Abstract
1,4-butanediamine (BEA) is incorporated into FASnI3 (FA=formamidinium) to develop a series of lead-free low-dimensional Dion–Jacobson-phase perovskites, (BEA)FAn−1SnnI3n+1. The broadness of the (BEA)FA2Sn3I10 band gap appears to be influenced by the structural distortion owing to high symmetry. The introduction of BEA ligand stabilizes the low-dimensional perovskite structure (formation energy ca. 106 j mol−1), which inhibits the oxidation of Sn2+. The compact (BEA)FA2Sn3I10 dominated film enables a weakened carrier localization mechanism with a charge transfer time of only 0.36 ps among the quantum wells, resulting in a carrier diffusion length over 450 nm for electrons and 340 nm for holes, respectively. Solar cell fabrication with (BEA)FA2Sn3I10 delivers a power conversion efficiency (PCE) of 6.43 % with negligible hysteresis. The devices can retain over 90 % of their initial PCE after 1000 h without encapsulation under N2 environment.
| Original language | English |
|---|---|
| Pages (from-to) | 6909-6914 |
| Number of pages | 6 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 59 |
| Issue number | 17 |
| DOIs | |
| State | Published - 20 Apr 2020 |
| Externally published | Yes |
Keywords
- Dion–Jacobson phase
- charge transfer
- lead-free perovskites
- low-dimensional perovskites
- solar cells