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arXiv · 2009.04727

Hydration of NH$_4^+$ in Water: Bifurcated Hydrogen Bonding Structures and Fast Rotational Dynamics

Jianqing Guo·Liying Zhou·Andrea Zen·Angelos Michaelides·Xifan Wu·Enge Wang·Limei Xu·Ji Chen
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Abstract

Understanding the hydration and diffusion of ions in water at the molecular level is a topic of widespread importance. The ammonium ion (NH$_4^+$) is an exemplar system that has received attention for decades because of its complex hydration structure and relevance in industry. Here we report a study of the hydration and the rotational diffusion of NH$_4^+$ in water using ab initio molecular dynamics simulations and quantum Monte Carlo calculations. We find that the hydration structure of NH$_4^+$ features bifurcated hydrogen bonds, which leads to a rotational mechanism involving the simultaneous switching of a pair of bifurcated hydrogen bonds. The proposed hydration structure and rotational mechanism are supported by existing experimental measurements, and they also help to rationalize the measured fast rotation of NH$_4^+$ in water. This study highlights how subtle changes in the electronic structure of hydrogen bonds impacts the hydration structure, which consequently affects the dynamics of ions and molecules in hydrogen bonded systems.

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Jianqing Guo, Liying Zhou, Andrea Zen, Angelos Michaelides, Xifan Wu, Enge Wang, Limei Xu, Ji Chen. 2020-09-10. Hydration of NH$_4^+$ in Water: Bifurcated Hydrogen Bonding Structures and Fast Rotational Dynamics. https://doi.org/10.1103/physrevlett.125.106001

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