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Photoexcitation control process

The photoexcited CVD process, being free of ion bombardment damage, allows selective excitation of reactant gas in a surface process only. Then the film growth process would treat as heterogeneous gas-phase reactions on the solid surface, which consist of series processes, i.e., surface chemical reaction of adsorption species and transportation of gas phase. We would control each process independently to grow stoichiometric BP films. [Pg.585]

Once the mechanisms of dynamic processes are understood, it becomes possible to think about controlling them so that we can make desirable processes to occur more efficiently. Especially when we use a laser field, nonadiabatic transitions are induced among the so-called dressed states and we can control the transitions among them by appropriately designing the laser parameters [33 1]. The dressed states mean molecular potential energy curves shifted up or down by the amount of photon energy. Even the ordinary type of photoexcitation can be... [Pg.97]

As mentioned earlier, a great deal of literature has dealt with the properties of heterogeneous liquid systems such as microemulsions, micelles, vesicles, and lipid bilayers in photosynthetic processes [114,115,119]. At externally polarizable ITIES, the control on the Galvani potential difference offers an extra variable, which allows tuning reaction paths and rates. For instance, the rather high interfacial reactivity of photoexcited porphyrin species has proved to be able to promote processes such as the one shown in Fig. 3(b). The inhibition of back ET upon addition of hexacyanoferrate in the photoreaction of Fig. 17 is an example of a photosynthetic reaction at polarizable ITIES [87,166]. At Galvani potential differences close to 0 V, a direct redox reaction involving an equimolar ratio of the hexacyanoferrate couple and TCNQ features an uphill ET of approximately 0.10 eV (see Fig. 4). However, the excited state of the porphyrin heterodimer can readily inject an electron into TCNQ and subsequently receive an electron from ferrocyanide. For illumination at 543 nm (2.3 eV), the overall photoprocess corresponds to a 4% conversion efficiency. [Pg.227]

It has been shown that the influence of photoexcited fullerene C60 on the processes of free-radical oxidation depends on the type of the cell and on the composition of composite. So, in thymocytes in the presence of photoexcited fullerene C60 as well as fullerene C60-containing composites, the content of primary and final LPO products did not alter compared to the control. In malignant cells the intensification of LPO processes was registered, and its level depends on the type of cells. So, in thymocytes in the presence of photoexcited fullerene C60 in suspension of EAC cells the decrease in the content of diene conjugates simultaneously with the increase in the... [Pg.130]

Regardless of the nature of the surface state it is clear that it can capture an electron from the conduction band producing cathodic current. This cathodic current balances the anodic current produced when the photoexcited holes produced the oxidized surface state. The net result of these two processes is electron-hole recombination leading to no net current. This recombination process is what controls the voltage of photocurrent onset as can be seen in curve 2 of Figure 5. [Pg.112]

Matrix isolation experimental techniques [1-10] stand out among many other modern chemical research methods with regard to their ability to provide direct comparisons with quantum mechanical calculations. The use of photoexcitation methods to induce reactions [7-9] as well as the applications of multiple spectroscopic techniques to study such photochemical reactions allows for close control of the reaction parameters. Most of the high temperature and entropy effects, otherwise very large in thermochemical reactions, are therefore not present here and thus some of the limitations associated with applications of precise quantum mechanical calculations to kinetic processes disappear. [Pg.106]

Longitudinal diffusion term, Bin A term in chromatographic band-broadening models that accounts for longitudinal diffusion. Lower control limit, LCL The lower boundai7 that has been set for satisfactory performance of a process or measurement. Luminescence Radiation resulting from photoexcitation (photoluminescence), chemical excitation (chemiluminescence), or theiTnal excitation (thermoluminescence). [Pg.1112]

Such a process can produce 02( Ag) with 80% efficiency and similar reactions involving peroxide decomposition have been documented [21]. Of particular interest is the use of the decomposition of the endoperoxides of aromatic compounds, which, when appropriately substituted can be used in water [22] and of water soluble phosphite/ozone adducts [23]. Such chemical methods can provide a critical control for reactions in which photoexcitation of a sensitizer is suspected of doing more than just produce 02(1Ag). A prime example involves the rose bengal sensitized photooxidation of relatively unreactive alkenes [24],... [Pg.220]


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