Abstract
UV–visible broadband light harvesting ability is critical for photodetectors, and all inorganic perovskite CsPbBr3 is regarded as a promising candidate as the response active material. Herein, a saturated-solution crystallization method is employed to synthesize CsPbBr3 single crystal. Temperature-dependent photoluminescence spectra with one-photon and two-photon excitation are systematically investigated, determining a large exciton binding energy of 39.8 meV. This allows the stable excitonic emission of CsPbBr3 single crystal at room temperature. Subsequently, an asymmetric structure CsPbBr3 photodetector is fabricated by using InGa alloy as the Ohmic electrode and Au as the Schottky electrode. At -8 V, the device exhibits a prominent response to the irradiation from UV to green band with a maximum responsivity of 2.56 A/W, an external quantum efficiency of 580 %, and a detectivity of 1.24 × 1013 Hz1/2 W−1. In addition, the CsPbBr3 photodetector also presents rapid response speeds at both reverse and forward bias voltages and self-powered characteristics owing to the Schottky depletion layer underneath the Au electrode. The demonstration of asymmetric metal-semiconductor-metal (MSM) structure photodetector presents a promising pathway toward next-generation CsPbBr3 optoelectronic devices.
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