Uncertainty principle, electron-transfer

If we increase the accuracy with which the position of the electron is determined by decreasing the wavelength of the light that is used to observe the electron, then the photon has a greater momentum, since p = hiA. The photon can then transfer a larger amount of momentum to the electron, and so the uncertainty in the momentum of the electron increases. Thus any reduction in the uncertainty in the position of the electron is accompanied by an increase in the uncertainty in the momentum of the electron, in accordance with the uncertainty principle relationship. We may summarize by saying that there is no way of accurately measuring simultaneously both the position and velocity of an electron the more closely we attempt to measure its position, the more we disturb its motion and the less accurately therefore we are able to define its velocity. 

The events taking place in the RCs within the timescale of ps and sub-ps ranges usually involve vibrational relaxation, internal conversion, and photo-induced electron and energy transfers. It is important to note that in order to observe such ultrafast processes, ultrashort pulse laser spectroscopic techniques are often employed. In such cases, from the uncertainty principle AEAt Ti/2, one can see that a number of states can be coherently (or simultaneously) excited. In this case, the observed time-resolved spectra contain the information of the dynamics of both populations and coherences (or phases) of the system. Due to the dynamical contribution of coherences, the quantum beat is often observed in the fs time-resolved experiments. 

Figure 5.4, one can easily understand why the interfacial electron transfer should take place in the 10-100 fsec range because this ET process should be faster than the photo-luminescence of the dye molecules and energy transfer between the molecules. Recently Zimmermann et al. [58] have employed the 20 fsec laser pulses to study the ET dynamics in the DTB-Pe/TiC>2 system and for comparison, they have also studied the excited-state dynamics of free perylene in toluene solution. Limited by the 20 fsec pulse-duration, from the uncertainty principle, they can only observe the vibrational coherences (i.e., vibrational wave packets) of low-frequency modes (see Figure 5.5). Six significant modes, 275, 360, 420, 460, 500 and 625 cm-1, have been resolved from the Fourier transform spectra of ultrashort pulse measurements. The Fourier transform spectrum has also been compared with the Raman spectrum. A good agreement can be seen (Figure 5.5). For detail of the analysis of the quantum beat, refer to Figures 5.5-5.7 of Zimmermann et al. s paper [58], These modes should play an important role not only in ET dynamics or excited-state dynamics, but also in absorption spectra. Therefore, the steady state absorption spectra of DTB-Pe, both in...

For the electron, the uncertainty in position is far larger than the diameter of the atom, which is about 100 pm. Therefore, the concept of a trajectory—the simultaneous possession of a precise position and momentum—is untenable. However, the degree of uncertainty is completely negligible for all practical purposes in the case of the bacterium. Indeed, the position of the cell can be known to within 0.05 per cent of the diameter of a hydrogen atom. It follows that the uncertainty principle plays no direct role in cell biology. However, it plays a major role in the description of the motion of electrons around nuclei in atoms and molecules and, is we shall see soon, the transfer of electrons between molecules and proteins during metabolism. 

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