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      Multimolecular assemblies on high surface area metal oxides and their role in interfacial energy and electron transfer

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          Abstract

          High surface area metal oxides offer a unique substrate for the assembly of multiple molecular components at an interface.

          Abstract

          High surface area metal oxides offer a unique substrate for the assembly of multiple molecular components at an interface. The choice of molecules, metal oxide, and the nature of the assembly method can have a profound influence on the mechanism, rate, and efficiency of photoinduced energy and electron transfer events at the interface. Owing to their diversity and high level of control, these interfacial assemblies are of interest for numerous applications including solar energy conversion, photoelectrosynthesis, photo-writable memory, and more. Although these assemblies are generated with very different goals in mind, they rely on similar surface binding motifs and molecular structure–property relationships. Therefore, the goal of this review is to summarize the various strategies ( i.e. co-deposition, axial coordination, metal ion linkages, electrostatics, host–guest interactions, etc.) for assembling chromophores, hosts, electron donors/acceptors, and insulating co-adsorbent molecules on mesoporous metal oxide substrates. The assembly, synthesis, and characterization, as well as subsequent photoinduced events ( i.e. cross-surface energy/electron transfer, interchromophore energy transfer, electron injection, and others) are discussed for the various assembly strategies.

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          Dye-sensitized solar cells.

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            Semiconductor Clusters, Nanocrystals, and Quantum Dots

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              Porphyrin-sensitized solar cells with cobalt (II/III)-based redox electrolyte exceed 12 percent efficiency.

              The iodide/triiodide redox shuttle has limited the efficiencies accessible in dye-sensitized solar cells. Here, we report mesoscopic solar cells that incorporate a Co((II/III))tris(bipyridyl)-based redox electrolyte in conjunction with a custom synthesized donor-π-bridge-acceptor zinc porphyrin dye as sensitizer (designated YD2-o-C8). The specific molecular design of YD2-o-C8 greatly retards the rate of interfacial back electron transfer from the conduction band of the nanocrystalline titanium dioxide film to the oxidized cobalt mediator, which enables attainment of strikingly high photovoltages approaching 1 volt. Because the YD2-o-C8 porphyrin harvests sunlight across the visible spectrum, large photocurrents are generated. Cosensitization of YD2-o-C8 with another organic dye further enhances the performance of the device, leading to a measured power conversion efficiency of 12.3% under simulated air mass 1.5 global sunlight.
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                Author and article information

                Journal
                CSRVBR
                Chemical Society Reviews
                Chem. Soc. Rev.
                Royal Society of Chemistry (RSC)
                0306-0012
                1460-4744
                2018
                2018
                : 47
                : 1
                : 104-148
                Affiliations
                [1 ]Department of Chemistry and Biochemistry
                [2 ]Florida State University
                [3 ]Tallahassee
                [4 ]USA
                [5 ]Materials Science and Engineering
                [6 ]Max Planck Institute for Solid State Research
                Article
                10.1039/C7CS00565B
                d7f038d2-de49-4b7c-8f22-75c8f278c1e4
                © 2018

                http://rsc.li/journals-terms-of-use

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