Cell potential force

The potential of the reaction is given as = (cathodic — anodic reaction) = 0.337 — (—0.440) = +0.777 V. The positive value of the standard cell potential indicates that the reaction is spontaneous as written (see Electrochemical processing). In other words, at thermodynamic equihbrium the concentration of copper ion in the solution is very small. The standard cell potentials are, of course, only guides to be used in practice, as rarely are conditions sufftciendy controlled to be called standard. Other factors may alter the driving force of the reaction, eg, cementation using aluminum metal is usually quite anomalous. Aluminum tends to form a relatively inert oxide coating that can reduce actual cell potential. 

By the half-cell potentials, we conclude the Zn-Zn+2 half-reaction has the greater tendency to release electrons. It will tend to transfer an electron to silver ion, forcing (54) in the reverse direction. Hence we obtain the net reaction by subtracting (54) from (52). But remember that this subtraction must be in the proportion that causes no net gain or loss of electrons. If two electrons are lost per atom of zinc oxidized in (52), then we must double half-reaction (54) so that two electrons will be consumed. 

The electrochemical detection of pH can be carried out by voltammetry (amper-ometry) or potentiometry. Voltammetry is the measurement of the current potential relationship in an electrochemical cell. In voltammetry, the potential is applied to the electrochemical cell to force electrochemical reactions at the electrode-electrolyte interface. In potentiometry, the potential is measured between a pH electrode and a reference electrode of an electrochemical cell in response to the activity of an electrolyte in a solution under the condition of zero current. Since no current passes through the cell while the potential is measured, potentiometry is an equilibrium method. 

A schematic diagram of a typical pH electrode system is shown in Fig. 10.1. The cell potential, i.e. the electromotive force, is measured between a pH electrode and a reference electrode in a test solution. The pH electrode responds to the activity or concentration of hydrogen ions in the solution. The reference electrode has a very stable half-cell potential. The most commonly used reference electrodes for potentiometry are the silver/silver chloride electrodes (Ag/AgCl) and the saturated calomel electrodes (SCE). 

To calculate the properties of a perfect crystal, the pair potentials required are set up, and the ions and shells are allocated to positions in the unit cell. The forces on the... 

Much less is known about the role of the SR in excitation—contraction coupling in the rat ureter, where InsP3 release predominates, but as will be discussed below its role in Ca2+ signalling in single cells has been studied. It is expected from this that the SR s contribution will be to potentiate force production. 

Potentiometry deals with the electromotive force (EMF) generated in a galvanic cell where a spontaneous chemical reaction is taking place. In practice, potentiometry employs the EMF response of a galvanostatic cell that is based on the measurement of an electrochemical cell potential under zero-current conditions to determine the concentration of analytes in measuring samples. Because an electrode potential generated on the metal electrode surface,... 

An electrical potential difference between the electrodes of an electrochemical cell (called the cell potential) causes a flow of electrons in the circuit that connects those electrodes and therefore produces electrical work. If the cell operates under reversible conditions and at constant composition, the work produced reaches a maximum value and, at constant temperature and pressure, can be identified with the Gibbs energy change of the net chemical process that occurs at the electrodes [180,316]. This is only achieved when the cell potential is balanced by the potential of an external source, so that the net current is zero. The value of this potential is known as the zero-current cell potential or the electromotive force (emf) of the cell, and it is represented by E. The relationship between E and the reaction Gibbs energy is given by... 

While this potential cannot he determined for a single electrode, a potential can be derived if the potential of the other electrode in a cell is defined, i.e. the potential of the standard hydrogen electrode (SHE) is arbitrarily taken as 0.(XXX)V. In this way. a potential scale can then be devised for single electrode potentials - see Section 3.2. t The abbreviation emf , in upright script, is often used in other lextNmks as a direct , i.e. non-variable, acronym for the electromotive force. Note, however, that in this present text it is used to represent a variable (cell potential) and is therefore. shown in italic script. 

The acronym emf derives from the somewhat archaic term electromotive force . Physicists tend to employ the term potential difference (and abbreviate it to pd ). Another term that is used is fceii (cell potential). 

For the Daniell cell, the overall (cell) potential, or cell electromotive force ( ) is given by the so-called Nernst equation [1] (Eq. 6.5). 

