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首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Photoluminescence developed from polystyrene and CdS/polystyrene nanocomposite films in picosecond time range by repetitional irradiation of excitation femtosecond pulses in PL up conversion measurements
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Photoluminescence developed from polystyrene and CdS/polystyrene nanocomposite films in picosecond time range by repetitional irradiation of excitation femtosecond pulses in PL up conversion measurements

机译:在PL上转换测量中,通过重复照射激发飞秒脉冲,在皮秒级时间范围内从聚苯乙烯和CdS /聚苯乙烯纳米复合材料薄膜产生的光致发光

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A CdS/SPS nanocomposite film in which CdS nanoparticles were embedded into partially sulfonated polystyrene (SPS) was synthesized and its subpicosecond time resolved photoluminescence (photoluminescence up conversion: PL Up-C) measurements were carried out. A similar measurement was also done for pure SPS and polystyrene (PS) films that were used as the matrix. For a CdS/SPS, PL Up-C signals (sum frequency signal; SFS) were observed at the first measurement. They were also observed for pure SPS and PS films by repetitional measurements though they were not observed at the first measurement. It seems that the development of SFS for SPS and PS films is due to relatively stable luminescent substances formed from themselves by exposing them to intense femtosecond laser pulse (for excitation) during the measurements. The SFS development process was also readily observed for a CdS/SPS film by reducing excitation pulse intensity in the measurements. Therefore, PL that was observed for a CdS/SPS film is also mainly due to luminescent substances formed from the SPS matrix but CdS nanoparticles. CdS nanoparticles embedded into a SPS film may act as an accelerator for PL development from the SPS matrix. The origin of PL may be several luminescent substances formed by photo- or thermal-degradation of SPS via multiphoton (probably two photons) absorption of SPS itself and/or photo-excitation of CdS nanoparticles. Although the luminescent substances could not be assigned, they might be oxidative decomposition products of SPS that have long conjugated π bonds with a PS main polymer chain that absorbs the excitation femtosecond pulse (λ_(max)= 396 nm).
机译:合成了将CdS纳米颗粒嵌入部分磺化聚苯乙烯(SPS)中的CdS / SPS纳米复合膜,并进行了亚皮秒时间分辨的光致发光(光致发光上转换:PL Up-C)的测量。还对用作基质的纯SPS和聚苯乙烯(PS)膜进行了类似的测量。对于CdS / SPS,在第一次测量时观察到PL Up-C信号(和频信号; SFS)。通过重复测量也可以观察到它们是纯SPS和PS膜,尽管在第一次测量中没有观察到它们。似乎用于SPS和PS膜的SFS的开发是由于在测量过程中将它们暴露于强烈的飞秒激光脉冲(用于激发)中,从而形成了相对稳定的发光物质。通过降低测量中的激发脉冲强度,也很容易观察到CdS / SPS膜的SFS显影过程。因此,对于CdS / SPS膜观察到的PL也主要归因于由SPS基质但由CdS纳米颗粒形成的发光物质。嵌入SPS膜中的CdS纳米粒子可以充当从SPS基质中PL发育的促进剂。 PL的起源可能是通过SPS自身的多光子(可能是两个光子)吸收和/或CdS纳米粒子的光激发,通过SPS的光降解或热降解而形成的几种发光物质。尽管无法分配发光物质,但它们可能是SPS的氧化分解产物,它们与吸收飞秒飞秒脉冲(λ_(max)= 396 nm)的PS主聚合物链具有长共轭π键。

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