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 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.
Original language | American English |
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Article number | 1800973 |
Number of pages | 6 |
Journal | Advanced Materials |
Volume | 30 |
Issue number | 34 |
DOIs | |
State | Published - 2018 |
Bibliographical note
Publisher Copyright:© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
NREL Publication Number
- NREL/JA-5900-71096
Keywords
- Chemical doping
- Iodine diffusion
- Moisture stability
- Perovskite solar cells