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The simulations summarized in Figure 2, consistent with the experimental UV-visible absorption measurements, are consistent with the excitation of the longitudinal mode of silver nanostructures.
This red-shift in energy implies the formation of a triangular structure, which is ascribed to the in-plane dipole resonance mode of silver nanoprisms as shown in Figure 2a.
First, the smaller form has a larger ratio of surface area to volume, which dramatically increases the potential for silver ions to be released the primary mode of silver and nanosilver toxicity.
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Individual and collective plasmonic modes of silver NPs aggregates were investigated at nanometer scale by means of EFTEM.
The aim of this paper was to explore the potential modes of silver NP (AgNP) interaction with NOM and a model EPS.
The individual and collective LSPR modes of silver nanoparticle aggregated by covalent binding by means of bifunctional molecular linkers are described in this study.
These features can be attributed to scattering by vibrational modes of silver oxide, Ag2O [27], formed on the surface of the island film during high-temperature annealing.
We attribute this to the well-known dipolar mode of single silver NPs [20 22].
In this work, we show that the growth mode of the silver can be controlled by the deposition condition.
The second peak could be attributed to the transverse plasmon mode of Ag NWs, and the peak position is related to the dimensions of silver nanostructures [79].
Absorption peak of Ag NWs at 380 nm corresponds to transverse plasmon mode of Ag NWs, and the shoulder peak at ~355 nm can be attributed to long nanowires which exhibit similar optical properties to bulk silver [ 30].
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