Wei Zheng, Han Liu, Xiaoyu Liu, Ruirui Shi, Xinyi Han, Xiaojia Wang, Teng Long, Yuhai Zhang, Hua Wang, William W. Yu, Chuanjian Zhou
{"title":"通过在过氧化物纳米晶-聚甲基三氟丙基硅氧烷之间采用相互促进策略实现超稳定 X 射线成像","authors":"Wei Zheng, Han Liu, Xiaoyu Liu, Ruirui Shi, Xinyi Han, Xiaojia Wang, Teng Long, Yuhai Zhang, Hua Wang, William W. Yu, Chuanjian Zhou","doi":"10.1002/adfm.202418944","DOIUrl":null,"url":null,"abstract":"The instability of halide perovskite nanocrystals (PNCs) and related composite polymer films posed considerable challenges for application in flexible optoelectronic devices. Herein, perovskite nanocrystal-polymethyltrifluoropropylsiloxane (PNCs-PMFS) composites are developed that exhibit outstanding optical stability and irradiation resistance through a mutually reinforcing strategy. The photoluminescence (PL) intensity of PNCs-PMFS remained stable after four heating cycles, whereas perovskite nanocrystal-polydimethylsiloxane (PNCs-PDMS) composites exhibited a 31% decrease in PL intensity. Moreover, PNCs-PMFS demonstrated superior luminescence stability under UV and X-ray irradiation due to strong ion-dipole interactions between PNCs and trifluoromethyl (CF<sub>3</sub>) dipoles. Under γ-ray irradiation (300 kGy), PNCs-PMFS retained 73% (2.86 MPa) of the initial mechanical strength, while PMFS without PNCs retained only 51%. This enhancement is attributed to the effective reduction of free radical concentration in the system by PNCs, as confirmed by electron spin resonance (ESR) and curing curve. Density-functional theory (DFT) calculations further indicated that PNCs adsorbed free radicals, thereby facilitating interfacial charge transfer and forming a stable resonance structure. These advancements enabled PNCs-PMFS to serve as scintillation screens for X-ray detection and imaging, achieving a spatial resolution of 19.0 lp mm<sup>−1</sup> and a detection limit of 3.78 µGy s<sup>−1</sup>, offering novel insights for designing of X-ray detectors in high-energy radiation environments.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"32 1","pages":""},"PeriodicalIF":18.5000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ultra Stable X-Ray Imaging Through a Mutually Reinforcing Strategy Between Perovskite Nanocrystal-Polymethyltrifluoropropylsiloxane\",\"authors\":\"Wei Zheng, Han Liu, Xiaoyu Liu, Ruirui Shi, Xinyi Han, Xiaojia Wang, Teng Long, Yuhai Zhang, Hua Wang, William W. 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Under γ-ray irradiation (300 kGy), PNCs-PMFS retained 73% (2.86 MPa) of the initial mechanical strength, while PMFS without PNCs retained only 51%. This enhancement is attributed to the effective reduction of free radical concentration in the system by PNCs, as confirmed by electron spin resonance (ESR) and curing curve. Density-functional theory (DFT) calculations further indicated that PNCs adsorbed free radicals, thereby facilitating interfacial charge transfer and forming a stable resonance structure. 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Ultra Stable X-Ray Imaging Through a Mutually Reinforcing Strategy Between Perovskite Nanocrystal-Polymethyltrifluoropropylsiloxane
The instability of halide perovskite nanocrystals (PNCs) and related composite polymer films posed considerable challenges for application in flexible optoelectronic devices. Herein, perovskite nanocrystal-polymethyltrifluoropropylsiloxane (PNCs-PMFS) composites are developed that exhibit outstanding optical stability and irradiation resistance through a mutually reinforcing strategy. The photoluminescence (PL) intensity of PNCs-PMFS remained stable after four heating cycles, whereas perovskite nanocrystal-polydimethylsiloxane (PNCs-PDMS) composites exhibited a 31% decrease in PL intensity. Moreover, PNCs-PMFS demonstrated superior luminescence stability under UV and X-ray irradiation due to strong ion-dipole interactions between PNCs and trifluoromethyl (CF3) dipoles. Under γ-ray irradiation (300 kGy), PNCs-PMFS retained 73% (2.86 MPa) of the initial mechanical strength, while PMFS without PNCs retained only 51%. This enhancement is attributed to the effective reduction of free radical concentration in the system by PNCs, as confirmed by electron spin resonance (ESR) and curing curve. Density-functional theory (DFT) calculations further indicated that PNCs adsorbed free radicals, thereby facilitating interfacial charge transfer and forming a stable resonance structure. These advancements enabled PNCs-PMFS to serve as scintillation screens for X-ray detection and imaging, achieving a spatial resolution of 19.0 lp mm−1 and a detection limit of 3.78 µGy s−1, offering novel insights for designing of X-ray detectors in high-energy radiation environments.
期刊介绍:
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