An electrocatalyst comprising molybdenum disulfide nanosheets with dispersed iron phosphide nanoparticles is described. The molybdenum disulfide nanosheets may have an average length in a range of 300 nm-1 μm and the iron phosphide nanoparticles may have an average diameter in a range of 5-20 nm. The electrocatalyst may have an electroactive surface area in a range of 10-50 mF.Math.cm.sup.−2 when deposited on a working electrode for use in a hydrogen evolution reaction.

Various embodiments include a method for producing a gas diffusion electrode, the method comprising: providing a raw electrode layer comprising an electrically non-conducting web; adapting a thickness of the raw electrode layer; and applying a non-solvent to the raw electrode layer.

A manganese oxide, a manganese oxide/carbon mixture and a manganese oxide composite electrode material, having high catalytic activity produced at low cost, to be used as an anode catalyst for oxygen evolution in water electrolysis, and their production methods, are provided. A manganese oxide for an oxygen evolution electrode catalyst in water electrolysis is provided, which is a manganese oxide having a metallic valence of higher than 3.0 and at most 4.0, having an average primary particle size of at most 80 nm and an average secondary particle size of at most 25 μm, a manganese oxide/carbon mixture for an oxygen evolution electrode catalyst in water electrolysis, having a proportion of manganese oxide to the total of the manganese oxide and electrically conductive carbon of from 0.5 to 40 wt %, and a manganese oxide composite electrode material which includes an electrically conductive substrate constituted by fibers.

A manganese oxide, a manganese oxide/carbon mixture and a manganese oxide composite electrode material, having high catalytic activity produced at low cost, to be used as an anode catalyst for oxygen evolution in water electrolysis, and their production methods, are provided. A manganese oxide for an oxygen evolution electrode catalyst in water electrolysis is provided, which is a manganese oxide having a metallic valence of higher than 3.0 and at most 4.0, having an average primary particle size of at most 80 nm and an average secondary particle size of at most 25 μm, a manganese oxide/carbon mixture for an oxygen evolution electrode catalyst in water electrolysis, having a proportion of manganese oxide to the total of the manganese oxide and electrically conductive carbon of from 0.5 to 40 wt %, and a manganese oxide composite electrode material which includes an electrically conductive substrate constituted by fibers.

A method of producing methanol from methane in which hot-electrons generated under an external electric field in a process taking place in a multi-layer heterostructure comprising a nanoporous layer drive the conversion from methane to methanol. The structure generates hot electrons by providing spatial enhancement of the electric field, and purges hot holes which are created when hot electrons depart. This combination enhances heterogeneous catalysis of the conversion reaction.

A method for making a metal oxyhydroxide electrocatalytic material comprises titrating a precursor solution with a (bi)carbonate salt, the precursor solution comprising a first metal salt and a solvent, wherein the titration induces reactions between the (bi)carbonate salt and the first metal salt to provide first metal carbonate species in the titrated precursor solution; and exposing the titrated precursor solution to microwave radiation to decompose the first metal carbonate species to form the metal oxyhydroxide electrocatalytic material and carbon dioxide. Mixed metal oxyhydroxide electrocatalytic materials such as nickel-iron oxyhydroxide may be formed. Also provided are the materials themselves, electrocatalytic systems comprising the materials, and methods of using the materials and systems.

Methods of making improved bioelectrodes are provided capable of functionalizing electrode materials in less than 24 hours. Pre-seeding the electrode with electricigenic microbes forms an electricigenic biofilm on the electrode to maximize surface coverage by electricigenic microbes and reduce the number of fastidious organisms. The method results in bioelectrodes that are functionalized in less than 24 hours and that can generate higher yields of current from a wide range of substrates. Methods for treating wastewater by removing fermentative inhibitors and generating current are provided. The bioelectrodes generated are tailored to efficiently oxidize substrates, such as the fermentative inhibitors, in the wastewater targeted for removal from the wastewater. Improved electrodes are generated rapidly with high coulombic efficiency. Bioelectrochemical systems (BESs) containing the improved electrodes are also provided.

A durable composite diamond electrode is disclosed which comprise at least a relatively thicker conductive UNCD (Ultrananocrystalline Diamond) layer, with low deposition cost, on a substrate underlying a relatively thinner conductive MCD (Microcrystalline Diamond) layer. The electrode exhibits long life and superior delamination resistance under extremely stressed electrochemical oxidation conditions. It is hypothesized that this improvement in electrode reliability is due to a combination of stress relief by the composite film with the slightly softer underlying UNCD root layer and the electrochemically durable overlying MCD shield layer, an effective disruption mechanism of the fracture propagation between the compositing layers, and thermal expansion coefficient match between the diamond layers and the substrate. The diamond composite electrode can be applied to any electrochemical application requiring extreme voltages/current densities, extreme reliability or biomedical inertness such as electrochemical systems to generate ozone, hydroxyl radicals, or biomedical electrode applications.

A photoelectrode for a photoelectrochemical cell is disclosed. The photoelectrode comprises a back-contact solar cell comprising emitter and collector contacts being spaced apart by first openings. The emitter and collector contacts are respectively collected in an emitter busbar and a collector busbar. The photoelectrode further comprises a contact passivation layer to separate the emitter and collector contacts from the electrolyte when in use. The contact passivation layer further comprises second openings in correspondence with the first openings. The photoelectrode further comprises a resin layer covering the openings and a portion of the contact passivation layer such that in use only charge carriers from the emitter contacts traverse the contact passivation layer in its way to the electrolyte while charge carriers from the collector contacts are collected in the collector busbar. An electrocatalyst layer is further provided covering respectively the resin layer and/or the contact passivation layer.

An electrochemical gas generator for ammonia with the use of ionic liquids containing nitrate ions as the electrolyte and to the use of the gas generator for generating gaseous ammonia, especially for testing the function of and/or calibrating gas sensors.