The chemical stabilities of hybrid perovskite materials demand further improvement toward long-term and large-scale photovoltaic applications. Herein, the enhanced chemical stability of CH3 NH3 PbI3 is reported by doping the… Click to show full abstract
The chemical stabilities of hybrid perovskite materials demand further improvement toward long-term and large-scale photovoltaic applications. Herein, the enhanced chemical stability of CH3 NH3 PbI3 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 CH3 NH3 PbI3 films exhibited >140-fold stability improvement over pristine CH3 NH3 PbI3 films. As the PbSe-doped CH3 NH3 PbI3 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.
               
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