Enhanced yield-mobility products in hybrid halide Ruddlesden-Popper compounds with aromatic ammonium spacers.

Dalton Trans

Materials Department, University of California, Santa Barbara, California 93106, USA. and Materials Research Laboratory, University of California, Santa Barbara, California 93106, USA and Department of Chemistry and Biochemistry, University of California, Santa Barbara, California 93106, USA.

Published: October 2019

Hybrid halide Ruddlesden-Popper compounds are related to three-dimensional hybrid AMX perovskites (e.g. where A is a monovalent cation, M is a divalent metal cation, and X is a halogen) with the general formula LAMX where L is a monovalent spacer cation. The crystal structure comprises perovskite-like layers separated by organic cation spacers. Here two Ruddlesden-Popper compounds with a conjugated cation, 2-(4-biphenyl)ethylammonium (BPEA) prepared by solvothermal and solvent evaporation techniques are reported. The structures of the two compounds: (BPEA)PbI and (BPEA)(CHNH)PbI, were solved by X-ray crystallography. The aromatic rings of the BPEA groups are well-separated in the organic layers leading to optical properties comparable to n = 1 and 2 hybrid halide Ruddlesden-Popper compounds with simpler alkyl ammonium cations. The ambient stability of both compounds over time was also confirmed by powder X-ray diffraction. Finally, the transient photoconductance, measured by time-resolved microwave conductivity, show that the compounds have maximum yield-mobility products respectively of 0.07 cm V s and 1.11 cm V s for (BPEA)PbI and (BPEA)(CHNH)PbI, both slightly enhanced over what has been measured for compounds with n-butylammonium spacer cations.

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http://dx.doi.org/10.1039/c9dt03074cDOI Listing

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