Big Chemical Encyclopedia

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

Articles Figures Tables About

Photon introduced

In this chapter, the foundations of equilibrium statistical mechanics are introduced and applied to ideal and weakly interacting systems. The coimection between statistical mechanics and thennodynamics is made by introducing ensemble methods. The role of mechanics, both quantum and classical, is described. In particular, the concept and use of the density of states is utilized. Applications are made to ideal quantum and classical gases, ideal gas of diatomic molecules, photons and the black body radiation, phonons in a hannonic solid, conduction electrons in metals and the Bose—Einstein condensation. Introductory aspects of the density... [Pg.435]

The second way to achieve quadrahire is to introduce another field, E, (called a local oscillator) designed in frequency and wavevector to conjugate (go into quadrahire) in its complex representation with the new field of interest. Thus in the heterodyne case, the signal photons are derived fromcr. jy i. or Sj (lieterodyne) x x X... [Pg.1182]

In this chapter we review some of the most important developments in recent years in connection with the use of optical teclmiques for the characterization of surfaces. We start with an overview of the different approaches available to tire use of IR spectroscopy. Next, we briefly introduce some new optical characterization methods that rely on the use of lasers, including nonlinear spectroscopies. The following section addresses the use of x-rays for diffraction studies aimed at structural detenninations. Lastly, passing reference is made to other optical teclmiques such as ellipsometry and NMR, and to spectroscopies that only partly depend on photons. [Pg.1780]

When the states P1 and P2 are described as linear combinations of CSFs as introduced earlier ( Fi = Zk CiKK), these matrix elements can be expressed in terms of CSF-based matrix elements < K I eri IOl >. The fact that the electric dipole operator is a one-electron operator, in combination with the SC rules, guarantees that only states for which the dominant determinants differ by at most a single spin-orbital (i.e., those which are "singly excited") can be connected via electric dipole transitions through first order (i.e., in a one-photon transition to which the < Fi Ii eri F2 > matrix elements pertain). It is for this reason that light with energy adequate to ionize or excite deep core electrons in atoms or molecules usually causes such ionization or excitation rather than double ionization or excitation of valence-level electrons the latter are two-electron events. [Pg.288]

The first-order El "golden-rule" expression for the rates of photon-induced transitions can be recast into a form in which certain specific physical models are easily introduced and insights are easily gained. Moreover, by using so-called equilibrium averaged time correlation functions, it is possible to obtain rate expressions appropriate to a... [Pg.416]

If a sample solution is introduced into the center of the plasma, the constituent molecules are bombarded by the energetic atoms, ions, electrons, and even photons from the plasma itself. Under these vigorous conditions, sample molecules are both ionized and fragmented repeatedly until only their constituent elemental atoms or ions survive. The ions are drawn off into a mass analyzer for measurement of abundances and mJz values. Plasma torches provide a powerful method for introducing and ionizing a wide range of sample types into a mass spectrometer (inductively coupled plasma mass spectrometry, ICP/MS). [Pg.87]

The third common level is often invoked in simplified interpretations of the quantum mechanical theory. In this simplified interpretation, the Raman spectrum is seen as a photon absorption-photon emission process. A molecule in a lower level k absorbs a photon of incident radiation and undergoes a transition to the third common level r. The molecules in r return instantaneously to a lower level n emitting light of frequency differing from the laser frequency by —>< . This is the frequency for the Stokes process. The frequency for the anti-Stokes process would be + < . As the population of an upper level n is less than level k the intensity of the Stokes lines would be expected to be greater than the intensity of the anti-Stokes lines. This approach is inconsistent with the quantum mechanical treatment in which the third common level is introduced as a mathematical expedient and is not involved directly in the scattering process (9). [Pg.297]

Figure 7.3 shows the two-beam photon-force measurement system using a coaxial illumination photon force measurement system. Two microparticles dispersed in a liquid are optically trapped by two focused near-infrared beams ( 1 pm spot size) of a CW Nd YAG laser under an optical microscope (1064 nm, 1.2 MWcm , lOOX oil-immersion objective, NA = 1.4). The particles are positioned sufficiently far from the surface of a glass slide in order to neglect the interaction between the particles and the substrate. Green and red beams from a green LD laser (532 nm, 21 kWcm ) and a He-Ne laser (632.8 nm, 21 kW cm ) are introduced coaxially into the microscope and slightly focused onto each microparticle as an illumination light (the irradiated area was about 3 pm in diameter). The sizes of the illumination areas for the green and red beams are almost the same as the diameter of the microparticles (see Figure 7.4). The back scattered light from the surface of each microparticle is... Figure 7.3 shows the two-beam photon-force measurement system using a coaxial illumination photon force measurement system. Two microparticles dispersed in a liquid are optically trapped by two focused near-infrared beams ( 1 pm spot size) of a CW Nd YAG laser under an optical microscope (1064 nm, 1.2 MWcm , lOOX oil-immersion objective, NA = 1.4). The particles are positioned sufficiently far from the surface of a glass slide in order to neglect the interaction between the particles and the substrate. Green and red beams from a green LD laser (532 nm, 21 kWcm ) and a He-Ne laser (632.8 nm, 21 kW cm ) are introduced coaxially into the microscope and slightly focused onto each microparticle as an illumination light (the irradiated area was about 3 pm in diameter). The sizes of the illumination areas for the green and red beams are almost the same as the diameter of the microparticles (see Figure 7.4). The back scattered light from the surface of each microparticle is...
We introduced the technique for measuring the weak interaction forces acting between two particles using the photon force measurement method. Compared with the previous typically used methods, such as cross-correlation analysis, this technique makes it possible to evaluate the interaction forces without a priori information, such as media viscosity, particle mass and size. In this chapter, we focused especially on the hydrodynamic force as the interaction between particles and measured the interaction force by the potential analysis method when changing the distance between particles. As a result, when the particles were dose to each other, the two-dimensional plots of the kinetic potentials for each particle were distorted in the diagonal direction due to the increase in the interaction force. From the results, we evaluated the interaction coeffidents and confirmed that the dependence of the... [Pg.129]

