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In order to estimate the electrocatalytic performance of the TR-MoSx toward I3 − reduction, CV analysis was performed using a potential interval ranging from −0.4 to 1.0 vs Ag/AgCl and a scan rate of 50 mV s−1.
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All these polyporphines of type II demonstrate a very broad range of their redox activity, without any potential interval of non-electroactivity.
By means of cyclic voltammetry, we demonstrate a wider potential interval of highly reversible redox activity for these doped films, as compared to purely tungstate films.
Potentiostatic depositions were performed from both Fe(II) and Fe III) solutions in a broad potential interval (from −1.5 to −2.3 V vs Pt) to define the threshold value for iron reduction and film formation: the best results were obtained at −1.7 V vs Pt for Fe(II) solution and at −2.3 V vs Pt for Fe(III) one.
The condition where (w_{c} = 0.2;{text{m}}) for a patch of (R = 10;{text{km}}) (cycle of 0.6 m) leads to a slip event of ~M6, with a potential recurrence interval of several tens of years if the tectonic convergence speed is fast enough.
During the primary screen we identified a potential Rho1-interacting interval in 83A-B that we were not able to verify with an overlapping deficiency, although we did limit the potential interval to 17 protein-coding genes through non-interacting deficiencies.
Films of type II possess a high redox activity and electronic conductivity within the whole potential interval of above 3 V in the width.
Figure 3 presents the CVs of the Pt/Ti, NiS/Ti, and NiS/Pt/Ti CEs under I-/I3- electrolyte system in the potential interval of -0.4 to 0.4 V vs. Pt taken at a scan rate of 50 mV s-1 [20].
In potential interval from −0.10 V to −1.40 V, the electrochemical redox process of Ziram occurred in two parts.
In the potential interval −0.185 > Ecat ≥ −0.285 V, energetic conditions are large enough to allow the immediate decomposition of bornite, forming chalcocite in a more quantitative manner.
The presence of the PNEA and PAni coatings on Fe electrode restricts dissolution potential interval according to linear anodic potentiodynamic polarization curves obtained in 0.5 M H2SO4.
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