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Voltammetry electrolyte

Recently, Bond and coworkers developed a very versatile method of studying the voltammetry of solids in which insoluble microcrystals are immobilized on an electrode surface that is then placed in an electrolyte. Voltammetry reveals that nu-cleation and crystal growth phenomena can accompany redox switching [133]. Systems of this kind have been used to probe the dynamics of crystal growth, the effect of the charge, and structure of the complex on crystallization [134] as well as the dynamics of charge transport through the films [135]. [Pg.181]

Flavin adenine dinucleotide (FAD) has been electropolymerized using cyclic voltammetry. Cyclic voltammograms of poly (FAD) modified electrode were demonstrated dramatic anodic current increasing when the electrolyte solution contained NADH compare with the absence of pyridine nucleotide. [Pg.363]

In stripping voltammetry the stripping potential of a given ion is generally close to the polarographic half-wave potential of that ion in solutions with similar supporting electrolytes. Thus, typical stripping potentials in a 0.05M potassium chloride base solution are as follows Zn, — 1.00 V Cd, -0.07 V Pb, -0.45 V Bi, -0.10 V Cu(II), -0.05 V. [Pg.835]

Using dilatometry in parallel with cyclic voltammetry (CV) measurements in lmolL 1 LiC104 EC-l,2-dimethoxy-ethane (DME), Besenhard et al. [87] found that over the voltage range of about 0.8-0.3 V (vs. Li/Li+), the HOPG crystal expands by up to 150 percent. Some of this expansion seems to be reversible, as up to 50 percent contraction due to partial deintercalation of solvated lithium cations was observed on the return step of the CV. It was concluded [87] that film formation occurs via chemical reduction of a solvated graphite intercalation compound (GIC) and that the permselective film (SEI) in fact penetrates into the bulk of the HOPG. It is important to repeat the tests conducted by Besenhard et al. [87] in other EC-based electrolytes in order to determine the severity of this phenomenon. [Pg.435]

Sodium-silicate glass, 151 Sol-gel films, 120, 173 Solid electrodes, 110 Solid state devices, 160 Solvents, 102 Speciation, 84 Spectroelectrochenristry, 40 Spherical electrode, 6, 8, 9, 61 Square-wave voltammetry, 72, 92 Staircase voltammetry, 74 Standard potential, 3 Standard rate constant, 12, 18 Stripping analysis, 75, 79, 110 Supporting electrolyte, 102 Surface-active agents, 79... [Pg.209]

Although cyclic voltammetry in a variety of electrolyte systems, and with a variety of doped polymers, has shown strong effects due to ion transport, it has provided little understanding. In fact, one of the important uses of ion transport data from the techniques discussed in the preceding subsections is that they help to provide an understanding of the cyclic voltammetry behavior of conducting polymer films. Their importance will... [Pg.580]

C.G. Vayenas, A. loannides, and S. Bebelis, Solid Electrolyte Cyclic Voltammetry for in situ Investigation of Catalyst Surfaces, J. Catal. 129, 67-87 (1991). [Pg.107]

J. Yi, A. Kaloyannis, and C.G. Vayenas, High Temperature cyclic voltammetry of Pt electrodes in solid electrolyte cells, Electrochim. Acta 38(17), 2533-2539 (1993). [Pg.184]

They first reported and studied permanent NEMCA and via cyclic voltammetry established the dependence of metal/solid electrolyte capacitance on porous metal film mass, which confirms the O2" backspillover promoting mechanism. [Pg.560]


See other pages where Voltammetry electrolyte is mentioned: [Pg.176]    [Pg.1191]    [Pg.176]    [Pg.1191]    [Pg.538]    [Pg.270]    [Pg.144]    [Pg.224]    [Pg.624]    [Pg.871]    [Pg.146]    [Pg.440]    [Pg.602]    [Pg.109]    [Pg.1038]    [Pg.36]    [Pg.82]    [Pg.323]    [Pg.326]    [Pg.327]    [Pg.233]    [Pg.233]    [Pg.202]    [Pg.240]    [Pg.267]    [Pg.268]    [Pg.273]    [Pg.99]    [Pg.72]    [Pg.126]    [Pg.131]    [Pg.158]    [Pg.176]    [Pg.213]    [Pg.319]   
See also in sourсe #XX -- [ Pg.785 ]




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Cyclic voltammetry supporting electrolyte

Solid Electrolyte Cyclic Voltammetry

Stripping Voltammetry at Two Immiscible Liquid Electrolyte Solutions

Voltammetry supporting electrolytes

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