A device for removing ions from a solution. The device includes first and second end plates, an anion exchange membrane positioned between the first and second end plates, a first multiple of two or more first cation intercalation electrodes positioned between the first end plate and the anion exchange membrane, and one or more second intercalation electrodes positioned between the second end plate and the anion exchange membrane. The first multiple of two or more first cation intercalation electrodes and the one or more second intercalation electrodes are configured to receive an electric bias of current or voltage such that the first multiple of two or more first cation intercalation electrodes and the one or more second intercalation electrodes store and release ions from the solution.

A device for removing ions from a solution. The device includes first and second flow channels between an anion exchange membrane and first and second flow plates, respectively. The first flow channel has a first land volume positioned between the first land regions and the anion exchange membrane. The first flow channel has a first channel volume positioned between the anion exchange membrane and the first channel regions and spaced apart from the anion exchange membrane. The second flow channel has a second land volume positioned between the second land regions and the anion exchange membrane. The second flow channel has a second channel volume positioned between the anion exchange membrane and the second channel regions and spaced apart from the anion exchange membrane. The device also includes an intercalation material positioned within the first land and channel volumes or the second land and channel volumes.

A system and a method for separation of ions from ions-containing medium is disclosed herein, that utilizes capacitive-faradaic fuel cells (CFFC) particles coated at least partially with catalysts capable of catalyzing redox reactions provided a reductant (fuel) and/or an oxidant, thereby polarizing the particles to more effectively absorb charged species (ions) from the water upon introducing, e.g., H.sub.2 gas or O.sub.2 gas, in the medium during the adsorption or regeneration. The same concept is utilized in a hybrid electrochemical cell for providing a system and a method for generating and converting electrochemical energy.

The present disclosure provides methods, electrodes, and systems for electrochemical oxidation of polyfluoroalkyl and perfluroalkyl (PFAS) contaminants using Magnéli phase titanium suboxide ceramic electrodes/membranes. Magneli phase titanium suboxide ceramic electrodes/membranes can be porous and can be included in reactive electrochemical membrane filtration systems for filtration, concentration, and oxidation of PFASs and other contaminants.

The invented bio-electrical system is a housing-electrode which allows insertion of another electrode for various electrochemical and bio-electrical applications. Together with other invented elements as well as standard components, the system is fully scalable, modular, and allows production and collection of gases under pressure. It can be built in many shapes, such as the embodied tubular shape. The design allows operation on unstable ground, for example on ships. Flow of electrolyte can be regulated and directed in cascaded reactions by opening and closing the compartments of the outer or the inner electrodes using the provided electrode holders. The redox conditions inside the system can be controlled using off-the-shelf power supplies which are controlled using the provided algorithm. Gas collection can be regulated based on the level of liquid inside the system using the provided float switches or conductivity probes even as the system is moving or operated under zero-gravity conditions.

A device for removing ions from a solution. The device includes first and second intercalation hosts, an anion exchange membrane, a first compartment extending between the first intercalation host and the anion exchange membrane, and a second compartment extending between the second intercalation host and the anion exchange membrane. The first and/or second intercalation hosts include a mixture of first and second intercalation materials. The first and/or second intercalation hosts may include layers (e.g., alternating layers) of the first and second intercalation materials. The first and second intercalation materials are different.

An electrode for use in a device configured to remove ions from a solution. The electrode includes an intercalation material including a binary transition metal Prussian blue analogue compound, a ternary transition metal Prussian blue analogue compound, or a combination thereof. The binary compound may have a general formula: A.sub.xB.sub.yC.sub.z[Fe(CN).sub.6], where A=Li, Na, or K; B=Mn, Fe, Ni, Cu, or Zn; C=Mn, Fe, Ni, Cu, or Zn; 0≤x≤1; 0≤y≤1; and 0≤z≤1. The ternary compound may have the general formula: A.sub.xB.sub.yC.sub.zD.sub.w[Fe(CN).sub.6], where A=Li, Na, or K; B=Mn, Fe, Ni, Cu, or Zn; C=Mn, Fe, Ni, Cu, or Zn; D=Mn, Fe, Ni, Cu, or Zn; 0≤x≤1; 0≤y≤1; 0≤z≤1; 0≤w≤1.

There is disclosed a method of making an electrode for an electrochemical reactor including the steps of providing a template and depositing electrode material such that the electrode material is in contact with the template. This template is provided in a form that produces channels in the electrode material. There is also disclosed an electrode for an electrochemical reactor which includes electrode material and a template, with the template occupying channels in the electrode material.

A method of making copper sulfide electrode material comprising steps of: 1) stirring and dissolving copper(ii) nitrate hydrate (Cu(NO.sub.3)2.3H.sub.2O) and Thiourea (CH.sub.4N.sub.2S) in a mixed solution consisting of ethylene glycol and deionized water; 2) adding hexadecyl trimethyl ammonium bromide (C.sub.19H.sub.42N.Br) to mixture A; 3) placing the mixture B into a roaster, raising a temperature of the roaster to 100° C. to 180° C. for 10 hours to 18 hours; 4) washing the crude CuS by using a mixed fluid of ethanol absolute (C.sub.2H.sub.6O) and deionized water to be cooled in a room temperature, placing the crude CuS in the roaster and raising a temperature of the roaster to 50° C. to 80° C.; 5) producing cathode electrode of asymmetric capacitive deionization module by using the copper sulfide electrode material; 6) producing anode electrode of asymmetric capacitive deionization module by using activated carbon electrode material.

A water treatment apparatus including: discharge treatment units each including a ground electrode and a discharge electrode opposing the ground electrode, and water to be treated is treated by forming a discharge between the ground electrode and the discharge electrode, and generating ozone by the discharge, and moreover causing the water to be treated to contact the discharge; a water reservoir portion that collects, in the interior of the treatment tank, the water to be treated having been subject to water treatment by one of the discharge treatment units; and an ozone supply section that supplies the ozone in the treatment tank to the water to be treated in the water reservoir portion are provided, and wherein the water to be treated passes through the plurality of discharge treatment units as a continuous flow.