Effect of Co-Solvents on the Crystallization and Phase Distribution of Mixed-Dimensional Perovskites

Alessandro Caiazzo, Kunal Datta, Junke Jiang, María C. Gélvez-Rueda, Junyu Li, Riccardo Ollearo, J.M. Vicent-Luna, Shuxia Tao, Ferdinand C. Grozema, Martijn M. Wienk, René A.J. Janssen (Corresponding author)

Onderzoeksoutput: Bijdrage aan tijdschriftTijdschriftartikelAcademicpeer review

Samenvatting

Solution-processed quasi-2D perovskites are promising for stable and efficient solar cells because of their superior environmental stability compared to 3D perovskites and tunable optoelectronic properties. Changing the number of inorganic layers (n) sandwiched between the organic spacers allows for tuning of the bandgap. However, narrowing the phase distribution around a specific n-value is a challenge. In-situ UV–vis–NIR absorption spectroscopy is used to time-resolve the crystallization dynamics of quasi-2D butylammonium-based (BA) perovskites with <n> = 4, processed from N,N-dimethylformamide (DMF) in the presence of different co-solvents. By combining with photoluminescence, transient absorption, and grazing-incidence wide-angle X-ray scattering, the crystallization is correlated to the distribution of phases with different n-values. Infrared spectroscopy and density functional theory reveal that the phase distribution correlates with perovskite precursor—co-solvent interaction energies and that stronger interactions shift the phase distribution towards smaller n-values. Careful tuning of the solvent/co-solvent ratio provides a more homogeneous phase distribution, with highly oriented perovskite crystals and suppressed formation of n = 1–2 phases, providing a power conversion efficiency for BA2MA3Pb4I13 solar cells that increases from 3.5% when processed from DMF to over 11% and 10% when processed from DMF/dimethyl sulfoxide and DMF/N-methyl-2-pyrrolidone mixtures, respectively.
Originele taal-2Engels
Artikelnummer2102144
Aantal pagina's12
TijdschriftAdvanced Energy Materials
Volume11
Nummer van het tijdschrift42
Vroegere onlinedatum5 okt 2021
DOI's
StatusGepubliceerd - 11 nov 2021

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