Cell potential (E ) A measure of how far a redox reaction is from equilibrium. It is reported in units of volts. The higher the E, the greater the driving force for reaction. 

The sum of these two half-cell potentials is the electromotive force (EMF) of the cell ... 

The multilayered Cu/Co systems discussed here can be grown as described next (6b). Electrolyte composition is based on a cobalt/copper ratio of 100 1 and consists of a solution of 0.34 M cobalt sulfate, 0.003 M copper sulfate, and 30g/L boric acid. The pH is fixed around 3.0, and there is no forced convection while deposition is carried out. The electrodeposition may usually be carried out potentiostatically at 45°C between —1.40 V versus SCE for the cobalt and —0.65 V versus SCE for the copper with an 3 cell potential interrupt between the cobalt-to-copper transition to avoid cobalt dissolution, which can occur when there is no interrupt. 

In a similar though less diabolical manner, the electrons produced at the anode of a voltaic cell have a natural tendency to flow along the circuit to a location with lower potential the cathode. This potential difference between the two electrodes causes the electromotive force, or EMF, of the cell. EMF is also often referred to as the cell potential and is denoted fj.g,. The cell potential varies with temperature and concentration of products and reactants and is measured in volts (V). The standard cell potential, or E° gn, is the that occurs when concentrations of solutions ire all at 1 M and the cell is at standard temperature and pressure (STP). 

A positive standard cell potential tells you that the cathode is at a higher potential than the anode, and the reaction is therefore spontaneous. What do you do with a cell that has a negative " gii Electrochemical cells that rely on such nonspontaneous reactions cire called electrolytic cells. The redox reactions in electroljdic cells rely on a process called electrolysis. These reactions require that a current be passed through the solution, forcing it to split into components that then fuel the redox reaction. Such cells are created by applying a current source, such as a battery, to electrodes placed in a solution of molten salt, or salt heated until it melts. This splits the ions that make up the salt. 

Cell potential The driving force in a galvanic cell that pulls electrons from the reducing agent in one compartment to the oxidizing agent in the other. 

The cell potential is sometimes called the electromotive force (emf) of the cell or, more colloquially, its voltage. 

Cell potential, which is also called electromotive force (emf), is always positive. Compare with standard potential. 

P The driving force of a cell / V I reaction, measured in volts and called cell voltage, cell potential, or electromotive force, is a function of the natural tendency of one substance to lose electrons and of a second substance to gain electrons. The greater these tendencies, the higher the cell voltage. 

We ve now seen two quantitative measures of the driving force of a chemical reaction the cell potential E (an electrochemical quantity) and the free-energy change AG (a thermochemical quantity, Section 17.7). The values of AG and E are directly proportional and are related by the equation... 

The cell potential E (also called the cell voltage or electromotive force) is an electrical measure of the driving force of the cell reaction. Cell potentials depend on temperature, ion concentrations, and gas pressures. The standard cell potential E° is the cell potential when reactants and products are in their standard states. Cell potentials are related to free-energy changes by the equations AG = —nFE and AG° = —mFE°, where F = 96,500 C/mol e is the faraday, the charge on 1 mol of electrons. 

An oxidation-reduction reaction that is not spontaneous, for which the calculated cell potential is negative, may be induced by electrolysis. This reaction can be due to an external electrical potential to force electrons into the couple undergoing reduction and to extract electrons from the couple undergoing oxidation. The minimum external potential required for electrolysis is the value of the calculated cell potential for the reaction. 

Apart from the ease of precise control in an electrochemical path to synthesis, there is the unique feature of being able to force the electrode reaction to take place against its own AG. This is because the principal rule of chemical equilibria is AG = 0, but in electrochemical equilibria, the equilibrium condition is AG = -nFEKV Thus, if the cell potential is exactly rev, the chemical reaction in the cell is at equilibrium and nothing happens. However (in contrast to what can be done chemically), moving the potential of the working electrode in a more negative direction than its reversible potential stimulates the reaction to take off in a cathodic direction at a fixed rate i.e., it acts to reduce the reactant ... 

In an electrolytic cell, electrical energy is used to force a current through the cell to produce a chemical change for which the cell potential is negative ... 

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