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      Integrating MXene nanosheets with cobalt-tipped carbon nanotubes for an efficient oxygen reduction reaction

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          Abstract

          A metal–organic-framework-engaged strategy is proposed for the fabrication of cobalt-tipped carbon nanotube/Ti 3C 2 nanosheet composites for an efficient oxygen reduction reaction.

          Abstract

          The oxygen reduction reaction (ORR) plays a key role in many renewable energy conversion and storage technologies. As the state-of-the-art ORR electrocatalysts, Pt-based electrocatalysts suffer from high price, low earth abundance and poor stability. Developing high performance noble-metal-free ORR electrocatalysts as alternatives for Pt is highly desirable but still remains a significant challenge. In this work, we reported a metal–organic-framework-engaged strategy for the fabrication of cobalt-tipped carbon nanotube/Ti 3C 2 nanosheet composites (Co-CNT/Ti 3C 2), in which ZIF-67 particles were in situ grown on Ti 3C 2 nanosheets and then were converted to cobalt-tipped carbon nanotubes through a pyrolysis process. The Ti 3C 2 nanosheets not only served as two-dimensional conductive scaffolds for the growth of Co-CNTs but also balanced the tradeoff between graphitization of carbon and the surface area. Benefiting from the abundant Co–N/C active sites, reasonably high graphitization of carbon and suitable surface areas, the optimized Co-CNT/Ti 3C 2 manifested comparable ORR activity (half-wave potential of 0.82 V and diffusion-limiting current density of 5.55 mA cm −2) but superior stability to commercial Pt/C (half-wave potential of 0.82 V and diffusion-limiting current density of 5.30 mA cm −2), providing great opportunity for its application in renewable conversion and storage technologies.

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          Most cited references51

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          Design of electrocatalysts for oxygen- and hydrogen-involving energy conversion reactions.

          A fundamental change has been achieved in understanding surface electrochemistry due to the profound knowledge of the nature of electrocatalytic processes accumulated over the past several decades and to the recent technological advances in spectroscopy and high resolution imaging. Nowadays one can preferably design electrocatalysts based on the deep theoretical knowledge of electronic structures, via computer-guided engineering of the surface and (electro)chemical properties of materials, followed by the synthesis of practical materials with high performance for specific reactions. This review provides insights into both theoretical and experimental electrochemistry toward a better understanding of a series of key clean energy conversion reactions including oxygen reduction reaction (ORR), oxygen evolution reaction (OER), and hydrogen evolution reaction (HER). The emphasis of this review is on the origin of the electrocatalytic activity of nanostructured catalysts toward the aforementioned reactions by correlating the apparent electrode performance with their intrinsic electrochemical properties. Also, a rational design of electrocatalysts is proposed starting from the most fundamental aspects of the electronic structure engineering to a more practical level of nanotechnological fabrication.
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            Toward the rational design of non-precious transition metal oxides for oxygen electrocatalysis

            The rational design of non-precious transition metal perovskite oxide catalysts holds exceptional promise for understanding and mastering the kinetics of oxygen electrocatalysis instrumental to artificial photosynthesis, solar fuels, fuel cells, electrolyzers, and metal–air batteries. In this Review, we discuss the state-of-the-art understanding of non-precious transition metal oxides that catalyze the oxygen reduction and evolution reactions. Understanding and mastering the kinetics of oxygen electrocatalysis is instrumental to making use of photosynthesis, advancing solar fuels, fuel cells, electrolyzers, and metal–air batteries. We first present key insights, assumptions and limitations of well-known activity descriptors and reaction mechanisms in the past four decades. The turnover frequency of crystalline oxides as promising catalysts is also put into perspective with amorphous oxides and photosystem II. Particular attention is paid to electronic structure parameters that can potentially govern the adsorbate binding strength and thus provide simple rationales and design principles to predict new catalyst chemistries with enhanced activity. We share new perspective synthesizing mechanism and electronic descriptors developed from both molecular orbital and solid state band structure principles. We conclude with an outlook on the opportunities in future research within this rapidly developing field.
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              Flexible MXene/Carbon Nanotube Composite Paper with High Volumetric Capacitance

              Free-standing and flexible sandwich-like MXene/carbon nanotube (CNT) paper, composed of alternating MXene and CNT layers, is fabricated using a simple filtration method. These sandwich-like papers exhibit high volumetric capacitances, good rate performances, and excellent cycling stability when employed as electrodes in supercapacitors.
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                Author and article information

                Contributors
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                January 15 2019
                2019
                : 7
                : 3
                : 1281-1286
                Affiliations
                [1 ]Institute of Functional Nano & Soft Materials (FUNSOM)
                [2 ]Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices
                [3 ]Joint International Research Laboratory of Carbon-Based Functional Materials and Devices
                [4 ]Soochow University
                [5 ]Suzhou
                Article
                10.1039/C8TA10574J
                02c04263-3b83-4789-b9c4-dfa4c8a632c5
                © 2019

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

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