626results about "Indirect fuel cells" patented technology

Redox flow devices are described in which at least one of the positive electrode or negative electrode-active materials is a semi-solid or is a condensed ion-storing electroactive material, and in which at least one of the electrode-active materials is transported to and from an assembly at which the electrochemical reaction occurs, producing electrical energy. The electronic conductivity of the semi-solid is increased by the addition of conductive particles to suspensions and/or via the surface modification of the solid in semi-solids (e.g., by coating the solid with a more electron conductive coating material to increase the power of the device). High energy density and high power redox flow devices are disclosed. The redox flow devices described herein can also include one or more inventive design features. In addition, inventive chemistries for use in redox flow devices are also described.

A vanadium redox cell having a positive half cell containing a positive half cell solution comprising a supporting electrolyte selected from H₂SO₄, HBr/HCl mixtures and one or more ions selected from the group vanadium (EI), Vanadium (IV), Vanadium (V), Br₃ and Br₂Cl; a negative half cell containing a negative half cell solution comprising a supporting electrolyte selected from H₂SO₄, HBr and HBr/HCl mixtures and one or more vanadium ions selected from the group Vanadium (II), Vanadium (III) and Vanadium (FV) and a perfluorinated cast cation exchange membrane or separator disposed between the positive and negative half cells and in contact with the positive and negative half cell solutions.

The present invention provides high capacity and high voltage Li-ion batteries that have a carbonaceous cathode and a nonaqueous electrolyte solution comprising LiF salt and an anion receptor that binds the fluoride ion. The batteries can comprise dual intercalating electrode Li ion batteries. Methods of the present invention use a cathode and electrode pair, wherein each of the electrodes reversibly intercalate ions provided by a LiF salt to make a high voltage and high specific capacity dual intercalating electrode Li-ion battery. The present methods and systems provide high-capacity batteries particularly useful in powering devices where minimizing battery mass is important.

A redox flow battery comprising an electrode cell including a negative electrode cell, a positive electrode cell and a separator for separating them, in which at least one of the negative electrode cell and the positive electrode cell includes a slurry type electrode solution, a porous current collector and a casing; a tank for storing the slurry type electrode solution; and a pipe for circulating the slurry type electrode solution between the tank and the electrode cell.

An energy storage system includes a vanadium redox battery that interfaces with a control system to optimize performance and efficiency. The control system calculates optimal pump speeds, electrolyte temperature ranges, and charge and discharge rates. The control system instructs the vanadium redox battery to operate in accordance with the prescribed parameters. The control system further calculates optimal temperature ranges and charge and discharge rates for the vanadium redox battery.

A bio-implantable electrochemical cell system for active implantable medical devices. In one embodiment, the fuel cell includes an electrode structure consisting of immobilized anode and cathode enzymes deposited on nanostructured high-surface-area metal nanowires or carbon nanotube electrodes. The anode enzyme comprises immobilized glucose oxidase and the cathode enzyme comprises immobilized laccase. Glucose is oxidized at the surface of the anode and oxygen is reduced at the surface of the cathode. The coupled glucose oxidation-oxygen reduction reactions provide a self-generating current source. In another embodiment, the nanowires or carbon nanotubes, along with the adjacent surface anode and cathode electrodes, are coated with immobilized glucose oxidase and immobilized laccase containing biocolloidal substrates, respectively. This results in the precise construction of an enzyme architecture with control at the molecular level, while increasing the reactive surface area and corresponding output power by at least two orders of magnitude.

Embodiments of the invention generally provide for flow battery cells and systems containing a plurality of flow battery cells, and methods for improving metal plating within the flow battery cell, such as by flowing and exposing the catholyte to various types of cathodes. In one embodiment, a flow battery cell is provided which includes a cathodic half cell and an anodic half cell separated by an electrolyte membrane, wherein the cathodic half cell contains a plurality of cathodic wires extending perpendicular or substantially perpendicular to and within the catholyte pathway and in contact with the catholyte, and each of the cathodic wires extends parallel or substantially parallel to each other. In some examples, the plurality of cathodic wires may have at least two arrays of cathodic wires, each array contains at least one row of cathodic wires, and each row extends along the catholyte pathway.

A stack for use in a flow battery, the stack comprising an odd number of interior elements positioned between two end elements, the two end elements each including an electrode, and the odd number of interior elements including membrane elements alternating with electrode elements, wherein the membrane elements include an interior frame and a membrane, the electrode elements include the interior frame and an electrode, wherein the interior frame is rotated by 180° from the frame of the membrane elements.

The invention discloses a preparation method for commercial vanadium battery electrolyte. According to the preparation method, vanadium electrolyte is prepared by one step through a chemical method; the preparation method comprises the following steps: dissolving raw materials containing vanadium by using an alkali; adjusting a pH (Potential of Hydrogen) value by acid-alkali regulation; repeatedly precipitating the vanadium to remove impurity elements; then roasting to obtain an oxide of the vanadium; finally, dissolving the oxide of the vanadium by using concentrated sulfuric acid to obtain the vanadium electrolyte. With the adoption of the method, impurities including iron, chrome, silicon, manganese and the like can be removed effectively and a process flow is shortened; the vanadium yield is improved, the impurity content is reduced and the process flow is shortened; the product purity can also be improved. The preparation method for the commercial vanadium battery electrolyte has important meanings on production technology levels and market competitiveness of the vanadium electrolyte; the method has good economic benefits and social benefits.

