An electrochemical chlorine gas sensor is disclosed with a working electrode, a counter electrode, and a reference electrode. The working electrode may be coated with a nanoporous gold layer, a first solution comprising an ionic liquid, and a second solution that may be selected from a Nation solution, a chitosan solution, an agar solution, or combinations thereof. The reference and counter electrodes may be further coated with the ionic liquid.

A measuring electrode for chemical liquid in semiconductor process that measures a chemical liquid used for a semiconductor process comprises a first body having a first internal liquid chamber into which a first internal liquid is filled, and a flow tube for a part or all of which a responsive glass is used and that forms a flow channel where a chemical liquid as being a measuring object flows, wherein the flow tube is so arranged to penetrate the first body and the responsive glass makes contact with the first internal liquid in the first internal liquid chamber.

A measuring device 1 according to the present disclosure measures a state of a solution L. The measuring device 1 includes a measuring unit 10 that outputs a measurement signal associated with the state of the solution L, a protection unit 20 attached to the measuring unit 10, and a controller 40 that obtains the information on the state of the solution L on the basis of a measurement signal output from the measuring unit 10. The measuring unit 10 has a first part P1 in a usable state that contributes to output of the measurement signal by coming into contact with the solution L, and a second part that is isolated from the solution L by the protection unit 20 and is in a standby state for measurement.

An electrochemical detection system for determining a concentration of a gas in exhaust gases of a combustion process. The system includes an electrolyte, a reference electrode, and a sense electrode that cooperate to form an electrochemical sensor that exposes both the reference electrode and the sense electrode to the exhaust gases. The electrochemical sensor is configured to output a sensor signal indicative of a species concentration of a species gas in the exhaust gases. The sensor signal exhibits a transient error in response to a change in a reference concentration of a reference gas in the exhaust gases. The processor is configured to determine the species concentration based on the sensor signal, and to determine an estimate of the transient error based on an operating condition of the combustion process.

The invention discloses a metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor, comprising a three-electrode system composed of a working electrode, a counter electrode, and a reference electrode. The surface of the working electrode is coated with a metal nanoparticles/nanocellulose composites. The surface of the nanocellulose is modified with a strong cationic conducting polymer. The invention promotes the sensitivity and selectivity of glucose sensing with the linear range of 4 μM-15 mM and the detection limit of 1.4 μM. Therefore, the sensor possesses high sensitivity, high response speed, stable performance and high anti-interference ability. The preparation method of the metal nanoparticles/nanocellulose composites-based non-enzymatic electrochemical glucose sensor is simple and the cost is low. And enzyme is introduced into the preparation process.

Electrochemical impedance-based label-free and rapid biosensor for select bodily fluid biomolecule levels. Monoclonal antibodies to of biomolecule such as Cortisol were covalently attached to a 16-mercaptohexadecanoic acid functionalized gold working electrode using zero-length crosslinkers N-(3-dimethylaminopropyl)-N-ethylcarbodiimide and 10 mM N-hydroxysulfosuccinimide. Cortisol was detected in phosphate buffered saline (simulated tear fluid) using a simple ferrocyanide reagent with a lower limit of detection of 18.73 pM and less than 10% relative standard deviation.

A sensor element includes a layered body that includes a measurement-object gas flowing portion which a measurement object gas is introduced and flowed in and a reference electrode that is formed inside of the layered body and a reference gas introducing layer made of a porous material that introduces a reference gas being used as a standard for detection of a specific gas concentration in the measurement-object gas and that flows the reference gas to the reference electrode, the reference gas introducing layer including an inlet portion serving as an inlet of the reference gas and one or more gas flowing spaces provided over a region from the inlet portion to the reference electrode in a direction in which the reference gas is flowed.

Techniques for increasing the lifespan of a nanopore DNA sensing device are disclosed. A related method may include forming a first electrode, forming a second electrode, disposing the first electrode and second electrode within an insulator, and disposing a lipid bilayer having a nanopore between the first electrode and second electrode. The forming of the second electrode may comprise forming a silver (Ag) layer, pressing a mold into the Ag layer to form a pattern in the Ag layer, removing the mold from the Ag layer, and exposing the Ag layer to an electrolyte.

Artifacts from the presence of a reference electrode in a thin-film cell configuration can be minimized or eliminated by providing the surface of a reference electrode with a specified surface resistivity. Theoretical considerations are set forth that show that for a given wire size, there is a theoretical surface resistance (or resistivity) that negates all artifacts from the presence of the reference wire. The theory and the experimental results hold for a electrochemical cell in a thin-film configuration.

A method of making a reversible hydrogen electrode comprises filling a housing with electrolyte, the housing having an open end, a closed end and a platinum wire having an internal portion in the housing and an external portion extending through the closed end to an exterior of the housing. The housing is inverted into a container of electrolyte and a counter electrode is placed into the container of electrolyte, the counter electrode being metal. A power source is attached to the external portion of the platinum wire and the counter electrode. The power source is run for a period of time to produce electrolysis. Hydrogen is formed at the internal portion of the platinum wire and oxygen is formed at the counter electrode. A single hydrogen bubble is formed in the housing, the platinum wire extending through the single hydrogen bubble.