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Electrochemical cell Construction

Kline G., KamK., Canfield D. and Parkinson B. A. (1981), Efficient and stable photo-electrochemical cells constructed with WSei and MoSei photoanodes , Solar Energy Mat. 4, 301-308. [Pg.34]

In situ spectroelectrochemical studies can also be carried out on chiral CEP films deposited on ITO-coated glass electrodes inserted in electrochemical cells constructed in quartz cuvettes, allowing detailed studies of the changes in the CEP structures upon redox switching between different oxidation states. [Pg.48]

Detector E, Metrohm 1096/2, platinum working electrode +0.4 V, Ag/AgCl reference electrode following post-column reaction. The column effluent passed through an electrochemical cell (construction details in paper) and the bromide was oxidized to bromine at 3 pA. The mixture flowed through a 20 s reaction coil (3.9 m ( ) X 0.33 mm ID) to the detector. [Pg.428]

In Chapter 5, the instrumentation of RDE technique including electrode design and electrochemical cell construction have been presented, which are also applicable to RRDE technique. [Pg.210]

Potentiometric electrochemical cells are constructed such that one of the half-cells provides a known reference potential, and the potential of the other half-cell indicates the analyte s concentration. By convention, the reference electrode is taken to be the anode thus, the shorthand notation for a potentiometric electrochemical cell is... [Pg.471]

Instrumentation Controlled-current coulometry normally is carried out using a galvanostat and an electrochemical cell consisting of a working electrode and a counterelectrode. The working electrode, which often is constructed from Pt, is also... [Pg.500]

All flashlight batteries, button batteries, compact rechargeable batteries and vehicle storage batteries operate under the same basic principles. An electrochemical cell is constructed of two chemicals with different electron-attracting capabilities. Called an electrochemical couple, these two chemicals, itntncrscd in an electrolyte (material that carries the flow of energy between electrodes), are connected to each other through an external circuit. [Pg.114]

There are two major types of electrochemical cells primary batteries and secondaiy, or storage, batteries. Primary hatteiy construction allows for only one continuous or intermittent discharge secondary hattei y construction, on the other hand, allows for recharging as well. Since the charging process is the... [Pg.117]

There are distinct differences in the electrochemical behavior of lithium cells constructed with /1-Mn02 electrodes prepared by acid treatment and those containing Li[Mn2]04 electrodes [120].Cells with A-Mn02 electrodes show an essentially featureless voltage profile at 4V on the initial discharge on subsequent cycling, the cells show a profile more consistent with that expected from an Li[Mn2]04 electrode. [Pg.311]

The majority of electrochemical cells to have been constructed are based on PEO, PAN, or PVdF [101]. Recently, the Yuasa Corporation have commercialized solid polymer electrolyte batteries, primarily for use in devices such as smart cards, ID cards, etc. To date, the batteries which have been manufactured and marketed are primary lithium batteries based on a plasticized polymer electrolyte, but a similar secondary battery is expected [120]. [Pg.516]

Measurement of E° and Activities Electrochemical cells can be constructed to measure E° and thermodynamic properties such as K, AG, AH, AS, A V, and ACP for a reaction. Consider as an example the cell shown schematically in Figure 9.4.x The cathode consists of an Ag metal rod coated with AgCl(s). The anode is a Pt metal rod around which H2(g) is bubbled. The two electrodes are... [Pg.479]

In this part of Chapter 12, we study electrolysis, the process of driving a reaction in a nonspontaneous direction by using an electric current. First, we see how electrochemical cells are constructed for electrolysis and how to predict the potential needed to bring electrolysis about. Then, we examine the products of electrolysis and see how to predict the amount of products to expect for a given flow ot electric current. [Pg.630]

