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首页> 外文期刊>RSC Advances >Dazzling green emission from graphene oxide nanosheet-embedded co-doped Ce3+ and Tb3+:PVA polymer nanocomposites for photonic applications
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Dazzling green emission from graphene oxide nanosheet-embedded co-doped Ce3+ and Tb3+:PVA polymer nanocomposites for photonic applications

机译:从石墨烯氧化物纳米末端的共掺杂CE3 +和Tb3 +:PVA聚合物纳米复合材料的光调应用令人眼花缭乱

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摘要

Novel dazzling green emission has been obtained from graphene oxide nanosheet-embedded Ce3+ and Tb3+:PVA polymer nanocomposites under UV excitation. We have successfully synthesized Tb3+:PVA, Ce3+ + Tb3+:PVA and Ce3+ + Tb3+ + graphene oxide nanosheet (GO NS):PVA polymer films by the solution casting method. For these polymer films, their XRD and FTIR spectral profiles have been analyzed for structure details and ion-polymer interaction mechanism. Tb3+ doped at different concentrations in the PVA polymer films displayed a green emission at 546 nm (D-5(4) -> F-7(5)) and under 370 nm (F-7(6) -> L-5(10)) excitation. Upon co-doping with Ce3+ to the Tb3+:PVA polymer film, it exhibits enriched green emission compared to the single Tb3+:PVA under the same excitation due to energy transfer from Ce3+ to Tb3+. Surprisingly a common excitation band has been found at 370 nm for Tb3+, Ce3+ and the GO NS. After good dispersion of the GO NS in the co-doped Ce3+ + Tb3+:PVA polymer films, the photoluminescence properties are remarkably enhanced and a prominent green emission is observed at 370 nm. The green emission of Tb3+ is significantly enhanced though an efficient energy transfer process from Ce3+ to Tb3+ and the GO NS to Tb3+. A possible energy transfer mechanism is clearly demonstrated by several fluorescence methods and lifetime decay dynamics. From these results, these GO NS-embedded Ce3+ + Tb3+:PVA polymer films could be suggested as promising candidates for green luminescent materials for photonic devices.
机译:在紫外线激发下,从石墨烯氧化物纳米片嵌入式CE3 +和TB3 +:PVA聚合物纳米复合材料中获得了新的令人眼花缭乱的绿色发射。我们已成功合成TB3 +:PVA,CE3 + + TB3 +:PVA和CE3 + + TB3 + +含石墨烯纳米液(GO NS):PVA聚合物膜通过溶液浇铸方法。对于这些聚合物薄膜,已经分析了它们的XRD和FTIR光谱谱的结构细节和离子聚合物相互作用机理。在PVA聚合物膜中以不同浓度掺杂的Tb3 +在546nm(d-5(4) - > f-7(5))和370nm以下的绿色发射(F-7(6) - > l-5( 10))激发。在将CE3 +共掺杂至TB3 +:PVA聚合物膜时,它与单个TB3 +:PVA相比,它表现出富集的绿色发射,其由于CE3 +至Tb3 +的能量转移而在相同的激励下。令人惊讶的是,对于TB3 +,CE3 +和Go NS,已经发现了370nm的常见激发带。在共掺杂Ce3 + + Tb3 +:PVA聚合物膜中良好的去NS分散后,光致发光性质显着增强,并且在370nm处观察到突出的绿色发射。尽管来自CE3 +至Tb3 +的有效能量转移过程和Go NS至TB3 +,但TB3 +的绿色发射明显增强。通过几种荧光方法和寿命衰减动态清楚地证明了可能的能量转移机制。从这些结果来看,可以建议这些GO NS-嵌入式CE3 + + TB3 +:PVA聚合物薄膜作为光子器件的绿色发光材料的有希望的候选者。

著录项

  • 来源
    《RSC Advances》 |2016年第59期|共14页
  • 作者单位

    Yeungnam Univ Coll Sci Dept Chem Gyongsan 38541 Gyeongbuk South Korea;

    Sri Venkateswara Univ Dept Phys Tirupati 517502 Andhra Pradesh India;

    Sri Venkateswara Univ Dept Phys Tirupati 517502 Andhra Pradesh India;

    Yeungnam Univ Coll Sci Dept Chem Gyongsan 38541 Gyeongbuk South Korea;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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