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      Heterostructured BN@Co‐C@C Endowing Polyester Composites Excellent Thermal Conductivity and Microwave Absorption at C Band

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          Abstract

          The trends of miniaturization, lightweight, and high integration in electronics have brought serious issues in heat dissipation and electromagnetic compatibility and also limited the simultaneous use of thermally conductive and microwave absorption materials. Therefore, it is imperative to design materials that possess those dual functions. In this work, one‐pot method is used to anchor zeolitic imidazolate framework ZIF‐67 coated with polydopamine (PDA) on boron nitride (BN) to obtain BN@ZIF‐67@PDA. The pyrolysis product BN@Co‐C@C is used as heterostructured thermally conductive/microwave absorption fillers and blended with polyethylene terephthalate (PET) to prepare BN@Co‐C@C/PET composites. When the mass ratio of BN to ZIF‐67@PDA is 7.5:1 and the mass fraction of BN 7.5@Co‐C@C is 45 wt%, the BN 7.5@Co‐C@C/PET composites exhibit excellent thermal conductivities and microwave absorption performances. The thermal conductivity coefficient is 5.37 W m −1 K −1, which is 35.8 times higher than that of PET (0.15 W m −1 K −1), and also higher than that of 45 wt% (BN 7.5/Co‐C@C)/PET composites (4.03 W m −1 K −1) prepared by directly mixing. The minimum reflection loss of 45 wt% BN 7.5@Co‐C@C/PET composites are −63.1 dB at 4.72 GHz, and the corresponding effective absorption bandwidth is 1.28 GHz (4.08–5.36 GHz), achieving excellent microwave absorption performance at C band.

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          Catalyst-free synthesis of nitrogen-doped graphene via thermal annealing graphite oxide with melamine and its excellent electrocatalysis.

          The electronic and chemical properties of graphene can be modulated by chemical doping foreign atoms and functional moieties. The general approach to the synthesis of nitrogen-doped graphene (NG), such as chemical vapor deposition (CVD) performed in gas phases, requires transitional metal catalysts which could contaminate the resultant products and thus affect their properties. In this paper, we propose a facile, catalyst-free thermal annealing approach for large-scale synthesis of NG using low-cost industrial material melamine as the nitrogen source. This approach can completely avoid the contamination of transition metal catalysts, and thus the intrinsic catalytic performance of pure NGs can be investigated. Detailed X-ray photoelectron spectrum analysis of the resultant products shows that the atomic percentage of nitrogen in doped graphene samples can be adjusted up to 10.1%. Such a high doping level has not been reported previously. High-resolution N1s spectra reveal that the as-made NG mainly contains pyridine-like nitrogen atoms. Electrochemical characterizations clearly demonstrate excellent electrocatalytic activity of NG toward the oxygen reduction reaction (ORR) in alkaline electrolytes, which is independent of nitrogen doping level. The present catalyst-free approach opens up the possibility for the synthesis of NG in gram-scale for electronic devices and cathodic materials for fuel cells and biosensors.
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            Hollow Engineering to Co@N‐Doped Carbon Nanocages via Synergistic Protecting‐Etching Strategy for Ultrahigh Microwave Absorption

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              Multidimension‐Controllable Synthesis of MOF‐Derived Co@N‐Doped Carbon Composite with Magnetic‐Dielectric Synergy toward Strong Microwave Absorption

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                Author and article information

                Contributors
                Journal
                Advanced Functional Materials
                Adv Funct Materials
                Wiley
                1616-301X
                1616-3028
                January 09 2024
                Affiliations
                [1 ] Shaanxi Key Laboratory of Macromolecular Science and Technology School of Chemistry and Chemical Engineering Northwestern Polytechnical University Xi'an Shaanxi 710072 P. R. China
                [2 ] School of Materials Science and Engineering South China University of Technology Guangzhou Guangdong 510640 P. R. China
                Article
                10.1002/adfm.202313544
                27bbcb4d-c77d-402a-b81a-03476f466b79
                © 2024

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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