posted on 2019-09-27, 15:35authored byTobias Morawietz, Andres S. Urbina, Patrick K. Wise, Xiangen Wu, Wanjun Lu, Dor Ben-Amotz, Thomas E. Markland
Molecules
with an excess number of hydrogen-bonding partners play
a crucial role in fundamental chemical processes, ranging from anomalous
diffusion in supercooled water to transport of aqueous proton defects
and ordering of water around hydrophobic solutes. Here we show that
overcoordinated hydrogen-bond environments can be identified in both
the ambient and supercooled regimes of liquid water by combining experimental
Raman multivariate curve resolution measurements and machine learning
accelerated quantum simulations. In particular, we find that OH groups
appearing in spectral regions usually associated with non-hydrogen-bonded
species actually correspond to hydrogen bonds formed in overcoordinated
environments. We further show that only these species exhibit a turnover
in population as a function of temperature, which is robust and persists
under both constant pressure and density conditions. This work thus
provides a new tool to identify, interpret, and elucidate the spectral
signatures of crowded hydrogen-bond networks.