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  2. Differential pulse voltammetry - Wikipedia

    en.wikipedia.org/wiki/Differential_pulse_voltammetry

    The system of this measurement is usually the same as that of standard voltammetry.The potential between the working electrode and the reference electrode is changed as a pulse from an initial potential to an interlevel potential and remains at the interlevel potential for about 5 to 100 milliseconds; then it changes to the final potential, which is different from the initial potential.

  3. Randles–Sevcik equation - Wikipedia

    en.wikipedia.org/wiki/Randles–Sevcik_equation

    In electrochemistry, the Randles–ŠevĨík equation describes the effect of scan rate on the peak current (i p) for a cyclic voltammetry experiment. For simple redox events where the reaction is electrochemically reversible, and the products and reactants are both soluble, such as the ferrocene/ferrocenium couple, i p depends not only on the concentration and diffusional properties of the ...

  4. Voltammetry - Wikipedia

    en.wikipedia.org/wiki/Voltammetry

    In practice it can be important to have a working electrode with known dimensions and surface characteristics. As a result, it is common to clean and polish working electrodes regularly. The auxiliary electrode can be almost anything as long as it doesn't react with the bulk of the analyte solution and conducts well.

  5. Auxiliary electrode - Wikipedia

    en.wikipedia.org/wiki/Auxiliary_electrode

    In electrochemistry, the auxiliary electrode, often also called the counter electrode, is an electrode used in a three-electrode electrochemical cell for voltammetric analysis or other reactions in which an electric current is expected to flow.

  6. Electroanalytical methods - Wikipedia

    en.wikipedia.org/wiki/Electroanalytical_methods

    In practice, the analyte solution is usually disposed of since it is difficult to separate the analyte from the bulk electrolyte, and the experiment requires a small amount of analyte. A normal experiment may involve 1–10 mL solution with an analyte concentration between 1 and 10 mmol/L.

  7. Cyclic voltammetry - Wikipedia

    en.wikipedia.org/wiki/Cyclic_voltammetry

    In electrochemistry, cyclic voltammetry (CV) is a type of voltammetric measurement where the potential of the working electrode is ramped linearly versus time. Unlike in linear sweep voltammetry , after the set potential is reached in a CV experiment, the working electrode 's potential is ramped in the opposite direction to return to the ...

  8. Reference electrode - Wikipedia

    en.wikipedia.org/wiki/Reference_electrode

    2) Hydrogen gas, 3) Acid solution with an activity of H + = 1 mol/L, 4) Hydroseal for prevention of oxygen interference, 5) Reservoir via which the second half-element of the galvanic cell should be attached. The connection can be direct, through a narrow tube to reduce mixing, or through a salt bridge, depending on the other electrode and ...

  9. Cottrell equation - Wikipedia

    en.wikipedia.org/wiki/Cottrell_equation

    In electrochemistry, the Cottrell equation describes the change in electric current with respect to time in a controlled potential experiment, such as chronoamperometry. Specifically it describes the current response when the potential is a step function in time.