Abstract: Provided are electrochemical cells and electrolytes used to build such cells. An electrolyte includes at least one salt having a molecular weight less than about 250. Such salts allow forming electrolytes with higher salt concentrations and ensure high conductivity and ion transport in these electrolytes. The low molecular weight salt may have a concentration of at least about 0.5M and may be combined with one or more other salts, such as linear and cyclic imide salts and/or methide salts. The concentration of these additional salts may be less than that of the low molecular weight salt, in some embodiments, twice less. The additional salts may have a molecular weight greater than about 250. The electrolyte may also include one or more fluorinated solvents and may be capable of maintaining single phase solutions at between about ?30° C. to about 80° C.

Abstract: High-purity crystalline ferric phosphate material with desirable characteristics for use in synthesis of nano-sized LFP cathode material are described. The ferric phosphate dihydrate material has as disclosed herein has a molar ratio of phosphorous to iron is from about 1.001 to about 1.05, a surface area of from about 25 m2/g to about 65 m2/g, and is substantially free of metallic or magnetic impurities. Methods of synthesizing high-purity crystalline ferric phosphate material with desirable characteristics for use in synthesis of nano-sized LFP cathode material are also described. In some embodiments, one or more magnetic traps are used during the reaction process and/or after the formation of the final product to remove magnetic impurities. In some embodiments, a synthetic method of ferric phosphate using multiple steps is described, wherein the intermediate of the synthesis is isolated and purified to improve the purity of the ferric phosphate material.

Abstract: Improved positive electrode material and methods for making the same are described. Lithium-iron-manganese phosphate materials, doped with one or more dopant Co, Ni, V, and Nb, and methods for making the same are described. The improved positive electrode material of the present invention is capable of exhibiting improved energy density and/or specific capacity for use in wide range of applications. In certain embodiments, energy density of greater than 340 mWh/g is possible.

Abstract: Systems and methods for assessing operation of analog digital converters (ADCs) of a battery pack supplying power to a vehicle are disclosed. One example system comprises, a first ADC for determining a voltage of at least one battery cell; a second ADC for determining a voltage of a plurality of battery cells; and a controller performing an action in response to comparing an output of said first ADC to an output of said second ADC.

Abstract: Systems and methods for assessing voltage threshold detection circuitry of individual battery cells within a battery pack supplying power to a vehicle are disclosed. One example system comprises, a plurality of battery cells within a battery pack, a plurality of voltage threshold detecting circuits detecting voltage of the plurality of battery cells, a voltage of a first battery cell of the plurality of battery cells coupled to a first voltage threshold detecting circuit of the plurality of voltage threshold detecting circuits, and a network that selectively couples a second battery cell to the first voltage detecting circuit while the first battery cell is coupled to the first voltage detecting circuit.

Abstract: The present disclosure relates to anode materials having high surface areas and improved cycle performance made by surface treatments of spheroidized graphite powders. The surface treatments provide a high surface area protective coating over the spheroidized graphite powder. The anodes made according to the disclosed embodiments have improved cycle life and long term high temperature storage performance. In the disclosed embodiments, a spheroidized graphite powder is coated with a high surface area protective coating. The high surface area protective coating improves the performance and durability of an anode made from disclosed material. The high surface area protective coating can include polymers, metal compounds and/or hard carbon. Further, in some embodiments, a protective coating, that may or may not have a high surface area but does have increased durability, can be formed by heat treating the spheroidized graphite in oxidizing or inert atmospheres.

Abstract: Provided are electrochemical cells and electrolytes used to build such cells. The electrolytes include ion-supplying salts and fluorinated solvents capable of maintaining single phase solutions with the salts at between about ?30° C. to about 80° C. The fluorinated solvents, such as fluorinated carbonates, fluorinated esters, and fluorinated esters, are less flammable than their non-fluorinated counterparts and increase safety characteristics of cells containing these solvents. The amount of fluorinated solvents in electrolytes may be between about 30% and 80% by weight not accounting weight of the salts. Fluorinated salts, such as fluoroalkyl-substituted LiPF6, fluoroalkyl-substituted LiBF4 salts, linear and cyclic imide salts as well as methide salts including fluorinated alkyl groups, may be used due to their solubility in the fluorinated solvents.

Abstract: Provided herein are methods for processing electrochemically active materials and resulting active material structures for use in rechargeable batteries. The resulting active materials structures include carbon containing coatings that partially or completely cover the surface of the active material structures. In a typical embodiment, the method includes providing a solution of carbon containing precursor in a solvent, dispersing electrochemically active material in the solution to form a mixture, removing the solvent from the mixture to form electrochemically active material coated with the carbon containing precursor, and heating the electrochemically active material coated with the carbon containing precursor in an inert atmosphere at a temperature sufficient to at least partially convert the carbon containing precursor into a carbon coating.

Abstract: Systems and methods for controlling the output of a battery pack are disclosed. In one example, a battery pack contactor is opened in response to battery pack current. The system and method may reduce battery pack degradation and increase system flexibility.

Abstract: A battery system comprises a battery cell having a cell body and a voltage terminal extending out of the cell body and having first and second terminal edges; a busbar to which an upper end of the voltage terminal is electrically connected; and a zipper fuse formed in a portion of the terminal between the cell body and the busbar, wherein the zipper fuse comprises an array of perforations through the voltage terminal and extending across the voltage terminal from the first edge to the second edge.

