Showing posts with label Under. Show all posts
Showing posts with label Under. Show all posts

Thursday, 3 November 2011

Liquid can turn into solid under high electric field, physicists show in simulations

ScienceDaily (Oct. 12, 2011) — Physicists have demonstrated in simulations that under the influence of sufficiently high electric fields, liquid droplets of certain materials will undergo solidification, forming crystallites at temperature and pressure conditions that correspond to liquid droplets at field-free conditions. This electric-field-induced phase transformation is termed electrocrystallization.

The study, performed by scientists at the Georgia Institute of Technology, appears online and is scheduled as a feature and cover article in the 42nd issue of Volume 115 of the Journal of Physical Chemistry C.

"We show that with a strong electric field, you can induce a phase transition without altering the thermodynamic parameters," said Uzi Landman, Regents' and Institute Professor in the School of Physics, F.E. Callaway Chair and director of the Center for Computational Materials Science (CCMS) at Georgia Tech.

In these simulations, Landman and Senior Research Scientists David Luedtke and Jianping Gao at the CCMS set out first to explore a phenomenon described by Sir Geoffrey Ingram Taylor in 1964 in the course of his study of the effect of lightning on raindrops, expressed as changes in the shape of liquid drops when passing through an electric field. While liquid drops under field-free conditions are spherical, they alter their shape in response to an applied electric field to become needle-like liquid drops. Instead of the water droplets used in the almost decade-old laboratory experiments of Taylor, the Georgia Tech researchers focused their theoretical study on a 10 nanometer (nm) diameter liquid droplet of formamide, which is a material made of small polar molecules each characterized by a dipole moment that is more than twice as large as that of a water molecule.

With the use of molecular dynamics simulations developed at the CCMS, which allow scientists to track the evolution of materials systems with ultra-high resolution in space and time, the physicists explored the response of the formamide nano-droplet to an applied electric field of variable strength. Influenced by a field of less than 0.5V/nm, the spherical droplet elongated only slightly. However, when the strength of the field was raised to a critical value close to 0.5 V/nm, the simulated droplet was found to undergo a shape transition resulting in a needle-like liquid droplet with its long axis -- oriented along the direction of the applied field -- measuring about 12 times larger than the perpendicular (cross-sectional) small axis of the needle-like droplet. The value of the critical field found in the simulations agrees well with the prediction obtained almost half a decade ago by Taylor from general macroscopic considerations.

Past the shape transition further increase of the applied electric field yielded a slow, gradual increase of the aspect ratio between the long and short axes of the needle-like droplet, with the formamide molecules exhibiting liquid diffusional motions.

"Here came the Eureka moment," said Landman. "When the field strength in the simulations was ramped up even further, reaching a value close to 1.5V/nm, the liquid needle underwent a solidification phase transition, exhibited by freezing of the diffusional motion, and culminating in the formation of a formamide single crystal characterized by a structure that differs from that of the x-ray crystallographic one determined years ago under zero-field conditions. Now, who ordered that?" he added.

Further analysis has shown that the crystallization transition involved arrangement of the molecules into a particular spatial ordered lattice, which optimizes the interactions between the positive and negative ends of the dipoles of neighboring molecules, resulting in minimization of the free energy of the resulting rigid crystalline needle. When the electric field applied to the droplet was subsequently decreased, the crystalline needle remelted and at zero-field the liquid droplet reverted to a spherical shape. The field reversal process was found to exhibit a hysteresis.

Analysis of the microscopic structural changes that underlie the response of the droplet to the applied field revealed that accompanying the shape transition at 0.5 V/nm is a sharp increase in the degree of reorientation of the molecular electric dipoles, which after the transition lie preferentially along the direction of the applied electric field and coincide with the long axis of the needle-­­like liquid droplet. The directional dipole reorientation, which is essentially complete subsequent to the higher field electrocrystallization transition, breaks the symmetry and transforms the droplet into a field-induced ferroelectric state where it possesses a large net electric dipole, in contrast to its unpolarized state at zero-field conditions.

