Preparation of plate-form manganese oxide by selective lithium extraction from monoclinic Li2MnO3 under hydrothermal conditions

Hydrothermal lithium extraction from well-crystallized Li2MnO3 crystals was studied by scanning electron microscopy (SEM) observation, chemical, and X-ray diffraction analyses. Monoclinic Li2MnO3 polyhedral crystals were prepared in an LiCl flux at 650 degreesC. The lithium extraction was carried out in a variety of H2SO4 solutions with mole ratios of H+ in the solution to Li+ in the solid ([H+](l)/[Li+](s)) of 0.1, 0.15, 0.25, 0.50, 0.75, and 1.0 under a hydrothermal condition at 140 degreesC, The lithium extraction from Li2MnO3 proceeds consuming equimolar H+ in the solution by the mechanism of a Li+/H+ ion exchange reaction when [H+](l)/[Li+](s) less than or equal to 0.15 and by the mechanism of a mixture of the Li+/H+ ion exchange reaction and lithium dissolution when 0.25 less than or equal to [H+](l)/[Li+](s) less than or equal to 0.75. The lithium-extracted phase preserves the crystal structure of Li2MnO3 with a partial contraction of the lattice when 0.25 less than or equal to [H+](l)/[Li+](s) less than or equal to 0.75. SEM observation showed that the lithium extraction brings about a cleavage of the Li2MnO3 particle along the (001) plane to result in a unique form in which platelike particles are stacked, preserving the polyhedral outline. High-magnification SEM observation showed that the platelike particles consist of an aggregate of subplates with nanometer thickness in parallel arrangement. Slit-shaped mesopores were formed among the subplates. gamma -MnO2 was formed as a final product when [H+](l)/[Li+](s) = 1. A structural model is proposed to explain the mechanism of lithium extraction as well as the cleavage of the particle.