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Quantization levels

The three-dimensional particle in a box corresponds to the real life problem of gas molecules in a container, and is also sometimes used as a first approximation for the free conduction electrons in a metal. As we found for one dimension (Section 2.3), the allowed energy levels are extremely closely spaced in macroscopically sized boxes. For many purposes they can be regarded as a continuum, with no discernible energy gaps. Nevertheless, there are problems, for example in the theory of metals and in the calculation of thermodynamic properties of gases, where it is essential to take note of the existence of discrete quantized levels, rather than a true continuum. [Pg.50]

G. Barbieri, S. Depaquit, and J. P. Vigier, Spectroscopy of baryons and resonances considered as quantized levels of a relativistic rotator, Nuovo Cimento, Ser. X 30 (1963). [Pg.194]

Table number Quantization levels Table size Number of bits per pair of zeroes... [Pg.49]

The bit allocation is derived from the SMR-values which have been calculated in the psychoacoustic model. This is done in an iterative fashion. The objective is to minimize the noise-to-mask ratio over every subband and the whole frame. In each iteration step the number of quantization levels is increased for the subband with the worst (maximum) noise-to-mask ratio. This is repeated until all available bits have been spent. [Pg.54]

Coloured sodium chloride crystals are due to the formation of non-stoichiometric vacancies in the anion lattice. This vacancy is capable of trapping an electron, which can then move between a number of quantized levels. These transitions occur in the visible region and generate the yellow colour. This type of vacancy in the anion sublattice of an alkali metal halide is called a Farbenzcentre or F centre. F centres can be generated by irradiation to ionize the anion, or by exposure of the lattice to excess alkali-metal cation vapour. Both procedures result in more alkali-metal cations than halide anions in the lattice. [Pg.141]

Photo-induced electron transfer reactions from quantum well electrodes into a redox system in solution represent an intriguing research area of photoelectrochemistry. Several aspects of quantized semiconductor electrodes are of interest, including the question of hot carrier transfer from quantum well electrodes into solution. The most interesting question here is whether an electron transfer from higher quantized levels to the oxidized species of the redox system can occur, as illustrated in Fig. 9.31. In order to accomplish such a hot electron transfer, the rate of electron transfer must be competitive with the rate of electron relaxation. It has been shown that quantization can slow down the carrier cooling dynamics and make hot carrier transfer competitive with carrier cooling. [Pg.294]

As a starting point for the experiments discussed in this paper, we want to prepare the %e" ion in a particular internal state and in the lowest quantized level of vibrational motion in the trap - the zero-point state. The ion can be optically pumped into a particular internal state using polarized light. Preparation in the zero-point state of motion is achieved with laser cooling. [Pg.46]

The quantization of transition state energy levels is not simply a mathematical device to add quantum effects to the partition functions. The quantized levels actually show up as structure in the exact quantum mechanical rate constants as functions of total energy [51]. The interpretation of this structure provides clear evidence for quantized dynamical bottlenecks, both near to and distant from the saddle points, as reviewed elsewhere [52]. Quantized variational transition states have also been observed in molecular beam scattering experiments [53]. Analysis of the reactive flux in state-to-state terms from reactant states to transition state levels to product states provides the ultimate limit of resolution allowed by quantum mechanics [53,54]. Quantized energy levels of the variational transition state have been used to rederive TST using the language of quantum mechanical resonance scattering theory [55]. [Pg.77]


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