材料科学
掺杂剂
异质结
钙钛矿(结构)
卤化物
兴奋剂
光电子学
碘化物
纳米技术
太阳能电池
化学工程
无机化学
工程类
化学
作者
Yongming Sha,Enbing Bi,Yao Zhang,Pengbin Ru,Weiyu Kong,Peng Zhang,Xudong Yang,Han Chen,Liyuan Han
标识
DOI:10.1002/aenm.202003301
摘要
Abstract Perovskite solar cell (PSC) modules employing a hole transport layer (HTL) without unstable dopants possess high potential for improving operational stability. However, the low efficiencies of the devices greatly limit their commercial applications owing to the lower efficacy of the dopant‐free HTL, introduced by the unintentional n ‐doping effect of volatile ions from the halide‐rich perovskite surface. Here, a scalable heterostructure integrated by a methylammonium‐free perovskite film with an iodide‐rich surface, an ultrathin interlayer of bridge‐jointed graphene oxide nanosheets (BJ‐GO), and an HTL without additional ionic dopants is developed. In this heterostructure, the iodide ions are physically immobilized by the compact 2D network, and lead defects are chemically passivated by multiple coordination bonds. Moreover, the BJ‐GO with tunable surface energy enables a highly ordered HTL a considerably improved carrier mobility by an order of magnitude. Finally, the PSC module with an area of 35.80 cm 2 employing this heterostructure shows a certified efficiency of 15.3%. The encapsulated PSC modules retain over 91% of initial efficiency after the damp heat test at 85 °C and ≈85% relative humidity for 1000 h, while maintaining 90% of the initial value for 1000 h at the maximum power point under continuous 1‐Sun illumination at 60 °C.
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