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This charge is attributed to OH-adsorption on the Bi-covered Pt(111) surface rather than to a change in valence state of the adsorbed Bi, as was previously suggested.
At all temperatures, the expected increase in thermal-induced charge is attributed to the delocalization of holes (or/and electrons) in potential hills (or/and potential wells) which accurately accounts for the total electric and dielectric behavior through DNA molecule.
The observed decrease in surface charge is attributed to the screening of negatively charged Ag NPs by surface-bound Hb molecules, which may establish electrostatic interactions between the surface ions and the positively charged amino acid residues of the Hb (histidine, lysine) [60, 61].
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The residual energetic disorder encountered by charges is attributed to significant paracrystalline disorder in the π−π stacking distances within the aggregates (g ≈ 6 8%)[ 101] and manifests itself in moderate activation energies of the mobility or energetic width of trap distributions (Ea = 72 ± 24 meV).
The heat variations of the Li/LiMn2O4 cell during charging were attributed to the LiMn2O4 phase transition and order/disorder changes.
All hydrogens were added to the protein and partial charges were attributed to the protein atoms using Amber99 force field [25].
These negative surface charges are attributed to the negatively charged citrate capping at this pH.
This difference in the discharge rate capability behaviour of the pristine and ball-milled graphites with charge rate is attributed to the interplay of two different charge storage mechanisms: Li-ion intercalation and Li-ion adsorption that co-exist; but the later becomes more significant for milled samples.
The high dispersion in the recorded charge values is attributed to an existing exponential relationship between the voltage gate and the current of the transistor in the working region selected in this application (region near the transistor cut-off value) (Fig. S3, Supporting Information).
The basal surface of kaolinites is believed to carry a constant structural charge, which is attributed to the isomorphous substitution of Si4+ by Al3+.
Therefore, the reason for the large charge capacity is attributed to delithiation of the LiCoPO4 coincident with the decomposition of the electrolyte.
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