School of Chemistry, University of Bristol, Bristol, BS8 1TS, UK.
Phys Chem Chem Phys. 2012 Mar 7;14(9):3037-47. doi: 10.1039/c2cp23999j. Epub 2012 Jan 27.
The cavity enhanced Raman scattering spectrum recorded from an aerosol droplet provides a unique fingerprint of droplet radius and refractive index, assuming that the droplet is homogeneous in composition. Aerosol optical tweezers are used in this study to capture a single droplet and a Raman fingerprint is recorded using the trapping laser as the source for the Raman excitation. We report here the retrieval of the real part of the refractive index with an uncertainty of ± 0.0012 (better than ± 0.11%), simultaneously measuring the size of the micrometre sized liquid droplet with a precision of better than 1 nm (< ± 0.05% error). In addition, the equilibrium size of the droplet is shown to depend on the laser irradiance due to optical absorption, which elevates the droplet temperature above that of the ambient gas phase. Modulation of the illuminating laser power leads to a modulation in droplet size as the temperature elevation is altered. By measuring induced size changes of <1 nm, we show that the imaginary part of the refractive index can be retrieved even when less than 10 × 10(-9) with an accuracy of better than ± 0.5 × 10(-9). The combination of these measurements allows the complex refractive index of a droplet to be retrieved with high accuracy, with the possibility of making extremely sensitive optical absorption measurements on aerosol samples and the testing of frequently used mixing rules for treating aerosol optical properties. More generally, this method provides an extremely sensitive approach for measuring refractive indices, particularly under solute supersaturation conditions that cannot be accessed by simple bulk-phase measurements.
从气溶胶液滴中记录的腔增强拉曼散射光谱提供了液滴半径和折射率的独特指纹,假设液滴在组成上是均匀的。在这项研究中,气溶胶光镊用于捕获单个液滴,并使用捕获激光作为拉曼激发源记录拉曼指纹。我们在这里报告了折射率实部的检索,其不确定度为±0.0012(优于±0.11%),同时以优于 1nm 的精度(<±0.05%的误差)测量了微米级液滴的尺寸。此外,由于光吸收,液滴的平衡尺寸显示出依赖于激光辐照度,这会将液滴温度升高到环境气相以上。通过测量<1nm 的诱导尺寸变化,我们表明即使折射率的虚部小于 10×10(-9),也可以以优于±0.5×10(-9)的精度检索到它。这些测量的组合允许以高精度检索液滴的复折射率,有可能对气溶胶样品进行极其灵敏的光吸收测量,并测试经常用于处理气溶胶光学性质的混合规则。更一般地说,这种方法提供了一种非常灵敏的测量折射率的方法,特别是在简单的体相测量无法达到的溶质过饱和度条件下。