Chemistry: electrical current producing apparatus – product – and – Current producing cell – elements – subcombinations and... – Electrode
Reexamination Certificate
1997-12-19
2001-04-03
Nuzzolillo, Maria (Department: 1745)
Chemistry: electrical current producing apparatus, product, and
Current producing cell, elements, subcombinations and...
Electrode
C429S218100
Reexamination Certificate
active
06210831
ABSTRACT:
TECHNICAL FIELD
The present invention relates generally to the field of cathodes and rechargeable electric current producing cells. More particularly, the present invention pertains to solid composite cathodes which comprise (a) an electroactive sulfur-containing material which, in its oxidized state, comprises a polysulfide moiety of the formula, —S
m
—, wherein m is an integer from 3 to 10; and, (b) a non-electroactive particulate material having a strong adsorption of soluble polysulfides. This strongly adsorbing particulate material significantly reduces or retards the diffusion of sulfur-containing electroactive materials from the cathode into the electrolyte and other cell components when incorporated into the cathode of an electric current producing cell. The present invention also pertains to electric current producing cells comprising such composite cathodes, and methods of making such solid composite cathodes and electric current producing cells.
BACKGROUND
Throughout this application, various publications, patents, and published patent applications are referred to by an identifying citation. The disclosures of the publications, patents, and published patent applications referenced in this application are hereby incorporated by reference into the present disclosure to more fully describe the state of the art to which this invention pertains.
As the rapid evolution of portable electronic devices continues, the need for safe, long-lasting, high capacity rechargeable batteries becomes increasingly evident. Under such circumstances, high energy density lithium secondary batteries are rapidly being developed that will eventually replace the conventional lead acid, nickel-cadmium, and nickel metal hydride batteries in many applications. In recent years, there has been considerable interest in developing high energy density cathode active materials and alkali metals as anode active materials for high energy density lithium secondary batteries to meet these needs.
Lithium and sulfur are highly desirable as the electrochemically active materials for the anode and cathode, respectively, of rechargeable or secondary battery cells because they provide nearly the highest energy density on a weight (2500 Wh/kg) or volume (2800 Wh/l) basis possible of any of the known combinations of materials. To obtain high energy densities, the lithium can be present as the pure metal, in an alloy or in an intercalated form, and the sulfur can be present as elemental sulfur or as a component in an organic or inorganic material with a high sulfur content, preferably greater than 50 weight percent sulfur.
Hereinafter, anodes containing the element lithium in any form are referred to as lithium-containing anodes. Cathodes containing the element sulfur in any form are hereinafter referred to as sulfur-containing cathodes.
Many battery systems comprising alkali metal containing anodes and sulfur-containing cathodes have been described. Exemplary of high temperature cells incorporating molten alkali metal anodes and molten sulfur cathodes separated by a solid electrolyte are those described in U.S. Pat. Nos. 3,993,503, 4,237,200 and 4,683,179. For operation, these storage cells must be heated to temperatures greater than about 320° C. Of considerable recent interest are cells comprising alkali metal anodes and cathodes containing elemental sulfur that operate at considerably lower temperatures, particularly those with solid cathodes operating at ambient temperatures. Rechargeable lithium sulfur battery cells operating at room temperature have been described by Peled et al. in
J. Power Sources,
1989, 26, 269-271, wherein the solid sulfur-containing cathodes are comprised of a porous carbon loaded with elemental sulfur. The nature of the porous carbon was not described, but cells constructed with these cathodes provided only a maximum of 50 cycles. The decline in capacity with cycling was attributed to loss of cathode active material.
U.S. Pat. No. 3,639,174 to Kegelman describes solid composite cathodes comprising elemental sulfur and a particulate electrical conductor. U.S. Pat. No. 4,303,748 to Armand et al. discloses solid composite cathodes containing an ionically conductive material together with elemental sulfur, transition metal salts, or other cathode active materials for use with lithium or other anodes in which, for example, the active sulfur or other cathode active material and the inert compounds with electrical conduction, such as graphite powder, are both particles of between 1 and 500 microns in diameter. Further examples of cathodes comprising elemental sulfur, an electrically conductive material and an ionically conductive material that operate in the temperature range from −40° C. to 145° C. are described in U.S. Pat. Nos. 5,523,179, 5,532,077, 5,582,623 and 5,686,201 to Chu. U.S. Pat. Nos. 5,552,244 and 5,506,072 to Griffin et al. describe metal-sulfur batteries using a cathode comprising a mixture of finely divided sulfur and graphite packed around a conductive electrode and covered with a porous separator. A minimum of 10 weight percent of graphite is needed to achieve sufficient conductivity in the cathode structure. No function other than providing conductivity is described for the graphite.
In spite of the many known systems, as for example described above, employing a solid cathode comprising elemental sulfur in rechargeable alkali metal sulfur battery systems has been problematic in obtaining good electrochemical efficiency and capacity, cycle life, and safety of the cells owing to the diffusion of sulfur active materials from the sulfur-containing cathode into the electrolyte and anode components. This has been particularly true in battery cells comprising a sulfur-containing cathode in combination with a lithium-containing anode. U.S. Pat. No. 3,907,591 to Lauck and an article by Yamin et al. in
J. Power Sources,
1983, 9, 281-287 describe the reduction of elemental sulfur during the discharging of a lithium/sulfur cell to soluble lithium polysulfides in high concentrations in the electrolyte. Even partial reduction of the solid sulfur in the cathode forms polysulfides, such as lithium octasulfide, that are soluble in the organic electrolytes. In battery cells, these soluble polysulfides diffuse from the cathode into the surrounding electrolyte and may react with the lithium anode leading to its fast depletion. This leads to reduced capacity of the battery cell.
In attempts to reduce the problems associated with the generation of soluble polysulfides in alkali metal battery cells comprising elemental sulfur, battery cells have been developed utilizing cathodes comprised of sulfur-containing materials in which sulfur is chemically bound to an organic or carbon polymer backbone or to a low molecular weight organic compound. One such class of electroactive sulfur-containing materials has been referred to as organo-sulfur materials. Herein, the term “organo-sulfur materials” means a material containing organic sulfur compounds with only single or double carbon-sulfur bonds or sulfur-sulfur bonds forming disulfide (—S—S—) linkages.
U.S. Pat. Nos. 4,833,048 and 4,917,974 to Dejonghe et al. disclose liquid sulfur-containing cathodes comprising organo-sulfur materials of the formula, (R(S)
y
)
n
, where y=1 to 6; R is one or more different aliphatic or aromatic organic moieties having 1 to 20 carbon atoms; and n is greater than 1. U.S. Pat. No. 5,162,175 to Visco et al. describes the use of 1 to 20 weight percent of conductor particles, such as carbon black, in solid composite cathodes containing organo-sulfur materials having disulfide electroactive groups. These organo-sulfur materials undergo polymerization (dimerization) and de-polymerization (disulfide cleavage) upon the formation and breaking of the disulfide bonds. The de-polymerization which occurs during the discharging of the cell results in lower molecular weight polymeric and monomeric species, namely soluble anionic organic sulfides, which may dissolve into the electrolyte and cause self discharge, redu
Boguslavsky Leonid I.
Deng Zhongyi
Gorkovenko Alexander
Mukherjee Shyama P.
Skotheim Terje A.
Moltech Corporation
Morrison & Foerster / LLP
Nuzzolillo Maria
Tsang Susy
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