Lattice-Gradient Perovskite KTaO<sub>3</sub> Films for an Ultrastable and Low-Dose X-Ray Detector.
basic_science · Level V
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- Record sourced from PubMed, PMID 37796177.
- Also identified by DOI 10.1002/adma.202211026.
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Abstract
Conventional indirect X-ray detectors employ scintillating phosphors to convert X-ray photons into photodiode-detectable visible photons, leading to low conversion efficiencies, low spatial resolutions, and optical crosstalk. Consequently, X-ray detectors that directly convert photons into electric signals have long been desired for high-performance medical imaging and industrial inspection. Although emerging hybrid inorganic-organic halide perovskites, such as CH<sub>3</sub> NH<sub>3</sub> PbI<sub>3</sub> and CH<sub>3</sub> NH<sub>3</sub> PbBr<sub>3</sub> , exhibit high sensitivity, they have salient drawbacks including structural instability, ion motion, and the use of toxic Pb. Here, this work reports an ultrastable, low-dose X-ray detector comprising KTaO<sub>3</sub> perovskite films epitaxially grown on a Nb-doped strontium titanate substrate using a low-cost solution method. The detector exhibits a stable photocurrent under high-dose irradiation, high-temperature (200 °C), and aqueous conditions. Moreover, the prototype KTaO<sub>3</sub> -film-based detector exhibits a 150-fold higher sensitivity (3150 µC Gy<sub>air</sub> <sup>-1</sup> cm<sup>-2</sup> ) and 150-fold lower detection limit (<40 nGy<sub>air</sub> s<sup>-1</sup> ) than those of commercial α-Se-based direct detectors. Systematic investigations reveal that the high stability of the detector originates from the strong covalent bonds within the KTaO<sub>3</sub> film, whereas the low detection limit is due to a lattice-gradient-driven built-in electric field and the high insulating property of KTaO<sub>3</sub> film. This study unveils a new path toward the fabrication of green, stable, and low-dose X-ray detectors using oxide perovskite films, which have significant application potential in medical imaging and security operations.