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Retarding Thermal Degradation in Hybrid Perovskites by Ionic Liquid Additives
Authors:Rui Xia  Zhaofu Fei  Nikita Drigo  Felix D Bobbink  Zhangjun Huang  Rokas Jasi nas  Marius Franckevi ius  Vidmantas Gulbinas  Mounir Mensi  Xiaodong Fang  Cristina Roldn‐Carmona  Mohammad Khaja Nazeeruddin  Paul J Dyson
Affiliation:Rui Xia,Zhaofu Fei,Nikita Drigo,Felix D. Bobbink,Zhangjun Huang,Rokas Jasiūnas,Marius Franckevi?ius,Vidmantas Gulbinas,Mounir Mensi,Xiaodong Fang,Cristina Roldán‐Carmona,Mohammad Khaja Nazeeruddin,Paul J. Dyson
Abstract:Recent years have witnessed considerable progress in the development of solar cells based on lead halide perovskite materials. However, their intrinsic instability remains a limitation. In this context, the interplay between the thermal degradation and the hydrophobicity of perovskite materials is investigated. To this end, the salt 1‐(4‐ethenylbenzyl)‐3‐(3,3,4,4,5,5,6,6,7,7,8,8,8‐tridecafluorooctylimidazolium iodide (ETI), is employed as an additive in hybrid perovskites, endowing the photoactive materials with high thermal stability and hydrophobicity. The ETI additive inhibits methylammonium (MA) permeation in methylammonium lead triiodide (MAPbI3) occurring due to intrinsic thermal degradation, by inhibiting out‐diffusion of the MA+ cation, preserving the pristine material and preventing decomposition. With this simple approach, high efficiency solar cells based on the unstable MAPbI3 perovskite are markedly stabilized under maximum power point tracking, leading to greater than twice the preserved efficiency after 700 h of continuous light illumination and heating (60 °C). These results suggest a strategy to tackle the intrinsic thermal decomposition of MAI, an essential component in all state‐of‐the‐art perovskite compositions.
Keywords:additive  imidazolium salt  ionic liquid  perovskite  solar cell  stability
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