Working with a team at the University of Illinois at Chicago, the researchers developed a scalable method for making a material that can reversibly store magnesium ions at high-voltage, the defining feature of a cathode. While it is at an early stage, the researchers say it is a significant development in moving towards magnesium-based batteries. To date, very few inorganic materials have shown reversible magnesium removal and insertion, which is key for the magnesium battery to function.
"Lithium-ion technology is reaching the boundary of its capability, so it's important to look for other chemistries that will allow us to build batteries with a bigger storage capacity and a slimmer design," said Dr Ian Johnson in UCL's Chemistry department. "Magnesium battery technology has been championed as a possible solution to provide longer-lasting phone and electric car batteries, but getting a practical material to use as a cathode has been a challenge."
One factor limiting lithium-ion batteries is the anode. Low-capacity carbon anodes have to be used in lithium-ion batteries for safety reasons, as the use of pure lithium metal anodes can cause dangerous short circuits and fires. In contrast, magnesium metal anodes are much safer, so partnering magnesium metal with a functioning cathode material would make a battery smaller and store more energy. Previous research using computational models predicted that magnesium chromium oxide (MgCr2O4) could be a promising candidate for Mg battery cathodes.
The UCL researchers produced a ~5 nm, disordered magnesium chromium oxide material in a very rapid and relatively low temperature reaction. The team at Chicago then compared its magnesium activity with a conventional, ordered magnesium chromium oxide material ~7 nm wide.
They used a range of different techniques including X-ray diffraction and X-ray absorption spectroscopy to see the structural and chemical changes when the two materials were tested for magnesium activity in a cell.