Ma Q, Boulet C, Tipping R H
NASA/Goddard Institute for Space Studies and Department of Applied Physics and Applied Mathematics, Columbia University, 2880 Broadway, New York, New York 10025, USA.
Institut des Sciences Moléculaires d'Orsay (ISMO), CNRS (UMR8214) et Université Paris-Sud Bât 350, Campus d'Orsay F-91405, France.
J Chem Phys. 2014 Mar 14;140(10):104304. doi: 10.1063/1.4867417.
The refinement of the Robert-Bonamy (RB) formalism by considering the line coupling for isotropic Raman Q lines of linear molecules developed in our previous study [Q. Ma, C. Boulet, and R. H. Tipping, J. Chem. Phys. 139, 034305 (2013)] has been extended to infrared P and R lines. In these calculations, the main task is to derive diagonal and off-diagonal matrix elements of the Liouville operator iS1 - S2 introduced in the formalism. When one considers the line coupling for isotropic Raman Q lines where their initial and final rotational quantum numbers are identical, the derivations of off-diagonal elements do not require extra correlation functions of the Ŝ operator and their Fourier transforms except for those used in deriving diagonal elements. In contrast, the derivations for infrared P and R lines become more difficult because they require a lot of new correlation functions and their Fourier transforms. By introducing two dimensional correlation functions labeled by two tensor ranks and making variable changes to become even functions, the derivations only require the latters' two dimensional Fourier transforms evaluated at two modulation frequencies characterizing the averaged energy gap and the frequency detuning between the two coupled transitions. With the coordinate representation, it is easy to accurately derive these two dimensional correlation functions. Meanwhile, by using the sampling theory one is able to effectively evaluate their two dimensional Fourier transforms. Thus, the obstacles in considering the line coupling for P and R lines have been overcome. Numerical calculations have been carried out for the half-widths of both the isotropic Raman Q lines and the infrared P and R lines of C2H2 broadened by N2. In comparison with values derived from the RB formalism, new calculated values are significantly reduced and become closer to measurements.
通过考虑我们之前的研究[Q. Ma, C. Boulet, and R. H. Tipping, J. Chem. Phys. 139, 034305 (2013)]中所发展的线性分子各向同性拉曼Q线的线耦合,对罗伯特 - 博纳米(RB)形式体系的改进已扩展到红外P线和R线。在这些计算中,主要任务是推导该形式体系中引入的刘维尔算子iS1 - S2的对角和非对角矩阵元。当考虑各向同性拉曼Q线的线耦合时,其初始和最终转动量子数相同,除了用于推导对角元的那些函数外,非对角元的推导不需要ŝ算子的额外关联函数及其傅里叶变换。相比之下,红外P线和R线的推导变得更加困难,因为它们需要许多新的关联函数及其傅里叶变换。通过引入由两个张量秩标记的二维关联函数并进行变量变换使其成为偶函数,推导仅需要在表征平均能隙和两个耦合跃迁之间频率失谐的两个调制频率处对后者的二维傅里叶变换进行求值。利用坐标表示,很容易准确推导这些二维关联函数。同时,通过使用采样理论能够有效地评估它们的二维傅里叶变换。因此,克服了考虑P线和R线线耦合时的障碍。已经对N2加宽的C2H2的各向同性拉曼Q线以及红外P线和R线的半高宽进行了数值计算。与从RB形式体系导出的值相比,新的计算值显著降低并且更接近测量值。