Porous Mixed-Metal Oxide Li-Ion Battery Electrodes by Shear-Induced Co-assembly of Precursors and Tailored Polymer Particles

Due to their various applications, metal oxides are of high interest for fundamental research and commercial usage. Per applications as catalysts or electrochemical devices, the tailored design of metal oxides featuring a high specific surface area and additional functionalities is of the utmost importance for the performance of the resulting materials. We report a new method for preparing free-standing films consisting of hierarchically porous metal oxides (titanium and niobium based) by combining emulsion polymerization and shear-induced monodisperse particle self-assembly in the presence of sol-gel precursors. After thermal treatment, the resulting porous materials can be used as electrodes in Li-ion batteries. The titanium and niobium sol-gel precursors were partially immobilized to the surface of organic core-interlayer particles featuring hydroxyl groups to obtain hybrid organic-inorganic particles through the melt-shear organization process. Free-standing particle-based films, in analogy to elastomeric opal alms and colloidal crystals, can be prepared in a convenient one-step preparation process. After thermal treatment, ordered pores are obtained, while the pristine metal oxide precursor shell can be converted to the (mixed) metal oxide matrix. Heat treatment under CO2 leads to mixed-TiNb oxide/carbon hybrid materials. The highly porous derivative structure enhances electrolyte permeation. When tested as Li-ion battery electrodes, it shows a specific capacity of 335 mAh.g(-1) at a rate of 10 mA.g(-1). After 1000 cycles at 250 mA.g(-1), the electrodes still provided a specific capacity of 191 mAh.g(-1).

Automated summary

A new method for preparing free-standing films of metal oxides for use as electrodes in Li-ion batteries is reported. This method combines emulsion polymerization and shear-induced monodisperse particle self-assembly. The resulting porous materials have ordered pores and a high specific surface area, and can be converted to metal oxide matrices. Heat treatment under CO2 leads to mixed-TiNb oxide/carbon hybrid materials, with enhanced electrolyte permeation. When tested as Li-ion battery electrodes, the materials showed a specific capacity of 335 mAh.g(-1) at a rate of 10 mA.g(-1) and retained a specific capacity of 191 mAh.g(-1) after 1000 cycles at 250 mA.g(-1).