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Divalent Anionic Doping in Perovskite Solar Cells for Enhanced Chemical Stability
Advanced Materials ( IF 29.4 ) Pub Date : 2018-07-08 , DOI: 10.1002/adma.201800973
Jue Gong 1 , Mengjin Yang 2 , Dominic Rebollar 1 , Jordan Rucinski 1 , Zachary Liveris 1 , Kai Zhu 2 , Tao Xu 1
Affiliation  

The chemical stabilities of hybrid perovskite materials demand further improvement toward long‐term and large‐scale photovoltaic applications. Herein, the enhanced chemical stability of CH3NH3PbI3 is reported by doping the divalent anion Se2− in the form of PbSe in precursor solutions to enhance the hydrogen‐bonding‐like interactions between the organic cations and the inorganic framework. As a result, in 100% humidity at 40 °C, the 10% w/w PbSe‐doped CH3NH3PbI3 films exhibited >140‐fold stability improvement over pristine CH3NH3PbI3 films. As the PbSe‐doped CH3NH3PbI3 films maintained the perovskite structure, a top efficiency of 10.4% with 70% retention after 700 h aging in ambient air is achieved with an unencapsulated 10% w/w PbSe:MAPbI3‐based cell. As a bonus, the incorporated Se2− also effectively suppresses iodine diffusion, leading to enhanced chemical stability of the silver electrodes.

中文翻译:

钙钛矿太阳能电池中的二价阴离子掺杂可增强化学稳定性

钙钛矿杂化材料的化学稳定性需要进一步改善,以适应长期和大规模的光伏应用。在本文中,通过在前体溶液中掺入PbSe形式的二价阴离子Se 2−来增强有机阳离子与无机骨架之间的氢键样相互作用,从而提高了CH 3 NH 3 PbI 3的化学稳定性。结果,在40°C的100%湿度下,掺有10%w / w PbSe的CH 3 NH 3 PbI 3膜的稳定性比原始CH 3 NH 3 PbI 3膜高140倍以上。作为PbSe掺杂的CH 3NH 3 PbI 3膜保持钙钛矿结构,在未封装的10%w / w PbSe:MAPbI 3基电池中,在环境空气中老化700小时后,最高效率为10.4%,保留率达70%。另外,掺入的Se 2-还可有效抑制碘扩散,从而提高银电极的化学稳定性。
更新日期:2018-07-08
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