Low-dimensional metal halides, which possess efficient luminescent properties, have garnered significant interest in the fields of optoelectronics and radiation detection. This study introduces novel lead-free silver-based metal halide material, CsAgCl 2 microcrystals (MCs). These MCs have a one-dimensional atomic chain structure and a unique [AgCl 5 ] 4- tetragonal shared triangular configuration. CsAgCl 2 MCs exhibit excellent performance as X-ray scintillators due to their bright broadband yellow emission and fast decay time in the microsecond range. The large Stokes shift of 350 nm is produced by self-trapped exciton emission. In X-ray scintillation applications, CsAgCl 2 MCs demonstrate a high light yield of 13280 photons/MeV and a wide range of linear scintillation response. It is noteworthy that the CsAgCl 2 MCs maintain good stability under both atmospheric conditions and continuous X-ray irradiation. The sample was used in an X-ray imaging screen, which clearly presented the X-ray projection image of a wooden stick. As a result, this research not only contributes to the collection of lead-free metal halide scintillators but also indicates that CsAgCl 2 MCs have a wide range of future applications and potential in areas such as medical imaging, scientific research, and diagnostic and detection technologies.
Low-dimensional organic–inorganic metal halides, especially lead-free perovskites, are attracting increasing attention because of their environmentally friendly processing, flexible structures, chemical stability, and promising nonlinear optical properties. Herein, we report a new stable polar 0D lead-free hybrid bismuth chloride to enable the second-harmonic generation (SHG) active material (BTA)3Bi2Cl9 (BTA = benzyltriethylammonium, C6H5CH2N(C2H5)3+) that was obtained by the antisolvent vapor diffusion method and crystallized in the polar Cc space group. Its structure features organic cations surrounded by face-sharing [Bi2Cl9]3− dimers. (BTA)3Bi2Cl9 exhibits a wide direct bandgap (3.21 eV) and a strong phase-matchable SHG conversion efficiency (1.39 × KDP). Theoretical calculation reveals that the SHG response is owing to the synergistic effect of distorted inorganic [Bi2Cl9]3− anions and polar organic BTA+ cations. This work not only enriches the family of organic–inorganic A3M2X9 (A = monovalent cations; M = trivalent metal ions; and X = halide ions) NLO crystals but also provides the possibilities for further designing novel lead-free semiconducting piezoelectric, pyroelectric and ferroelectric materials.
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