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      Heterophase fcc-2H-fcc gold nanorods

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          Abstract

          The crystal phase-based heterostructures of noble metal nanomaterials are of great research interest for various applications, such as plasmonics and catalysis. However, the synthesis of unusual crystal phases of noble metals still remains a great challenge, making the construction of heterophase noble metal nanostructures difficult. Here, we report a one-pot wet-chemical synthesis of well-defined heterophase fcc-2H-fcc gold nanorods (fcc: face-centred cubic; 2H: hexagonal close-packed with stacking sequence of “AB”) at mild conditions. Single particle-level experiments and theoretical investigations reveal that the heterophase gold nanorods demonstrate a distinct optical property compared to that of the conventional fcc gold nanorods. Moreover, the heterophase gold nanorods possess superior electrocatalytic activity for the carbon dioxide reduction reaction over their fcc counterparts under ambient conditions. First-principles calculations suggest that the boosted catalytic performance stems from the energetically favourable adsorption of reaction intermediates, endowed by the unique heterophase characteristic of gold nanorods.

          Abstract

          The crystal phase-based heterostructures of noble metal nanomaterials are of interest for various applications. Here, the authors report the wet-chemical synthesis of gold nanorods with a well-defined fcc-2H-fcc heterophase, which possess unique optical and catalytic properties.

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          Most cited references39

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          Quantum dot-induced phase stabilization of α-CsPbI3 perovskite for high-efficiency photovoltaics.

          We show nanoscale phase stabilization of CsPbI3 quantum dots (QDs) to low temperatures that can be used as the active component of efficient optoelectronic devices. CsPbI3 is an all-inorganic analog to the hybrid organic cation halide perovskites, but the cubic phase of bulk CsPbI3 (α-CsPbI3)-the variant with desirable band gap-is only stable at high temperatures. We describe the formation of α-CsPbI3 QD films that are phase-stable for months in ambient air. The films exhibit long-range electronic transport and were used to fabricate colloidal perovskite QD photovoltaic cells with an open-circuit voltage of 1.23 volts and efficiency of 10.77%. These devices also function as light-emitting diodes with low turn-on voltage and tunable emission.
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            Recent Advances in Inorganic Heterogeneous Electrocatalysts for Reduction of Carbon Dioxide.

            In view of the climate changes caused by the continuously rising levels of atmospheric CO2 , advanced technologies associated with CO2 conversion are highly desirable. In recent decades, electrochemical reduction of CO2 has been extensively studied since it can reduce CO2 to value-added chemicals and fuels. Considering the sluggish reaction kinetics of the CO2 molecule, efficient and robust electrocatalysts are required to promote this conversion reaction. Here, recent progress and opportunities in inorganic heterogeneous electrocatalysts for CO2 reduction are discussed, from the viewpoint of both experimental and computational aspects. Based on elemental composition, the inorganic catalysts presented here are classified into four groups: metals, transition-metal oxides, transition-metal chalcogenides, and carbon-based materials. However, despite encouraging accomplishments made in this area, substantial advances in CO2 electrolysis are still needed to meet the criteria for practical applications. Therefore, in the last part, several promising strategies, including surface engineering, chemical modification, nanostructured catalysts, and composite materials, are proposed to facilitate the future development of CO2 electroreduction.
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              Monodisperse Au nanoparticles for selective electrocatalytic reduction of CO2 to CO.

