|
Photochemical carbon dioxide reduction harnesses solar energy to convert CO2 into higher-energy products. The chemical conversion of CO2 already occurs on an industrial scale in the manufacture of solvents such as formic acid, but photochemical reduction differs in that it relies on a renewable energy source, the sun. Because CO2 is a greenhouse gas, there is environmental interest in producing artificial systems that are efficient photocatalysts, but the low turn-over rates of current methods have prohibited wide-scale industrial application. ==Overview== Photochemical reduction follows from chemical reduction (redox). But, it differs in that the electrons used for reduction are generated from the photoexcitation of another molecule, called a photosensitizer. To harness the sun's energy, the photosensitizer must be able to absorb light within the visible and ultraviolet spectrum. 〔Crabtree, R.-H.; “The Organometallic Chemistry of the Transition Metals, 4th ed.” John Wiley & Sons: New York, 2005. ISBN 978-0-471-66256-3〕 Molecular sensitizers that meet this criterion often include a metal center, as the d-orbital splitting in organometallic species often falls within the energy range of far-UV and visible light. The reduction process begins with excitation of the photosensitizer, as mentioned. This causes the movement of an electron from the metal center into the functional ligands. This movement is termed a metal-to-ligand charge transfer (MLCT). Back-electron transfer from the ligands to the metal after the charge transfer, which yields no net result, is prevented by including an electron-donating species in solution. Successful photosensitizers have a long-lived excited state, usually due to the interconversion from singlet to triplet states, that allow time for electron donors to interact with the metal center. Common donors in photochemical reduction include triethylamine (TEA), triethanolamine (TEOA), and 1-benzyl-1,4-dihydronicotinamide (BNAH). After excitation, CO2 coordinates or otherwise interacts with the inner coordination sphere of the reduced metal. The mechanistic details for this reduction process have not been fully determined, but commonly observed products include formate, formic acid, carbon monoxide, and methanol. Note that light absorption and catalytic reduction may occur at the same metal center or on different metal centers. That is, a photosensitizer and catalyst may be tethered through an organic linkage that provides for electronic communication between the species. In this case, the two metal centers form a bimetallic supramolecular complex. And, the excited electron that had resided on the functional ligands of photosensitizer passes through the ancillary ligands to the catalytic center, which becomes a one-electron reduced (OER) species. The advantage of dividing the two processes among different centers is in the ability to tune each center for a particular task, whether through selecting different metals or ligands. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Photochemical carbon dioxide reduction」の詳細全文を読む スポンサード リンク
|