Hybrid halide perovskites recently emerged as promising
semiconductor
materials for high-mobility field-effect transistors and detectors
due to their unique optoelectronic properties. However, iontronics
in these materials play a significant role in charge carrier dynamics.
In addition, the impact of grain boundaries and trap density on the
dielectric properties and the alternate current (AC) ionic conductivity
has been one of the most debated topics. In this work, we have studied
the electro-ionic dynamics in perovskite single crystals (SCs) using
temperature-dependent impedance spectroscopy and the transient photovoltage
(TPV) technique. The device capacitances are temperature-independent,
revealing that the temperature is only accelerating the migration
of ions (MA+ and Br–) but not increasing
the number of ion migrations in single crystals. Moreover, the ions
in perovskite single crystals are not trapped at the grain boundaries,
and hence all of the ions participate in the conduction; this leads
to a higher increase in conductivity resulting in the super-linear
power law (SPL) region at a higher frequency. Furthermore, TPV measurements
also confirmed the temperature independence recombination lifetime
in these materials. The maximum values of responsivity (R), detectivity (D), and external quantum efficiency
(EQE) are 12.35 mA/W, 5.89 × 109 Jones, and 38.8%,
respectively. This work will be beneficial for understanding charge
carrier dynamics in single-crystal field-effect transistors (FETs)
and detectors.