Spatially resolved studies of the phases and morphology of methylammonium and formamidinium lead tri-halide perovskites
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GALKOWSKI , Krzysztof, MITIOGLU, Anatolie, SURRENTE, Alessandro, YANG, Zhuo, MAUDE, Duncan Kennedy, KOSSACKI, Piotr, EPERON , Giles E., WANG, Jacob Tse Wei, SNAITH, Henry James, PŁOCHOCKA, Paulina, NICHOLAS, Robin John. Spatially resolved studies of the phases and morphology of methylammonium and formamidinium lead tri-halide perovskites. In: Nanoscale, 2017, nr. 9(9), pp. 3222-3230. ISSN 2040-3364. DOI: https://doi.org/10.1039/c7nr00355b
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Nanoscale
Numărul 9(9) / 2017 / ISSN 2040-3364 /ISSNe 2040-3372

Spatially resolved studies of the phases and morphology of methylammonium and formamidinium lead tri-halide perovskites

DOI:https://doi.org/10.1039/c7nr00355b

Pag. 3222-3230

Galkowski Krzysztof1, Mitioglu Anatolie1, Surrente Alessandro1, Yang Zhuo1, Maude Duncan Kennedy1, Kossacki Piotr2, Eperon Giles E.3, Wang Jacob Tse Wei3, Snaith Henry James3, Płochocka Paulina1, Nicholas Robin John3
 
1 LNCMI, CNRS-UJF-UPS-INSA, Grenoble and Toulouse,
2 Warsaw University,
3 University of Oxford
 
 
Disponibil în IBN: 19 martie 2022


Rezumat

The family of organic-inorganic tri-halide perovskites including MA (MethylAmmonium)PbI3, MAPbI3-xClx, FA (FormAmidinium)PbI3 and FAPbBr3 are having a tremendous impact on the field of photovoltaic cells due to the combination of their ease of deposition and high energy conversion efficiencies. Device performance, however, is known to be still significantly affected by the presence of inhomogeneities. Here we report on a study of temperature dependent micro-photoluminescence which shows a strong spatial inhomogeneity related to the presence of microcrystalline grains, which can be both bright and dark. In all of the tri-iodide based materials there is evidence that the tetragonal to orthorhombic phase transition observed around 160 K does not occur uniformly across the sample with domain formation related to the underlying microcrystallite grains, some of which remain in the high temperature, tetragonal, phase even at very low temperatures. At low temperature the tetragonal domains can be significantly influenced by local defects in the layers or the introduction of residual levels of chlorine in mixed halide layers or dopant atoms such as aluminium. We see that improvements in room temperature energy conversion efficiency appear to be directly related to reductions in the proportions of the layer which remain in the tetragonal phase at low temperature. In FAPbBr3 a more macroscopic domain structure is observed with large numbers of grains forming phase correlated regions.

Cuvinte-cheie
energy conversion, perovskite, Photoelectrochemical cells, photovoltaic cells, temperature