Higher-order shear and normal deformation theory is used in this paper to account thickness stretching effect for free vibration analysis of the cylindrical micro/nano shell subjected to an applied voltage and uniform...Higher-order shear and normal deformation theory is used in this paper to account thickness stretching effect for free vibration analysis of the cylindrical micro/nano shell subjected to an applied voltage and uniform temperature rising.Size dependency is included in governing equations based on the modified couple stress theory.Hamilton’s principle is used to derive governing equations of the cylindrical micro/nano shell.Solution procedure is developed using Navier technique for simply-supported boundary conditions.The numerical results are presented to investigate the effect of significant parameters such as some dimensionless geometric parameters,material properties,applied voltages and temperature rising on the free vibration responses.展开更多
Experimental vibrational spectra of heavy light XH stretching vibrations of simple molecules have been analyzed using the local mode model.In addition,the bond dipole approach,which assumes that the transition dipole ...Experimental vibrational spectra of heavy light XH stretching vibrations of simple molecules have been analyzed using the local mode model.In addition,the bond dipole approach,which assumes that the transition dipole moment(TDM)of the XH stretching mode is aligned along the XH bond,has helped analyze experimental spectra.We performed theoretical calculations of the XH stretching vibrations of HOD,HND^−,HCD,HSD,HPD^−,and HSiD using local mode model and multi-dimensional normal modes.We found that consistent with previous notions,a localized 1D picture to treat the XH stretching vibration is valid even for analyzing the TDM tilt angle.In addition,while the TDM of the OH stretching fundamental transition tilted away from the OH bond in the direction away from the OD bond,that for the XH stretching fundamental of HSD,HND^−,HPD^−,HCD,and HSiD tilted away from the OH bond but toward the OD bond.This shows that bond dipole approximation may not be a good approximation for the present systems and that the heavy atom X can affect the transition dipole moment direction.The variation of the dipole moment was analyzed using the atoms-in-molecule method.展开更多
The influence of vibration on the spatiotemporal structure of the pattern in dielectric barrier discharge is studied for the first time.The spatiotemporal structure of the pattern investigated by an intensified charge...The influence of vibration on the spatiotemporal structure of the pattern in dielectric barrier discharge is studied for the first time.The spatiotemporal structure of the pattern investigated by an intensified charge-coupled device shows that it is an interleaving of three sublattices, whose discharge sequence is small rods–halos–large spots in each half-cycle of the applied voltage.The result of the photomultiplier indicates that the small rods are composed of moving filaments.The moving mode of the moving filaments is determined to be antisymmetric stretching vibration by analyzing a series of consecutive images taken by a high-speed video camera.The antisymmetric stretching vibration affects the distribution of wall charges and leads to the halos.Furthermore, large spots are discharged only at the centers of the squares consisting of vibrating filaments.The vibration mechanism of the vibrating filaments is dependent on the electric field of wall charges.展开更多
We apply the strong-field Lewenstein model to demonstrate the high-order harmonic generation of CO2 with three vibrational modes（balance vibration,bending vibration,and stretching vibration） driven by an intense las...We apply the strong-field Lewenstein model to demonstrate the high-order harmonic generation of CO2 with three vibrational modes（balance vibration,bending vibration,and stretching vibration） driven by an intense laser field.The results show that the intensity of harmonic spectra is sensitive to molecular vibrational modes,and the high harmonic efficiency with stretching vibrational mode is the strongest.The underlying physical mechanism of the harmonic emission can be well explained by the corresponding ionization yield and the time-frequency analysis.Finally,we demonstrate the attosecond pulse generation with different vibrational modes and an isolated attosecond pulse with a duration of about 112 as is generated.展开更多
The Raman and infrared spectra of all-trans-astaxanthin （AXT） in dimethyl sulfoxide （DMSO） solvent were investigated experimentally and theoretically. Density functional cal-culations of the Raman spectra predict ...The Raman and infrared spectra of all-trans-astaxanthin （AXT） in dimethyl sulfoxide （DMSO） solvent were investigated experimentally and theoretically. Density functional cal-culations of the Raman spectra predict the splitting of the υ1 band into υ1-1 and υ1-2 compo-nents. The absence of splitting in Raman experimental spectra is ascribed to the competition between the two symmetric C=C stretching vibrations of the backbone chain. The υ1 band is very sensitive to the excitation wavelength： resonance excitation stimulates the higher-frequency υ1-2 mode, and off-resonance excitation corresponds to the lower-frequency υ1-1 mode. Analyses of the intramolecular hydrogen bonding between C=O and O-H in the AXT/DMSO system reveal that the C4=O1...H1-O3 and C4＇=O2...H2-O4 bonds are strengthened and weakened, respectively, in the electronically excited state compared with those in the ground state. This result reveals significant variations of the AXT molecular structure in different electronic states.展开更多
基金The authors would like to thank the Iranian Nanotechnology Development Committee for their financial support.
