卤化物
原位
兴奋剂
钙钛矿(结构)
材料科学
光电子学
铅(地质)
纳米技术
化学
结晶学
无机化学
地貌学
地质学
有机化学
作者
Sishen Xie,Yongrun Dong,Changsheng Wang,Wen Li,Hao Hu,Jinkun Xue,Zequan Li,Wei Gao,Bingsuo Zou
标识
DOI:10.1002/admt.202501431
摘要
Abstract In situ fabrication techniques enable the synthesis of non‐lead double perovskite halide composite optical films (COFs) with excellent optical properties at low temperatures via simple processes. However, most studies are based on rigid polymers as matrices, and there is a lack of exploration on narrow‐band emission COFs. This study proposes an improved in situ growth strategy, successfully synthesizing Sb 3 ⁺‐doped Cs 2 KTbCl 6 lead‐free double perovskite halide COFs within a self‐healing polyurethane (ISSPU) matrix featuring synergistic dynamic disulfide bonds and high‐density hydrogen bonds. These films achieving narrow‐band emission with a full width at half maximum (FWHM) of 7.54 nm and a maximum photoluminescence quantum yield (PLQY) of 27.08%, also exhibits excellent tensile strength (31.13 MPa), fracture elongation (987%), and cyclic tensile stability, along with thermal‐induced self‐healing capability. Leveraging the excellent narrow‐band green luminescence and self‐healing properties of the COFs, this material demonstrates significant application potential in optical anti‐counterfeiting and flexible wearable devices.
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