A crystal of iron sulfide grown in the University of Minnesota lab to extremely high purity using a method called chemical vapor transport. Photo: Leighton et al.In a breakthrough new study, scientists and engineers at the University of Minnesota have electrically transformed the abundant and low-cost non-magnetic material iron sulfide, also known as ‘fool's gold’ or pyrite, into a magnetic material.
This is the first time that scientists have electrically transformed an entirely non-magnetic material into a magnetic one, and it could be the first step in creating valuable new magnetic materials for more energy-efficient computer memory devices. The researchers report their work in a paper in Science Advances.
"Most people knowledgeable in magnetism would probably say it was impossible to electrically transform a non-magnetic material into a magnetic one. When we looked a little deeper, however, we saw a potential route, and made it happen," said Chris Leighton, the lead researcher on the study and a professor in the Department of Chemical Engineering and Materials Science.
Leighton and his colleagues have been studying iron sulfide for more than a decade for possible use in solar cells. Sulfur in particular is a highly abundant and low-cost by-product of petroleum production. Unfortunately, scientists and engineers haven't found a way to make the material efficient enough to realize low-cost, earth-abundant solar cells.
"We really went back to the iron sulfide material to try to figure out the fundamental roadblocks to cheap, non-toxic solar cells," Leighton said. "Meanwhile, my group was also working in the emerging field of magnetoionics, where we try to use electrical voltages to control magnetic properties of materials for potential applications in magnetic data storage devices. At some point we realized we should be combining these two research directions, and it paid off."
According to Leighton, their goal was to manipulate the magnetic properties of materials with a voltage alone, with very little electrical current, which is important for making magnetic devices more energy efficient. Progress to date had included turning ferromagnetism, the most technologically important form of magnetism, on and off in other types of magnetic materials. Iron sulfide, however, offered the prospect of electrically inducing ferromagnetism in an entirely non-magnetic material.
In the study, the researchers took advantage of a technique called electrolyte gating. They took the non-magnetic iron sulfide material and put it in a device in contact with an ionic solution, or electrolyte. By applying as little as 1 volt (less voltage than a household battery), they were able to move positively charged molecules to the interface between the electrolyte and the iron sulfide, and induce magnetism. Importantly, they were able to turn off the voltage and return the material to its non-magnetic state, meaning they can reversibly switch the magnetism on and off.
"We were pretty surprised it worked," Leighton said. "By applying the voltage, we essentially pour electrons into the material. It turns out that if you get high enough concentrations of electrons, the material wants to spontaneously become ferromagnetic, which we were able to understand with theory. This has lots of potential. Having done it with iron sulfide, we guess we can do it with other materials as well."
Leighton said they would never have imagined trying this approach if it wasn't for his team's research into iron sulfide for solar cells and the work on magnetoionics. "It was the perfect convergence of two areas of research," he said.
The next step will involve trying to replicate the process at higher temperatures, which the team's preliminary data suggest should certainly be possible. The researchers also hope to try the process with other materials and to demonstrate potential for real devices.
This story is adapted from material from the University of Minnesota, with editorial changes made by Materials Today. The views expressed in this article do not necessarily represent those of Elsevier. Link to original source.