High charge carrier mobility in CsPbBr3 single crystals investigated by Time of Flight technique
Anastasiia Sakahtska a b, Kostiantyn Sakhatskyi a b, Andrii Kanak a b, Gebhard Matt a b, Sergii Yakunin a b, Maksym Kovalenko a b
a Laboratory of Inorganic Chemistry, Department of Chemistry and Applied Biosciences, ETH Zürich, Switzerland; Laboratory for Transport at Nanoscale Interfaces, Empa – Swiss Federal Laboratories for Materials Science and Technology, CH-8600 Dübendorf, Switzerland
b Laboratory for Thin Films and Photovoltaics, Empa – Swiss Federal Laboratories for Materials Sci-ence and Technology, Überlandstrasse 129, CH-8600 Dübendorf, Switzerland
Proceedings of Asia-Pacific Conference on Perovskite, Organic Photovoltaics&Optoelectronics (IPEROP25)
Kyoto, Japan, 2025 January 19th - 21st
Organizers: Atsushi Wakamiya and Hideo Ohkita
Oral, Anastasiia Sakahtska, presentation 040
Publication date: 4th October 2024

CsPbBr3 single crystal X-ray and gamma-ray detectors match state-of-the-art performance with a few exceptions, particularly the detection speed is insufficient for photon counting medical imaging. The slow perovskite response is intrinsically limited by the low charge carrier mobility (µ), reported in CsPbBr3 to be 10-30 times smaller than that of CdTe. By using Time of Flight (ToF) technique with alternative voltage biasing (AC) mode CsPbBr3 crystals grown by the modified Bridgman method demonstrated two component hole mobility with median high mobility of 300 cm2V-1s-1 (while the best achieved - 520 cm2V-1s-1) and low mobility of 30 cm2V-1s-1. The fast component is quenched due to ionic migration and the reaction of the Bi electrode with Br- ions, while applying DC bias mode, commonly used in perovskite hard radiation detectors. Additionally, we examine the influence of temperature on charge carrier mobility. The reported mobility is the highest among lead-based perovskites and shows promise for applications with fast response requirements.

 

The work was financially supported by the Swiss Innovation Agency (Innosuisse) under grant agreement 46894.1 IP-ENG and by ETH Zürich through the ETH + Project SynMatLab: Laboratory for Multiscale Materials Synthesis.

 

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