A new technique for understanding quantum effects in water

Oct 03, 2011
A snapshot taken from a path integral molecular dynamics simulation of liquid water. The oxygen atoms are shown by red spheres and the hydrogen atoms are shown by multiple white spheres (bubbles) which represent their positional uncertainty in the quantum simulation.

It covers over two thirds of our planet, is essential for life on Earth and its chemical formula is one of the few most people can name, but we still have much to learn about the structure of H2O. Now, scientists working in Grenoble have developed a new technique using oxygen isotopes to study in detail the structure of disordered oxide materials such as water in biological processes or glasses in lasers and telecommunication devices. This new technique allowed a team from the Institut Laue-Langevin (ILL), University of Bath, Oak Ridge National Laboratory and Stanford University to validate a new theoretical model for water's structure by measuring subtle differences between the molecular organisation of light and heavy water that result from quantum mechanics.

At ILL the structural properties of materials are probed by using neutrons, which act like “super x-rays”, via a technique known as . As neutrons pass through materials they are often bounced (or scattered) by atomic nuclei which alters their trajectories, and these scattered neutrons can then be detected to create detailed maps of a sample’s molecular structure. To find out more about the positions of particular atoms within a sample, scientists use a trick called isotopic substitution where the scattering length (or ability to bounce neutrons) of a particular element is ‘tuned’ by substituting one of its isotopes for another. This allows them to zero in on the structure around the atoms of the chosen element.

In modern structural analysis, researchers commonly interchange hydrogen with its heavier isotope deuterium to probe the locations of atoms in or other hydrogen containing materials. This technique of ‘H/D substitution’ is also commonly used in the analysis of hydrogen-storage materials or fuel cells. However, there are problems with using H/D substitution in neutron scattering. The lighter hydrogen isotope is comparable in mass to the neutron which generates imprecise scattering data and makes determination of structure more difficult. Also, you can’t use H/D substitution to study the difference between the positions of hydrogen atoms in H2O versus deuterium atoms in D2O as the technique assumes that H and D atoms have the same positions.

Oxygen has three isotopes: 16O, 17O and 18O and, like hydrogen, is a ubiquitous element on Earth and plays an important role across scientific disciplines. It is often found in structurally disordered materials like silicates in planetary science, glasses for lasers and optical communications, oxide layers in silicon-based electronic devices and water in biological processes. However, it was generally believed that the difference in scattering length between these isotopes is too small to make isotopic substitution with neutron scattering feasible.

The team at ILL challenged this assumption via neutron interferometry – a technique where , acting as coherent quantum waves, allow for a very precise measurement of the scattering lengths of atoms in a sample. With the highly sensitive equipment at ILL, the team showed that the difference between the scattering lengths of two of the oxygen isotopes was actually six times larger than the literature suggested.

Professor Philip Salmon, from the University of Bath, said: “With this larger contrast, we showed the difference in the scattering lengths of the was just about large enough to make neutron scattering a plausible technique for studying the structure of .“

In order to demonstrate the powerful potential of their new technique, the team turned to the structure of the best-known oxide in nature - liquid water where the imprecise results from hydrogen isotope substitution had created some uncertainty. In particular, the team were interested in comparing structural differences between light water (H2O) and (D2O).

“The structure and dynamics of water have long been controversial subjects since they can have profound effects on , and there can be dramatic differences between heavy and light water. For example, most organisms eventually perish in a D2O environment, whereas they thrive in H2O“, said Dr Henry Fischer, a physicist at ILL who worked alongside Prof Salmon on this paper.

Using oxygen isotope substitution, Prof Salmon and his team at ILL analysed the difference between the lengths of the O-H and O-D bonds within water molecules. They found that the O-H bonds were ½ % longer than the O-D bonds – the first time anyone had measured with such pin-point accuracy this important difference between the molecular structures of light and heavy water.

Their findings were then compared with predictions using path-integral methods to see if they could clarify some uncertainty around the structural model for liquid water. Earlier mathematical models often assumed simple rigid molecules, where the bond lengths do not vary, but it turns out that such models are not sufficient to account for the quantum effects leading to the observed structural differences between H2O and D2O. Quantum mechanics gives a fuzzy uncertainty to the positions of the H and D atoms in a water molecule, and since D is twice as heavy as H, the fuzzy effect is not as strong for D as compared to H. This leads to the observed structural differences which can be predicted using a more appropriate flexible model for the water molecule.

Salmon and his team thus identified the type of theoretical model that is needed for understanding the true structure of water, and confirmed that this model can explain the structural differences between H2O and D2O due to quantum mechanics.

Explore further: Asteroid impacts on Earth make structurally bizarre diamonds

More information: Phys. Rev. Lett., 107, 145501 (30 September, 2011) prl.aps.org/abstract/PRL/v107/i14/e145501

Provided by Institut Laue-Langevin

5 /5 (4 votes)
add to favorites email to friend print save as pdf

Related Stories

Neutron scattering confirms DNA is as stretchy as nylon

Sep 08, 2011

(PhysOrg.com) -- Neutron scientists at the Institut Laue-Langevin (ILL, France) have measured how fast sound travels along DNA to determine its ‘stiffness’. These findings help to explain how DNA folds, coils and ...

In Brief: Unmasking elusive hydrogen

Jun 24, 2011

Researchers used the SEQUOIA inelastic spectrometer at the Spallation Neutron Source to map the dynamics of hydrogen atoms in a natural crystal of muscovite.

Physicists Devise New Technique for Detecting Heavy Water

Jun 13, 2006

Scientists at the California Institute of Technology have created a new method of detecting heavy water that is 30 times more sensitive than any other existing method. The detection method could be helpful in the fight against ...

Recommended for you

New terahertz device could strengthen security

Nov 21, 2014

We are all familiar with the hassles that accompany air travel. We shuffle through long lines, remove our shoes, and carry liquids in regulation-sized tubes. And even after all the effort, we still wonder if these procedures ...

CERN makes public first data of LHC experiments

Nov 21, 2014

CERN today launched its Open Data Portal where data from real collision events, produced by experiments at the Large Hadron Collider (LHC) will for the first time be made openly available to all. It is expected ...

User comments : 2

Adjust slider to filter visible comments by rank

Display comments: newest first

not rated yet Oct 03, 2011
testing my inability to post on 'certain' subjects.(I'm being blocked)
not rated yet Oct 03, 2011
ok. I'm just being paranoid, which is nothing new. Nothing to say except:

"Water is ashes". :p

Please sign in to add a comment. Registration is free, and takes less than a minute. Read more

Click here to reset your password.
Sign in to get notified via email when new comments are made.