Researchers use Argonne X-rays to better understand the phases of a quantum material

Understanding the mysterious properties of materials requires the ability to precisely measure the atoms of those materials as they go through changes. For example, scientists are not certain why quantum materials become superconducting at low temperatures. To find out, they need the most advanced instruments available to catch the atoms in the act. 

The Advanced Photon Source (APS), a U.S. Department of Energy (DOE) Office of Science user facility at DOE’s Argonne National Laboratory, is one such instrument. Or rather, it’s more than 70 such instruments, able to explore materials with a variety of X-ray techniques and, when needed, combine those techniques to deliver a more comprehensive result. 

“The integration of the improved beams, the sample environment and the combination of techniques available at the APS will make further breakthroughs with these materials possible.” – Philip J. Ryan, Argonne National Laboratory

Recently a collaboration between DOE’s SLAC National Accelerator Laboratory and Argonne used the ultrabright X-ray beams of the APS to uncover tantalizing insights about strontium titanate, a material that was once used as a diamond substitute in jewelry and now has the potential to unlock our understanding of an array of quantum behaviors.

The research team built extremely thin, flexible strontium titanate membranes and, using a sample apparatus developed by the beamline staff, stretched it, in the process turning on what is known as a ferroelectric state. In that state, the material generates its own electric field, somewhat similar to how a permanent magnet generates its own magnetic field. APS X-ray beams were able to capture the movement of the ions in the material as it was repeatedly strained to ​“tune” the material in and out of a ferroelectric state.

“Our apparatus allows us to precisely control the strain placed on the material,” said Yongseong Choi, a physicist who works at the APS. ​“That and the combination of X-ray techniques we used gave us an extraordinary insight into the behavior of this material as it transitions through controlled phases.”

The team used two beamlines at the APS. They performed linear X-ray dichroism at beamline 4-ID-Dto determine the change in the spacing between the atoms, and X-ray diffraction at beamline 6-ID-Bto determine the strain on the material. Combining these results enabled the team to precisely track the arrangement of electrons in the material as its positively charged titanium ions were separated from its negatively charged oxygen ions, creating an electric field. 

While the ability to turn on ferroelectricity — as well as superconductivity through the addition of impurities — makes strontium titanate promising for applications in next generation computing, data storage and superconducting devices, this well-known material also offers us a prototype to study fundamental quantum behaviors in a plethora of structurally similar materials.

What the research team found when they lowered the material temperature to cryogenic temperatures — lower than 200 degrees Fahrenheit below zero – was a transition into a quantum state. In this state, quantum fluctuations — random, temporary changes in energy levels — present themselves. At lower temperatures under applied strain strontium titanate began to shift to a state in which quantum fluctuations, rather than thermal motion, drove the order of nearby ions in the material.

Stretching the material is an excellent tuning parameter altering those quantum fluctuations. Introducing strain as a control element gives scientists more ways to explore the material’s properties. A better understanding of this transition could help researchers tailor strontium titanate and other quantum materials for different applications, such as microelectronic switches or capacitors.

Read more on APS website

Image: An artist’s illustration of X-ray probes of strontium titanate.

Credit: Greg Stewart/SLAC National Accelerator Laboratory

Keeping Water-Treatment Membranes from Fouling Out

When you use a membrane for water treatment, junk builds up on the membrane surface—a process called fouling—which makes the treatment less efficient. In this work, researchers studied how membranes are fouled by interactions between natural organic matter and positively charged ions (such as calcium cations) that are commonly found in water from dissolved minerals and salts.

“Fouling has been studied since membranes emerged for use in water purification decades ago, but it still remains one of the largest challenges in water treatment,” said the study’s first author, Matthew Landsman, an ALS collaborative postdoctoral fellow from the University of Texas at Austin’s Center for Materials for Water and Energy Systems (M-WET), a DOE Energy Frontier Research Center (EFRC). “Our research aimed to understand the molecular-level mechanisms that influence membrane fouling by natural organic matter so that we can establish design rules for making better membranes.”

After running laboratory fouling experiments on membranes at UT Austin, the team used synchrotron characterization techniques at the Advanced Light Source (ALS) and Brookhaven’s National Synchrotron Light Source II (NSLS-II) to analyze the surface and bulk compositions of the fouled membranes. At ALS Beamline 7.3.3, wide angle x-ray scattering (WAXS) was used to see if any inorganic contaminants, such as calcium carbonate, were precipitating on the membranes. At NSLS-II, soft and tender x-ray scattering experiments determined the distribution of calcium in the fouling layers.

Read more on the BNL website

Image: Top: Water-treatment facilities use arrays of cylindrical elements containing rolled-up membranes to filter contaminants from water. Bottom inset: In this experiment, such membranes were used to filter water containing ions (reddish spheres) and natural organic matter (green-brown blobs). The fouled membranes were analyzed using various x-ray probes, revealing (for example) how calcium cations form bridges between organic molecules, causing them to aggregate and reduce flow through the membrane.