Advanced partial nucleation for single-phase FA0.92MA0.08PbI3-based high-efficiency perovskite solar cells
To date, extensive research has been carried out, with considerable success, on the development of high-performance perovskite solar cells (PSCs). Owing to its wide absorption range and remarkable thermal stability, the mixed-cation perovskite FA x MA 1− x PbI 3 (formamidinium/methylammonium lead io...
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Veröffentlicht in: | Science China materials 2019-12, Vol.62 (12), p.1846-1856 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | To date, extensive research has been carried out, with considerable success, on the development of high-performance perovskite solar cells (PSCs). Owing to its wide absorption range and remarkable thermal stability, the mixed-cation perovskite FA
x
MA
1−
x
PbI
3
(formamidinium/methylammonium lead iodide) promises high performance. However, the ratio of the mixed cations in the perovskite film has proved difficult to control with precursor solution. In addition, the FA
x
MA
1−
x
PbI
3
films contain a high percentage of MA
+
and suffer from serious phase separation and high trap states, resulting in inferior photovoltaic performance. In this study, to suppress phase separation, a post-processing method was developed to partially nucleate before annealing, by treating the as-prepared intermediate phase FAI-PbI
2
-DMSO (DMSO: dimethylsulfoxide) with mixed FAI/MAI solution. It was found that in the final perovskite, FA
0.92
MA
0.08
PbI
3
, defects were substantially reduced because the analogous molecular structure initiated ion exchange in the post-processed thin perovskite films, which advanced partial nucleation. As a result, the increased light harvesting and reduced trap states contributed to the enhancement of open-circuit voltage and short-circuit current. The PSCs produced by the post-processing method presented reliable reproducibility, with a maximum power conversion efficiency of 20.80% and a degradation of ∼30% for 80 days in standard atmospheric conditions. |
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ISSN: | 2095-8226 2199-4501 |
DOI: | 10.1007/s40843-019-1186-4 |