Abstract
Metal halide perovskite absorbers with wide bandgaps (1.6-1.7 eV) that are suitable for tandem devices typically require high Br concentrations; this renders the material prone to halide segregation and degradation. Inorganic, bromine-free CsPbI3 has a wide bandgap of 1.7 eV and does not suffer from halide segregation; however, these active layers are not stable at room temperature. Here, we report a method to create stable tetragonal perovskites with a bandgap near 1.7 eV: we add small amounts of large A-site cations having ionic radii between 272 and 278 pm - dimethylammonium (DMA) and guanidinium (Gua) - into the crystal lattice. When we deploy perovskites using mixed Cs and these large organic cations, we achieve stable, wide bandgap perovskites with power conversion efficiencies of 15.2% and VOC of 1.19 V. This study extends materials selection for wide bandgap Cs-based perovskites.
Original language | English (US) |
---|---|
Pages (from-to) | 869-872 |
Number of pages | 4 |
Journal | ACS Materials Letters |
Volume | 2 |
Issue number | 7 |
DOIs | |
State | Published - Jul 6 2020 |
Funding
This work was supported by Ontario Research Fund-Research Excellence program (ORF7-Ministry of Research and Innovation, Ontario Research Fund-Research Excellence Round 7) and US Department of the Navy, Office of Naval Research (Grant Award No. N00014-17-1-2524).
ASJC Scopus subject areas
- General Chemical Engineering
- Biomedical Engineering
- General Materials Science