Stolte Nore, Daru János, Forbert Harald, Behler Jörg, Marx Dominik
Lehrstuhl für Theoretische Chemie, Ruhr-Universität Bochum, 44780 Bochum, Germany.
Department of Organic Chemistry, Eötvös Loránd University, 1117 Budapest, Hungary.
J Phys Chem Lett. 2024 Dec 12;15(49):12144-12150. doi: 10.1021/acs.jpclett.4c02925. Epub 2024 Nov 28.
Isotopic substitution, which can be realized in both experiment and computer simulations, is a direct approach to assess the role of nuclear quantum effects on the structure and dynamics of matter. However, the impact of nuclear quantum effects on the structure of liquid water as probed in experiment by comparing normal to heavy water has remained controversial. To settle this issue, we employ a highly accurate machine-learned high-dimensional neural network potential to perform converged coupled cluster-quality path integral simulations of liquid HO versus DO at ambient conditions. We find substantial H/D quantum effects on the rotational and translational dynamics of water, in close agreement with the experimental benchmarks. However, in stark contrast to the role for dynamics, H/D quantum effects turn out to be small, on the order of 1/1000 Å, on both average intramolecular and H-bonding structures of water. The most probable structure of water remains nearly unaffected by nuclear quantum effects, but effects on fluctuations away from average are appreciable, rendering HO substantially more "liquid" than DO.
同位素取代在实验和计算机模拟中都可以实现,是评估核量子效应在物质结构和动力学中作用的直接方法。然而,通过比较普通水和重水在实验中探究核量子效应对液态水结构的影响一直存在争议。为了解决这个问题,我们采用高精度的机器学习高维神经网络势,在环境条件下对液态HO与DO进行收敛的耦合簇质量路径积分模拟。我们发现H/D量子效应在水的旋转和平移动力学方面有显著影响,与实验基准密切一致。然而,与动力学中的作用形成鲜明对比的是,H/D量子效应在水的平均分子内结构和氢键结构上都很小,约为1/1000 Å。水最可能的结构几乎不受核量子效应的影响,但对偏离平均值的涨落的影响是显著的,使得HO比DO更具“液态”。