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Electronic flow cells

Wet the inside of the electronic flow cell with the supplied soap solution by pushing on the button several times. [Pg.247]

Taken as a group, PV cells comprise soHd-state devices in which photons of light coUide with atoms and transfer thek energy to electrons. These electrons flow into wkes that ate connected to the cells, thereby providing current to electrical loads. [Pg.104]

If electron flow between the electrodes is toward the sample half-cell, reduction occurs spontaneously in the sample half-cell, and the reduction potential is said to be positive. If electron flow between the electrodes is away from the sample half-cell and toward the reference cell, the reduction potential is said to be negative because electron loss (oxidation) is occurring in the sample halfcell. Strictly speaking, the standard reduction potential, is the electromotive force generated at 25°C and pH 7.0 by a sample half-cell (containing 1 M concentrations of the oxidized and reduced species) with respect to a reference half-cell. (Note that the reduction potential of the hydrogen half-cell is pH-dependent. The standard reduction potential, 0.0 V, assumes 1 MH. The hydrogen half-cell measured at pH 7.0 has an of —0.421 V.)... [Pg.676]

Figure 21.2a shows a sample/reference half-cell pair for measurement of the standard reduction potential of the acetaldehyde/ethanol couple. Because electrons flow toward the reference half-cell and away from the sample half-cell, the standard reduction potential is negative, specifically —0.197 V. In contrast, the fumarate/succinate couple and the Fe /Fe couple both cause electrons to flow from the reference half-cell to the sample half-cell that is, reduction occurs spontaneously in each system, and the reduction potentials of both are thus positive. The standard reduction potential for the Fe /Fe half-cell is much larger than that for the fumarate/ succinate half-cell, with values of + 0.771 V and +0.031 V, respectively. For each half-cell, a half-cell reaction describes the reaction taking place. For the fumarate/succinate half-cell coupled to a H Hg reference half-cell, the reaction occurring is indeed a reduction of fumarate. [Pg.676]

In the experiments to be described, in each case the half-cell was coupled to a Ag/AgOl half-cell, which in each case formed the positive electrode of the cell that is to say, on closing the external circuit, electrons flowed in the external circuit from the amalgam electrode to the silver electrode. This was the situation whether the solvent was water, or methanol, or a mixture of methanol and water. [Pg.220]

This proton exchange membrane is used in both hydrogen and methanol fuel cells, in which a catalyst at the anode produces hydrogen from the methanol. Because the membrane allows the protons, but not the electrons, to travel through it, the protons flow through the porous membrane to the cathode, where they combine with oxygen to form water, while the electrons flow through an external circuit. [Pg.639]

In a galvanic cell, electrons flow downhill from a region of higher electrical potential to a region of lower electrical potential. [Pg.1381]

The difference in electrical potential between two electrodes is the cell potential, designated E and measured in volts (V). The magnitude of E increases as the amount of charge imbalance between the two electrodes increases. For any galvanic cell, the value of E and the direction of electron flow can be determined experimentally by inserting a voltmeter in the external circuit. [Pg.1381]

Defining a reference value for the SHE makes it possible to determine E ° values of all other redox half-reactions. As an example. Figure 19-14 shows a cell in which a standard hydrogen electrode is connected to a copper electrode in contact with a 1.00 M solution of C U . Measurements on this cell show that the SHE is at higher electrical potential than the copper electrode, indicating that electrons flow from the SHE to the Cu... [Pg.1383]

C19-0072. A cell is setup with two Cu wire electrodes, one immersed in a 1.0 M solution of C11NO3, the other in a 1.0 M solution of Cu (N03)2. Determine E° oi this cell, identify the anode, and draw a picture that shows the direction of electron flow at each electrode and in the external circuit. [Pg.1420]

Identify the two half-reactions, (b) Determine the potential of this cell, (c) Identify the anode and cathode, (d) Redraw the sketch to show the direction of electron flow and the molecular processes occurring at each electrode. [Pg.1424]

Figure 8.31. Principle of a Polymer Electrolyte Membrane (PEM) fuel cell. A Nation membrane sandwiched between electrodes separates hydrogen and oxygen. Hydrogen is oxidized into protons and electrons at the anode on the left. Electrons flow through the outer circuit, while protons diffuse through the... Figure 8.31. Principle of a Polymer Electrolyte Membrane (PEM) fuel cell. A Nation membrane sandwiched between electrodes separates hydrogen and oxygen. Hydrogen is oxidized into protons and electrons at the anode on the left. Electrons flow through the outer circuit, while protons diffuse through the...
Fig. 5.2 The n-Cd(Se,Te)/aqueous Cs2Sx/SnS solar cell. P, S, and L indicate the direction of electron flow through the photoelectrode, tin electrode, and external load, respectively (a) in an illuminated cell and (b) in the dark. For electrolytes, m represents molal. Electron transfer is driven both through an external load and also into electrochemical storage by reduction of SnS to metaUic tin. In the dark, the potential drop below that of tin sulfide reduction induces spontaneous oxidation of tin and electron flow through the external load. Independent of illumination conditions, electrons are driven through the load in the same direction, ensuring continuous power output. (Reproduced with permission from Macmillan Publishers Ltd [Nature] [60], Copyright 2009)... Fig. 5.2 The n-Cd(Se,Te)/aqueous Cs2Sx/SnS solar cell. P, S, and L indicate the direction of electron flow through the photoelectrode, tin electrode, and external load, respectively (a) in an illuminated cell and (b) in the dark. For electrolytes, m represents molal. Electron transfer is driven both through an external load and also into electrochemical storage by reduction of SnS to metaUic tin. In the dark, the potential drop below that of tin sulfide reduction induces spontaneous oxidation of tin and electron flow through the external load. Independent of illumination conditions, electrons are driven through the load in the same direction, ensuring continuous power output. (Reproduced with permission from Macmillan Publishers Ltd [Nature] [60], Copyright 2009)...
The silver-zinc cell is a storage battery After discharge, it can be recharged by forcing through it an electric cnrrent in the reverse direction. In this process the two electrode reactions (19.3) and (19.4) as well as the overall reaction (19.2) go from right to left electrons flowing in the sense of arrow r in Fig. 19.1. [Pg.345]

The diagram shows a student s setup for a voltaic cell. Which change would help ensure that electron flow would continue indefinitely ... [Pg.41]

In the above process electrons will be consumed and will have to be generated by a net electron flow along the externally used connecting wire from the electrode Zn in the Cu-Zn cell. In order for electrons to be produced at the electrode Zn, the electrode reaction at Zn must be reversed ... [Pg.648]

Ans. In direct current, the electrons flow in the same direction all the time. In alternating current, the electrons flow one way for a short period of time (typically s) and then they flow the other way. To get any electrolysis that is not immediately undone, direct current is required. Direct current is also used in cars because cells generate direct current. [Pg.236]


See other pages where Electronic flow cells is mentioned: [Pg.93]    [Pg.44]    [Pg.505]    [Pg.394]    [Pg.116]    [Pg.231]    [Pg.218]    [Pg.483]    [Pg.484]    [Pg.504]    [Pg.1374]    [Pg.1386]    [Pg.1390]    [Pg.1408]    [Pg.218]    [Pg.219]    [Pg.417]    [Pg.469]    [Pg.293]    [Pg.805]    [Pg.649]    [Pg.673]    [Pg.97]    [Pg.441]    [Pg.62]    [Pg.5]    [Pg.66]    [Pg.230]    [Pg.299]    [Pg.225]    [Pg.226]   
See also in sourсe #XX -- [ Pg.53 ]




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