The need for higher energy density batteries has spawned recent renewed interest in alternatives to lithium ion batteries, including multivalent chemistries that theoretically can provide twice the volumetric capacity if two electrons can be transferred per intercalating ion. Initial investigations of these chemistries have been limited to date by the lack of understanding of the compatibility between intercalation electrode materials, electrolytes, and current collectors. This work describes the utilization of hybrid cells to evaluate multivalent cathodes, consisting of high surface area carbon anodes and multivalent nonaqueous electrolytes that are compatible with oxide intercalation electrodes. In particular, electrolyte and current collector compatibility was investigated, and it was found that the carbon and active material play an important role in determining the compatibility of PF6-based multivalent electrolytes with carbon-based current collectors. Through the exploration of electrolytes that are compatible with the cathode, new cell chemistries and configurations can be developed, including a magnesium-ion battery with two intercalation host electrodes, which may expand the known Mg-based systems beyond the present state of the art sulfide-based cathodes with organohalide-magnesium based electrolytes.

Titanium-based ceramic supports designed for polymer electrolyte membrane fuel cells were synthesized, and catalytic activity was explored using electrochemical analysis. Synthesis of high surface area TiO2 and TiO supports was accomplished by rapidly heating a gel of polyethyleneimine-bound titanium in a tube furnace under a forming gas atmosphere. X-ray diffraction analysis revealed anatase phase formation for the TiO2 materials and crystallite sizes of less than 10 nm in both cases. Subsequent disposition of platinum through an incipient wetness approach leads to highly dispersed crystallites of platinum, less than 6 nm each, on the conductive supports. Scanning Electron Microscope (SEM)/energy dispersive x-ray analysis results showed a highly uniform Ti and Pt distribution on the surface of both materials. The supports without platinum are highly stable to acidic aqueous conditions and show no signs of oxygen reduction reactivity (ORR). However, once the 20 wt% platinum is added to the material, ORR activity comparable to XC-72-based materials is observed.

Currently, there are a variety of techniques to deposit metal thin films ranging from high vacuum techniques such as chemical vapor deposition (CVD) and physical vapor deposition (PVD), through to solution methods like sol-gel. While the vacuum techniques can be limited by size and cost, sol-gel can be limited be the availability of appropriate precursors. All of these techniques have the further limitation that they cannot be used to coat porous materials conformally.

Polymer assisted deposition (PAD) addresses some of the limitations of sol-gel and costs of high vacuum techniques. PAD utilizes an aqueous polymer to bind a metal or metal complex that serves both to encapsulate the metal to prevent chemical reaction and maintain an even distribution of the metal in solution. Another advantage that PAD has is that the same solution can be used as precursors for the growth of metal oxide or reduced metal films. Herein, we report on the utility of PAD in preparing metal oxide films used to conformally coat porous material and reduced metal films.