材料科学
钙钛矿(结构)
光电子学
带隙
能量转换效率
光伏
光伏系统
结晶度
激子
发光二极管
量子效率
二极管
卤化物
化学工程
凝聚态物理
无机化学
生物
物理
工程类
复合材料
化学
生态学
作者
Rong Yang,Renzhi Li,Yu Cao,Yingqiang Wei,Yanfeng Miao,Wen Liang Tan,Xuechen Jiao,Hong Chen,Liangdong Zhang,Qing Chen,Huotian Zhang,Wei Zou,Yuming Wang,Ming Yang,Chang Yi,Nana Wang,Feng Gao,Christopher R. McNeill,Tianshi Qin,Jianpu Wang
标识
DOI:10.1002/adma.201804771
摘要
Abstract Quasi‐2D layered organometal halide perovskites have recently emerged as promising candidates for solar cells, because of their intrinsic stability compared to 3D analogs. However, relatively low power conversion efficiency (PCE) limits the application of 2D layered perovskites in photovoltaics, due to large energy band gap, high exciton binding energy, and poor interlayer charge transport. Here, efficient and water‐stable quasi‐2D perovskite solar cells with a peak PCE of 18.20% by using 3‐bromobenzylammonium iodide are demonstrated. The unencapsulated devices sustain over 82% of their initial efficiency after 2400 h under relative humidity of ≈40%, and show almost unchanged photovoltaic parameters after immersion into water for 60 s. The robust performance of perovskite solar cells results from the quasi‐2D perovskite films with hydrophobic nature and a high degree of electronic order and high crystallinity, which consists of both ordered large‐bandgap perovskites with the vertical growth in the bottom region and oriented small‐bandgap components in the top region. Moreover, due to the suppressed nonradiative recombination, the unencapsulated photovoltaic devices can work well as light‐emitting diodes (LEDs), exhibiting an external quantum efficiency of 3.85% and a long operational lifetime of ≈96 h at a high current density of 200 mA cm −2 in air.
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