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      Structural models of the biological oxygen-evolving complex: achievements, insights, and challenges for biomimicry

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          Abstract

          Recent developments on structural mimics for the oxygen-evolving complex of photosystem II are reviewed and discussed.

          Abstract

          The oxygen-evolving complex (OEC) in Photosystem II (PS-II) of oxygenic photosynthesis catalyzes the oxidation of water into dioxygen, protons and electrons, a reaction that underpins solar to chemical energy conversion in the biosphere. The inorganic core of the OEC is an oxo-bridged cluster that comprises four Mn and one Ca ions, Mn 4CaO 5. Deciphering the structure of this cluster and its immediate environment has been the aim of intense experimental efforts that span decades of research. The constantly improving structural definition of the OEC in the last fifteen years has offered opportunities to better understand its properties and function; it has also provided ever clearer and more well-defined targets for biomimetic synthetic chemistry. Here we present a critical overview of the most recent advances in molecular structural models of the OEC, focusing mostly on successful research efforts reported after the availability of atomically resolved crystallographic models of PS-II. We delineate the properties that have been targeted in biomimetic studies and analyze which structural aspects have by now been reproduced in synthetic systems. In combination with in-depth theoretical studies, the availability of novel synthetic structural analogues has led to considerable insight into structure–property correlations despite the lack of catalytic activity. Nevertheless, there are important features of the OEC that remain inaccessible to synthetic chemistry. Principal among them are the unique type of restricted structural flexibility and the highly structured and stable ligand sphere which enable the tightly controlled interplay of geometry, spin state and reactivity that is the hallmark of the OEC.

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          New Approach to the Theory of Superexchange Interactions

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              The artificial leaf.

              To convert the energy of sunlight into chemical energy, the leaf splits water via the photosynthetic process to produce molecular oxygen and hydrogen, which is in a form of separated protons and electrons. The primary steps of natural photosynthesis involve the absorption of sunlight and its conversion into spatially separated electron-hole pairs. The holes of this wireless current are captured by the oxygen evolving complex (OEC) of photosystem II (PSII) to oxidize water to oxygen. The electrons and protons produced as a byproduct of the OEC reaction are captured by ferrodoxin of photosystem I. With the aid of ferrodoxin-NADP(+) reductase, they are used to produce hydrogen in the form of NADPH. For a synthetic material to realize the solar energy conversion function of the leaf, the light-absorbing material must capture a solar photon to generate a wireless current that is harnessed by catalysts, which drive the four electron/hole fuel-forming water-splitting reaction under benign conditions and under 1 sun (100 mW/cm(2)) illumination. This Account describes the construction of an artificial leaf comprising earth-abundant elements by interfacing a triple junction, amorphous silicon photovoltaic with hydrogen- and oxygen-evolving catalysts made from a ternary alloy (NiMoZn) and a cobalt-phosphate cluster (Co-OEC), respectively. The latter captures the structural and functional attributes of the PSII-OEC. Similar to the PSII-OEC, the Co-OEC self-assembles upon oxidation of an earth-abundant metal ion from 2+ to 3+, may operate in natural water at room temperature, and is self-healing. The Co-OEC also activates H(2)O by a proton-coupled electron transfer mechanism in which the Co-OEC is increased by four hole equivalents akin to the S-state pumping of the Kok cycle of PSII. X-ray absorption spectroscopy studies have established that the Co-OEC is a structural relative of Mn(3)CaO(4)-Mn cubane of the PSII-OEC, where Co replaces Mn and the cubane is extended in a corner-sharing, head-to-tail dimer. The ability to perform the oxygen-evolving reaction in water at neutral or near-neutral conditions has several consequences for the construction of the artificial leaf. The NiMoZn alloy may be used in place of Pt to generate hydrogen. To stabilize silicon in water, its surface is coated with a conducting metal oxide onto which the Co-OEC may be deposited. The net result is that immersing a triple-junction Si wafer coated with NiMoZn and Co-OEC in water and holding it up to sunlight can effect direct solar energy conversion via water splitting. By constructing a simple, stand-alone device composed of earth-abundant materials, the artificial leaf provides a means for an inexpensive and highly distributed solar-to-fuels system that employs low-cost systems engineering and manufacturing. Through this type of system, solar energy can become a viable energy supply to those in the non-legacy world.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                GRCHFJ
                Green Chemistry
                Green Chem.
                Royal Society of Chemistry (RSC)
                1463-9262
                1463-9270
                2017
                2017
                : 19
                : 10
                : 2309-2325
                Affiliations
                [1 ]Max Planck Institute for Chemical Energy Conversion
                [2 ]45470 Mülheim an der Ruhr
                [3 ]Germany
                Article
                10.1039/C7GC00425G
                efc3c7d7-bcce-4908-8881-43a268c604ad
                © 2017

                http://creativecommons.org/licenses/by/3.0/

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