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The deposition scan rate affects the capacitive behaviour of mixed oxide electrodes through its effects on layer morphology and surface structure.
The use of an SPE resulted in good stabilisation of the Co + Ni mixed oxide electrodes during electrolysis of the electrolyte-free water.
The mechanism of the chloride electrooxidation was investigated by CV and radiotracer techniques, as well as PC simulation methods on RuO2/TiO2 mixed oxide electrodes.
A systematic investigation was conducted on the mechanism and electrocatalytic properties of O2 and Cl2 evolution on mixed oxide electrodes of nominal composition: Ti/[Ru 0.3 Ti 0.6 Ce(0.1−x)]O2[Nb2O5](x) (0 ≤ x ≤ 0.1).
Mixed oxide electrodes with nominal composition Ti/[Ru 0.3 Ti 0.6 Ce 0.1−x)]O2[Nb2O5](x), (0≤x≤0.1) were prepared through a process of thermal decomposition (450 °C) of chloride precursor mixture solutions.
We study in particular the effect of the deposition scan rate and of the Ni II) to Mn II) molar ratio in the deposition bath on the capacitive behaviour of mixed oxide electrodes.
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The adsorbed intermediate of the chloride electrochemical oxidation process on a RuO2TiO2 mixed oxide electrode was studied by cv technique in a large range of sweep rate.
It was found that covering of the cathode by a mixed oxide electrode increased NO decomposition even in the presence of excess oxygen.
The study of the electrochemical behaviour of mixed spinel oxide electrodes, obtained by the partial replacement of Fe by Ni and/or Mn in the cobalt ferrite CoFe2O4 is presented.
This phenomenon in the mixed oxide nanotube electrode can be attributed to the retention of energy by WOx during high photon influx and releasing it during photon starvation condition.
A three electrode electrochemical cell was designed with these mixed oxide thin films as the working electrode, platinum mesh as counter electrode and the saturated calomel as the reference electrode with 0.01 M HCl solution diluted in distilled water as electrolyte.
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