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      Piezo‐Photocatalysis over Metal–Organic Frameworks: Promoting Photocatalytic Activity by Piezoelectric Effect

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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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            Metal-organic frameworks (MOFs).

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              Particulate Photocatalysts for Light-Driven Water Splitting: Mechanisms, Challenges, and Design Strategies

              Solar-driven water splitting provides a leading approach to store the abundant yet intermittent solar energy and produce hydrogen as a clean and sustainable energy carrier. A straightforward route to light-driven water splitting is to apply self-supported particulate photocatalysts, which is expected to allow solar hydrogen to be competitive with fossil-fuel-derived hydrogen on a levelized cost basis. More importantly, the powder-based systems can lend themselves to making functional panels on a large scale while retaining the intrinsic activity of the photocatalyst. However, all attempts to generate hydrogen via powder-based solar water-splitting systems to date have unfortunately fallen short of the efficiency values required for practical applications. Photocatalysis on photocatalyst particles involves three sequential steps: (i) absorption of photons with higher energies than the bandgap of the photocatalysts, leading to the excitation of electron-hole pairs in the particles, (ii) charge separation and migration of these photoexcited carriers, and (iii) surface chemical reactions based on these carriers. In this review, we focus on the challenges of each step and summarize material design strategies to overcome the obstacles and limitations. This review illustrates that it is possible to employ the fundamental principles underlying photosynthesis and the tools of chemical and materials science to design and prepare photocatalysts for overall water splitting.
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Advanced Materials
                Advanced Materials
                Wiley
                0935-9648
                1521-4095
                December 2021
                October 13 2021
                December 2021
                : 33
                : 51
                : 2106308
                Affiliations
                [1 ]College of Chemistry and Environmental Engineering Shenzhen University Shenzhen Guangdong 518060 P. R. China
                [2 ]Hefei National Laboratory for Physical Sciences at the Microscale CAS Key Laboratory of Soft Matter Chemistry Department of Chemistry University of Science and Technology of China Hefei Anhui 230026 P. R. China
                [3 ]Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province College of Optoelectronic Engineering Shenzhen University Shenzhen Guangdong 518060 P. R. China
                [4 ]School of Chemistry and Environmental Engineering Hanshan Normal University Chaozhou Guangdong 521041 P. R. China
                [5 ]Xinjiang Key Laboratory of Explosives Safety Science Xinjiang Technical Institute of Physics and Chemistry Key Laboratory of Functional Materials and Devices for Special Environments Chinese Academy of Sciences Urumqi Xinjiang 830011 P. R. China
                [6 ]Nanjing Institute of Environmental Sciences Ministry of Ecology and Environment Nanjing Jiangsu 210042 P. R. China
                Article
                10.1002/adma.202106308
                07b4e417-b3a2-42fb-abfc-d911f9a3d49d
                © 2021

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

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