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SERS active substrates of gold nanoparticles embedded in the pool of 5-CB liquid crystal molecules organized in Langmuir-Reverse Schaefer films: A facile fabrication route to make the topological defects useful

机译:嵌入在Langmuir-反向Schaefer膜中的5-CB液晶分子池中嵌入的金纳米粒子的SERS活性基质:一种使拓扑缺陷有用的简便制造途径

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This paper reports for the first time, fabrications of SERS active substrates I and II from Langmuir Reverse Schaefer (L-R Sh) films of 5-CB nematic liquid crystal molecules immersed in gold nanocolloids for 36 and 48 h respectively. Under parallel or slightly crossed polarizations, the POM images of these two substrates exhibit micro aggregated textures embedded in the pool of 5-CB molecules. Under crossed polarizations, the aggregated textures disappear with the appearance of bright birefringent defects of various sizes and shapes. The rationale behind the evolution of such micro aggregated textures and spatial locations of birefringent defects in these substrates are suggested. The FESEM images of the substrates exhibit distinctive patterns driven by the birefringent defects and confirm trapping of gold nanoparticles within the defect sites. The instabilities appeared in the patterns are estimated from statistical considerations in terms of Hurst exponent and phase space trajectories. The chaotic domains prevailing in these substrates are confirmed from the Lyapunov exponents. The efficacies of both the substrates as efficient SERS sensing platform have been tested to detect 4-MPy molecules at trace concentration. The as prepared substrates can be used as "lab on a chip" for chemical and biochemical sensing at ultralow concentrations.
机译:本文首次报道了分别在金纳米胶体中浸入36和48 h的5-CB向列液晶分子的Langmuir Reverse Schaefer(L-R Sh)膜制备SERS活性基底I和II的过程。在平行或略微交叉的极化下,这两个底物的POM图像显示嵌入在5-CB分子池中的微聚集纹理。在交叉偏振下,聚集的纹理消失,并出现各种尺寸和形状的明亮双折射缺陷。提出了这样的微观聚集结构和这些基材中双折射缺陷的空间位置演变的原理。基材的FESEM图像显示出由双折射缺陷驱动的独特图案,并确认了金纳米颗粒在缺陷部位的捕获。根据Hurst指数和相空间轨迹的统计考虑,可以估算出模式中出现的不稳定性。这些底物中普遍存在的混沌域由李雅普诺夫指数证实。已经测试了两种底物作为高效SERS传感平台的功效,可检测痕量浓度的4-MPy分子。所制备的底物可用作“芯片实验室”,以超低浓度进行化学和生化传感。

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