Reference electrodes for non-aqueous solvents are always troublesome because the necessary salt bridge may add considerable errors by undefined junction potentials. Leakage of components of the reference compartment, water in particular, into the working electrode compartment is a further problem. Whenever electrochemical cells of very small dimensions have to be designed, the construction of a suitable reference electrode system may be very difficult. Thus, an ideal reference electrode would be a simple wire introduced into the test cell. The usefulness of redox modified electrodes as reference electrodes in this respect has been studied in some detail... [Pg.80]

Electrochemical cells can be constructed using an almost limitless combination of electrodes and solutions, and each combination generates a specific potential. Keeping track of the electrical potentials of all cells under all possible situations would be extremely tedious without a set of standard reference conditions. By definition, the standard electrical potential is the potential developed by a cell In which all chemical species are present under standard thermodynamic conditions. Recall that standard conditions for thermodynamic properties include concentrations of 1 M for solutes in solution and pressures of 1 bar for gases. Chemists use the same standard conditions for electrochemical properties. As in thermodynamics, standard conditions are designated with a superscript °. A standard electrical potential is designated E °. [Pg.1381]

Figure 12.2 The electrochemical cell has a 25 p-m Teflon spacer sandwiched between the electrode and a window (Cap2 or Mgp2) to provide an electrolyte layer of known and controlled thickness. Working, reference, and auxiliary electrodes are indicated. Construction materials are glass and Teflon. Figure 12.2 The electrochemical cell has a 25 p-m Teflon spacer sandwiched between the electrode and a window (Cap2 or Mgp2) to provide an electrolyte layer of known and controlled thickness. Working, reference, and auxiliary electrodes are indicated. Construction materials are glass and Teflon.
An electrochemical cell was constructed by connecting the copper wire attached at the back of the Ti02 electrode to the platinum black cathode through a load. The two compartments were connected through an agar salt bridge that allows the exchange of ionic... [Pg.246]

Air quality measuring systems that detect for example the leading substance C02 (refer to chapter 53.3.3) do not require the high accuracy of expensive measuring systems. Therefore, not much effort needs to be put in the development and construction of C02 detectors. In general the accuracy of such systems amounts to 10%, which is achievable for the cost of an electrochemical cell. Fast measurements aren t needed but nevertheless averaging to increase accuracy is possible and recommended. [Pg.150]

Morita and co-workers (60) have constructed a STM that employs a unique 3D scanner and 3D positioner that is constructed from several piezoelectric cubes. This microscope was subsequently equipped with an electrochemical cell that allows disconnection of the tip and conventional 3 electrode voltammetry to be performed (61). Itaya et. al. have gained similar capabilities by modifying their aforementioned STM (Itaya, K. Higaki, K. Sugawara, S. Chem. Lett.. in press). [Pg.178]

In summary, we construct a simple electrochemical cell in which the silver to be cleaned is the cathode (Equation (7.2)) and aluminium foil as the anode supplies the electrons via Equation (7.1). [Pg.282]

Sometimes electrochemists are forced to construct electrochemical cells without water, e.g. if the analyte is water sensitive or merely insoluble. In these cases, we construct the cell with an organic solvent, the usual choice being the liquids acetonitrile, propylene carbonate (I), N,/V-dirrielhylformamide (DMF) or di-methylsulphoxide (DMSO), each of which is quite polar because of its high dielectric constant e. [Pg.302]

A reaction in an electrochemical cell comprises two half-cell reactions. Even when we want to focus on a single half-cell, we must construct a whole cell and determine its cell emf, which is dehned as (positive electrode) - E(negative electrode) - Only when we know both the emf and the value of one of the two electrode potentials can we calculate the unknown electrode potential. [Pg.328]

A student constructed an electrochemical cell as shown in Figure 1 ... [Pg.327]

The cell construction provides (i) a uniform internal distribution of up to four separate electrolytes, (ii) cooling and heating facilities (useful temperature range ca. - 40 °C up to -I- 250 °C), (iii) gas supply, and (iv) different turbulent promotors to improve transport performances. The versatility of off-the-shelf cells, paired with increasing experience of integrating electrolytic cells into industrial processes thus reduces the obstacles and risks for the scale-up. Furthermore, electrochemical units lend themselves well to modular construction, thus CPI plant expansion is a chance for this new technique. [Pg.137]