Where is the Hamiltonian for the interaction of the nucleus with the photon, /> is the initial (excited) state of the nucleus, g the final (ground) state and T the inverse of the natural lifetime of state /). We introduce an integral form of the denominator of Eq. (92) by ... [Pg.109]

The constant h and the hypothesis that energy is quantized in integral multiples of hv had previously been introduced by M. Planck (1900) in his study of blackbody radiation. In terms of the angular frequency a> deflned in equation (1.2), the energy E of a photon is... [Pg.18]

Albert Einstein s 1905 work on the photoelectric effect paved the way for one of the greatest advances of twentieth-century science, the theory of quantum mechanics. Light had always been regarded as a wave. Quantum mechanics introduced the concept of light being transmitted in wave packets, or photons, that have particle-like qualities as well as wave-like qualities. [Pg.33]

This chapter deals mainly with (multi)hyphenated techniques comprising wet sample preparation steps (e.g. SFE, SPE) and/or separation techniques (GC, SFC, HPLC, SEC, TLC, CE). Other hyphenated techniques involve thermal-spectroscopic and gas or heat extraction methods (TG, TD, HS, Py, LD, etc.). Also, spectroscopic couplings (e.g. LIBS-LIF) are of interest. Hyphenation of UV spectroscopy and mass spectrometry forms the family of laser mass-spectrometric (LAMS) methods, such as REMPI-ToFMS and MALDI-ToFMS. In REMPI-ToFMS the connecting element between UV spectroscopy and mass spectrometry is laser-induced REMPI ionisation. An intermediate state of the molecule of interest is selectively excited by absorption of a laser photon (the wavelength of a tuneable laser is set in resonance with the transition). The excited molecules are subsequently ionised by absorption of an additional laser photon. Therefore the ionisation selectivity is introduced by the resonance absorption of the first photon, i.e. by UV spectroscopy. However, conventional UV spectra of polyatomic molecules exhibit relatively broad and continuous spectral features, allowing only a medium selectivity. Supersonic jet cooling of the sample molecules (to 5-50 K) reduces the line width of their... [Pg.428]

Figure 1. Schematic illustration of two-pathway control in the (a) frequency and (b) time domains. In case (a) the ground state is excited to a coupled continuum by either one photon of frequency CO3 or three photons of frequency C >i. Control is achieved by introducing a phase lag between the two fields. In case (b) a two-pulse sequence has sufficient bandwidth to excite a superposition of two intermediate states. Control is achieved by introducing a delay, At, between the pulses, resulting in a phase difference of to At. Figure 1. Schematic illustration of two-pathway control in the (a) frequency and (b) time domains. In case (a) the ground state is excited to a coupled continuum by either one photon of frequency CO3 or three photons of frequency C >i. Control is achieved by introducing a phase lag between the two fields. In case (b) a two-pulse sequence has sufficient bandwidth to excite a superposition of two intermediate states. Control is achieved by introducing a delay, At, between the pulses, resulting in a phase difference of to At.
In this section we first (Section IV A) derive a formal expression for the channel phase, applicable to a general, isolated molecule experiment. Of particular interest are bound-free experiments where the continuum can be accessed via both a direct and a resonance-mediated process, since these scenarios give rise to rich structure of 8 ( ), and since they have been the topic of most experiments on the phase problem. In Section IVB we focus specifically on the case considered in Section III, where the two excitation pathways are one- and three-photon fields of equal total photon energy. We note the form of 8 (E) = 813(E) in this case and reformulate it in terms of physical parameters. Section IVC considers several limiting cases of 813 that allow useful insight into the physical processes that determine its energy dependence. In the concluding subsection of Section V we note briefly the modifications of the theory that are introduced in the presence of a dissipative environment. [Pg.160]

It is interesting to note (see Eqs. (59)—(61)) that pure decoherence introduces dependence of the channel phase on the final state energies. This dependence can be utilized to obtain new insights into the resonance properties, as illustrated in Fig. 16. Here we explore the photon energy dependence of 8/ for final state... [Pg.181]


See other pages where Photon introduced is mentioned: [Pg.129]    [Pg.131]    [Pg.131]    [Pg.129]    [Pg.131]    [Pg.131]    [Pg.209]    [Pg.524]    [Pg.2859]    [Pg.259]    [Pg.295]    [Pg.295]    [Pg.57]    [Pg.129]    [Pg.153]    [Pg.298]    [Pg.10]    [Pg.86]    [Pg.199]    [Pg.123]    [Pg.266]    [Pg.550]    [Pg.562]    [Pg.277]    [Pg.9]    [Pg.371]    [Pg.482]    [Pg.150]    [Pg.289]    [Pg.120]    [Pg.130]    [Pg.360]    [Pg.386]    [Pg.509]    [Pg.163]    [Pg.183]    [Pg.184]    [Pg.333]   
See also in sourсe #XX -- [ Pg.6 ]




SEARCH



Introduced

© 2024 chempedia.info