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1 Fe(CN)6(4-) ion at the surface of a platinum rotating disk electrode.
2 ed previously for other electrodes including rotating disk electrodes.
5 and catalysts deposited onto a glassy carbon rotating disk electrode) and in situ (in a membrane elec
6 -GDI) were studied using cyclic voltammetry, rotating disk electrode, and flow injection analysis.
9 f external mass transfer resistances using a rotating disk electrode exhibited only a 5% reduction in
10 oscopic electrochemical responses, including rotating disk electrode measurements of the catalytic ac
11 current values, derived from microelectrode/rotating disk electrode measurements or transient peak c
14 dation/evolution activity obtained using the rotating disk electrode method is found to decrease with
20 spectrophotometer (RSS) was coupled to a Au rotating disk electrode (RDE) for monitoring at near-nor
23 ain or with 10% CB) were further examined in rotating disk electrode (RDE) tests that minimized mass
25 ed the classical Koutecky-Levich model for a rotating disk electrode (RDE) to a general heterogeneous
26 hydrodynamic diffusion of the ss-HSDNA/rGOae rotating disk electrode (RDE) toward AFB1 detection usin
27 possess a USL as well as at the surface of a rotating disk electrode (RDE) used to measure chemical f
34 f dioxygen in neutral aqueous solutions at a rotating disk electrode to be oxidized at a concentric A
35 reaction is conducted on a polymer film on a rotating disk electrode under potentiostatic condition s
38 ammetry over steady-state techniques such as rotating disk electrode voltammetry and microdisk electr
40 mediator and NADH has been characterized via rotating disk electrode voltammetry, and it has been fou
41 gas analyses, scanning electron microscopy, rotating disk electrode voltammetry, demonstrate that Li
42 methodology is proposed, in the framework of rotating disk electrode voltammetry, to analyze the curr
46 er microdisk electrode or a 3 mm diameter Pt rotating disk electrode, while peak currents at a macrod
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