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Electrochemistry, which studies the interaction between electrical energy and chemical changes. This technique allows us to analyse reactions that involve electron transfer processes ( redox reactions).
EC-AFM allows to perform in-situ AFM measurements in an electrochemical cell, in order to investigate the actual changes in the electrode surface morphology during electrochemical reactions. The solid-liquid interface is thus investigated. [ 1 ]
RRS effect (Resonance Raman Scaterring) The Raman resonance effect produces an increase in Raman intensity up to 10 6 times. In this phenomenon, the monochromatic light interaction with the sample produces the transition of the molecules from the fundamental state to an excited electronic state, instead of a virtual state as in normal Raman spectroscopy.
In electrochemistry, the Randles–Ševčík 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 ...
where k f and k b are the reaction rate constants, with units of frequency (1/time) and c o and c r are the surface concentrations (mol/area) of the oxidized and reduced molecules, respectively (written as c o (0,t) and c r (0,t) in the previous section). The net rate of reaction v and net current density j are then: [Note 2]
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.
Electrochemical reactions occur in electrolytic solutions—for example electroplating, etching, batteries, and so on.On the electrode surface, many atoms, molecules, and ions adsorb and affect the reactions.
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. It was derived by Frederick Gardner Cottrell in 1903. [1]