              We report selective electrocatalytic reduction of carbon dioxide to carbon monoxide on gold nanoparticles (NPs) in 0.5 M KHCO3 at 25 °C. Among monodisperse 4, 6, 8, and 10 nm NPs tested, the 8 nm Au NPs show the maximum Faradaic efficiency (FE) (up to 90% at -0.67 V vs reversible hydrogen electrode, RHE). Density functional theory calculations suggest that more edge sites (active for CO evolution) than corner sites (active for the competitive H2 evolution reaction) on the Au NP surface facilitates the stabilization of the reduction intermediates, such as COOH*, and the formation of CO. This mechanism is further supported by the fact that Au NPs embedded in a matrix of butyl-3-methylimidazolium hexafluorophosphate for more efficient COOH* stabilization exhibit even higher reaction activity (3 A/g mass activity) and selectivity (97% FE) at -0.52 V (vs RHE). The work demonstrates the great potentials of using monodisperse Au NPs to optimize the available reaction intermediate binding sites for efficient and selective electrocatalytic reduction of CO2 to CO.
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                Author and article information

                Contributors
                hmzheng@lbl.gov
                hua.zhang@cityu.edu.hk
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                3 July 2020
                3 July 2020
                2020
                : 11
                : 3293
                Affiliations
                [1 ]ISNI 0000 0004 1792 6846, GRID grid.35030.35, Department of Chemistry, , City University of Hong Kong, ; Hong Kong, China
                [2 ]ISNI 0000 0004 1792 6846, GRID grid.35030.35, Hong Kong Branch of National Precious Metals Material Engineering Research Center (NPMM), , City University of Hong Kong, ; Hong Kong, China
                [3 ]ISNI 0000 0001 2224 0361, GRID grid.59025.3b, Center for Programmable Materials, School of Materials Science and Engineering, , Nanyang Technological University, ; 50 Nanyang Avenue, Singapore, 639798 Singapore
                [4 ]ISNI 0000 0001 2231 4551, GRID grid.184769.5, Materials Sciences Division, , Lawrence Berkeley National Laboratory, ; Berkeley, CA 94720 USA
                [5 ]ISNI 0000 0001 2180 6431, GRID grid.4280.e, Department of Materials Science and Engineering, , National University of Singapore, ; 9 Engineering Drive 1, Singapore, 117575 Singapore
                [6 ]ISNI 0000 0004 0637 0221, GRID grid.185448.4, Institute of Materials Research and Engineering, , Agency for Science, Technology, and Research (A*STAR), ; 2 Fusionopolis Way, Singapore, 138634 Singapore
                [7 ]ISNI 0000 0004 1761 0489, GRID grid.263826.b, School of Physics, , Southeast University, ; 211189 Nanjing, China
                [8 ]ISNI 0000 0004 0637 0221, GRID grid.185448.4, Institute of High Performance Computing, , Agency for Science, Technology, and Research (A*STAR), ; 1 Fusionopolis Way, #16-16 Connexis, Singapore, 138632 Singapore
                [9 ]ISNI 0000 0001 2231 4551, GRID grid.184769.5, National Center for Electron Microscopy, Molecular Foundry, , Lawrence Berkeley National Laboratory, ; Berkeley, CA 94720 USA
                [10 ]ISNI 0000 0004 0637 0221, GRID grid.185448.4, Singapore Institute of Manufacturing Technology, , Agency for Science, Technology, and Research (A*STAR), ; 71 Nanyang Drive, Singapore, 638075 Singapore
                [11 ]ISNI 0000 0001 2181 7878, GRID grid.47840.3f, Department of Materials Science and Engineering, , University of California, ; Berkeley, CA 94720 USA
                Author information
                http://orcid.org/0000-0003-3133-6503
                http://orcid.org/0000-0003-0821-7469
                http://orcid.org/0000-0001-6743-9251
                http://orcid.org/0000-0002-6762-9976
                http://orcid.org/0000-0002-2546-005X
                http://orcid.org/0000-0002-2487-4250
                http://orcid.org/0000-0003-3813-4170
                http://orcid.org/0000-0001-9518-740X
                Article
                17068
                10.1038/s41467-020-17068-w
                7335101
                32620898
                8061bf8b-d699-4347-8725-e62a0143d01e
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 17 January 2020
                : 5 June 2020
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                © The Author(s) 2020

                Uncategorized
                electrocatalysis,structural properties
                Uncategorized
                electrocatalysis, structural properties

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