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      Localized surface plasmon resonance effect enhanced Cu/TiO 2 core–shell catalyst for boosting CO 2 hydrogenation reaction

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          Abstract

          Inexpensive and nontoxic Cu/TiO 2 catalysts based on the LSPR effect for boosting the CO 2 hydrogenation reaction.

          Abstract

          Photothermal catalysis is a promising strategy for converting CO 2 into high value-added chemical feedstocks. Its current major challenges lie in improving CO 2 conversion efficiency and product selectivity. In this work, a series of Cu/TiO 2 core–shell catalysts were prepared using the hard template method. The Cu 10/TiO 2 catalyst exhibited excellent performance for the photothermal conversion of CO 2 to CO in the presence of H 2 under Xe lamp irradiation (CO 2 conversion, 30.6%; CO selectivity, ∼100%; CO maximum yield, 87.1 mmol h −1 g cat −1). Results indicated that the Cu/TiO 2 catalyst has a good photo-to-thermal conversion ability based on the significant LSPR effect, and the existence of hot electrons makes the reaction follow the carbonate pathway efficiently. This article successfully achieves efficient CO 2 reduction under inexpensive and non-toxic conditions. In addition, it also provides unique insights into the study of the LSPR effect in the field of photothermal catalysis.

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          Double-slit photoelectron interference in strong-field ionization of the neon dimer

          Wave-particle duality is an inherent peculiarity of the quantum world. The double-slit experiment has been frequently used for understanding different aspects of this fundamental concept. The occurrence of interference rests on the lack of which-way information and on the absence of decoherence mechanisms, which could scramble the wave fronts. Here, we report on the observation of two-center interference in the molecular-frame photoelectron momentum distribution upon ionization of the neon dimer by a strong laser field. Postselection of ions, which are measured in coincidence with electrons, allows choosing the symmetry of the residual ion, leading to observation of both, gerade and ungerade, types of interference.
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            Reporting physisorption data for gas/solid systems with special reference to the determination of surface area and porosity (Recommendations 1984)

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              In situ click chemistry generation of cyclooxygenase-2 inhibitors

              Cyclooxygenase-2 isozyme is a promising anti-inflammatory drug target, and overexpression of this enzyme is also associated with several cancers and neurodegenerative diseases. The amino-acid sequence and structural similarity between inducible cyclooxygenase-2 and housekeeping cyclooxygenase-1 isoforms present a significant challenge to design selective cyclooxygenase-2 inhibitors. Herein, we describe the use of the cyclooxygenase-2 active site as a reaction vessel for the in situ generation of its own highly specific inhibitors. Multi-component competitive-binding studies confirmed that the cyclooxygenase-2 isozyme can judiciously select most appropriate chemical building blocks from a pool of chemicals to build its own highly potent inhibitor. Herein, with the use of kinetic target-guided synthesis, also termed as in situ click chemistry, we describe the discovery of two highly potent and selective cyclooxygenase-2 isozyme inhibitors. The in vivo anti-inflammatory activity of these two novel small molecules is significantly higher than that of widely used selective cyclooxygenase-2 inhibitors.
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                Author and article information

                Contributors
                Journal
                CSTAGD
                Catalysis Science & Technology
                Catal. Sci. Technol.
                Royal Society of Chemistry (RSC)
                2044-4753
                2044-4761
                October 17 2022
                2022
                : 12
                : 20
                : 6155-6162
                Affiliations
                [1 ]TJU-NIMS International Collaboration Laboratory, School of Materials Science and Engineering, Tianjin University, Tianjin 300072, P. R. China
                [2 ]School of Chemical and Environmental Engineering, Liaoning University of Technology, Jinzhou 121001, China
                [3 ]International Center for Materials Nanoarchitectonics (WPI-MANA), National Institutes for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan
                Article
                10.1039/D2CY01327D
                dfad5e3d-f050-4892-ae70-45be6697f5f5
                © 2022

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

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