Despite the high performance of lead-halide perovskite-based X-ray detectors, the toxicity and instability of lead require the development of lead-free perovskites for X-ray detection applications. Here, we demonstrate lead-free and environmentally friendly, all-inorganic millimeter-sized Cs2AgBiCl6 double perovskite single crystal (SC) for X-ray detection and imaging. The high dark resistivity (3.1 × 1010 Ω cm), high carrier mobility-lifetime product (5.36 × 10–4 cm2 V–1), and lower trap density (1.18 × 109 cm–3) in these double perovskite SCs render them a potential material for X-ray detection. The fabricated vertical structured X-ray detector exhibits a sensitivity of 325.78 μC Gy air–1 cm–2 and a limit of detection of 241 nGy s–1. Additionally, the Cs2AgBiCl6 SCs exhibit self-powered X-ray detection at zero bias with a sensitivity of 7 μC Gy air–1 cm–2. Moreover, the fabricated perovskite X-ray detector exhibits a stable and robust performance under continuous X-ray irradiation and long-term ambient storage. Further, we demonstrated the imaging capability of the Cs2AgBiCl6 X-ray detector using a metal test object and obtained a distortion-free image. Our findings demonstrate that the Cs2AgBiCl6 single crystal-based X-ray detectors have great potential as practical X-ray detectors and imaging for medical radiography.
In this work, we report, the synthesis of Boron and Sulfur co-doped graphene quantum dots (BS-GQDs) and its applicability as a label-free fluorescence sensing probe for the highly sensitive and selective detection of dopamine (DA). Upon addition of DA, the fluorescence intensity of BS-GQDs were effectively quenched over a wide concentration range of DA (0–340 μM) with an ultra-low detection limit of 3.6 μM. The quenching mechanism involved photoinduced electron transfer process from BS-GQDs to dopamine-quinone, produced by the oxidization of DA under alkaline conditions. The proposed sensing mechanism was probed using a detailed study of UV–Vis absorbance, steady state and time resolved fluorescence spectroscopy. The high selectivity of the fluorescent sensor towards DA is established. Our study opens up the possibility of designing a low-cost biosensor which will be suitable for detecting DA in real samples.
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