The energy density and power density of lightweight aerospace batterie
s utilizing the nickel oxide electrode are often limited by the micros
tructures of both the collector and the resulting active deposit inion
the collector. Heretofore, these two microstructures have been intima
tely linked to one another by the materials used to prepare the collec
tor grid as well as the methods and conditions used to deposit the act
ive material. Significant weight and performance advantages have been
demonstrated by Britton and Reid at NASA-LeRC using FIBREX nickel mats
of similar to 28-32 mu m diameter. Work in our laboratory has investi
gated the potential performance advantages offered by nickel fiber com
posite electrodes containing a mixture of fibers as small as 2 mu m di
ameter (available from Memtec America Corporation). These electrode co
llectors possess in excess of an order of magnitude more surface area
per gram of collector than FIBREX nickel. The increase in surface area
of the collector roughly translates into an order of magnitude thinne
r layer of active material. Performance data and advantages of these t
hin layer structures will be presented. Attributes and limitations of
their electrode microstructure to independently control void volume, p
ore structure of the NI(OH)(2) deposition, and resulting electrical pr
operties will be discussed.