1968
DOI: 10.1016/0013-4686(68)80024-6
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Double-layer effect correction in chronoamperometry with linear potential sweep

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1969
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Cited by 11 publications
(5 citation statements)
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“…4 (Bottom)) reiterates the capacitive effect due to the presence of active substances in the soil mixture double-layer. To understand the current change effect better, we can incorporate the following equation: 40,41…”
Section: Resultsmentioning
confidence: 99%
“…4 (Bottom)) reiterates the capacitive effect due to the presence of active substances in the soil mixture double-layer. To understand the current change effect better, we can incorporate the following equation: 40,41…”
Section: Resultsmentioning
confidence: 99%
“…Tracking antibody-antigen interactions via chronoamperometry.-Chronoamperometry (CA) has been widely studied and utilized as a modality to probe current-time dependence for diffusion limited processes at the electrode surface. 40,41 Traditionally, it has been used as a mechanism to visualize the electrochemical impacts of redox reaction processes and non-faradaic diffusion behavior. In this study-CA was employed to monitor the double layer modulation due to antibody-antigen binding with an input step bias of 250 mV/500 mV applied towards electrode 1 of the IDE microelectrode for 30 s. This capacitive dominant current was captured at the min-max position within 0.01 s of the bias applied.…”
Section: Resultsmentioning
confidence: 99%
“…The potential ( ) in the diffuse double layer can have a rather significant effect on mass transport so that Fick's laws require modi-fication. A rederivation of the current-voltage relation, including this effect, was completed for irreversible charge transfer reactions (72). Calculated rate constants for zinc(II) reduction in several electrolyte solutions were about two orders of magnitude smaller than constants obtained from equations that neglected the potential.…”
Section: Controlled Potentialmentioning
confidence: 99%
“…Inorganic. Nucleation of mercury on platinum (376) and cadmium, indium, and thallium on solid mercury (395); surface oxidation of platinum (174,178,256,339) and gold (256), and surface oxide reduction on platinum metals (357); hydrogen on platinum single crystal faces (141,836); cadmium and lead in various electrolyte solutions (136); dissolution of mercury in cyanide (845); homogeneous reactions of cadmium cyanide (342) and nitrilotriacetate (346) complexes; adsorption effects on cadmium, lead, copper(II), and vanadium(III) (206); adsorption of cadmium in presence of iodide and bromide (18); mechanism of solid cadmium electrode (166); adsorption and rates of cadmium and thallium (193); mechanism of solid zinc electrode ( 185); effect of potential on zinc reduction (72); nucleation and orientation of copper (109); copper(I) (56) and nickel(II) (9) reduction in fused salts; inhibition of copper and iron by surface active agents (315); (149); diffusion of iodide in alcohols, effect of liquid structure at electrode surface (288); lithium amalgam electrode rate in dimethyl sulfoxide (77); oxygen reduction on mercury (377); oxygen reduction in nonaqueous solvents (375); formation of NO+ from nitrous acid (162); silver iodide solid electrolyte on graphite and platinum surfaces (172); silver rubidium iodide solid electrolyte on silver electrode (21); silver oxidation to Ag20 and AgO (355,356); catalytic oxidation of ammine complexes of chromium (II) to (III) (51) and of vanadium(III) to (V) (52) by chlorite ion.…”
Section: Controlled Potentialmentioning
confidence: 99%