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      Nitrogen-doped porous carbon nanosheets derived from poly(ionic liquid)s: hierarchical pore structures for efficient CO2capture and dye removal

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          Abstract

          Nitrogen-doped porous carbon nanosheets were synthesized viaan activation- or post-treatment-free approach, which delivered high CO 2and dye adsorption capacities.

          Abstract

          Poly(ionic liquid) has recently served as an important precursor for nitrogen-doped functional porous carbons. It was applied here in a facile one-pot approach to synthesize nitrogen-doped porous carbon nanosheets (NPCNSs) using C 3N 4nanosheets as sacrificial templates. C 3N 4nanosheets are found to improve the carbonization yield and nitrogen content of NPCNSs and additionally facilitate the formation of a unique pore structure. Without post-treatments or activation steps, the as-synthesized NPCNS readily reaches a specific surface area above 1100 m 2g −1with hierarchical micro-/meso-/macropore structures while keeping a high nitrogen content (17.4 wt%). More significantly, the NPCNS is able to deliver not only a high CO 2adsorption capacity with outstanding reversibility, but also an unprecedented capacity in methylene blue uptake by 962.1 mg g −1, which is among the few highest ever reported for wastewater, with excellent reusability.

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          Exploration of the active center structure of nitrogen-doped graphene-based catalysts for oxygen reduction reaction

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            Nitrogen-doped porous carbon nanofiber webs as anodes for lithium ion batteries with a superhigh capacity and rate capability.

            Nitrogen-doped carbon nanofiber webs (CNFWs) with high surface areas are successfully prepared by carbonization-activation of polypyrrole nanofiber webs with KOH. The as-obtained CNFWs exhibit a superhigh reversible capacity of 943 mAh g(-1) at a current density of 2 A g(-1) even after 600 cycles, which is ascribed to the novel porous nanostructure and high-level nitrogen doping. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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              Mesoporous metal-nitrogen-doped carbon electrocatalysts for highly efficient oxygen reduction reaction.

              A family of mesoporous nonprecious metal (NPM) catalysts for oxygen reduction reaction (ORR) in acidic media, including cobalt-nitrogen-doped carbon (C-N-Co) and iron-nitrogen-doped carbon (C-N-Fe), was prepared from vitamin B12 (VB12) and the polyaniline-Fe (PANI-Fe) complex, respectively. Silica nanoparticles, ordered mesoporous silica SBA-15, and montmorillonite were used as templates for achieving mesoporous structures. The most active mesoporous catalyst was fabricated from VB12 and silica nanoparticles and exhibited a remarkable ORR activity in acidic medium (half-wave potential of 0.79 V, only ∼58 mV deviation from Pt/C), high selectivity (electron-transfer number >3.95), and excellent electrochemical stability (only 9 mV negative shift of half-wave potential after 10,000 potential cycles). The unprecedented performance of these NPM catalysts in ORR was attributed to their well-defined porous structures with a narrow mesopore size distribution, high Brunauer-Emmett-Teller surface area (up to 572 m(2)/g), and homogeneous distribution of abundant metal-Nx active sites.
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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2016
                2016
                : 4
                : 19
                : 7313-7321
                Affiliations
                [1 ]Department of Colloid Chemistry
                [2 ]Max Planck Institute of Colloids and Interfaces Am Mühlenberg 1 OT Golm
                [3 ]D-14476 Potsdam
                [4 ]Germany
                Article
                10.1039/C6TA01945E
                51a9c3e0-8ebd-46ad-8e98-f15b5feb18fb
                © 2016
                History

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