The rules of stoichiometry also apply in this case. In electrochemical cells, we must consider not only the stoichiometry related to chemical formulas, but also the stoichiometry related to electric currents. The half-reaction under consideration not only involves 1 mol of each of the copper species, but also 2 mol of electrons. We can construct a mole ratio that includes moles of electrons or we could construct a mole ratio using faradays. A faradav (F) is a mole of electrons. Thus, we could use either of the following ratios for the copper half-reaction ... [Pg.273]

Electrochemical cells are constructed, and their cell potentials are determined with a voltmeter. Electroplating is accomplished by using an external power supply, usually a battery, to plate a metal onto an electrode. (See Electrochemistry chapter.)... [Pg.296]

Generally, irrespective of the technique for which they are used, electrochemical cells are constructed in a way which minimizes the resistance of the solution. The problem is particularly accentuated for those techniques which require high current flows (large-scale electrolysis and fast voltammetric techniques). When current flows in an electrochemical cell there is always an error in the potential due to the non-compensated solution resistance. The error is equal to / Rnc (see Chapter 1, Section 3). This implies that if, for example, a given potential is applied in order to initiate a cathodic process, the effective potential of the working electrode will be less negative compared to the nominally set value by a amount equal to i Rnc. Consequently, for high current values, even when Rnc is very small, the control of the potential can be critical. [Pg.142]

The success of an electrolysis process depends on the choice of a suitable electrochemical cell and optimal operation conditions because there is a widespread variety of electrolyte composition, cell constructions, electrode materials, and electrochemical reaction parameters. [Pg.29]

The objective of this chapter is to study some essential practical aspects, which have to be considered. First, as necessary background information, the different alternatives for electrochemical cell operation are discussed in general. Then follows an overview of properties of electrode materials, electrolyte components, and cell separators. Finally, examples of cell constructions are shown. [Pg.29]

For choosing a suitable cell construction and optimal reaction conditions in the cell, it is inevitable to consider the fundamental correlations between electrode potential and cell current and their influence on selectivity and yield of the electrochemical reactions. Therefore, a simplified overview is given here. The detailed theory is elucidated in Chapter 1. [Pg.31]

A fundamental improvement in the facilities for studying electrode processes of reactive intermediates was the purification technique of Parker and Hammerich [8, 9]. They used neutral, highly activated alumina suspended in the solvent-electrolyte system as a scavenger of spurious impurities. Thus, it was possible to generate a large number of dianions of aromatic hydrocarbons in common electrolytic solvents containing tetraalkylammonium ions. It was the first time that such dianions were stable in the timescale of slow-sweep voltammetry. As the presence of alumina in the solvent-electrolyte systems may produce adsorption effects at the electrode, or in some cases chemisorption and decomposition of the electroactive species, Kiesele constructed a new electrochemical cell with an integrated alumina column [29]. [Pg.96]

The design and construction of an electrochemical cell derives from consideration of the system being examined. Potential sources of contamination must be carefully evaluated. Cell components are typically made of inert materials such as Teflon or Kel-F. Alternatively, electrolyte contact with confining materials may be avoided altogether by letting the cell be defined by the geometry of a hanging meniscus. The latter method has been incor-... [Pg.244]


See other pages where Electrochemical cell Construction is mentioned: [Pg.47]    [Pg.283]    [Pg.61]    [Pg.193]    [Pg.669]    [Pg.47]    [Pg.283]    [Pg.61]    [Pg.193]    [Pg.669]    [Pg.314]    [Pg.168]    [Pg.209]    [Pg.299]    [Pg.240]    [Pg.687]    [Pg.626]    [Pg.138]    [Pg.166]    [Pg.167]    [Pg.376]    [Pg.16]    [Pg.321]   
See also in sourсe #XX -- [ Pg.136 ]




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