Abstract:
In an example of a method for making a silicon-based active electrode material, a silicon active material precursor is introduced into a carrier gas. Another active material precursor is introduced into the carrier gas prior to, simultaneously with or subsequent to the silicon active material precursor. The other active material precursor is selected from a tin active material precursor, an aluminum active material precursor, a graphene active material precursor, and combinations thereof. The carrier gas containing the precursors is exposed to plasma vaporization, and a material is formed. The material includes i) an alloy of phase separated silicon and tin and/or aluminum, or ii) a graphene layer having silicon nanoparticles and tin nanoparticles, aluminum nanoparticles, or combinations of tin and aluminum nanoparticles deposited on a surface thereof, or iii) a graphene layer having an alloy of phase separated silicon and tin, aluminum, or tin and aluminum deposited on a surface thereof.
Abstract:
A negative electrode material includes an active material, which is present in an amount ranging from about 60 wt % to about 95 wt % of a total wt % of the negative electrode material. The negative electrode material further includes a polyimide binder, which is present in an amount ranging from about 1 wt % to about 20 wt % of the total wt % of the negative electrode material. The polyimide binder contains a repeating unit, where a backbone structure of each repeating unit has no ether group present and no more than one carbonyl group present. The negative electrode material also includes a conductive filler, which is present in an amount ranging from about 3 wt % to about 20 wt % of the total wt % of the negative electrode material.
Abstract:
A surface coating method and a method for reducing irreversible capacity loss of a lithium rich transitional oxide electrode are disclosed herein. In an example of the surface coating method, a dispersion of a lithium rich transitional oxide powder and an oxide precursor or a phosphate precursor in a liquid is formed. The liquid is evaporated. The forming and evaporating steps are carried out in the absence of air to prevent precipitation of the oxide precursor or the phosphate precursor. Hydrolyzation of the oxide precursor or the phosphate precursor is controlled under predetermined conditions, and an intermediate product is formed. The intermediate product is annealed to form an oxide coated lithium rich transitional oxide powder or the phosphate coated lithium rich transitional oxide powder.
Abstract:
A method of operating a vehicle powertrain includes determining a selected powertrain operational mode. A demand fraction is determined. An internal combustion engine (ICE) is to output a maximum power when a gaseous fuel is conveyed to an injector of the ICE at a source pressure greater than a cutoff pressure. The source pressure in a container in fluid connection with the injector is determined. The gaseous fuel is received at the source pressure by the injector to inject the gaseous fuel into the ICE for combustion in response to the source pressure, demand fraction, or selected powertrain operation mode meeting a first set of criteria. The injector is prevented from injecting the gaseous fuel into the ICE and the powertrain is driven from an alternative power source in response to the source pressure, demand fraction, or selected powertrain operation mode meeting a second set of criteria.
Abstract:
A porous interlayer for a lithium-sulfur battery includes an electronic component and a negatively charged or chargeable lithium ion conducting component. The electronic component is selected from a carbon material, a conductive polymeric material, and combinations thereof. In an example, the porous interlayer may be disposed between a sulfur-based positive electrode and a porous polymer separator in a lithium-sulfur battery. In another example, the porous interlayer may be formed on a surface of a porous polymer separator.
Abstract:
A method for increasing capacity of a natural gas (NG) tank. The method includes selecting a container with a service pressure rating of about 3,000 or 3,600 psi. An NG adsorbent is in the container. The container has a maximum fill capacity. The method further includes cooling the adsorbent by Joule-Thomson cooling during filling of the container with NG from a filling source at greater than 3,600 psi. The container is filled to the maximum fill capacity at a fill rate to prevent a bulk temperature of the adsorbent from rising more than about 5° C. above an ambient temperature. A rate of heat transfer from the tank is less than a rate of heating from compression of the NG and adsorption during the filling. The NG adsorbent adsorbs a higher amount of NG than it would at higher than 5° C. above ambient.
Abstract:
Anodes including mesoporous hollow silicon particles are disclosed herein. A method for synthesizing the mesoporous hollow silicon particles is also disclosed herein. In one example of the method, a silicon dioxide sphere having a silicon dioxide solid core and a silicon dioxide mesoporous shell is formed. The silicon dioxide mesoporous shell is converted to a silicon mesoporous shell using magnesium vapor. The silicon dioxide solid core, any residual silicon dioxide, and any magnesium-containing by-products are removed to form the mesoporous, hollow silicon particle.
Abstract:
A battery with a sulfur-containing cathode, an anode, and a separator between the cathode and the anode has a coating comprising a single-lithium ion conductor on at least one of the cathode or the separator.
Abstract:
A thermal barrier component for an electrochemical cell according to various aspects of the present disclosure includes a functional material. The functional material includes at least one of a hydrate of a metal carbonate and a hydrate of a metal phosphate. The functional material is configured to release water vapor at a first temperature of greater than or equal to about 100° C. and decompose to release a gaseous fire retardant at a second temperature of greater than or equal to about 300° C. Another thermal barrier component according to various aspects of the present disclosure includes a hydrate and a fire retardant. The hydrate is configured to release water in an amount greater than or equal to about 1 kg at a first temperature of greater than or equal to about 100° C. The fire retardant is configured to decompose at a second temperature of greater than or equal to about 300° C.
Abstract:
A coated polymer separator for a battery cell is provided. The coated polymer separator includes a polymer separator including a first primary surface and a second primary surface. The coated polymer separator further includes a ceramic-based composite coating disposed on the first primary surface and the second primary surface. The ceramic-based composite coating includes lithiated zeolite particles and particles of a second ceramic material including an oxide.