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Poly(styrene-b-2-(N,N-dimethylamino)ethyl methacrylate) diblock copolymers: Micellization and application in the synthesis of photoluminescent CdS nanoparticles

机译:聚(苯乙烯-b-2-(N,N-二甲基氨基)甲基丙烯酸乙酯)二嵌段共聚物:胶束化及其在光致发光CdS纳米粒子合成中的应用

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摘要

Fluorescence studies on amphiphilic diblock copolymers of styrene and 2-(N,N-dimethyIamino)ethyl methacrylate using 1,8-anilinonaphthalenesulfonate (ANS) as fluorescent probe revealed the formation of stable micelles at extremely low polymer concentrations of ~0.05%. The micellar microenvironment was characterized by an average polarity of E_T(30) = 44-48 kcal mol~(-1), similar to the moderately polar solvents, and extremely high microviscosity. Increase in hydrophilic: hydrophobic ratio of the copolymers resulted in an increase in the average polarity and decrease in microviscosity. The micelles proved to be excellent hosts for the synthesis and stabilization of photoluminescent CdS nanoparticles with a high degree of quantum confinement and broad photoluminescence, dominated by trap-state emission. Moreover, the size and size-related steady-state optical properties of CdS nanoparticles were significantly dependent on the microenvironment of the host micelle. In contrast, the photoluminescence dynamics of the nanoparticles, involving time-scales from 100 ps to 100 ns, are similar in all cases. Interestingly, the nanoparticles exhibit a large time-dependent Stokes shift, 75% of which is complete within the first ~100 ps after the excitation. The extremely rapid Stokes shift is attributed to the decay of the initially formed band-edge excitons in a time-scale too fast to be affected by the microenvironment surrounding the particle.
机译:以1,8-苯胺基萘磺酸盐(ANS)为荧光探针,对苯乙烯和甲基丙烯酸2-(N,N-二甲基氨基)乙酯的两亲性二嵌段共聚物进行荧光研究,结果表明,在极低的聚合物浓度(〜0.05%)下,形成了稳定的胶束。胶束微环境的特征是平均极性为E_T(30)= 44-48 kcal mol〜(-1),类似于中等极性溶剂,并且具有极高的微粘度。共聚物的亲水:疏水比率的增加导致平均极性的增加和微粘度的降低。胶束被证明是具有高量子限制和宽泛光致发光特性的光致发光CdS纳米粒子的合成和稳定的极好宿主,其主要由陷阱态发射形成。此外,CdS纳米粒子的尺寸和与尺寸相关的稳态光学性质显着取决于宿主胶束的微环境。相反,在所有情况下,涉及从100 ps到100 ns的时间尺度的纳米粒子的光致发光动力学都是相似的。有趣的是,纳米粒子表现出较大的时间依赖性斯托克斯位移,其中的75%在激发后的最初约100 ps内完成。极快的斯托克斯位移归因于最初形成的带边激子在时间尺度上的衰变,其速度太快而无法受到粒子周围微环境的影响。

著录项

  • 来源
    《Materials Chemistry and Physics.》 |2009年第3期|578-585|共8页
  • 作者单位

    Department of Chemistry, Visva-Bharati University, Santiniketan 731 235, India;

    Department of Chemistry, Visva-Bharati University, Santiniketan 731 235, India;

    Polymer Science Unit, Indian Association for the Cultivation of Sciences, Kolkata 700 032, India;

    Department of Chemistry, Visva-Bharati University, Santiniketan 731 235, India;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    micelles; microenvironment; nanoparticles; photoluminescence;

    机译:胶束微环境纳米粒子光致发光;

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