Hydrothermal synthesis of cubic α-Fe2O3 microparticles using glycine: Surface characterization, reaction mechanism and electrochemical activity
This article was originally published as: Yin, C., Minakshi, M., Ralph, D., Jiang, Z., Xie, Z. , & Guo, H. (2011). Hydrothermal synthesis of cubic α-Fe2O3 microparticles using glycine: Surface characterization, reaction mechanism and electrochemical activity. Journal of Alloys and Compounds, 509(41), 9821-9825. Original article available here
Cubic α-Fe2O3 (hematite) microparticles (side lengths = 0.3–1.3 μm) have been synthesized using glycine and ferric chloride via a simple one-step hydrothermal reaction. Their morphological, mineralogical and surface properties have been determined using scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffractometry (XRD) and X-ray photoelectron spectroscopy (XPS). XRD analysis indicated that the synthesized α-Fe2O3 microparticles were minerallogically pure. An increase in hydrothermal reaction duration from 10 to 24 h increased the atomic percentages of α-Fe2O3 on the surface of the microparticles by almost 8%. The mechanism concerning reactions of species to produce this microparticles precipitate was elucidated based on thermodynamics and ionic equilibrium aspects. In the electrochemical analysis, the synthesized α-Fe2O3 microparticles (as cathode material) exhibit an approximate charge capacity of 160 mAh/g and excellent coulombic efficiency of 94%.