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Research Uncovers the Spontaneous Polarization of Novel Ultrathin Materials

by | Nov 14, 2018 | Blog

Many materials exhibit new properties when in the form of thin films composed of just a few atomic layers.  Most people are familiar with graphene, the two-dimensional form of graphite, but thin film versions of other materials also have the potential to facilitate technological breakthroughs.

For example, a class of three-dimensional materials called Group-IV monochalcogenides are semiconductors that perform in applications such as thermoelectrics and optoelectronics among others. Researchers are now creating two-dimensional versions of these materials, in the hope that they will offer improved performance or even new applications.

Recently, a research team that includes Salvador Barraza-Lopez, associate professor of physics at the U of A and Taneshwor Kaloni, a former post-doctoral researcher in Barraza Lopez’s lab, has shed light on the behavior of one of these ultrathin materials known as tin telluride (SnTe). Barraza Lopez and his colleagues at the Max-Planck Institute of Microstructure Physics in Germany, the Key Laboratory of Low-Dimensional Quantum Physics and the Collaborative Innovation Center of Quantum Matter in China and the RIKEN Center for Emergent Matter Science in Japan recently published a paper on their findings in the journal Advanced Materials.

The researchers used a variable temperature scanning tunneling microscope to study the structure and polarization of SnTe thin films grown on graphene substrates. They studied the material at a range of temperatures, from 4.7 Kelvin to over 400 Kelvin. They discovered that when SnTe is only a few atomic layers thick, it forms a layered structure that is different from the bulk, rhombic-shaped version of the material. The Arkansas team contributed to this research by providing calculations that account for the quantum mechanical nature of these atomic structures, using a method known as density functional theory.

The atoms in ultrathin SnTe create electric dipoles oriented along opposite directions in every other atomic layer, which makes the material anti-polar, as opposed to the bulk sample in which all layers point along the same direction. Moreover, the transition temperature, which is the temperature at which the material loses this spontaneous polarization, is much higher than that of the bulk material.

“[These findings] underline the potential of atomically thin g-SnTe films for the development of novel spontaneous polarization-based devices,” said the researchers in the paper.

This work was funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)–Project number PA 1812/2-1, the National Natural Science Foundation of China (Grant No. 51561145005) and the Ministry of Science and Technology of China (Grant No. 2016YFA0301002). Work performed at Arkansas was supported by the U.S. Department of Energy, Office of Basic Energy Sciences, under the Early Career Award DE-SC0016139. Calculations were carried out at Trestles (funded by multiple grants from the National Science Foundation, a grant from the Arkansas Economic Development Commission, and the U of A Office of the Vice Provost for Research and Innovation.)

About The Author

Camilla Shumaker is the director of science and research communications. She graduated Summa Cum Laude with a bachelor's degree in English from the University of Arkansas in 2001. She also holds a Master of Fine Arts in Creative Writing from the U of A. From 2010 through 2017, she was the director of communications in the U of A College of Engineering. Camilla can be reached at camillas@uark.edu or (479) 575-7422.

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