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Therefore, it is crucial to choose the appropriately applied potential for the electropolymerization process.
The detection limit, linear calibration range, and applied potential for CySH and iodate detection are listed in Table 1.
The photocurrent density versus time (J T) under an externally applied potential for all samples at 1.23 V versus RHE is shown in Fig. 4b.
To obtain high sensitivity and to minimize possible interferences, -0.2 V was chosen as the optimum applied potential for further investigations.
The applied potential for the hydrogen evolution is as low as 0.8 V for phosphmolybdic acid and 0.6 V for phosphotungstic acid.
The relation between photocurrent and applied potential for the anodic film has been analyzed by the Gartner model, from which the values of the absorption coefficients of t-PbO were found to be much larger than that of t-PbO single crystals.
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Furthermore, Figure 7 clearly shows the comparison curves of the photocurrent densities versus applied potentials for three different TiO2 photoanodes (TNTAs, BTs, and PCTs) under Xe lamp irradiation (100 mW/cm2) in 1 M KOH electrolyte [43].
This subsequently leads to the lowest reported applied potentials for CO2 reduction to formate on Ag electrodes to date with high Faradaic efficiencies.
The experimental conditions, applied potential and pH, for ethanol monitoring were optimised, and ethanol was determined amperometrically at −0.3 V vs. SCE at pH 7.5.
The graphene oxide was reduced electrochemically in phosphate buffer solution by applying potential of −0.8 V for different times.
The results provide evidence for adaptation of complex communities to optimize applied potential, while reducing energy input for electrolysis.
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