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Nano Focus: Nanoscale study helps explain materials’ ability to convert waste heat to electricity

Published online by Cambridge University Press:  18 February 2011

Abstract

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Other
Copyright
Copyright © Materials Research Society 2011

An international team of researchers has discovered that a class of materials known to convert heat to electricity and vice versa behaves unexpectedly at the nanoscale in response to changes in temperature. The discovery—described in the December 17, 2010, issue of Science (DOI: 10.1126/science.1192759; p. 1660)—is an “opposite-direction” phase transition that helps explain the strong thermoelectric response of these materials. It may also help scientists identify other useful thermoelectrics, and could further their application in capturing energy lost as heat, for example, in automotive and factory exhaust.

The scientists—from Brookhaven National Laboratory, Columbia University, Argonne National Laboratory, Los Alamos National Laboratory, Northwestern University, and the Swiss Federal Institute of Technology—were studying lead chalcogenides (lead paired with tellurium, selenium, or sulfur) using newly available experimental techniques and theoretical approaches that allow them to “see” and model behavior of individual atoms at the nanoscale. With those tools they were able to observe subtle changes in atomic arrangements invisible to conventional probes of structure.

Simon Billinge, a physicist at Brookhaven Lab and Columbia University’s School of Engineering and Applied Science and a lead author on the Science paper, said that the development of localized atomic distortions upon cooling is normal. He said, “What we discovered in lead chalcogenides is the opposite behavior: At the very lowest temperature, there were no atomic displacements, nothing—but on warming, displacements appear!”

The lead materials were made in a purified powder form. The researchers then bombarded the samples with neutrons using the Lujan Neutron Scattering Center at Los Alamos as a source. Detectors gather information about how these beams scatter off the sample to produce diffraction patterns that indicate positions and arrangements of the atoms. Further mathematical and computational analysis of the data allowed the scientists to model and interpret what was happening at the atomic level over a range of temperatures.

Brookhaven physicist Emil S. Božin, first author on the article, was the first to notice the odd behavior in the data. “If we had just looked at the average structure, we never would have observed this effect. Our analysis of atomic pair distribution functions gives us a much more local view—the distance from one particular atom to its nearest neighbors—rather than just the average,” Božin said. The detailed analysis revealed that, as the material got warmer, these distances were changing on a tiny scale—about 0.025 nm—demonstrating that individual atoms were becoming displaced.

The displacements can be pictured as tiny arrows with the points indicating the orientations of the atoms. Upon heating, these dipoles appear and flip back and forth, or fluctuate.

According to the scientists, it is this random flipping behavior that is key to the materials’ ability to convert heat into electricity.

Billinge said, “This low thermal conductivity allows a large temperature gradient to be maintained across the sample, which is crucial to the thermoelectric properties.”

When one side of the material comes in contact with heat—for example, in the exhaust system of a car—the gradient will cause charge carriers in the thermoelectric material (e.g., electrons) to diffuse from the hot side to the cold side. Capturing this thermally induced electric current could put the “waste” heat to use.

According to the research team, this work may help scientists search for other thermoelectric materials with exceptional properties, since it links the good thermoelectric response to the existence of fluctuating dipoles.

Other members of the research team are C.D. Malliakas, P. Souvatzis, T. Proffen, N.A. Spaldin, and M.G. Kanatzidis.