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Wavelength nonresonant

Principles and Characteristics Atomic fluorescence spectrometry (AFS) is based on excitation of atoms by radiation of a suitable wavelength (absorption), and detection and measurement of the resultant de-excitation (fluorescence). The only process of analytical importance is resonance fluorescence, in which the excitation and fluorescence lines have the same wavelength. Nonresonance transitions are not particularly analytically useful, and involve absorption and fluorescence photons of different energies (wavelength). [Pg.624]

In atomic fluorescence spectrometry (AFS), the analyte is introduced into an atomizer (flame, plasma, glow discharge, furnace) and excited by monochromatic radiation emitted by a primary source. The latter can be a continuous source (xenon lamp) or a line source (hollow cathode lamp, electrodeless discharge lamp, or tuned laser). Subsequently, the fluorescence radiation, which may be of the same wavelength (resonance fluorescence) or of longer wavelength (nonresonance fluorescence), is measured. [Pg.713]

When the exciting frequency is nonresonant (distant from any electronic transition), the differential scattering cross section at wavelength X is as in equation 8 ... [Pg.318]

Here we summarize our investigations on the nonlinear optical properties of CdTe QDs in the nonresonant wavelength region, in which the size dependence of will be... [Pg.156]

Third-order nonlinear optical properties of CdTe QDs were examined by Z-scan and FWM experiments in the nonresonant wavelength region. We found that the two-photon absorption cross section, a, is as high as 10 GM, although this value decreases with decreasing size. In addition, the nonlinear response is comparable to the pulse width of a fs laser and the figures of merit (FOM = Re Xqd/ Xqd)... [Pg.166]

Raman spectroscopy is primarily useful as a diagnostic, inasmuch as the vibrational Raman spectrum is directly related to molecular structure and bonding. The major development since 1965 in spontaneous, c.w. Raman spectroscopy has been the observation and exploitation by chemists of the resonance Raman effect. This advance, pioneered in chemical applications by Long and Loehr (15a) and by Spiro and Strekas (15b), overcomes the inherently feeble nature of normal (nonresonant) Raman scattering and allows observation of Raman spectra of dilute chemical systems. Because the observation of the resonance effect requires selection of a laser wavelength at or near an electronic transition of the sample, developments in resonance Raman spectroscopy have closely paralleled the increasing availability of widely tunable and line-selectable lasers. [Pg.466]

Fig. 16.3 Simulation of transmission spectrum for a four resonator array. FDTD simulation showing the steady state electric field distributions when the device is excited at the (a) resonant wavelength and (b) nonresonant wavelength. Note that the color levels in this image are scaled to the maximum field intensity in each image not to each other. The field levels in (b) are roughly of 20 times greater magnitude than those shown in (a), (c) Output spectrum for a device consisting of a waveguide with four evanescently coupled side cavities adjacent to it. Here each resonator consists of a cavity with four holes on either side. Reprinted from Ref. 37 with permission. 2008 Optical Society of America... Fig. 16.3 Simulation of transmission spectrum for a four resonator array. FDTD simulation showing the steady state electric field distributions when the device is excited at the (a) resonant wavelength and (b) nonresonant wavelength. Note that the color levels in this image are scaled to the maximum field intensity in each image not to each other. The field levels in (b) are roughly of 20 times greater magnitude than those shown in (a), (c) Output spectrum for a device consisting of a waveguide with four evanescently coupled side cavities adjacent to it. Here each resonator consists of a cavity with four holes on either side. Reprinted from Ref. 37 with permission. 2008 Optical Society of America...
Fig. 1.19. Quenching of the coherent vibrational oscillations of MDMO-PPV upon photoinduced charge transfer. The AT/T dynamics for pure MDMO-PPV (continuous line) and for MDMO-PPV/PCBM (1 3 wt. ratio) (dashed line), excited by a sub-10-fs pulse, was recorded at the probe wavelength of 610 nm. The inset shows the Fourier transform of the oscillatory component of the MDMO-PPV signal, the nonresonant Raman spectrum of MDMO-PPV (excitation 1064 nm) and the resonant Raman spectrum of an MDMO-PPV/PCBM sample (excitation 457 nm). For the resonant Raman spectrum of MDMO-PPV, it was necessary to quench the strong background luminescence by adding PCBM... Fig. 1.19. Quenching of the coherent vibrational oscillations of MDMO-PPV upon photoinduced charge transfer. The AT/T dynamics for pure MDMO-PPV (continuous line) and for MDMO-PPV/PCBM (1 3 wt. ratio) (dashed line), excited by a sub-10-fs pulse, was recorded at the probe wavelength of 610 nm. The inset shows the Fourier transform of the oscillatory component of the MDMO-PPV signal, the nonresonant Raman spectrum of MDMO-PPV (excitation 1064 nm) and the resonant Raman spectrum of an MDMO-PPV/PCBM sample (excitation 457 nm). For the resonant Raman spectrum of MDMO-PPV, it was necessary to quench the strong background luminescence by adding PCBM...
Spectroscopy is traditionally performed in a static (nonresonant) fashion A transition (absorption or emission) is observed as a function of the frequency or wavelength of light. However, if one uses an electromagnetic wave,... [Pg.239]


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