Download Applied Photochemistry: When Light Meets Molecules by Giacomo Bergamini, Serena Silvi PDF

By Giacomo Bergamini, Serena Silvi

This monograph good points what occurs while gentle meets molecules. This edited quantity includes contributions from a global array of participants, and it truly is divided into sections representing a range of rigorously focussed and attached photochemistry issues: strength, know-how, drugs, environmental sciences, and artwork. In each one part a number of chapters illustrates appropriate features of every box, corresponding to synthetic photosynthesis and solar power conversion (energy), mild emitting units and photochromic dyes (technology), and photodynamic remedy and sun filters (medicine). geared toward scholars of all degrees and researchers energetic in photochemistry.

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The array self assembles in solution by side-to-face axial coordination of the pyridyl groups of the free-base “pillars” to the four zinc porphyrin units of the metallacycles [67]. In A9, the energy absorbed by the zinc porphyrin units is transferred to the free-base ones in 36 ps with an efficiency of ca 50 % (because of intercomponent competing electron transfer processes) [68]. Related structures can also be assembled following the same strategy, using perylene bisimide pillars instead of porphyrin-based ones [69].

47a): (i) the reduction potential of the excited sensitizer (*P1) must be more negative than the CB edge potential of the ntype SC and (ii) the redox potential of the P1+/P1 redox couple should be more positive than the oxidation potentials of the WOC. The approach adopted herein is similar to the one used in n-type dye-sensitized solar cells (n-DSSCs), [141, 142] in which a redox mediator, instead of the WOC, is used to regenerate the oxidized dye and the electrons in the CB are employed at a suitable cathode for the reduction of the oxidized component of the redox mediator thus completing a whole circuit.

Importantly, the water oxidation mechanism not only involves electron removal steps (each one accompanied by a proton loss) but requires a fundamental chemical step, namely the formation of the oxygen-oxygen bond. , a metal-aquo starting complex, the 34 Fig. 29 Mechanisms for oxygen-oxygen bond formation: (a) water nucleophilic attack, (b) coupling between two M-O radicals M. Natali and F. Scandola a b H M O + O 2M H O H M O O M + O2 H M O O 2M + M O2 O-O bond formation process may occur by two different mechanisms (Fig.

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