Beyond silicon: Researchers solve a materials mystery key to next-gen electronic devices

// Materials Science & Engineering

Tags: Faculty, research

From left: MS&E postdoctoral researcher Jungwoo Lee, physics graduate student Neil Campbell, MS&E postdoctoral researcher Hyungwoo Lee, MS&E Professor Chang-Beom Eom, and Physics Professor Mark Rzchowski. Photo: Renee Meiller.

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Lennon and McCartney. Abbott and Costello. Peanut butter and jelly.

Think of one half of any famous duo, and the other half likely comes to mind.

Not only do they complement each other, but together, they work better.

The same is true in the burgeoning field of oxide electronics materials. Boasting a wide array of behaviors, including electronic, magnetic and superconducting, these multifunctional materials are poised to expand the way we think about the functions of traditional silicon-based electronic devices such as cell phones or computers.

Yet until now, a critical aspect has been missing—one that complements the function of electrons in oxide electronics. And a team led by University of Wisconsin-Madison materials scientist Chang-Beom Eom has directly observed that missing second half of the duo necessary to move oxide electronics materials forward.

Materials science and engineering postdoctoral researcher Hyungwoo Lee looks at the inside of a thin film deposition system during oxide thin-film heterostructure growth. Photo: Renee Meiller.

It’s called a two-dimensional hole gas—a counterpart to something known as a two-dimensional electron gas. For more than a decade, researchers have recognized a hole gas appearance was possible, but haven’t been able to create it experimentally.

Writing in the Feb. 5, 2018, issue of the journal Nature Materials, Eom and his collaborators provided evidence of a hole gas coexisting with the electron gas. They designed an ultrathin material, known as a thin film structure, specifically for this research.

“The 2D hole gas was not possible primarily because perfect-enough crystals could not be grown,” says Eom, the Theodore H. Geballe Professor and Harvey D. Spangler Distinguished Professor of materials science and engineering at UW-Madison. “Inside, there were defects that killed the hole gas.”

Eom is a world expert in material growth, using techniques that allow him to meticulously build, or “grow,” each layer of a material with atomic precision. That expertise, combined with insight into the interaction between layers in their structure, was key in identifying the elusive 2D hole gas. “We were able to design the correct structure and make near-perfect crystals, all without defects that degrade the hole gas,” he says.

Also important in identifying the hole gas was the almost-symmetrical way in which Eom assembled the various layers—something like a club sandwich. While other researchers have made the material in a bi-layer structure, Eom designed a triple layer. He alternated layers of strontium oxide and titanium dioxide on the bottom, then layers of lanthanum oxide and aluminum oxide, then added additional layers of strontium oxide and titanium dioxide on the top.

As a result, the hole gas forms at the interface of the layers on the top, while the electron gas forms at the interface of the layers on the bottom—the first demonstration of a very powerful complementary pair.

Just as people 50 years ago likely could not have envisioned communicating via wireless devices, the advance sets forth a platform that can enable new concepts—applications that today remain beyond our wildest dreams.

“We’re not just improving the performance of devices,” says Eom. “So, not improving a cell phone, for example—but envisioning an entirely new device made possible by this advance. This is the beginning of an exciting new path.”

Eom’s collaborators from UW-Madison include Physics Professor Mark Rzchowski and graduate students in materials science and engineering and physics, as well as collaborators from The Ohio State University, the University of Nebraska at Lincoln, Argonne National Laboratory, and Sungkyunkwan University and Pohang University of Science and Technology in Korea.

The authors acknowledge support from the National Science Foundation under DMREF Grant No. DMR-1629270 and Grant No. DMR-1420645 and Grant No. DMR-1305193; AFOSR FA9550-15-1-0334 and AOARD FA2386-15-1-4046; and the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Award No. DE-FG02-06ER46327 and Contract No. DE-AC02-06CH11357.

Author: Renee Meiller