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      Multifunctional mixed valence N-doped CNT@MFe2O4 hybrid nanomaterials: from engineered one-pot coprecipitation to application in energy storage paper supercapacitors.

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          Abstract

          This work reports on the design of novel mixed valence hybrid N-doped carbon nanotubes/metal ferrite nanomaterials (MFe2O4, M(ii) = Mn, Fe, Co) with tailored composition, and magnetic and electrical properties through a straightforward eco-sustainable and less time consuming one-pot in situ coprecipitation process. The potentialities of this strategy rely on the lack of oxidative treatments to the support and thermal annealing, besides the use of aqueous conditions, a chelating base (isopropanolamine) and low temperatures. The process afforded the controlled nucleation/growth of the MFe2O4 nanoparticles (NPs), with sizes of 3.2-5.4 nm and superparamagnetic properties, on the surface of the N-doped carbon nanotubes (CNT-N) and their immobilization by covalent bonding. The nitrogen-based functionalities of CNT-N allied with the use of a coprecipitation agent with coordinating properties towards M(ii)/Fe(iii) cations were responsible for these achievements. To unravel the potentialities of the novel nanohybrids (CNT-N@M), they were tested as electrode active nanomaterials in the fabrication of all-solid-state asymmetric paper supercapacitors (SCs). All asymmetric SCs presented significantly higher performance than the symmetric CNT-N based one, with an enhancement of the energy density to up to 6.0× and of the power density to up to 4.3× due to the occurrence of both non-faradaic and faradaic charge storage mechanisms. Moreover, they led to enhanced volumetric energy density (up to 11.1×) and power density (up to 5.2×) compared with other solid-state hybrid paper SCs based on carbon materials recently reported in the literature. These results highlight the importance of conjugating a conductive support bearing N-based functionalities with MFe2O4 NPs featuring redox properties towards synergistically enhanced energy storage.

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          Author and article information

          Journal
          Nanoscale
          Nanoscale
          Royal Society of Chemistry (RSC)
          2040-3372
          2040-3364
          Jul 09 2018
          : 10
          : 26
          Affiliations
          [1 ] REQUIMTE/LAQV, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre s/n, 4169-007 Porto, Portugal. clara.pereira@fc.up.pt.
          [2 ] REQUIMTE/LAQV, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre s/n, 4169-007 Porto, Portugal. clara.pereira@fc.up.pt and IFIMUP and IN - Institute of Nanoscience and Nanotechnology, Departamento de Física e Astronomia, Faculdade de Ciências, Universidade do Porto, 4169-007 Porto, Portugal. ampereira@fc.up.pt.
          [3 ] Instituto de Catálisis y Petroleoquímica, CSIC, C/ Marie Curie 2, Cantoblanco, 28049 Madrid, Spain.
          [4 ] Departamento de Química Inorgánica y Química Técnica, Facultad de Ciencias, UNED, Senda del Rey 9, 28040 Madrid, Spain.
          [5 ] Departamento de Química and CQ-VR, Universidade de Trás-os-Montes e Alto Douro, 5001-801 Vila Real, Portugal.
          [6 ] IFIMUP and IN - Institute of Nanoscience and Nanotechnology, Departamento de Física e Astronomia, Faculdade de Ciências, Universidade do Porto, 4169-007 Porto, Portugal. ampereira@fc.up.pt.
          Article
          10.1039/c8nr03533d
          29947627
          ce0d88bb-c961-4e03-bfa2-3d5b413002c7
          History

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