Piskulich Zeke A, Thompson Ward H
Department of Chemistry, University of Kansas, Lawrence, Kansas 66045, United States.
J Phys Chem Lett. 2020 Sep 17;11(18):7762-7768. doi: 10.1021/acs.jpclett.0c02301. Epub 2020 Sep 2.
The temperature derivative of the infrared (IR) spectrum of HOD/DO is directly calculated from simulations at a single temperature using a fluctuation theory approach. It is demonstrated, on the basis of an energetic decomposition of the derivative, that the blue shift with increasing temperature is associated with the competition between electrostatic and Lennard-Jones interactions. The same competition gives rise, where their contributions cancel, to a near isosbestic point. The derivative is further used to define an effective internal energy (and entropy) associated with the IR spectrum, and it is shown how a van't Hoff relation can be used to accurately predict the spectrum over a wide range of temperatures. These predictions also explain why a precise isosbestic point is not observed.
利用涨落理论方法,通过在单一温度下的模拟直接计算出HOD/DO红外(IR)光谱的温度导数。基于导数的能量分解表明,随着温度升高的蓝移与静电相互作用和 Lennard-Jones 相互作用之间的竞争有关。在它们的贡献相互抵消的地方,同样的竞争导致了一个近似等吸收点。该导数进一步用于定义与IR光谱相关的有效内能(和熵),并展示了如何使用范特霍夫关系在很宽的温度范围内准确预测光谱。这些预测也解释了为什么没有观察到精确的等吸收点。