The Science

Just like a shark, a new film detects minute changes in nearby electric fields while immersed in a harsh environment. The thin film contains samarium, nickel, and oxygen (SNO). When submerged in water and exposed to an electric bias, the film undergoes a reproducible and reversible change in its structure. That is, it incorporates protons into the lattice. This tiny change can be sensed as a voltage.

The Impact

Electrical resistance of the SNO sensor can be tuned when a small (millivolt level) electrical bias potential is applied. This property may aid the monitoring of electrical signals from maritime vessels and sea creatures.

Summary

Designing materials for sensors that function at peak performance in relatively harsh environments, such as saltwater, is of interest to technologies ranging from energy utilization and ocean monitoring to biological applications. One primary challenge in sensor design is to retain the structure and activity of the material as it interacts dynamically with the surrounding environment. Materials that respond to mild stimulation through temporary changes in their structure—or phase transitions—and that amplify signals could open up new avenues for sensing. Scientists discovered an electric-field-driven and reversible structural phase change in a thin samarium nickelate (SmNiO3) film while submerged in water. The discovery was made by a team of users of the Center for Nanoscale Materials (CNM), Advanced Photon Source (APS), National Energy Research Scientific Computing Center, and the Argonne Leadership Computing Facility (ALCF) from Purdue University. SNO is a commonly studied quantum material—materials with electronically cooperative behavior that can’t be explained by individual electron properties—because it is stable in salt water, does not corrode, and allows the exchange of protons with the surrounding water at room temperature. Numerical calculations of the molecular SNO-water interactions were performed on computing resources at the CNM and the ALCF to explain the sensing mechanism in detail. X-ray reflectivity and absorption spectroscopy were performed at the APS. In addition to performing as both self-regulating heating elements and pH sensors, devices made of this material can detect very small electric potentials in salt water. Therefore, such devices could be used in oceanic environments for monitoring electrical signals from maritime vessels and sea creatures.

Funding

The Army Research Office, National Science Foundation, Defense Advanced Research Projects Agency, Office of Naval Research, and Air Force Office of Scientific Research funded this research. Use of the Center for Nanoscale Materials and Advanced Photon Source, both Office of Science user facilities, was supported by the Department of Energy (DOE), the Office of Science, Office of Basic Energy Sciences. This research used resources of the National Energy Research Scientific Computing Center supported by the DOE Office of Science. An award of computer time was provided by the Innovative and Novel Computational Impact on Theory and Experiment (INCITE) program and used the resources of the Argonne Leadership Computing Facility at Argonne National Laboratory, which is supported by the DOE Office of Science. S.S.N. acknowledges support from the University of Massachusetts-Amherst through start-up funding. Part of the research was performed at the Canadian Light Source, which is supported by the Canada Foundation for Innovation, Natural Sciences and Engineering Research Council of Canada, the University of Saskatchewan, the Government of Saskatchewan, Western Economic Diversification Canada, the National Research Council Canada and the Canadian Institutes of Health Research.  

Publications

Z. Zhang, D. Schwanz, B. Narayanan, M. Kotiuga, J.A. Dura, M. Cherukara, H. Zhou, J.W. Freeland, J. Li, R. Sutarto, F. He, C. Wu, J. Zhu, Y. Sun, K. Ramadoss, S.S. Nonnenmann, N. Yu, R. Comin, K.M. Rabe, S.K.R.S. Sankaranarayanan, and S. Ramanathan, “Perovskite nickelates as electric field sensors in salt water.” Nature 553, 68 (2018). [DOI: 10.1038/nature25008]

Journal Link: Nature 553, 68 (2018). [DOI: 10.1038/nature25008]