Mixed valence Zn–Co-layered double hydroxides and their exfoliated nanosheets with electrode functionality

New phases of Zn–Co-layered double hydroxides (Zn–Co-LDHs) were synthesized for the first time via a co-precipitation reaction using hydrogen peroxide as an oxidant. According to powder X-ray diffraction and field emission-scanning electron microscopy, both nitrate- and sulfate-forms of the Zn–Co-LDHs crystallized with the brucite-type layer structure having interlayer nitrate and sulfate anions, respectively, and commonly showed plate-like morphology with a crystal size of several hundred nanometers. dc magnetic susceptibility measurements revealed that the Zn–Co-LDHs displayed ferromagnetic/antiferromagnetic transitions below 15 K and the magnetic moment calculated from the paramagnetic region (30–300 K) indicated the co-existence of weak field Co2+ and strong field Co3+ ions. The mixed oxidation state of Co2+/Co3+ was confirmed by the results of iodometry and X-ray absorption near-edge structure spectroscopy. The heat-treatment for the Zn–Co–LDHs at elevated temperatures produced mixed metal oxide nanocomposites composed of spinel ZnCo2O4 and wurzite ZnO phases. The colloidal suspension of exfoliated Zn–Co-LDH nanosheets could be synthesized by dispersion of the pristine LDH materials in formamide, which was confirmed by the Tyndall phenomenon, high resolution-transmission electron microscopy/selected area electron diffraction, and UV-vis spectroscopy. The Zn–Co-LDH film fabricated with the restacked nanosheets exhibited pseudocapacitive behavior with a large specific capacitance and a good capacitance retention. The present findings underscore that the newly synthesized mixed valence Zn–Co-LDH phases showed promising functionality as a supercapacitor electrode material and also showed interesting magnetic coupling behavior.