Along with the large-scale atomistic computer simulations, researchers formulated and evaluated an analytical free-energy model, which describes the balance between the polarization, interfacial tension and dielectric saturation contributions. This model was shown to yield results in agreement with the computer simulation experiments, thus providing a theoretical framework for understanding the response of dielectric droplets to applied fields.

"This investigation unveiled fascinating properties of a large group of materials under the influence of applied fields," Landman said. "Here the field-induced shape and crystallization transitions occurred because formamide, like water and many other materials, is characterized by a relatively large electric dipole moment. The study demonstrated the ability to employ external fields to direct and control the shape, the aggregation phase (that is, solid or liquid) and the properties of certain materials."

Along with the fundamental interest in understanding the microscopic origins of materials behavior, this may lead to development of applications of field-induced materials control in diverse areas, ranging from targeted drug delivery, nanoencapsulation, printing of nanostructures and surface patterning, to aerosol science, electrospray propulsion and environmental science.

This research was supported by a grant from the U.S. Air Force Office of Scientific Research.

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Story Source:

The above story is reprinted (with editorial adaptations by ScienceDaily staff) from materials provided by Georgia Institute of Technology.

Journal Reference:

William D. Luedtke, Jianping Gao, Uzi Landman. Dielectric Nanodroplets: Structure, Stability, Thermodynamics, Shape Transitions and Electrocrystallization in Applied Electric Fields. The Journal of Physical Chemistry C, 2011; 110901150249036 DOI: 10.1021/jp206673j

Note: If no author is given, the source is cited instead.

Disclaimer: Views expressed in this article do not necessarily reflect those of ScienceDaily or its staff.


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Wednesday, 13 July 2011

Under pressure, sodium, hydrogen could undergo a metamorphosis, emerging as superconductor

ScienceDaily (June 13, 2011) — In the search for superconductors, finding ways to compress hydrogen into a metal has been a point of focus ever since scientists predicted many years ago that electricity would flow, uninhibited, through such a material.

Liquid metallic hydrogen is thought to exist in the high-gravity interiors of Jupiter and Saturn. But so far, on Earth, researchers have been unable to use static compression techniques to squeeze hydrogen under high enough pressures to convert it into a metal. Shock-wave methods have been successful, but as experiments with diamond anvil cells have shown, hydrogen remains an insulator even under pressures equivalent to those found in Earth's core.

To circumvent the problem, a pair of University at Buffalo chemists has proposed an alternative solution for metallizing hydrogen: Add sodium to hydrogen, they say, and it just might be possible to convert the compound into a superconducting metal under significantly lower pressures.

The research, published June 10 in Physical Review Letters, details the findings of UB Assistant Professor Eva Zurek and UB postdoctoral associate Pio Baettig.

Using an open-source computer program that UB PhD student David Lonie designed, Zurek and Baettig looked for sodium polyhydrides that, under pressure, would be viable superconductor candidates. The program, XtalOpt , is an evolutionary algorithm that incorporates quantum mechanical calculations to determine the most stable geometries or crystal structures of solids.

In analyzing the results, Baettig and Zurek found that NaH9, which contains one sodium atom for every nine hydrogen atoms, is predicted to become metallic at an experimentally achievable pressure of about 250 gigapascals -- about 2.5 million times Earth's standard atmospheric pressure, but less than the pressure at Earth's core (about 3.5 million atmospheres).

"It is very basic research," says Zurek, a theoretical chemist. "But if one could potentially metallize hydrogen using the addition of sodium, it could ultimately help us better understand superconductors and lead to new approaches to designing a room-temperature superconductor."

By permitting electricity to travel freely, without resistance, such a superconductor could dramatically improve the efficiency of power transmission technologies.

Zurek, who joined UB in 2009, conducted research at Cornell University as a postdoctoral associate under Roald Hoffmann, a Nobel Prize-winning theoretical chemist whose research interests include the behavior of matter under high pressure.

In October 2009, Zurek co-authored a paper with Hoffman and other colleagues in the Proceedings of the National Academy of Sciences predicting that LiH6 -- a compound containing one lithium atom for every six hydrogen atoms -- could form as a stable metal at a pressure of around 1 million atmospheres.

Neither LiH6 and NaH9 exists naturally as stable compounds on Earth, but under high pressures, their structure is predicted to be stable.

