螺吡喃
材料科学
发光
光致变色
掺杂剂
纳米技术
三吡啶
光催化
聚合物
镧系元素
光化学
光电子学
兴奋剂
金属
有机化学
化学
复合材料
离子
冶金
催化作用
作者
Di Zhao,Lei Guo,Huanrong Li,Chunmei Yue,Bing Han,Kai Liu,Huanrong Li
标识
DOI:10.1002/adma.202405164
摘要
Abstract Photoluminescent metallopolymers displaying photo‐stimuli‐responsive properties are emerging as promising materials with versatile applications in photo‐rewritable patterns, wearable UV sensors, and optical encryption anti‐counterfeiting. However, integrating these materials into practical applications that require fast response times, lightweight qualities, fatigue resistance, and multiple encryption capabilities poses challenges. In this study, luminescent photochromic lanthanide (Ln) metallopolymers with rapid self‐healing properties are developed by cross‐linking terpyridine (Tpy)‐ and spiropyran (SP)‐ functionalized polyurethane chains through Ln‐Tpy coordination bonds and H‐bonds among polymer chains. The resulting products exhibit a range of intriguing features: i) photo‐stimuli responsiveness using spiropyran monomers without additional dopants; ii) dual‐emitting performance under UV‐light due to Ln‐Tpy and open‐ring spiropyran moieties; iii) satisfactory mechanical properties and self‐healing abilities from polymer chains; iv) multiple control switches for luminescence colors through photostimulation or feed ratio adjustments. Leveraging these attributes, the developed material introduces novel opportunities for light‐writing applications, advanced information encryption, UV‐sensing wearable devices, and insights into designing multifunctional intelligent materials for the future.
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