An apparatus for estimating electrical properties of an electrolyzer includes a data processing system for estimating electrical values, for example a membrane resistance, of the electrolyzer based on a difference voltage, a current, and an initial value and an attenuation time constant of a double-layer capacitance voltage of the electrolyzer during a shutdown of the electrolyzer. The difference voltage is a difference between a voltage of the electrolyzer and a total reversible voltage of the electrolyzer. The initial value and the attenuation time constant of the double-layer capacitance voltage are estimated based on values of the difference voltage when the current is zero and thus the difference voltage equals the double-layer capacitance voltage. The electrical values can be estimated even if a stepwise interruption of the current of the electrolyzer is not possible.

An electrochemical cell comprises a first electrode, a second electrode, and a proton-conducting membrane between the first electrode and the second electrode. The first electrode comprises Pr(Co.sub.1-x-y-z, Ni.sub.x, Mn.sub.y, Fe.sub.z)O.sub.3-δ, wherein 0≤x≤0.9, 0≤y≤0.9, 0≤z≤0.9, and δ is an oxygen deficit. The second electrode comprises a cermet material including at least one metal and at least one perovskite. Related structures, apparatuses, systems, and methods are also described.

Electrocatalytic apparatus for the simultaneous conversion of methane and CO.sub.2 into methanol via an elctrochemical reactor operating at ambient temperature and pressure, said electrochemical reactor simultaneously converts CO.sub.2 to methanol by surficial catalytic reaction on the cathode, and methane to methanol by surficial catalytic reaction on the anode. The electrochemical reactor futher works with an electrolyte consisting of electrolytic complexes of water-soluable transition metals and small molecules as co-catalyst of the electrocatalytic reactions and facilitator of ionic transfer and solubility of CO.sub.2 and CH.sub.4 molecules in the electrolyte. The electrochemical reactor is further equipped with zero-gap membrane electrocatalytic electrode assemlics, the cathode and anode comprising two electrocatalytic mesoporous surfaces and being tubular and coaxial, delineating two regions, which are separated one from the other by an ion exchange membrane (27). The tubular electrodes pack vertically together, the external gaps being filled by an insulating material. The packed electrodes are electronically connected to the power source in a parallel electrical circuit.

Electrocatalytic apparatus for the simultaneous conversion of methane and CO.sub.2 into methanol via an elctrochemical reactor operating at ambient temperature and pressure, said electrochemical reactor simultaneously converts CO.sub.2 to methanol by surficial catalytic reaction on the cathode, and methane to methanol by surficial catalytic reaction on the anode. The electrochemical reactor futher works with an electrolyte consisting of electrolytic complexes of water-soluable transition metals and small molecules as co-catalyst of the electrocatalytic reactions and facilitator of ionic transfer and solubility of CO.sub.2 and CH.sub.4 molecules in the electrolyte. The electrochemical reactor is further equipped with zero-gap membrane electrocatalytic electrode assemlics, the cathode and anode comprising two electrocatalytic mesoporous surfaces and being tubular and coaxial, delineating two regions, which are separated one from the other by an ion exchange membrane (27). The tubular electrodes pack vertically together, the external gaps being filled by an insulating material. The packed electrodes are electronically connected to the power source in a parallel electrical circuit.

Methods and systems related to the field of carbon capture and utilization are disclosed. Disclosed electrolysis reactors can have a cathode area having a cathode output and a cathode input for an input fluid and an anode area having an anode input and an anode output. The carbon input fluid contains carbon dioxide. The cathode area reduces an oxygen-containing species into hydroxide ions and reacts them with the carbon dioxide to form anions containing carbon. The anode area oxidizes one or more oxidizable species to generate a protonating species. The electrolysis reactors can have a third output for a carbon output fluid. The electrolysis reactors can begin to produce carbon dioxide from the anions containing carbon and the protonating species in response to a potential of less than 1.23 V applied across the cathode terminal and the anode terminal.

One aspect of the invention provides a photoelectrochemical device including at least one electrochemical cell comprising an anode electrode and a cathode electrode; and a photovoltaic module integrated with the at least one electrochemical cell and adapted for converting energy of photons to electrical energy for driving the at least one electrochemical cell to facilitate redox reactions therein.

An electrochemical reduction device comprising: an electrode unit configured to include an electrolyte membrane, a reduction electrode that contains a reduction catalyst for hydrogenating at least one benzene ring of an aromatic compound, and an oxygen evolving electrode; a power control unit that applies a voltage Va between the reduction electrode and the oxygen evolving electrode; a concentration measurement unit that measures a concentration of an aromatic compound to be supplied to the reduction electrode; and a raw material supply amount adjustment unit that adjusts the amount of an organic liquid including an aromatic compound to be supplied to the reduction electrode per unit time based on the concentration measured by the concentration measurement unit.

An article comprising a first gas distribution layer (100), a first gas dispersion layer (200), or a first electrode layer, having first and second opposed major surfaces and a first adhesive layer having first and second opposed major surfaces, wherein the second major surface (102) of the first gas distribution layer (100), the second major surface (202) of the first gas dispersion layer (200), or the first major surface of the first electrode layer, as applicable, has a central area, wherein the first major surface of the first adhesive layer contacts at least the central area of the second major surface of the first gas distribution layer, the second major surface of the first gas dispersion layer, or the first major surface of the first electrode layer, as applicable, and wherein the first adhesive layer comprises a porous network of first adhesive including a continuous pore network extending between the first and second major surfaces of the first adhesive layer. The articles described herein are useful, for example, in membrane electrode assemblies, unitized electrode assemblies, and electrochemical devices (e.g., fuel cells, redox flow batteries, and electrolyzers).

The present invention provides a methanol generation device for generating methanol by reducing carbon dioxide, comprising: a container for storing an electrolyte solution containing carbon dioxide; a cathode electrode disposed in the container so as to be in contact with the electrolyte solution; an anode electrode disposed in the container so as to be in contact with the electrolyte solution; and an external power supply for applying a voltage so that a potential of the cathode electrode is negative with respect to a potential of the anode electrode. The cathode electrode has a region of Cu.sub.1-x-yNi.sub.xAu.sub.y (0<x, 0<y, and x+y<1). The anode electrode has a region of a metal or a metal compound.

Disclosed is a carbon dioxide utilization system capable of recharging and undergoing reactions. The system includes a cathode unit provided with a first aqueous solution accommodated in a first accommodation space, and a cathode at least a part of which is submerged in the first aqueous solution; an anode unit provided with an alkaline second aqueous solution accommodated in a second accommodation space, and a metal anode at least a part of which is submerged in the second aqueous solution; and a connection unit provided with a connection channel connecting the first and second accommodation spaces in open communication, and a porous ion transfer member, disposed in the connection channel, for blocking the movement of the first and second aqueous solutions but allowing the movement of ions.