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Nuclear Quantum Effects in Liquid Water Are Negligible for Structure but Significant for Dynamics
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abstract
Isotopic substitution, which can be realized both in experiment and computer simulations, is a direct approach to assess the role of nuclear quantum effects on the structure and dynamics of matter. Yet, 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 H$_2$O versus D$_2$O 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 unexpectedly small, on the order of 1/1000 \r{A}, on both intramolecular and H-bonding structure 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 H$_2$O substantially more "liquid" than D$_2$O.
Forward citations
Cited by 1 Pith paper
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When Theory Meets Experiment: What Does it Take to Accurately Predict $^1$H NMR Dipolar Relaxation Rates in Neat Liquid Water from Theory?
Using CCSD(T)-accurate path integral simulations of water, the authors predict the 1H NMR relaxation rate at 28 MHz as 0.278 s^-1, within the 0.280 ± 0.003 s^-1 experimental value.
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