y Chen
摘要
Low-dimensional/three-dimensional (LD/3D) perovskite heterojunctions have demonstrated exceptional promise in photovoltaics, yet their performance remains constrained by the inherent compromise between interfacial defect passivation and charge extraction efficiency. To address this challenge, we prompt the exploration of ammonium ligands with moderate reactivity to facilitate heterojunction charge transport while suppressing cation migration, thereby reconciling high efficiency with outstanding operational stability. Specially, we designed a π-conjugated quaternary ammonium ligand PCOZI (4-phenyl-1,3-oxazol-2-yl-heptyl-dimethylammonium iodide) as a surface modifier for 3D perovskite films, leading to the formation of a stable 1D (PCOZ)PbI3 protecting layer. The resulting near-conformal and structurally ordered interface effectively balances defect passivation with unimpeded charge transfer, significantly mitigating non-radiative recombination and ion redistribution under operational stressors. Remarkably, the optimized devices incorporating the PCOZI interlayer yield a record-breaking power conversion efficiency (PCE) of 26.33%, certified at 26.29%, setting a new benchmark for 1D/3D n-i-p PSCs, while the device also exhibits outstanding operational stability, retaining 94.2% of its initial efficiency after 1000 h of continuous operation under the ISOS-L-3 protocol. Notably, a minimodule with an aperture area of 10.24 cm2 also achieves a remarkable PCE of 23.15%, underscoring the scalability and practical relevance of this interfacial stabilization approach.
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