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      Three-dimensional annealed WO 3 nanowire/graphene foam as an electrocatalytic material for all vanadium redox flow batteries

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          Abstract

          This paper presents a three-dimensional annealed tungsten trioxide nanowire/graphene sheet (3D annealed WO 3 NWs/GS) foam as an excellent and low-cost electrocatalyst.

          Abstract

          This paper presents a three-dimensional annealed tungsten trioxide nanowire/graphene sheet (3D annealed WO 3 NWs/GS) foam as an excellent and low-cost electrocatalyst. It was prepared using vanadium redox flow battery (VRFB) electrodes through an in situ self-assembly of graphene sheets prepared by mild chemical reduction, followed by freeze-drying and annealing. The 3D annealed WO 3 NWs/GS foam exhibits the highest electrocatalytic activities toward V 2+/V 3+ and VO 2+/VO 2 + redox couples among all the tested samples. Charge–discharge tests further confirm that a single flow cell of a VRFB using the 3D annealed WO 3 NWs/GS foam demonstrates excellent energy efficiencies of 79.49% and 83.73% at current densities of 80 mA cm −2 and 40 mA cm −2, respectively, which are much higher than those of cells assembled with pristine graphite felt (GF) and 3D WO 3 NWs/GS foam without annealing treatment. Moreover, it shows no obvious degradation after 50 charge–discharge cycles. These results are attributed to the formation of new W–O–C bonds, confirming that the WO 3 NWs are anchored strongly to the GS, which is key to facilitating the redox reactions of the vanadium redox couples. Moreover, the 3D annealed WO 3 NWs/GS foam exhibits a 3D hierarchical porous structure, which can provide more surface electroactive sites to improve the electrochemical performance of VRFBs.

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          Most cited references58

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          Self-assembled graphene hydrogel via a one-step hydrothermal process.

          Self-assembly of two-dimensional graphene sheets is an important strategy for producing macroscopic graphene architectures for practical applications, such as thin films and layered paperlike materials. However, construction of graphene self-assembled macrostructures with three-dimensional networks has never been realized. In this paper, we prepared a self-assembled graphene hydrogel (SGH) via a convenient one-step hydrothermal method. The SGH is electrically conductive, mechanically strong, and thermally stable and exhibits a high specific capacitance. The high-performance SGH with inherent biocompatibility of carbon materials is attractive in the fields of biotechnology and electrochemistry, such as drug-delivery, tissue scaffolds, bionic nanocomposites, and supercapacitors.
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            Three dimensional macroporous architectures and aerogels built of carbon nanotubes and/or graphene: synthesis and applications.

            Carbon nanotubes and graphene are some of the most intensively explored carbon allotropes in materials science. This interest mainly resides in their unique properties with electrical conductivities as high as 10(4) S cm(-1), thermal conductivities as high as 5000 W m(-1) K and superior mechanical properties with elastic moduli on the order of 1 TPa for both of them. The possibility to translate the individual properties of these monodimensional (e.g. carbon nanotubes) and bidimensional (e.g. graphene) building units into two-dimensional free-standing thick and thin films has paved the way for using these allotropes in a number of applications (including photocatalysis, electrochemistry, electronics and optoelectronics, among others) as well as for the preparation of biological and chemical sensors. More recently and while recognizing the tremendous interest of these two-dimensional structures, researchers are noticing that the performance of certain devices can experience a significant enhancement by the use of three-dimensional architectures and/or aerogels because of the increase of active material per projected area. This is obviously the case as long as the nanometre-sized building units remain accessible so that the concept of hierarchical three-dimensional organization is critical to guarantee the mass transport and, as consequence, performance enhancement. Thus, this review aims to describe the different synthetic processes used for preparation of these three-dimensional architectures and/or aerogels containing either any or both allotropes, and the different fields of application in which the particular structure of these materials provided a significant enhancement in the efficacy as compared to their two-dimensional analogues or even opened the path to novel applications. The unprecedented compilation of information from both CNT- and graphene-based three-dimensional architectures and/or aerogels in a single revision is also of interest because it allows a straightforward comparison between the particular features provided by each allotrope.
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              Self-assembly and embedding of nanoparticles by in situ reduced graphene for preparation of a 3D graphene/nanoparticle aerogel.

              A 3D graphene architecture can be prepared via an in situ self-assembly of graphene prepared by a mild chemical reduction. Fe(3) O(4) nanoparticles are homogeneously dispersed into graphene oxide (GO) aqueous suspension and a 3D magnetic graphene/Fe(3) O(4) aerogel is prepared during the reduction of GO to graphene. This provides a general method to prepare 3D graphene/nanoparticle composites for a wide range of applications including catalysis and energy conversion.

                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                SEFUA7
                Sustainable Energy & Fuels
                Sustainable Energy Fuels
                2398-4902
                2017
                2017
                : 1
                : 10
                : 2091-2100
                Affiliations
                [1 ]Department of Materials Science and Engineering
                [2 ]National Taiwan University of Science and Technology
                [3 ]Taipei
                [4 ]Taiwan
                Article
                10.1039/C7SE00271H
                7ac3466a-dfa5-4f8c-9ad7-7939ef77e308
                © 2017

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

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