Journal
CHEMISTRY OF MATERIALS
Volume 32, Issue 6, Pages 2501-2507Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.9b05101
Keywords
-
Funding
- Office of Naval Research [N00014-17-1-2727]
- Defense Threat Reduction Agency [HDTRA1-14-10030]
Ask authors/readers for more resources
Halide perovskite solar cells have achieved unprecedented progress in efficiency and high-throughput module manufacturing; however, the stability of perovskite devices remains to be a major obstacle for their commercialization. Among various instability sources in perovskite solar cells, methylammonium (MA) has been identified to limit the thermal stability of perovskites with different band gaps. Formamidinium (FA) ions are frequently used to partially or fully replace MA ions for improved stability. Here, we show that FA ions can be less stable in precursor solution than MA ions. The -CH=NH double bonds of FA ions gradually converted into -CH=O under light in solution despite the fact that this reaction is not obvious in the solid state. The generation of -CH=O is confirmed by the FTIR measurements. FA ions containing perovskite solution stored in the dark shows comparable device efficiency with a fresh perovskite solution, while light soaking of FA-containing perovskite solution greatly impairs the device efficiency, confirming the light-induced FA degradation. This study highlights the importance of precursor solution stability and arouses the attention to avoid illumination during device fabrication.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available