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Quantum calculations of the IR spectrum of liquid water using ab initio and model potential and dipole moment surfaces and comparison with experiment

机译:从头算和模型势及偶极矩表面对液态水红外光谱的量子计算及与实验的比较

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The calculation and characterization of the IR spectrum of liquid water have remained a challenge for theory. In this paper, we address this challenge using a combination of ab initio approaches, namely, a quantum treatment of IR spectrum using the ab initio WHBB water potential energy surface and a refined ab initio dipole moment surface. The quantum treatment is based on the embedded local monomer method, in which the three intramolecular modes of each embedded H2O monomer are fully coupled and also coupled singly to each of six intermolecular modes. The new dipole moment surface consists of a previous spectroscopically accurate 1-body dipole moment surface and a newly fitted ab initio intrinsic 2-body dipole moment. A detailed analysis of the new dipole moment surface in terms of the coordinate dependence of the effective atomic charges is done along with tests of it for the water dimer and prism hexamer double-harmonic spectra against direct ab initio calculations. The liquid configurations are taken from previous molecular dynamics calculations of Skinner and co-workers, using the TIP4P plus E3B rigid monomer water potential. The IR spectrum of water at 300 K in the range of 0-4000 cm(-1) is calculated and compared with experiment, using the ab initio WHBB potential and new ab initio dipole moment, the q-TIP4P/F potential, which has a fixed-charged description of the dipole moment, and the TTM3-F potential and dipole moment surfaces. The newly calculated ab initio spectrum is in very good agreement with experiment throughout the above spectral range, both in band positions and intensities. This contrasts to results with the other potentials and dipole moments, especially the fixed-charge q-TIP4P/F model, which gives unrealistic intensities. The calculated ab initio spectrum is analyzed by examining the contribution of various transitions to each band. (C) 2015 AIP Publishing LLC.
机译:液态水的红外光谱的计算和表征仍然是理论上的挑战。在本文中,我们使用从头算方法的组合来应对这一挑战,即使用从头算WHBB水势能表面和精细的从头偶极矩表面对红外光谱进行量子处理。量子处理基于嵌入式局部单体方法,其中每个嵌入式H2O单体的三个分子内模式完全耦合,也分别与六个分子间模式耦合。新的偶极矩表面由以前的光谱精确的1体偶极矩表面和新安装的从头算起的固有2体偶极矩组成。根据有效原子电荷的坐标依赖性,对新偶极矩表面进行了详细分析,并针对水二聚体和棱镜六聚体双谐波光谱进行了针对直接从头算的测试。液体构型是使用TIP4P和E3B刚性单体水势从Skinner及其同事之前的分子动力学计算得出的。使用从头算起的WHBB势和新的从头算出的偶极矩q-TIP4P / F势,计算了300 K在0-4000 cm(-1)范围内的水的红外光谱并将其与实验进行比较偶极矩以及TTM3-F势和偶极矩表面的固定电荷描述。在整个上述光谱范围内,无论是在谱带位置还是强度上,新计算的从头算谱都与实验非常吻合。这与其他电位和偶极矩的结果形成对比,尤其是固定电荷的q-TIP4P / F模型,该模型给出了不切实际的强度。通过检查各种跃迁对每个频带的贡献来分析计算的从头算谱。 (C)2015 AIP Publishing LLC。

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