文摘Higher-order shear and normal deformation theory is used in this paper to account thickness stretching effect for free vibration analysis of the cylindrical micro/nano shell subjected to an applied voltage and uniform temperature rising.Size dependency is included in governing equations based on the modified couple stress theory.Hamilton’s principle is used to derive governing equations of the cylindrical micro/nano shell.Solution procedure is developed using Navier technique for simply-supported boundary conditions.The numerical results are presented to investigate the effect of significant parameters such as some dimensionless geometric parameters,material properties,applied voltages and temperature rising on the free vibration responses.
文摘Experimental vibrational spectra of heavy light XH stretching vibrations of simple molecules have been analyzed using the local mode model.In addition,the bond dipole approach,which assumes that the transition dipole moment(TDM)of the XH stretching mode is aligned along the XH bond,has helped analyze experimental spectra.We performed theoretical calculations of the XH stretching vibrations of HOD,HND^−,HCD,HSD,HPD^−,and HSiD using local mode model and multi-dimensional normal modes.We found that consistent with previous notions,a localized 1D picture to treat the XH stretching vibration is valid even for analyzing the TDM tilt angle.In addition,while the TDM of the OH stretching fundamental transition tilted away from the OH bond in the direction away from the OD bond,that for the XH stretching fundamental of HSD,HND^−,HPD^−,HCD,and HSiD tilted away from the OH bond but toward the OD bond.This shows that bond dipole approximation may not be a good approximation for the present systems and that the heavy atom X can affect the transition dipole moment direction.The variation of the dipole moment was analyzed using the atoms-in-molecule method.
文摘The influence of vibration on the spatiotemporal structure of the pattern in dielectric barrier discharge is studied for the first time.The spatiotemporal structure of the pattern investigated by an intensified charge-coupled device shows that it is an interleaving of three sublattices, whose discharge sequence is small rods–halos–large spots in each half-cycle of the applied voltage.The result of the photomultiplier indicates that the small rods are composed of moving filaments.The moving mode of the moving filaments is determined to be antisymmetric stretching vibration by analyzing a series of consecutive images taken by a high-speed video camera.The antisymmetric stretching vibration affects the distribution of wall charges and leads to the halos.Furthermore, large spots are discharged only at the centers of the squares consisting of vibrating filaments.The vibration mechanism of the vibrating filaments is dependent on the electric field of wall charges.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.61575077,11271158,and 11574117)
文摘We apply the strong-field Lewenstein model to demonstrate the high-order harmonic generation of CO2 with three vibrational modes（balance vibration,bending vibration,and stretching vibration） driven by an intense laser field.The results show that the intensity of harmonic spectra is sensitive to molecular vibrational modes,and the high harmonic efficiency with stretching vibrational mode is the strongest.The underlying physical mechanism of the harmonic emission can be well explained by the corresponding ionization yield and the time-frequency analysis.Finally,we demonstrate the attosecond pulse generation with different vibrational modes and an isolated attosecond pulse with a duration of about 112 as is generated.
文摘The Raman and infrared spectra of all-trans-astaxanthin （AXT） in dimethyl sulfoxide （DMSO） solvent were investigated experimentally and theoretically. Density functional cal-culations of the Raman spectra predict the splitting of the υ1 band into υ1-1 and υ1-2 compo-nents. The absence of splitting in Raman experimental spectra is ascribed to the competition between the two symmetric C=C stretching vibrations of the backbone chain. The υ1 band is very sensitive to the excitation wavelength： resonance excitation stimulates the higher-frequency υ1-2 mode, and off-resonance excitation corresponds to the lower-frequency υ1-1 mode. Analyses of the intramolecular hydrogen bonding between C=O and O-H in the AXT/DMSO system reveal that the C4=O1...H1-O3 and C4＇=O2...H2-O4 bonds are strengthened and weakened, respectively, in the electronically excited state compared with those in the ground state. This result reveals significant variations of the AXT molecular structure in different electronic states.