A prior to charge vanadium halide redox cell, a vanadium halide redox cell which is at a state of charge selected from the group consisting of a zero state of charge and a near zero state of charge and vanadium halide redox cell which are fully charged and partially charged are described. The prior to charge vanadium halide redox cell comprises a positive half cell containing a positive half cell solution comprising a halide electrolyte, vanadium (III) halide and vanadium (IV) halide, a negative half cell containing a negative half cell solution comprising a halide electrolyte, vanadium (III) halide and vanadium (N) halide wherein the amounts of vanadium (III) halide, vanadium (IV) halide and halide ions in the positive and negative half cell solutions are such that in a first charging step comprising charging the prior to charge vanadium halide redox cell, a vanadium halide redox cell having a state of charge selected from the group consisting of a zero state of charge and a near zero state of charge comprising predominantly vanadium (N) halide in the positive half cell solution and predominantly V(III) halide in the negative half cell solution can be prepared. The vanadium halide redox cell which is at a state of charge selected from the group consisting of a zero state of charge and a near zero state of charge comprises a positive half cell containing a positive half cell solution comprising a halide electrolyte and a vanadium halide which is predominantly vanadium (N) halide, a negative half cell containing a negative half cell solution comprising a halide electrolyte and a vanadium halide which is predominantly vanadium (III) halide wherein the amount of vanadium (N) halide in the positive half cell solution and the amount of vanadium (III) halide in the negative half cell solution are such that the vanadium halide redox cell is at a state of charge selected from the group consisting of a zero state of charge and a near zero state of charge. The vanadium halide redox cell which is fully charged comprises a positive half cell containing a positive half cell solution comprising a halide electrolyte, a polyhalide complex, vanadium (IV) halide and vanadium (V) halide, a negative half cell containing a negative half cell solution comprising a halide electrolyte and vanadium (II) halide wherein the molar concentration of vanadium (V) and polyhalide complex:molar concentration of vanadium (II) halide is about stoichiometrically balanced. The vanadium halide redox cell which is partially charged comprises a positive half cell containing a positive half cell solution comprising a halide electrolyte, a polyhalide complex, vanadium (IV) halide and vanadium (V) halide, a negative half cell containing a negative half cell solution comprising a halide electrolyte, vanadium (II) halide and vanadium (III) halide wherein the number of moles of moles of polyhalide complex and vanadium (V): number of moles of vanadium (II) halide is about stoichiometrically balanced.

A battery comprises an acid electrolyte in which a compound provides acidity to the electrolyte and further increases solubility of at least one metal in the redox pair. Especially preferred compounds include alkyl sulfonic acids and alkyl phosphonic acids, and particularly preferred redox coupled include Co³⁺/Zn⁰, Mn³⁺/Zn⁰, Ce⁴⁺/V²⁺, Ce⁴⁺/Ti³⁺, Ce⁴⁺/Zn⁰, and Pb⁴⁺/Pb⁰.

A flow battery includes a membrane having a thickness of less than approximately one hundred twenty five micrometers; and a solution having a reversible redox couple reactant, wherein the solution wets the membrane.

Disclosed is an electrolyte for batteries, comprising: (a) an electrolyte salt; (b) an organic solvent; (c) a first compound having an oxidation initiation voltage (vs. Li/Li⁺) higher than the operating voltage of a cathode; and (d) a second reversible compound having an oxidation initiation voltage higher than the operating voltage of the cathode, but lower than the oxidation initiation voltage of the first compound. Also disclosed is a lithium secondary battery comprising said electrolyte. In the lithium secondary battery, two compounds having different safety improvement actions at a voltage higher than the operating voltage of the cathode are used in combination as electrolyte components. Thus, the safety of the secondary battery in an overcharged state can be ensured, and at the same time, the deterioration of the battery can be prevented from occurring when it is repeatedly cycled, continuously charged and stored at high temperature for a long time.

The present invention provides a method of designing a redox flow battery system that can prevent system efficiency loss caused by weak generation power or load power at the time of electric charge or discharge, without using any lead storage battery, and can also provide further improved system efficiency. In the present invention, generating equipment that varies irregularly in output of power generation is provided with the redox flow battery to smooth the output of power generation. An average value of output distribution of the battery with respect to the smoothed output of power generation and standard deviation are determined. Then, at least either of a specified output of the battery and a specified output of the converter for converting the battery output is determined based on the standard deviation.

An electrode for use in a flow cell is presented. The electrode includes a metal plate for collecting current in the electrode that is bonded between a first and second plate.

The invention relates to a redox flow cell containing a polyhalide/halide redox couple in the positive half-cell electrolyte and a V(III)/V(II) redox couple in the negative half-cell electrolyte. The invention also relates to a method of producing electricity by discharging the fully charged or partially charged redox flow cell, and a method of charging the discharged or partially discharged redox flow cell.