摘要
Halide perovskites have emerged as highly promising materials for light absorption and emission, with significant potential in photovoltaics and optoelectronics. However, unintentional self-doping in solution-processed lead halide perovskite single crystals often degrades photodetector performance. In this study, we present an innovative precursor engineering approach aimed at controlling the self-doping characteristics of perovskite materials by optimizing the stoichiometry of the precursors. By precisely adjusting the PbCl2/MACl (MA = CH3NH3+) ratio, we achieved remarkable enhancements in MAPbCl3 single crystal performance. The crystal with a PbCl2/MACl molar ratio of 0.85 exhibited exceptional properties, including a high resistivity (2.7 × 108 Ω cm), outstanding carrier mobility (116.1 cm2 V−1 s−1), and ultralow trap state density (9.03 × 108 cm−3). Additionally, the fabricated MAPbCl3 single crystal ultraviolet photodetector (vertical architecture) demonstrated a high responsivity of 105 mA W−1 at 365 nm, with ultrafast response speed (rise time: 38.2 μs, fall time: 61.4 μs), surpassing all previously reported MAPbCl3 single crystal-based devices. These results highlight the superior quality of the optimized crystals, demonstrating their potential for use in high-performance optoelectronics and advancing perovskite integration into next-generation photonic and electronic technologies.
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