%0 Journal Article %A Nicholas H Bashian %A Mateusz J Zuba %A Ahamed Irshad %A Shona M Becwar %A Julija Vinckeviciute %A Warda Rahim %A Kent J Griffith %A Eric T McClure %A Joseph K Papp %A Bryan D McCloskey %A David O Scanlon %A Bradley F Chmelka %A Anton Van der Ven %A Sri R Narayan %A Louis F.J Piper %A Brent C Melot %B Chemistry of Materials %D 2021 %G eng %N 14 %P 5757 - 5768 %R 10.1021/acs.chemmater.1c01594 %T Electrochemical Oxidative Fluorination of an Oxide Perovskite %U https://pubs.acs.org/doi/10.1021/acs.chemmater.1c01594 %V 33 %8 07/2021 %! Chem. Mater. %X

We report on the electrochemical fluorination of the A-site vacant perovskite ReO₃ using high-temperature solid-state cells as well as room-temperature liquid electrolytes. Using galvanostatic oxidation and electrochemical impedance spectroscopy, we find that ReO₃ can be oxidized by approximately 0.5 equiv of electrons when in contact with fluoride-rich electrolytes. Results from our density functional theory calculations clearly rule out the most intuitive mechanism for charge compensation, whereby F-ions would simply insert onto the A-site of the perovskite structure. Operando X-ray diffraction, neutron total scattering measurements, X-ray spectroscopy, and solid-state ¹⁹F NMR with magic-angle spinning were, therefore, used to explore the mechanism by which fluoride ions react with the ReO₃ electrode during oxidation. Taken together, our results indicate that a complex structural transformation occurs following fluorination to stabilize the resulting material. While we find that this process of fluorinating ReO₃ appears to be only partially reversible, this work demonstrates a practical electrolyte and cell design that can be used to evaluate the mobility of small anions like fluoride that is robust at room temperature and opens new opportunities for exploring the electrochemical fluorination of many new materials.