Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Light excitation regime

In 1931 in her doctoral dissertation supervised by Max Bom, Maria Goppert-Mayer proposed the concept of the simultaneous absorption of two photons by a molecular system in one elementary action,(English translation Ref ). This prediction was based on the principles of the quantmn theory of radiation " as well as the concept of the intermediate energy level. Based on the formalism of summation over all eigenstates of the system, Maria Goppert-Mayer derived an expression for the two-photon absorption probability which, however, occurred to be too low to be experimentally observed in the incoherent light excitation regime. Hence, the unquestionable experimental confirmation took over thirty years. ... [Pg.695]

Overwhelmingly, the published research on Raman-based biofluid analysis uses excitation in the near-infrared regime in order to reduce fluorescence. Standard linewidth-narrowed diode lasers at 785 or 830 nm are most common. As noted in Chap. 1, several hundred milliwatts of multiple-spatial mode light can routinely be obtained from diode lasers, making them economical choices... [Pg.387]

At potentials near the photocurrent onset (roughly Fn,), a spiked response is seen with a characteristic overshoot when the light is turned off. At positive potentials near the plateau regime (again for the specific illustrative case of an n-type semiconductor), the response reverts to a rectangular profile that mimics the excitation waveform. Intermediate response patterns manifest at potentials in between. [Pg.2691]

Perhaps more challenging from both experimental and modeling perspectives is the -excitation case. Primary electron-hole pair separation occurs in the subnanosecond or picosecond time domain and light pulses with temporal resolution of 10 s (or better) are required. However, both nanosecond and picosecond light pulses have been employed [110 127] and although the analysis has been mostly confined to the slower (nanosecond) decay regime in the photocurrent (or photovoltage) transients, the rise-time domain has also been analyzed (see, e.g.. Ref. [256]). [Pg.2691]


See other pages where Light excitation regime is mentioned: [Pg.104]    [Pg.384]    [Pg.477]    [Pg.330]    [Pg.147]    [Pg.116]    [Pg.19]    [Pg.3872]    [Pg.1263]    [Pg.2420]    [Pg.2456]    [Pg.410]    [Pg.513]    [Pg.388]    [Pg.214]    [Pg.82]    [Pg.80]    [Pg.492]    [Pg.239]    [Pg.586]    [Pg.19]    [Pg.172]    [Pg.302]    [Pg.880]    [Pg.254]    [Pg.171]    [Pg.87]    [Pg.31]    [Pg.410]    [Pg.513]    [Pg.481]    [Pg.111]    [Pg.531]    [Pg.203]    [Pg.675]    [Pg.99]    [Pg.26]    [Pg.492]    [Pg.108]    [Pg.648]    [Pg.675]    [Pg.3]    [Pg.360]    [Pg.288]    [Pg.5]    [Pg.18]   
See also in sourсe #XX -- [ Pg.695 ]




SEARCH



Excitation light

© 2024 chempedia.info