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      Zeolitic imidazolate framework-67 and its derivatives for photocatalytic applications

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          The chemistry and applications of metal-organic frameworks.

          Crystalline metal-organic frameworks (MOFs) are formed by reticular synthesis, which creates strong bonds between inorganic and organic units. Careful selection of MOF constituents can yield crystals of ultrahigh porosity and high thermal and chemical stability. These characteristics allow the interior of MOFs to be chemically altered for use in gas separation, gas storage, and catalysis, among other applications. The precision commonly exercised in their chemical modification and the ability to expand their metrics without changing the underlying topology have not been achieved with other solids. MOFs whose chemical composition and shape of building units can be multiply varied within a particular structure already exist and may lead to materials that offer a synergistic combination of properties.
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            A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films

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              Photocatalyst releasing hydrogen from water.

              Direct splitting of water using a particulate photocatalyst would be a good way to produce clean and recyclable hydrogen on a large scale, and in the past 30 years various photocatalysts have been found that function under visible light. Here we describe an advance in the catalysis of the overall splitting of water under visible light: the new catalyst is a solid solution of gallium and zinc nitrogen oxide, (Ga(1-x)Zn(x))(N(1-x)O(x)), modified with nanoparticles of a mixed oxide of rhodium and chromium. The mixture functions as a promising and efficient photocatalyst in promoting the evolution of hydrogen gas.
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                Author and article information

                Contributors
                Journal
                Coordination Chemistry Reviews
                Coordination Chemistry Reviews
                Elsevier BV
                00108545
                March 2024
                March 2024
                : 502
                : 215612
                Article
                10.1016/j.ccr.2023.215612
                ef66b93f-f36d-4c5e-b090-0f85a38bfb75
                © 2024

                https://www.elsevier.com/tdm/userlicense/1.0/

                https://doi.org/10.15223/policy-017

                https://doi.org/10.15223/policy-037

                https://doi.org/10.15223/policy-012

                https://doi.org/10.15223/policy-029

                https://doi.org/10.15223/policy-004

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