Effect of halide-mixing on tolerance factor and charge-carrier dynamics in (CH3NH3PbBr3−xClx) perovskites powders
This work demonstrates a route to making mixed halide perovskite powders at room temperature by the anti-solvent-assisted crystallization method. Although, mixed halide CH 3 NH 3 PbBr 3− x Cl x perovskites have been prepared by different methods, however , to the best of our knowledge the anti-solve...
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Veröffentlicht in: | Journal of materials science. Materials in electronics 2020-11, Vol.31 (21), p.19415-19428 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This work demonstrates a route to making mixed halide perovskite powders at room temperature by the anti-solvent-assisted crystallization method. Although, mixed halide CH
3
NH
3
PbBr
3−
x
Cl
x
perovskites have been prepared by different methods, however
,
to the best of our knowledge the anti-solvent-assisted crystallization method is employed here for the first time to prepare mixed halide CH
3
NH
3
PbBr
3−
x
Cl
x
perovskite powders. Solution-processed methyl ammonium lead tribromide CH
3
NH
3
PbBr
3
(
x
= 0) and different amounts of chloride (Cl) containing mixed halide perovskites (CH
3
NH
3
PbBr
3−
x
Cl
x
) were prepared for compositions of
x
= 0.5, 1, 1.25, 1.75. It reveals that bulk CH
3
NH
3
PbBr
3−
x
Cl
x
samples are highly crystalline and exists in pure single cubic phase with an increased tolerance factor as compared to pure CH
3
NH
3
PbBr
3
. The CH
3
NH
3
PbBr
3
perovskite has space-group
Pm
-3
m
and a cell parameter of 5.930 Å (volume = 206 Å). The synthesis route adopted here gives access to hybrid perovskites powders with high Cl content and hence enables the band gap to be precisely tuned over a range from 2.26 to 2.49 eV. The powder samples display the subtle shifts in the emission spectra and the photoluminescence kinetics exhibits a decrease in average lifetime by increasing the Cl contents due to the presence of trap states in the structures that encourage non-radiative recombination of charge carrier. Conventionally, the CH
3
NH
3
PbBr
3
-based inverted solar cell architecture is prepared via mixing of the CH
3
NH
3
Br and PbBr
2
precursors. In contrast, herein, the precursor solutions are directly prepared from the CH
3
NH
3
PbBr
3
powder and the active layer of the inverted perovskite solar cells are then spin coated using this solution. The high
V
oc
value of the fabricated solar cells potentially makes it a promising candidate for tandem photovoltaic, photocatalytic water splitting, and semi-transparent photovoltaic applications. |
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ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-020-04475-4 |