Tag Archives: Yuki Nagata

How does ice melt? Layer by layer!

A Dec. 12, 2016 news item on ScienceDaily announces the answer to a problem scientists have been investigating for over a century but first, here are the questions,

We all know that water melts at 0°C. However, 150 years ago the famous physicist Michael Faraday discovered that at the surface of frozen ice, well below 0°C, a thin film of liquid-like water is present. This thin film makes ice slippery and is crucial for the motion of glaciers.

Since Faraday’s discovery, the properties of this water-like layer have been the research topic of scientists all over the world, which has entailed considerable controversy: at what temperature does the surface become liquid-like? How does the thickness of the layer dependent on temperature? How does the thickness of the layer increases with temperature? Continuously? Stepwise? Experiments to date have generally shown a very thin layer, which continuously grows in thickness up to 45 nm right below the bulk melting point at 0°C. This also illustrates why it has been so challenging to study this layer of liquid-like water on ice: 45 nm is about 1/1000th part of a human hair and is not discernible by eye.

Scientists of the Max Planck Institute for Polymer Research (MPI-P), in a collaboration with researchers from the Netherlands, the USA and Japan, have succeeded to study the properties of this quasi-liquid layer on ice at the molecular level using advanced surface-specific spectroscopy and computer simulations. The results are published in the latest edition of the scientific journal Proceedings of the National Academy of Science (PNAS).

Caption: Ice melts as described in the text layer by layer. Credit: © MPIP

A Dec. 12, 2016 Max Planck Institute for Polymer Research press release (also on EurekAlert), which originated the news item, goes on to answer the questions,

The team of scientists around Ellen Backus, group leader at MPI-P, investigated how the thin liquid layer is formed on ice, how it grows with increasing temperature, and if it is distinguishable from normal liquid water. These studies required well-defined ice crystal surfaces. Therefore much effort was put into creating ~10 cm large single crystals of ice, which could be cut in such a way that the surface structure was precisely known. To investigate whether the surface was solid or liquid, the team made use of the fact that water molecules in the liquid have a weaker interaction with each other compared to water molecules in ice. Using their interfacial spectroscopy, combined with the controlled heating of the ice crystal, the researchers were able to quantify the change in the interaction between water molecules directly at the interface between ice and air.

The experimental results, combined with the simulations, showed that the first molecular layer at the ice surface has already molten at temperatures as low as -38° C (235 K), the lowest temperature the researchers could experimentally investigate. Increasing the temperature to -16° C (257 K), the second layer becomes liquid. Contrary to popular belief, the surface melting of ice is not a continuous process, but occurs in a discontinuous, layer-by-layer fashion.

“A further important question for us was, whether one could distinguish between the properties of the quasi-liquid layer and those of normal water” says Mischa Bonn, co-author of the paper and director at the MPI-P. And indeed, the quasi-liquid layer at -4° C (269 K) shows a different spectroscopic response than supercooled water at the same temperature; in the quasi-liquid layer, the water molecules seem to interact more strongly than in liquid water.

The results are not only important for a fundamental understanding of ice, but also for climate science, where much research takes place on catalytic reactions on ice surfaces, for which the understanding of the ice surface structure is crucial.

Here’s a link to and a citation for the paper,

Experimental and theoretical evidence for bilayer-by-bilayer surface melting of crystalline ice by M. Alejandra Sánchez, Tanja Kling, Tatsuya Ishiyama, Marc-Jan van Zadel, Patrick J. Bisson, Markus Mezger, Mara N. Jochum, Jenée D. Cyran, Wilbert J. Smit, Huib J. Bakker, Mary Jane Shultz, Akihiro Morita, Davide Donadio, Yuki Nagata, Mischa Bonn, and Ellen H. G. Backus. Proceedings of the National Academy of Science, 2016 DOI: 10.1073/pnas.1612893114 Published online before print December 12, 2016

This paper appears to be open access.

Structural memory of water and the picosecond timescale

Water is a unique liquid and researchers from Germany and the Netherlands can detail at least part of why that’s so according to a Sept. 18, 2015 news item on Nanowerk,

A team of scientists from the Max Planck Institute for Polymer Research (MPI-P) in Mainz, Germany and FOM Institute AMOLF in the Netherlands have characterized the local structural dynamics of liquid water, i.e. how quickly water molecules change their binding state. Using innovative ultrafast vibrational spectroscopies, the researchers show why liquid water is so unique compared to other molecular liquids. …

With the help of a novel combination of ultrafast laser experiments, the scientists found that local structures persist in water for longer than a picosecond, a picosecond (ps) being one thousandth of one billionth of a second ((1012 s). This observation changes the general perception of water as a solvent.

A Sept. 18, 2015 Max Planck Institute for Polymer Research press release (also on EurekAlert), which originated the news item, details the research,

… “71% of the earth’s surface is covered with water. As most chemical and biological reactions on earth occur in water or at the air water interface in oceans or in clouds, the details of how water behaves at the molecular level are crucial. Our results show that water cannot be treated as a continuum, but that specific local structures exist and are likely very important” says Mischa Bonn, director at the MPI-P.

Water is a very special liquid with extremely fast dynamics. Water molecules wiggle and jiggle on sub-picosecond timescales, which make them undistinguishable on this timescale. While the existence of very short-lived local structures – e.g. two water molecules that are very close to one another, or are very far apart from each other – is known to occur, it was commonly believed that they lose the memory of their local structure within less than 0.1 picoseconds.

The proof for relatively long-lived local structures in liquid water was obtained by measuring the vibrations of the Oxygen-Hydrogen (O-H) bonds in water. For this purpose the team of scientists used ultrafast infrared spectroscopy, particularly focusing on water molecules that are weakly (or strongly) hydrogen-bonded to their neighboring water molecules. The scientists found that the vibrations live much longer (up to about 1 ps) for water molecules with a large separation, than for those that are very close (down to 0.2 ps). In other words, the weakly bound water molecules remain weakly bound for a remarkably long time.

Here’s a link to and a citation for the study,

Strong frequency dependence of vibrational relaxation in bulk and surface water reveals sub-picosecond structural heterogeneity by Sietse T. van der Post, Cho-Shuen Hsieh, Masanari Okuno, Yuki Nagata, Huib J. Bakker, Mischa Bonn & Johannes Hunger. Nature Communications 6, Article number: 8384 doi:10.1038/ncomms9384 Published 18 September 2015

This is an open access paper,