This disclosure relates to compositions and methods for improving the performance of batteries, such as lead-acid batteries, including reviving or rejuvenating a partially or totally dead battery, by adding an amount of nonionic, ground state metal nanoparticles to the electrolyte of the battery, and optionally recharging the battery by applying a voltage. The metal nanoparticles may be gold and coral-shaped and are added to provide a concentration within the electrolyte of 100 ppb to 2 ppm or more (e.g., up to 5 ppm, 10 ppm, 25 ppm, 50 ppm, or 100 ppm). The metal nanoparticles may be added to battery electrode paste applied to the electrodes to enhance newly manufactured or remanufactured batteries.

An aqueous electrolyte composition suitable for a lithium ion battery is provided. The aqueous electrolyte composition contains water, an ionic liquid which is a salt of a protonic cation and an anion comprising a fluoroalkylsulfonyl group and a lithium fluoroalkylsulfonyl salt. A lithium ion battery containing the aqueous electrolyte and a vehicle at least partially powered by the battery are also provided.

A meta-solid-state battery includes a first layer disposed on a first current collector, a second layer disposed on a second current collector, and third layer disposed between the first layer and the second layer. The first layer and the second layer are the cathode and anode electrodes. The third layer includes a first meta-solid-state electrolyte material. Each of the cathode and anode electrodes contain: an active material in an amount ranging from approximately 70% to 99.98% by weight, a carbon additive in an amount ranging from approximately 0.010% to 20% by weight, and a second meta-solid-state electrolyte material in an amount ranging from approximately 0.010% to 10% by weight. The first and second meta-solid-state electrolyte material include a gel polymer.

A method and/or electrochemical cell for utilising one or more gas diffusion electrodes (GDEs) in an electrochemical cell, the one or more gas diffusion electrodes have a wetting pressure and/or a bubble point exceeding 0.2 bar. The one or more gas diffusion electrodes can be subjected to a pressure differential between a liquid side and a gas side. A pressure on the liquid side of the GDE over the gas side does not exceed the wetting pressure of the GDE during operation (in cases where a liquid electrolyte side has higher pressure), and/or a pressure on the gas side of the GDE over the liquid side, does not exceeds the bubble point of the GDE (in cases where the gas side has the higher pressure).

A lead acid battery is described that makes it possible to suppress an increase in internal resistance and to accurately determine the state of charge or the state of degradation by a method of measuring the internal resistance. The lead acid battery includes an electrode plate group in which a plurality of positive electrode plates having a positive active material containing lead dioxide and a plurality of negative electrode plates having a negative active material containing metallic lead are alternately stacked with separators interposed therebetween. The electrode plate group is immersed in an electrolyte. The flatness of the positive electrode plates after chemical conversion is equal to or less than 4.0 mm

An electrochemical gas sensor (10) has a housing (20), a working electrode (51), a counterelectrode (52) and a reference electrode (53). The housing (20) has an electrolyte reservoir (30), a gas inlet orifice (21) and at least one gas outlet orifice (22). The electrolyte reservoir (30) is filled with a liquid electrolyte (40). The gas sensor (10) has a counterelectrode carrier (26). The counterelectrode (52) is suspended on the counterelectrode carrier (26) in such a way that the counterelectrode (52) is suspended in the electrolyte reservoir (30) and the electrolyte (40) flows around the counterelectrode (52) on all sides. Preferably, the electrolyte includes (I) a solvent, e.g. water, propylene carbonate, ethylene carbonate or mixtures thereof; (ii) a conductive salt, especially an ionic liquid; and/or (iii) an organic mediator, for example substituted quinones, anthraquinones, etc.

The present invention relates to novel lignin-derived compounds and compositions comprising the same and their use as redox flow battery electrolytes. The invention further provides a method for preparing said compounds and compositions as well as a redox flow battery comprising said compounds and compositions. Additionally, an assembly for carrying out the inventive method is provided.

Electrolytes including deep eutectic solvents (DES) are provided. In one example, DES has a formula Cat.sup.+X.sup.−.zY, where Cat.sup.+X.sup.− is a salt including a cation Cat.sup.+ and an anion X.sup.− having a hydrogen bond acceptor (HBA) component, Y is a molecule having a hydrogen bond donor (HBD) component that interacts with the HBA component of the anion X.sup.−, and z is a molar ratio of the HBD component of the molecule Y to the HBA component of the anion X.sup.−. The DES based electrolytes of the present disclosure have low volatility, non-flammability, wide electrochemical voltage window, and high ionic conductivity, and may be used in electrochemical devices including electrochemical energy storage devices.

A lead-based alloy containing alloying additions of bismuth, antimony, arsenic, and tin is used for the production of doped leady oxides, lead-acid battery active materials, lead-acid battery electrodes, and lead-acid batteries.

The present invention relates to a method of preparing a high-purity electrolyte solution for a vanadium redox flow battery using a catalytic reaction, and more specifically, to a method of preparing a high-purity electrolyte solution having a vanadium oxidation state of +3 to +5 from a mixture solution containing a vanadium precursor, a reducing agent, and an acidic solution, by using a catalyst. By using a catalyst and a reducing agent that does not leave impurities such as Zn.sup.2+, which are generated when preparing electrolyte solutions using an existing metal reducing agent, the high-purity electrolyte solution for a vanadium redox flow battery (VRFB) according to the present invention eliminates the need for an additional electrolysis process; does not form toxic substances during a reaction process, and thus is environmentally friendly; and is electrochemically desirable under milder process conditions than that of an existing process. In addition, the VRFB comprising the electrolyte solution prepared according to the present invention may be used to expand the utility of new renewable energy through price reduction of large-capacity energy storage devices.