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超越比尔定律:重新审视洛伦兹-洛伦茨方程。

Beyond Beer's Law: Revisiting the Lorentz-Lorenz Equation.

机构信息

Spectroscopy/Imaging, Leibniz Institute of Photonic Technology, Albert-Einstein-Str. 9, 07745, Jena, Germany.

Institute of Physical Chemistry and Abbe Center of Photonics, Friedrich Schiller University, Helmholtzweg 4, 07743, Jena, Germany.

出版信息

Chemphyschem. 2020 Jun 16;21(12):1218-1223. doi: 10.1002/cphc.202000301. Epub 2020 May 27.

Abstract

In this contribution we show how the Lorentz-Lorenz and the Clausius-Mosotti equations are related to Beer's law. Accordingly, the linear concentration dependence of absorbance is a consequence of neglecting the difference between the local and the applied electric field. Additionally, it is necessary to assume that the absorption index and the related refractive index change is small. By connecting the Lorentz-Lorenz equations with dispersion theory, it becomes obvious that the oscillators are coupled via the local field. We investigate this coupling with numerical examples and show that, as a consequence, the integrated absorbance of a single band is in general no longer linearly depending on the concentration. In practice, the deviations from Beer's law usually do not set in before the density reaches about one tenth of that of condensed matter. For solutions, the Lorentz-Lorenz equations predict a strong coupling also between the oscillators of solute and solvent. In particular, in the infrared spectral region, the absorption coefficients are prognosticated to be much higher due to this coupling compared to those in the gas phase.

摘要

在本贡献中,我们展示了洛伦兹-洛伦茨方程和克劳修斯-莫索蒂方程如何与比尔定律相关。因此,吸光度的线性浓度依赖性是忽略局部电场和应用电场之间差异的结果。此外,有必要假设吸收指数和相关折射率变化很小。通过将洛伦兹-洛伦茨方程与色散理论联系起来,很明显,振子通过局部场相互耦合。我们通过数值示例研究了这种耦合,并表明,结果是,单个带的积分吸光度通常不再线性依赖于浓度。在实践中,通常在密度达到凝聚态物质密度的十分之一左右之前,不会出现偏离比尔定律的情况。对于溶液,洛伦兹-洛伦茨方程还预测溶质和溶剂的振子之间存在很强的耦合。特别是在红外光谱区域,由于这种耦合,与气相相比,吸收系数预计会高得多。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/7317954/eeca68e14bb6/CPHC-21-1218-g001.jpg

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