"One of the things that I always like to emphasize is that chemistry is very different under high pressures," Zurek says. "Our chemical intuition is based upon our experience at one atmosphere. Under pressure, elements that do not usually combine on the Earth's surface may mix, or mix in different proportions. The insulator iodine becomes a metal, and sodium becomes insulating. Our aim is to use the results of computational experiments in order to help develop a chemical intuition under pressure, and to predict new materials with unusual properties."

Story Source:

The above story is reprinted (with editorial adaptations by ScienceDaily staff) from materials provided by University at Buffalo.

Note: If no author is given, the source is cited instead.

Disclaimer: Views expressed in this article do not necessarily reflect those of ScienceDaily or its staff.


View the original article here

Saturday, 9 July 2011

Under pressure, sodium, hydrogen could undergo a metamorphosis, emerging as superconductor

ScienceDaily (June 13, 2011) — In the search for superconductors, finding ways to compress hydrogen into a metal has been a point of focus ever since scientists predicted many years ago that electricity would flow, uninhibited, through such a material.

Liquid metallic hydrogen is thought to exist in the high-gravity interiors of Jupiter and Saturn. But so far, on Earth, researchers have been unable to use static compression techniques to squeeze hydrogen under high enough pressures to convert it into a metal. Shock-wave methods have been successful, but as experiments with diamond anvil cells have shown, hydrogen remains an insulator even under pressures equivalent to those found in Earth's core.

To circumvent the problem, a pair of University at Buffalo chemists has proposed an alternative solution for metallizing hydrogen: Add sodium to hydrogen, they say, and it just might be possible to convert the compound into a superconducting metal under significantly lower pressures.

The research, published June 10 in Physical Review Letters, details the findings of UB Assistant Professor Eva Zurek and UB postdoctoral associate Pio Baettig.

Using an open-source computer program that UB PhD student David Lonie designed, Zurek and Baettig looked for sodium polyhydrides that, under pressure, would be viable superconductor candidates. The program, XtalOpt , is an evolutionary algorithm that incorporates quantum mechanical calculations to determine the most stable geometries or crystal structures of solids.

In analyzing the results, Baettig and Zurek found that NaH9, which contains one sodium atom for every nine hydrogen atoms, is predicted to become metallic at an experimentally achievable pressure of about 250 gigapascals -- about 2.5 million times Earth's standard atmospheric pressure, but less than the pressure at Earth's core (about 3.5 million atmospheres).

"It is very basic research," says Zurek, a theoretical chemist. "But if one could potentially metallize hydrogen using the addition of sodium, it could ultimately help us better understand superconductors and lead to new approaches to designing a room-temperature superconductor."

By permitting electricity to travel freely, without resistance, such a superconductor could dramatically improve the efficiency of power transmission technologies.

Zurek, who joined UB in 2009, conducted research at Cornell University as a postdoctoral associate under Roald Hoffmann, a Nobel Prize-winning theoretical chemist whose research interests include the behavior of matter under high pressure.

In October 2009, Zurek co-authored a paper with Hoffman and other colleagues in the Proceedings of the National Academy of Sciences predicting that LiH6 -- a compound containing one lithium atom for every six hydrogen atoms -- could form as a stable metal at a pressure of around 1 million atmospheres.

Neither LiH6 and NaH9 exists naturally as stable compounds on Earth, but under high pressures, their structure is predicted to be stable.

"One of the things that I always like to emphasize is that chemistry is very different under high pressures," Zurek says. "Our chemical intuition is based upon our experience at one atmosphere. Under pressure, elements that do not usually combine on the Earth's surface may mix, or mix in different proportions. The insulator iodine becomes a metal, and sodium becomes insulating. Our aim is to use the results of computational experiments in order to help develop a chemical intuition under pressure, and to predict new materials with unusual properties."

Story Source:

The above story is reprinted (with editorial adaptations by ScienceDaily staff) from materials provided by University at Buffalo.

Note: If no author is given, the source is cited instead.

Disclaimer: Views expressed in this article do not necessarily reflect those of ScienceDaily or its staff.


View the original article here