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Graphene-supported Pt Sn increased the electrocatalytic activity, which is strongly influenced by the addition of Sn in its alloyed and oxidized forms, boosting the reaction more readily because of the lower oxidation potential.
Fe2O3/BiVO4 showed lower photocatalytic water splitting activity than pure BiVO4 because Fe2O3 had lower oxidation potential than BiVO4.
PTTAA formed in BFEE had lower oxidation potential (0.4 V) and better cycling stability.
The organoborate was found to have a much lower oxidation potential compared to the organoborane.
The lower oxidation potential of GC base pairs leads to the localization of holes [4, 9], which allows the formation and hopping conduction of polarons.
As the oxidation potential played a role of dissolving Ag atoms into the electrolyte, the lower oxidation potential resulted in the higher growth rate, and vice versa [20].
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The electrochemical chlorination fails for azulenes with lower oxidation potentials.
The results showed that all compounds presented lower oxidation potentials when compared to the commercial product BHT (Epa = 0.989 V).
Compared to bare glassy carbon, the carbon black-modified electrode exhibited greatly enhanced current densities and lower oxidation potentials for all three phenols.
The monomers have lower oxidation potentials (0.75 V and 0.80 V vs. Ag/AgCl for SNS-AB2 and SNS-AB3, respectively) when compared to their analogous.
Compared to Co3O4 and Mn2O3 catalysts with similar microstructures, the CoxMn3−xO4 catalysts had lower oxidation potentials and more redox-active sites, therefore demonstrating improved PMC activation for the degradation of 2,4-dichlorophenol (2,4-DCP).
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