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      Z-scheme AgBr@Ag/CoAl layered double hydroxide heterojunction for superior photocatalytic Cr(VI) reduction under visible light

      , , , ,
      Applied Clay Science
      Elsevier BV

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          All-solid-state Z-scheme photocatalytic systems.

          The current rapid industrial development causes the serious energy and environmental crises. Photocatalyts provide a potential strategy to solve these problems because these materials not only can directly convert solar energy into usable or storable energy resources but also can decompose organic pollutants under solar-light irradiation. However, the aforementioned applications require photocatalysts with a wide absorption range, long-term stability, high charge-separation efficiency and strong redox ability. Unfortunately, it is often difficult for a single-component photocatalyst to simultaneously fulfill all these requirements. The artificial heterogeneous Z-scheme photocatalytic systems, mimicking the natural photosynthesis process, overcome the drawbacks of single-component photocatalysts and satisfy those aforementioned requirements. Such multi-task systems have been extensively investigated in the past decade. Especially, the all-solid-state Z-scheme photocatalytic systems without redox pair have been widely used in the water splitting, solar cells, degradation of pollutants and CO2 conversion, which have a huge potential to solve the current energy and environmental crises facing the modern industrial development. Thus, this review gives a concise overview of the all-solid-state Z-scheme photocatalytic systems, including their composition, construction, optimization and applications.
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            Catalytic applications of layered double hydroxides: recent advances and perspectives.

            This review surveys recent advances in the applications of layered double hydroxides (LDHs) in heterogeneous catalysis. By virtue of the flexible tunability and uniform distribution of metal cations in the brucite-like layers and the facile exchangeability of intercalated anions, LDHs-both as directly prepared or after thermal treatment and/or reduction-have found many applications as stable and recyclable heterogeneous catalysts or catalyst supports for a variety of reactions with high industrial and academic importance. A major challenge in this rapidly growing field is to simultaneously improve the activity, selectivity and stability of these LDH-based materials by developing ways of tailoring the electronic structure of the catalysts and supports. Therefore, this Review article is mainly focused on the most recent developments in smart design strategies for LDH materials and the potential catalytic applications of the resulting materials.
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              Preparation of two dimensional layered double hydroxide nanosheets and their applications.

              Layered double hydroxides (LDHs) with their highly flexible and tunable chemical composition and physical properties have attracted tremendous attention in recent years. LDHs have found widespread application as catalysts, anion exchange materials, fire retardants, and nano-fillers in polymer nanocomposites. The ability to exfoliate LDHs into ultrathin nanosheets enables a range of new opportunities for multifunctional materials. In this review we summarize the current available LDH exfoliation methods. In particular, we highlight recent developments for the direct synthesis of single-layer LDH nanosheets, as well as the emerging applications of LDH nanosheets in catalyzing oxygen evolution reactions and preparing light emitting devices, supercapacitors, and flame retardant nanocomposites.
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                Author and article information

                Contributors
                Journal
                Applied Clay Science
                Applied Clay Science
                Elsevier BV
                01691317
                July 2020
                July 2020
                : 192
                : 105627
                Article
                10.1016/j.clay.2020.105627
                fb0c954b-d073-4d56-8db0-4133881f3f2f
                © 2020

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

                http://www.elsevier.com/open-access/userlicense/1.0/

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