Quantum Mechanical Foundations of Molecular Spectroscopy. Max Diem. Читать онлайн. Newlib. NEWLIB.NET

Автор: Max Diem
Издательство: John Wiley & Sons Limited
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Жанр произведения: Химия
Год издания: 0
isbn: 9783527829606
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comma normal nu right-parenthesis equals StartFraction 8 pi italic k upper T normal nu squared Over c cubed EndFraction"/>

      where the Boltzmann constant k = 1.381 × 10−23 [J/K]. This result indicated that the total energy radiated by a blackbody according to this “classical” model would increase with ν2 as shown by the dashed curve in Figure 1.2b. If this equation were correct, any temperature of a material above absolute zero would be impossible, since any material above 0 K would emit radiation according to Eq. (1.5), and the total energy emitted would be unrestricted and approach infinity. Particularly, toward higher frequency, more and more radiation would be emitted, and the blackbody would cool instantaneously to 0 K. Thus, any temperature above 0 K would be impossible. (For a more detailed discussion on this “ultraviolet catastrophe,” see Engel and Reid [2].)

      This is, of course, in contradiction with experimental results and was addressed by M. Planck (1901) who solved this conundrum by introducing the term 1/(ehν/kT − 1) into the blackbody equation, where h is Planck's constant:

      This, in itself, was a revolutionary thought since the wave properties of light had been established more than two centuries earlier and had been described in the late 1800s by Maxwell's equations in terms of electric and magnetic field contributions. Here arose for the first time the realization that two different descriptions of light, in terms of waves and particles, were appropriate depending on what questions were asked. A similar “particle–wave duality” was later postulated and confirmed for matter as well (see below). Thus, the work by Planck very early in the twentieth century is truly the birth of the ideas resulting in the formulation of quantum mechanics.

      Incidentally, the form of the expression

or
is fairly common‐place in classical physical chemistry. It compares the energy of an event, for example, a molecule leaving the liquid for the gaseous phase, with the energy content of the surroundings. For example, the vapor pressure of a pure liquid depends on a term
, where ΔHvap is the enthalpy of vaporization of the liquid, and RT = NkT is the energy at temperature T, R is the gas constant, and N is Avogadro's number. Similarly, the dependence of the reaction rate constant and the equilibrium constant on temperature is given by equivalent expressions that contain the activation energy or the reaction enthalpy, respectively, in the numerator of the exponent. In Eq. (1.6), the photon energy is divided by the energy content of the material emitting the photon and provides a likelihood of this event occurring.

      Figure 1.2 shows that the overall emitted energy increases with increasing temperature and that the peak wavelength of maximum intensity shifts toward lower wavelength (Wien's law). The total energy W radiated by a blackbody per unit area and unit time into a solid angle (the irradiance), integrated over all wavelengths, is proportional to the absolute temperature to the fourth power:

      (1.8)integral Subscript 0 Superscript infinity Baseline upper W normal d lamda equals sigma upper T Superscript 4

      (Stefan–Boltzmann law)

      The irradiance is expressed in units of left-bracket StartFraction upper W Over m squared s italic s r EndFraction right-bracket or left-bracket StartFraction photons Over m squared s italic s r EndFraction right-bracket.

      The implication of the aforementioned wave–particle duality will be discussed in the next section.