A method of depositing of a film on a substrate with controlled adhesion. The method comprises depositing the film including metal, wherein the metal is deposited on the substrate using physical vapor deposition at a pressure that achieves a pre-determined adhesion of the film to the substrate. The pre-determined adhesion allows processing of the film into a device while the film is adhered to the substrate but also allows removal of the device from the substrate.

A method of depositing of a film on a substrate with controlled adhesion. The method comprises depositing the film including metal, wherein the metal is deposited on the substrate using physical vapor deposition at a pressure that achieves a pre-determined adhesion of the film to the substrate. The pre-determined adhesion allows processing of the film into a device while the film is adhered to the substrate but also allows removal of the device from the substrate.

A microbial sensor, system and method that can be used to determine the chemical environment and/or substrate concentrations in saturated and unsaturated natural and environments, such as soils, aquifers and sediments are disclosed. The system may be used for monitoring municipal and industrial treatment facilities and sites where chemicals or contaminants were released to natural environments. The electrochemical microbial sensor system can be referenced using either a cathode exposed to oxygen or a reference cell (silver/silver chloride or calomel) for monitoring natural or man-made environments.

A microbial sensor, system and method that can be used to determine the chemical environment and/or substrate concentrations in saturated and unsaturated natural and environments, such as soils, aquifers and sediments are disclosed. The system may be used for monitoring municipal and industrial treatment facilities and sites where chemicals or contaminants were released to natural environments. The electrochemical microbial sensor system can be referenced using either a cathode exposed to oxygen or a reference cell (silver/silver chloride or calomel) for monitoring natural or man-made environments.

Provided are electronic biosensors based on graphene field effect transistors that utilize engineered hairpin probe DNA that allows for target recycling and hybridization chain reactions.

Provided are electronic biosensors based on graphene field effect transistors that utilize engineered hairpin probe DNA that allows for target recycling and hybridization chain reactions.

Various embodiments of the disclosure provide reference electrodes for use in electrochemical systems (e.g., electrochemical cells) that use molten salt media as the electrolyte of choice. The reference electrodes include a metal core with an outer, solid layer of the metal's oxide, silicide, or carbide. The oxide, silicide, or carbide outer layer may be formed uniformly and with sufficient durability to withstand exposure to molten salt material. The outer layer may be formed by processes configured to form (e.g., grow) the oxide, silicide, or carbide layer directly on the outer surface of the metal core with uniformity of the layer's composition and thickness all along the outer surface of the metal core. Related electrochemical systems are also disclosed.

A reference electrode which is stable over a wide range of temperatures, pressures and chemical conditions is provided. The subject reference electrode according to the present invention comprises a tubular enclosure composed of quartz having a distal, closed end and a proximal, open end. An insulating ceramic rod is seemingly connected to the opening in the closed distal end of the enclosure to form micro-cracks between the ceramic rod and the quartz enclosure (called a cracked junction, CJ). The CJ gives a very tortuous path for ion conduction from inside the reference electrode (RE) to a working electrode (WE). Inside the tubular enclosure is an electrical lead (e.g., a silver wire) disposed in an electrolyte comprising a mixture of alkaline metal salts (e.g., AgCl and KCl), extending from the electrolyte upward through a sealing means at the proximal end of the quartz enclosure.

A method for detecting glycoproteins in aqueous samples. The method includes putting an aqueous sample in contact with a diagnostic kit, obtaining an electrochemical pattern of the aqueous sample by applying an electrical potential to the diagnostic kit, and detecting a glycoprotein status of the aqueous sample based on the presence of a peak in the electrochemical pattern of the aqueous sample. The diagnostic kit includes a counter electrode, a reference electrode, and a working electrode including a label-free nanosensor deposited on a substrate. The label-free nanosensor includes a modified graphene oxide (GO) sheet and a signal amplifying agent loaded onto the modified GO sheet. The modified GO sheet includes a modifying agent conjugated to a GO sheet. The modifying agent includes 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC), N-hydroxysuccinimide (NHS), 8-hydroxyquinoline (8H), and hydroxylammonium chloride. The signal amplifying agent includes at least one of an amine-functionalized gold nanoparticle and a silver nanoparticle.

An immersion sensor is configured to determine the content of a chemical element in molten metal. The immersion sensor has an auxiliary electrochemical cell extending from an interior surface into the internal volume of a sampling chamber. The sampling chamber can be integrally-formed in a sensor head or in a separate refractory structure. The immersion sensor may be configured for the flow of molten metal into the internal volume of the sampling chamber and into contact with the auxiliary electrochemical cell.