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POROUS SOLIDS — NANOCOMPOSITES — SELF-ASSEMBLED FRAMEWORKS |
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3D-Nanostructured
Battery Components Development of small-footprint, high
energy density batteries would permit construction of autonomous miniaturized
devices (MEMS, actuators, sensors)
without bulky external power supplies. State-of-the-art thin
film Li+ batteries do not have the capacity per unit area necessary to
supply
the typical energy needed by a smart dust mote. Furthermore,
conventional lithium secondary batteries experience large capacity losses
during rapid
charging or discharging. At high charging or discharging rates,
fast lithium ion insertion at the surface and slow lithium ion transport
within
the electrode result in concentration polarization of lithium
throughout the electrode material. This causes a rise or drop in battery
voltage,
which leads to termination of the charge or discharge before
the maximum capacity of the electrode material is utilized. A revolutionary
improvement
can be effected by altering the battery geometry from 2D to 3D
and by incorporating nanostructure features in the electrode architecture.
In
work funded by an ONR MURI program, we have developed macroporous
electrode structures based on colloidal crystal templating. In these
materials,
charge-transport occurs on a nanometer scale, rather than a micrometer
scale to reduce diffusion paths for charge carriers, diffusion
polarization, and thereby charging times. Construction of such materials
is possible
via colloidal crystal templating methods to produce periodic
macroporous structures of each battery component. We have prepared several
electrode
compositions with 3D ordered macroporous (3DOM) structure, including
3DOM cathode materials (LiMn2O4, LiCoO2,
LiNiO2, V2O5) and anode materials
(C, lithiated SnO2). We have demonstrated significant
charge/discharge rate advantages due to the porous electrode
architecture with submicrometer
pores. 3D porous electrodes for lithium batteries have the potential
for significantly enhancing geometric capacities (capacities
per unit
area). A
nanoarchitectured cell design offers relatively large power densities
and small geometrical footprints, providing the opportunity
for significant gains for small systems. We are currently developing
methods of integrating electrode and electrolyte components within
a 3D interpenetrating structure. In addition to studying the
effects of
the unique material structure on electrochemical properties,
we are addressing fundamental issues of crystallization/polymerization
within the confinement
of macropores. Related Research: • Monolithic
Macroporous Carbon Electrodes for Lithium-Ion •
Zinc and Magnesium Manganese Oxides with High Lithium • Receptor-Based Chemical Sensors With Three-Dimensionally
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Fig. 2. The inside journal cover of Advanced Materials 2006, 18(13) shows an SEM image of a 3D-interpenetrating electrochemical cell with submicrometer features reported on p. 1750 of the journal. The pores of an inverse opal carbon electrode were coated with a conformal layer of a polymer separator and infiltrated with vanadia to form the opposite electrode after lithiation. The idealized scheme illustrates lithium ion transport between electrodes through the polymer membrane.
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