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This will make graphene receive the excited electronic and vibrational excitations resulting from Ag NPs and Rh123 molecules under laser excitation [14, 34].
Raman spectra demonstrated that the MR-GO monolayer beneath the Ag NPs can effectively quench the fluorescence signal emitted from the Ag films and dye molecules under laser excitation, resulting in a chemical enhancement (CM).
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Konar, A. et al. Polyatomic molecules under intense femtosecond laser irradiation.
Nsurf and Nbulk are the number of molecules for SERS, and the number of molecules for the bulk sample under laser illumination, respectively.
The main nonlinear optical mechanism in LC is collective reorientation of molecules in a bulk of LC under laser excitation that often appears with applied electric field.
We investigate the quantum dynamics of interacting polar molecules under the application of a short laser pulse.
In the MR-GO-Ag system, the presence of MR-GO monolayer not only effectively quenches the strong FL background from Rh123 and Ag films under laser excitation but also greatly increases Raman signal of Rh123 molecule.
Under laser excitation, the strong electromagnetic coupling produced between NPs will greatly increase the SERS intensity of adsorbed molecules.
Ion-trap quantum computing uses rotating magnetic fields to isolate individual molecules, and laser light rather than radio pulses to change the molecules' quantum states.
Furthermore, both the Au and Ag films have a strong photoluminescence (PL) background under laser excitation, which leads to a huge difficulty in obtaining the detailed molecular vibrational information, especially the fingerprints of FL molecules [9].
Under laser irradiation, Si NRs are positively charged.
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