Abstract: The present invention is directed to an electrochemical device for at least partially removing or reducing a target ionic species from an aqueous solution using faradaic immobilization, the electrochemical device including at least one first electrode and at least one second electrode with different void fraction and surface area properties, due to differences in void fraction (also referred to as void ratio) of the at least one first and the at least one second electrode, water flows through an electrode with a high porosity, while the aqueous solution does not flow through an electrode with a low porosity. The asymmetry of the electrodes provides a desired voltage distribution across the device, which equates to a different voltage at each electrode, to control the speciation of the target ionic species at the anode and the cathode.

Abstract: The present invention is directed to an electrochemical device for at least partially removing or reducing a target ionic species from an aqueous solution using faradaic immobilization, the electrochemical device including at least one first electrode and at least one second electrode with different void fraction and surface area properties, due to differences in void fraction (also referred to as void ratio) of the at least one first and the at least one second electrode, water flows through an electrode with a high porosity, while the aqueous solution does not flow through an electrode with a low porosity. The asymmetry of the electrodes provides a desired voltage distribution across the device, which equates to a different voltage at each electrode, to control the speciation of the target ionic species at the anode and the cathode.

Abstract: A method for removing a metal from a carbonaceous electrode includes providing a regeneration solution that includes an acid, an oxidizing agent, or a combination thereof. The method further includes applying the regeneration solution to the carbonaceous electrode, and oxidizing the metal on the surface of the carbonaceous electrode. The method also includes collecting the oxidized metal in the regeneration solution.

Abstract: The present invention is directed to an electrochemical device for at least partially removing or reducing a target ionic species from an aqueous solution using faradic immobilization, the electrochemical device including at least one first electrode and at least one second electrode with different void fraction and surface area properties, due to differences in void fraction (also referred to as void ratio) of the at least one first and the at least one second electrode, water flows through an electrode with a high porosity, while the aqueous solution does not flow through an electrode with a low porosity. The asymmetry of the electrodes provides a desired voltage distribution across the device, which equates to a different voltage at each electrode, to control the speciation of the target ionic species at the anode and the cathode.

Abstract: The present invention is directed to an electrochemical device for at least partially removing or reducing a target ionic species from an aqueous solution using faradaic immobilization, the electrochemical device including at least one first electrode and at least one second electrode with different void fraction and surface area properties, due to differences in void fraction (also referred to as void ratio) of the at least one first and the at least one second electrode, water flows through an electrode with a high porosity, while the aqueous solution does not flow through an electrode with a low porosity. The asymmetry of the electrodes provides a desired voltage distribution across the device, which equates to a different voltage at each electrode, to control the speciation of the target ionic species at the anode and the cathode.

Abstract: Applicant's faradic porosity cell combines adsorption (physical and capacitive) and faradic immobilization of a target species by optimizing electrode porosity, applied E, and Pourbaix operating regions. The optimization parameters are (i) physical adsorption; (ii) capacitive adsorption; (iii) electrochemical pH modulation; (iv) electrochemical peroxide (H2O2) generation; (v) electrodeposition (e.g., electroplating, electrophoretic deposition); (vi) electrochemical oxidation or reduction; (vii) precipitation; (viii) pore mouth diameter profile, and (ix) electrode spacing, and (xi) flow-by vs. flow-through vs. carbon block cell design.

Abstract: Applicant's faradic porosity cell combines adsorption (physical and capacitive) and faradic immobilization of a target species by optimizing electrode porosity, applied E, and Pourbaix operating regions. The optimization parameters are (i) physical adsorption; (ii) capacitive adsorption; (iii) electrochemical pH modulation; (iv) electrochemical peroxide (H2O2) generation; (v) electrodeposition (e.g., electroplating, electrophoretic deposition); (vi) electrochemical oxidation or reduction; (vii) precipitation; (viii) pore mouth diameter profile, and (ix) electrode spacing, and (xi) flow-by vs. flow-through vs. carbon block cell design.

Abstract: Disclosed are activated carbon electrodes fabricated according to a “pore mouth diameter mixture profile” that is optimized for a given electrochemical application. In a given pore mouth diameter mixture profile, the pore mouth diameter and conductivity of activated carbon are tightly controlled and provide unexpected long-term charging/discharging (aka “cycling”) performance. A given “pore mouth diameter mixture profile” optimizes a mixture of pore mouth diameters for a given electrochemical application, such as energy storage, desalination, deionization, hydrolysis, and dialysis, inter alia.

Abstract: Disclosed are activated carbon electrodes fabricated according to a “pore mouth diameter mixture profile” that is optimized for a given electrochemical application. In a given pore mouth diameter mixture profile, the pore mouth diameter and conductivity of activated carbon are tightly controlled and provide unexpected long-term charging/discharging (aka “cycling”) performance. A given “pore mouth diameter mixture profile” optimizes a mixture of pore mouth diameters for a given electrochemical application, such as energy storage, desalination, deionization, hydrolysis, and dialysis, inter alia.