Abstract: Provided are electrochemical cells and electrolytes used to build such cells. An electrolyte may include a fluoroalkyl-substituted LiPF6 salt or a fluoroalkyl-substituted LiBF4 salt. In some embodiments, at least one fluorinated alkyl of the salt has a chain length of from 1 to 8 or, more specifically, between about 2 and 8. These fluorinated alkyl groups, in particular, relatively large fluorinated alkyl groups improve solubility of these salts in fluorinated solvents that are less flammable than, for example, conventional carbonate solvents. At the same time, the size of fluoroalkyl-substituted salts should be limited to ensure adequate concentration of the salt in an electrolyte and low viscosity of the electrolyte. In some embodiments, the concentration of a fluoroalkyl-substituted salt is at least about 0.5M.

Abstract: A battery system comprises a plurality of battery subunits arranged in a stack, wherein each battery subunit among the plurality of battery subunits comprises a first battery cell, a heatsink, a second battery cell, and a compliant pad in that order with the heatsink between and in thermal contact with the first and second battery cells and with the compliant pad abutting the second battery cell.

Abstract: Provided herein are methods for processing electrochemically active materials for use in rechargeable batteries. The methods may also be practiced on electrodes and batteries containing such electrochemically active materials. In a typical embodiment, a method of chemically modifying the surface of an electrochemically active component of a battery is provided, the method including receiving the electrochemically active material and exposing the electrochemically active material to a gaseous reactant under conditions that chemically modify surfaces of the electrochemically active material that are accessible to the gaseous reactant, and thereby produce a modified electrochemically active material having improved properties for use in the battery.

Abstract: A battery housing is comprised of a unitary, seamless base member having a generally planar, quadrilateral bottom face with a side wall extending therefrom. The length dimension of the bottom face is at least twice the height of the side wall. The base member has an open top face. The housing includes a cover which closes the open top face and is engageable with the side wall of the base. An electrically resistive sealing gasket is configured to contact the cover member and the side wall so as to provide a fluid-tight seal. The components are mechanically interlocked by crimping or hemming. The housing is specifically configured to accommodate stacking of individual batteries into power assemblies, and the geometry of the housing optimizes thermal management. Further disclosed are batteries and battery assemblies including the housing.

Abstract: An electrode/separator assembly for use in an electrochemical cell includes a current collector; a porous composite electrode layer adhered to the current collector, said electrode layer comprising at least electroactive particles and a binder; and a porous composite separator layer comprising inorganic particles substantially uniformly distributed in a polymer matrix to form nanopores and having a pore volume fraction of at least 25%, wherein the separator layer is secured to the electrode layer by a solvent weld at the interface between the two layers, said weld comprising a mixture of the binder and the polymer. Methods of making and using the assembly are also described.

Abstract: Electrodes with a multilayer or monolayer composite separator are described. The multilayer composite separator comprises multiple individual composite separator layers. Each individual composite separator layer comprises inorganic particulate material(s) and organic polymer(s) with different inorganic particulate material/polymer weight ratios. The multilayer composite separator layer is constructed in a way such that the composite separator layer adjacent to the electrode active material contains a higher weight percentage of the inorganic particulate material and lower weight percentage of the organic polymer than the composite separator layer outermost from the electrode current collector. Laminated cells comprising a positive electrode, a negative electrode, a laminated multilayer or monolayer composite separator layer are described, wherein at least one of the electrodes has a multilayer or monolayer composite separator disposed onto the surface of the electrode.

Abstract: Systems and methods for controlling the output of a battery pack are disclosed. In one example, a battery pack contactor is closed after receiving a request to open the battery pack contactor during a power-up sequence. The system and method may reduce battery pack degradation.

Abstract: A composite material having utility for removing sulfur from a feedstock comprises a ceramic matrix having a relatively low melting point metal such as tin, zinc, lead or bismuth nanodispersed therein. The material may be prepared from a mixture of particles of a precursor of the ceramic matrix and precursor of the metal. The precursors are selected such that the melting point of the precursor of the ceramic is less than the melting point of the precursor of the metal. The mixture of precursor materials is heated to a temperature sufficient to melt the precursor of the ceramic material so as to coat it onto the precursor of the metal. The ceramic precursor is then reacted so as to convert it to a ceramic. Thereafter, the precursor of the metal is converted to a free metal which is retained within the ceramic matrix so as to prevent agglomeration.

Abstract: An insulation portion for an electrochemical cell having a plurality of slots into which bent electrode tabs are slid through during an assembly process of an electrochemical cell. A latch is disposed adjacent the slots and is movable from a resting position to a biased position to engage the electrode tabs. Attachment of the insulation portion to the electrochemical cell and bending of the electrode tabs can be robotically performed, such that controllers of an attachment device and bending device are in communication with each other.

Abstract: A method of determining state of charge of an energy delivery device includes sampling voltage values of the energy delivery device during relaxation of the device. The method further includes regressing an open circuit voltage value and the total overpotential being relaxed. The regression includes a predetermined time constant of relaxation associated with the energy delivery device. One embodiment uses the equation V(t)=OCV?? exp(?t/tau), where V(t) represents the sampled voltage values, t represents times at which each of the voltage values are sampled, OCV represents the open circuit voltage value of the energy delivery device, ?represents the overpotential value, and tau represents the time constant of relaxation. The method uses a predetermined profile that relates open circuit voltage of the energy delivery device to state of charge of the device, to determine a particular state of charge corresponding to the regressed open circuit voltage value.