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O2 Evolution (o2 + evolution)
Selected AbstractsEffects of Structural Variation on the Photocatalytic Performance of Hydrothermally Synthesized BiVO4,ADVANCED FUNCTIONAL MATERIALS, Issue 16 2006J. Yu Abstract Highly crystalline monoclinic scheelite BiVO4 powders are synthesized from aqueous Bi(NO3)3 and NH4VO3 solutions over a wide range of pH by a hydrothermal process. BiVO4 powders with various morphologies, surface textures, and grain shapes are selectively synthesized by adjusting the pH. The dependence of the Raman peak position and intensity on the synthesis conditions indicates that the symmetry distortions in the local structure of the synthesized BiVO4 are affected by the preparation conditions. These variations in the local structure result in the modification of the electronic structure of BiVO4, which results in a blue-shift in the UV-vis absorption spectrum of hydrothermally synthesized BiVO4 in comparison with a well-crystallized sample prepared by homogeneous coprecipitation. The photocatalytic activities for O2 evolution from an aqueous AgNO3 solution under visible-light irradiation are strongly dependent on the pH used in the synthesis. The differences in the photocatalytic activities between BiVO4 samples prepared under various conditions is attributed to the degree of structural distortion, leading to differences in the mobility of photogenerated holes formed in the valence band, which consists of Bi,6s and O,2p orbitals. [source] Auxotrophic mutant of the cyanobacterium Nostoc muscorum showing absolute requirement of Cs+ or Rb+ for diazotrophy and autotrophyJOURNAL OF BASIC MICROBIOLOGY, Issue 4 2006Santosh Bhargava Dr. Caesium-resistant (Cs+ -R) mutant clones of the cyanobacterium Nostoc muscorum were characterized for diazotrophic growth in a medium devoid of Cs+ or Rb+ or both. Cs+ -R phenotype suffered severe genetic damage of a pleiotropic nature affecting diazotrophic growth, chlorophyll a content, nitrogenase activity and photosynthetic O2 evolution. Mutation leading to development of Cs+ -R phenotype could be overcome by availability of Cs+/Rb+. Parent and mutant strains were similar with respect to their Cs+/Rb+ uptake. Available data suggests operation of an efficient coupling of the two incompatible reactions viz. oxygenic photosynthesis and oxygen sensitive N2 fixation in this cyanobacterium. (© 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Importance of AOX pathway in optimizing photosynthesis under high light stress: role of pyruvate and malate in activating AOXPHYSIOLOGIA PLANTARUM, Issue 1 2010Challabathula Dinakar The present study shows the importance of alternative oxidase (AOX) pathway in optimizing photosynthesis under high light (HL). The responses of photosynthesis and respiration were monitored as O2 evolution and O2 uptake in mesophyll protoplasts of pea pre-incubated under different light intensities. Under HL (3000 µmol m,2 s,1), mesophyll protoplasts showed remarkable decrease in the rates of NaHCO3 -dependent O2 evolution (indicator of photosynthetic carbon assimilation), while decrease in the rates of respiratory O2 uptake were marginal. While the capacity of AOX pathway increased significantly by two fold under HL, the capacity of cytochrome oxidase (COX) pathway decreased by >50% compared with capacities under darkness and normal light (NL). Further, the total cellular levels of pyruvate and malate, which are assimilatory products of active photosynthesis and stimulators of AOX activity, were increased remarkably parallel to the increase in AOX protein under HL. Upon restriction of AOX pathway using salicylhydroxamic acid (SHAM), the observed decrease in NaHCO3 -dependent O2 evolution or p -benzoquinone (BQ)-dependent O2 evolution [indicator of photosystem II (PSII) activity] and the increase in total cellular levels of pyruvate and malate were further aggravated/promoted under HL. The significance of raised malate and pyruvate levels in activation of AOX protein/AOX pathway, which in turn play an important role in dissipating excess chloroplastic reducing equivalents and sustenance of photosynthetic carbon assimilation to balance the effects of HL stress on photosynthesis, was depicted as a model. [source] The Mechanism of Water Oxidation: From Electrolysis via Homogeneous to Biological CatalysisCHEMCATCHEM, Issue 7 2010Holger Dau Prof. Abstract Striving for new solar fuels, the water oxidation reaction currently is considered to be a bottleneck, hampering progress in the development of applicable technologies for the conversion of light into storable fuels. This review compares and unifies viewpoints on water oxidation from various fields of catalysis research. The first part deals with the thermodynamic efficiency and mechanisms of electrochemical water splitting by metal oxides on electrode surfaces, explaining the recent concept of the potential-determining step. Subsequently, novel cobalt oxide-based catalysts for heterogeneous (electro)catalysis are discussed. These may share structural and functional properties with surface oxides, multinuclear molecular catalysts and the catalytic manganese,calcium complex of photosynthetic water oxidation. Recent developments in homogeneous water-oxidation catalysis are outlined with a focus on the discovery of mononuclear ruthenium (and non-ruthenium) complexes that efficiently mediate O2 evolution from water. Water oxidation in photosynthesis is the subject of a concise presentation of structure and function of the natural paragon,the manganese,calcium complex in photosystem,II,for which ideas concerning redox-potential leveling, proton removal, and OO bond formation mechanisms are discussed. The last part highlights common themes and unifying concepts. [source] | ||||||||||