Tag Archives: Timothy A. Miller

Research into phase changes in solids and control

A July 28, 2015 news item on ScienceDaily describes some practical reasons for research into phase changes from the Institute of Photonic Sciences (ICFO) in Spain in collaboration with Firtz-Haber-Institut der Max-Planck-Gesellschaft,

Rewritable CDs, DVDs and Blu-Ray discs owe their existence to phase-change materials, those materials that change their internal order when heated and whose structures can be switched back and forth between their crystalline and amorphous phases. Phase-change materials have even more exciting applications on the horizon, but our limited ability to precisely control their phase changes is a hurdle to the development of new technology.

A July 28, 2015 ICFO news release (also on EurekAlert), which originated the news item, describes the problem and the researchers’ solution,

One of the most popular and useful phase-change materials is GST, which consists of germanium, antimony, and tellurium. This material is particularly useful because it alternates between its crystalline and amorphous phases more quickly than any other material yet studied. These phase changes result from changes in the bonds between atoms, which also modify the electronic and optical properties of GST as well as its lattice structure. Specifically, resonant bonds, in which electrons participate in several neighboring bonds, influence the material’s electro-optical properties, while covalent bonds, in which electrons are shared between two atoms, influence its lattice structure. Most techniques that use GST simultaneously change both the electro-optical and structural properties. This is actually a considerable drawback since in the process of repeating structural transitions, such as heating and cooling the material, the lifetime of any device based on this material is drastically reduced.

In a study recently published in Nature Materials, researchers from the ICFO groups led by Prof. Simon Wall and ICREA Prof. at ICFO Valerio Pruneri, in collaboration with the Firtz-Haber-Institut der Max-Planck-Gesellschaft, have demonstrated how the material and electro-optical properties of GST change over fractions of a trillionth of a second as the phase of the material changes. Laser light was successfully used to alter the bonds controlling the electro-optical properties without meaningfully altering the bonds controlling the lattice. This new configuration allowed the rapid, reversible changes in the electro-optical properties that are important in device applications without reducing the lifetime of the device by changing its lattice structure. Moreover, the change in the electro-optical properties of GST measured in this study is more than ten times greater than that previously achieved by silicon materials used for the same purpose. This finding suggests that GST may be a good substitute for these commonly used silicon materials.

The results of this study may be expected to have far-reaching implications for the development of new technologies, including flexible displays, logic circuits, optical circuits, and universal memory for data storage. These results also indicate the potential of GST for other applications requiring materials with large changes in optical properties that can be achieved rapidly and with high precision.

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

Time-domain separation of optical properties from structural transitions in resonantly bonded materials by Lutz Waldecker, Timothy A. Miller, Miquel Rudé, Roman Bertoni, Johann Osmond,  Valerio Pruneri, Robert E. Simpson, Ralph Ernstorfer, & Simon Wall. Nature Materials (2015)
doi:10.1038/nmat4359 Published online 27 July 2015

This paper is behind a paywall.

Stress makes quantum dots ‘breathe’

A March 19, 2015 news item on ScienceDaily describes some new research on quantum dots,

Researchers at the Department of Energy’s SLAC National Accelerator Laboratory watched nanoscale semiconductor crystals expand and shrink in response to powerful pulses of laser light. This ultrafast “breathing” provides new insight about how such tiny structures change shape as they start to melt — information that can help guide researchers in tailoring their use for a range of applications.

In the experiment using SLAC’s Linac Coherent Light Source (LCLS) X-ray laser, a DOE Office of Science User Facility, researchers first exposed the nanocrystals to a burst of laser light, followed closely by an ultrabright X-ray pulse that recorded the resulting structural changes in atomic-scale detail at the onset of melting.

“This is the first time we could measure the details of how these ultrasmall materials react when strained to their limits,” said Aaron Lindenberg, an assistant professor at SLAC and Stanford who led the experiment. The results were published March 12 [2015] in Nature Communications.

A March 18, 2015 SLAC news release, which originated the news item, provides a general description of quantum dots,

The crystals studied at SLAC are known as “quantum dots” because they display unique traits at the nanoscale that defy the classical physics governing their properties at larger scales. The crystals can be tuned by changing their size and shape to emit specific colors of light, for example.

So scientists have worked to incorporate them in solar panels to make them more efficient and in computer displays to improve resolution while consuming less battery power. These materials have also been studied for potential use in batteries and fuel cells and for targeted drug delivery.

Scientists have also discovered that these and other nanomaterials, which may contain just tens or hundreds of atoms, can be far more damage-resistant than larger bits of the same materials because they exhibit a more perfect crystal structure at the tiniest scales. This property could prove useful in battery components, for example, as smaller particles may be able to withstand more charging cycles than larger ones before degrading.

The news release then goes on to describe the latest research showing the dots ‘breathe’ (Note: A link has been removed),

In the LCLS experiment, researchers studied spheres and nanowires made of cadmium sulfide and cadmium selenide that were just 3 to 5 nanometers, or billionths of a meter, across. The nanowires were up to 25 nanometers long. By comparison, amino acids – the building blocks of proteins – are about 1 nanometer in length, and individual atoms are measured in tenths of nanometers.

By examining the nanocrystals from many different angles with X-ray pulses, researchers reconstructed how they change shape when hit with an optical laser pulse. They were surprised to see the spheres and nanowires expand in width by about 1 percent and then quickly contract within femtoseconds, or quadrillionths of a second. They also found that the nanowires don’t expand in length, and showed that the way the crystals respond to strain was coupled to how their structure melts.

In an earlier, separate study, another team of researchers had used LCLS to explore the response of larger gold particles on longer timescales.

“In the future, we want to extend these experiments to more complex and technologically relevant nanostructures, and also to enable X-ray exploration of nanoscale devices while they are operating,” Lindenberg said. “Knowing how materials change under strain can be used together with simulations to design new materials with novel properties.”

Participating researchers were from SLAC, Stanford and two of their joint institutes, the Stanford Institute for Materials and Energy Sciences (SIMES) and Stanford PULSE Institute; University of California, Berkeley; University of Duisburg-Essen in Germany; and Argonne National Laboratory. The work was supported by the DOE Office of Science and the German Research Council.

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

Visualization of nanocrystal breathing modes at extreme strains by Erzsi Szilagyi, Joshua S. Wittenberg, Timothy A. Miller, Katie Lutker, Florian Quirin, Henrik Lemke, Diling Zhu, Matthieu Chollet, Joseph Robinson, Haidan Wen, Klaus Sokolowski-Tinten, & Aaron M. Lindenberg. Nature Communications 6, Article number: 6577 doi:10.1038/ncomms7577 Published 12 March 2015

This paper is behind a paywall but there is a free preview available through ReadCube Access.