Electrochemical methods for probing solid polymer electrolyte surface coatings on electrically conducting, active, three-dimensional electrode materials for use in lithium-ion batteries, to quantitatively determine the conformity, uniformity, and the presence of pinholes, and/or other defects in coatings, without requiring the detachment of the coating from the electrode or otherwise inducing damage to the coating, are described. Coated electrodes are submersed in an electrolyte solution containing a redox-active probe species which does not induce electrochemical damage to either the working electrode or the solid polymer electrolyte surface coating. For coated Cu.sub.2Sb working electrodes, molecules including a water-soluble redox active viologen moiety have been found to be effective. The current as a function of the applied potential for an uncoated working electrode is used as a baseline for testing solid polymer surface coatings on working electrodes, and the difference in the observed current between the electrodes for a given potential is a quantitative indicator of the ability of the probe species to access the surface of the working electrode through the solid polymer electrolyte coating.

Electrochemical methods for probing solid polymer electrolyte surface coatings on electrically conducting, active, three-dimensional electrode materials for use in lithium-ion batteries, to quantitatively determine the conformity, uniformity, and the presence of pinholes, and/or other defects in coatings, without requiring the detachment of the coating from the electrode or otherwise inducing damage to the coating, are described. Coated electrodes are submersed in an electrolyte solution containing a redox-active probe species which does not induce electrochemical damage to either the working electrode or the solid polymer electrolyte surface coating. For coated Cu.sub.2Sb working electrodes, molecules including a water-soluble redox active viologen moiety have been found to be effective. The current as a function of the applied potential for an uncoated working electrode is used as a baseline for testing solid polymer surface coatings on working electrodes, and the difference in the observed current between the electrodes for a given potential is a quantitative indicator of the ability of the probe species to access the surface of the working electrode through the solid polymer electrolyte coating.

Provided is a method of manufacturing a porous protective layer for a gas sensor. The porous protective layer according to one Example of the present invention is manufactured by a method of manufacturing a porous protective layer for a gas sensor including (1) a step of introducing a composition for forming a porous protective layer including a pore former and a ceramic powder, which includes particles having a degree of deformation of 1.5 or more expressed by the following Relational Formula 1 according to the present invention, onto a sensing electrode for a gas sensor, and (2) a step of sintering the introduced composition for forming a porous protective layer.

Disclosed herein are methods and compositions for detection of target small molecules in a mixed sample by performing a competition assay between the target and a surrogate and subsequently detecting the complex types in a nanopore device. Disclosed herein are competition assays for detection of small molecules using a nanopore. Target molecules of a sufficient size (>20 kDa) when passed through a solid-state nanopore cause a change in the current impedance, translocation time, or other measurable parameter. In the event the target molecule is not sufficiently big, and thus does not cause a noticeable change, an additional molecule/reagent can be used to aid in detection. This detection reagent would bind to the small molecule or to the “capture ligand-molecule complex” (e.g. peptide detection is aided by a monoclonal antibody (mAb) that recognizes a peptide/aptamer complex).

A wireless chemical sensor includes an electrical conductor and a material separated therefrom by an electric insulator. The electrical conductor is an unconnected open-circuit shaped for storage of an electric field and a magnetic field. In the presence of a time-varying magnetic field, the first electrical conductor resonates to generate harmonic electric and magnetic field responses. The material is positioned at a location lying within at least one of the electric and magnetic field responses so-generated. The material changes in electrical conductivity in the presence of a chemical-of-interest.

A wireless chemical sensor includes an electrical conductor and a material separated therefrom by an electric insulator. The electrical conductor is an unconnected open-circuit shaped for storage of an electric field and a magnetic field. In the presence of a time-varying magnetic field, the first electrical conductor resonates to generate harmonic electric and magnetic field responses. The material is positioned at a location lying within at least one of the electric and magnetic field responses so-generated. The material changes in electrical conductivity in the presence of a chemical-of-interest.

A device for separating a sample of cells suspended in a bio-compatible ferrofluid is described, The device includes a microfluidic channel having a sample inlet, at least one outlet and a length between the same inlet and the at least one outlet, wherein a sample can be added to the sample inlet and flow along the microfluidic channel length to the at least one outlet. The device includes a plurality of electrodes and a power source for applying a current to the plurality of electrodes to create a magnetic field pattern along the microfluidic channel length. The present invention also includes a method of using said device for separating at least one cell type.

For measuring concentrations of fluid-soluble gases with improved drift stability and low production costs, thus dispensing with tedious calibration and/or drift correction routines and re-membraning procedures, a sensor and a system are provided, comprising at least two electrodes, which are covered by sensor fluid at at least one detection site; and an ion-balancing means (50), for example a mixed-bed ion-exchange resin, in contact with the sensor fluid for removing polluting ions.

A gas concentration detection device includes a pump cell, a sensor cell, a monitor cell, a sensor current detection unit detecting a current outputted by the sensor cell, a monitor current detection unit detecting a current outputted by the monitor cell, a voltage adjustment unit adjusting a pump cell voltage applied to the pump cell, and a sensitivity determination unit determining a gas sensitivity of at least one of the sensor cell or the monitor cell. The voltage adjustment unit changes the pump cell voltage from a target voltage into a detection voltage where the concentration of the residual oxygen supplied to the sensor cell and the monitor cell is increased. The sensitivity determination unit determines the gas sensitivity based on a detection current detected by at least one of the sensor current detection unit or the monitor current detection unit in accordance with the concentration of the residual oxygen.

A test cartridge includes a membrane separating an internal space of the cartridge into a sample chamber and a second chamber. A first electrode is disposed within the sample chamber, and a second electrode is disposed within the second chamber. A device includes a dock and circuitry. The dock includes a first dock-terminal and a second dock-terminal, and is configured to receive the cartridge such that the circuitry is electrically connected to the electrodes via contact between terminals of the dock and terminals of the cartridge. The circuitry performs, while the cartridge remains docked with the dock: (a) a verification step that verifies an absence of nanopores in the membrane, (b) subsequently, a nanoporation subroutine, and (c) subsequently, an assay subroutine. The circuitry enables the nanoporation subroutine only if the verification step successfully verifies the absence of nanopores. Other embodiments are also described.