Band-Like Charge Transport in Cs2AgBiBr6 and Mixed Antimony-Bismuth Cs2AgBi1- xSbxBr6 Halide Double Perovskites

Journal Article (2018)
Author(s)

Eline M. Hutter (TU Delft - ChemE/Opto-electronic Materials, Stanford University)

Mariá C. Gélvez-Rueda (TU Delft - ChemE/Opto-electronic Materials)

D. Bartesaghi (TU Delft - ChemE/Opto-electronic Materials)

Ferdinand C. Grozema (TU Delft - ChemE/Opto-electronic Materials)

T.J. Savenije (TU Delft - ChemE/Opto-electronic Materials)

Research Group
ChemE/Opto-electronic Materials
Copyright
© 2018 E.M. Hutter, M.C. Gelvez Rueda, D. Bartesaghi, F.C. Grozema, T.J. Savenije
DOI related publication
https://doi.org/10.1021/acsomega.8b01705
More Info
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Publication Year
2018
Language
English
Copyright
© 2018 E.M. Hutter, M.C. Gelvez Rueda, D. Bartesaghi, F.C. Grozema, T.J. Savenije
Research Group
ChemE/Opto-electronic Materials
Issue number
9
Volume number
3
Pages (from-to)
11655-11662
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Abstract

Recently, halide double perovskites (HDPs), such as Cs2AgBiBr6, have been reported as promising nontoxic alternatives to lead halide perovskites. However, it remains unclear whether the charge-transport properties of these materials are as favorable as for lead-based perovskites. In this work, we study the mobilities of charges in Cs2AgBiBr6 and in mixed antimony-bismuth Cs2AgBi1-xSbxBr6, in which the band gap is tunable from 2.0 to 1.6 eV. Using temperature-dependent time-resolved microwave conductivity techniques, we find that the mobility is proportional to T-p (with p ≈ 1.5). Importantly, this indicates that phonon scattering is the dominant scattering mechanism determining the charge carrier mobility in these HDPs similar to the state-of-the-art lead-based perovskites. Finally, we show that wet chemical processing of Cs2AgBi1-xSbxBr6 powders is a successful route to prepare thin films of these materials, which paves the way toward photovoltaic devices based on nontoxic HDPs with tunable band gaps.