Electrochimica Acta, Vol.277, 20-29, 2018
Electrochemical and structural investigations of different polymorphs of TiO2 in magnesium and hybrid lithium/magnesium batteries
Commercial nanocrystalline TiO2 anatase and self-prepared TiO2(B) bronze synthesized by hydrothermal method were used as the cathode materials for Mg-ion and hybrid Li/Mg-ion batteries. The TiO2 anatase delivers high initial discharge/charge capacities of 225 mAh g(-1)/204mAhg(-1) in a mixture of Phenylmagnesium chloride-AlCl3/LiCl in tetrahydrofuran (APC/LiCl) hybrid electrolyte, while the TiO2(B) shows high initial discharge/charge capacities of 260 mAh g(-1)/231 mAh g(-1) in the same hybrid electrolyte. Low discharge capacities of 67 and 57 mAh g(-1) and strong polarization are observed for both TiO2 anatase and TiO2(B) samples in pure APC electrolyte, respectively. In situ synchrotron diffraction strongly identifies that in APC/LiCl hybrid electrolyte, the TiO2 anatase undergoes structural evolution via a solid solution and a two-phase reaction mechanism, while TiO2(B) exhibits a solid solution reaction during the discharge-charge processes. The analysis of X-ray photoelectron spectra for the TiO2 anatase and TiO2(B) cathodes in the discharged/charged states reveals a change of Mg/Ti as well as Li/Ti ratios at different stages, which may indicate a contribution of both Mg and Li to the charge storage mechanism in the hybrid electrolyte. (c) 2018 Elsevier Ltd. All rights reserved.
Keywords:TiO2 Hybrid lithium/magnesium batteries;In situ synchrotron;X-ray photoelectron spectroscopy (XPS);Electrochemical performance