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Surface interaction, polarization and molecular weight effects for a whispering gallery mode sensor.

机译:耳语画廊模式传感器的表面相互作用,极化和分子量效应。

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In this thesis, we investigate the use of an optical resonance of a microsphere in measuring the thickness and dielectric constant of a bio-nano-layer and in determining the molecular orientation of an adsorbate at the sphere surface. We also establish the molecular weight sensitivity of the resonance frequency shift.; The resonances of silica microspheres can be very narrow (i.e. high Quality Factor, Q and as a result are extremely sensitive to dielectric perturbations at the sphere surface. In particular, one may use the shift of the resonant frequency to detect the adsorption of bio-molecules with unprecedented sensitivity.; This work goes beyond the detection of nanoscopic bio-molecules to the characterization of polymer layers ∼100 nm in thickness. The possibility of enlarging the scope of the sensor is inspired by first order perturbation theory. The theory reveals that the evanescent field decay length influences resonance shifts and may be used as a nanoscopic ruler. Through this theoretical discussion, the idea of using the two light sources to stimulate resonances in an individual microsphere precipitated. Microsphere Wavelength Multiplexing (MWM) experiments proved the theory to be sound. The measurement of simultaneous shifts of two resonances at widely separated wavelengths allowed us to determine the thickness and the dielectric excess of an important bionanolayer (poly-L-lysine) even though its refractive index only exceeded that of the aqueous buffer solution by 0.0012.; We revisited protein adsorption and investigated the molecular weight MW sensitivity of the sensor. We found that the resonance shift is proportional to MW1/3. A new theoretical model explains the MW1/3 dependence and concludes that spherical protein covers 34% of the microsphere surface and the effective layer refractive index is 1.39.; We demonstrate polarization specific stimulation of resonances and measure TE and TM mode shifts by inducing a refractive index change in the medium. NaCl addition experiment confirms TM to TE shift ratio predicted by perturbation theory. The polarization specific measurement is applied to investigate the orientation of phenol molecule at the silica surface.
机译:在本文中,我们研究了微球光学共振在测量生物纳米层的厚度和介电常数以及确定球体表面吸附物分子取向方面的用途。我们还建立了共振频率偏移的分子量敏感性。二氧化硅微球的共振可能非常狭窄(即高品质因数,Q,因此对球表面的介电扰动极为敏感。特别是,人们可以利用共振频率的变化来检测生物微粒的吸附。分子,具有前所未有的灵敏性;这项工作不仅涉及到对纳米生物分子的检测,而且还包括对厚度约为100 nm的聚合物层进行表征的方法。一阶微扰理论启发了扩大传感器范围的可能性。 e逝场的衰减长度会影响共振位移,可以用作纳米尺。通过这一理论讨论,利用两个光源激发单个微球中沉淀的共振的想法通过微球波长多路复用(MWM)实验证明了该理论的有效性。声音。测量在很宽的波长下两个共振同时发生的位移使我们能够确定重要的生物纳米层(聚-L-赖氨酸)的厚度和介电过量,即使其折射率仅比缓冲水溶液的折射率高0.0012。我们重新研究了蛋白质吸附并研究了传感器的分子量MW灵敏度。我们发现共振位移与MW1 / 3成正比。一种新的理论模型解释了MW1 / 3的依赖性,并得出结论,球形蛋白覆盖了微球表面的34%,有效层折射率为1.39。我们演示了共振的偏振特定刺激,并通过诱导介质中的折射率变化来测量TE和TM模式转变。 NaCl的添加实验证实了扰动理论预测的TM与TE的位移比。极化比测量用于研究苯酚分子在二氧化硅表面的取向。

著录项

  • 作者

    Noto, Mayumi.;

  • 作者单位

    Polytechnic University.;

  • 授予单位 Polytechnic University.;
  • 学科 Chemistry Organic.; Chemistry Pharmaceutical.; Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 102 p.
  • 总页数 102
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;药物化学;高分子化学(高聚物);
  • 关键词

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