Novel materials with effective super dielectric constants for energy storage
Abstract
To test a theory of the recently discovered phenomenon of super dielectric
behavior at very low frequency, the dielectric constants of several ‘pastes’,
composed of porous alumina powders filled to the point of incipient wetness
with water containing dissolved sodium chloride, were measured. The effective
dielectric low frequency constants of some of the pastes were greater than
10¹⁰, dramatically higher than that of any material ever reported. Moreover,
the total energy density reported for one capacitor generated with NaCl-based
super dielectric material is marginally higher than found in any prior report.
These results are consistent with this recently postulated model of low frequency
super dielectric behavior in porous, non-conductive materials saturated
with ion-containing liquids: upon the application of an electric field, ions
dissolved in the saturating liquid contained in the pores will travel to the ends
of pore-filling liquid droplets creating giant dipoles. The fields of these giant
dipoles oppose the applied field, reducing the net field created per unit of
charge on the capacitor plates, effectively increasing charge/voltage ratio,
hence capacitance. This is simply a version of the theory of ‘polarizable media’
found in most classic texts on electromagnetism. Other observations reported
here include (1) the impact of ion concentration on dielectric values, (2) a
maximum voltage similar to that associated with the electrical breakdown of
water, (3) the loss of capacitance upon drying, (4) the recovery of capacitance
upon the addition of water to a dry super dielectric material, and (5) the linear
relationship between capacitance and inverse thickness. All observations are
consistent with the earlier proposed model of the super dielectric phenomenon.
An extrapolation of results suggests this technology can lead to energy
density greater than the best lithium-ion battery.
Description
The article of record as published may be found at http://dx.doi.org/10.1007/s11664-015-3641-8
Rights
This publication is a work of the U.S. Government as defined in Title 17, United States Code, Section 101. Copyright protection is not available for this work in the United States.Collections
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