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Abstract
The doping reactions of graphite oxide (GO) with 3-3′-diaminobenzidine (DAB) were studied using N, N′-dicyclohexylcarbodiimide (DCC), cyanuric chloride (CC) and hexafluorophosphate (HATU) as coupling agents. The bifunctionality of the coupling agents aid to interact GO functional groups with amino groups of DAB without being part of the final product. The doped materials (d-GO) and GO were characterized by thermogravimetric analysis, x-ray diffraction, FTIR/Raman spectroscopy, x-ray photoelectron, high-resolution electron microscopy and cyclic voltammetry. The GO-HATU material was more thermally stable than other graphitic material, with at 10% weight loss at 300 °C, this thermal stability is related to a more difficult intramolecular physisorbed water removal process than the other d-GO materials. GO-CC and GO-HATU materials presented 8.2 and 8.0 Å of interlayer spacing, which was associated with a good oxidation-doping process. Besides, these two materials showed modifications in the vibrations by FTIR technique, corresponding to epoxy and hydroxyl groups of the GO being more susceptible to react with the amino groups. Moreover, I D /I G ratio calculated by Raman Spectroscopy presents the following trend 0.70, 0.94, 0.97 and 1.04 for GO, GO-CC, GO-DCC and GO-HATU, respectively, this increase is related with a major disorder during the doping process. XPS analysis shows C–N and N=C bands for high resolution of C 1s and N 1s, respectively, for d-GO materials. This possibly suggests the formation of benzimidazoles during the oxidation-doping process, this generates a similar -non-lattice and -lattice oxygen amount for O 1s related to crosslinking between the functional groups of GO and DAB which improve the electronic mobility between the surface and the bulk of the final graphitic material. Finally, the obtained d-GO materials were investigated as a working electrode for electrochemical capacitors and all of them showed typical capacitive behaviour.
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1 Departamento de Ciencias Básicas, División de Ciencias Básicas e Ingeniería, Universidad Autónoma Metropolitana—Azcapotzalco, Av. San Pablo 180, Col. Reynosa Tamaulipas, Azcapotzalco, Ciudad de México, 02200, México
2 Departamento de Ciencias Básicas, División de Ciencias Básicas e Ingeniería, Universidad Autónoma Metropolitana—Azcapotzalco, Av. San Pablo 180, Col. Reynosa Tamaulipas, Azcapotzalco, Ciudad de México, 02200, México; Instituto de Física, Universidad Nacional Autónoma de México, Cuidad Universitaria, Ciudad de México, 20364, México
3 Instituto de Física, Universidad Nacional Autónoma de México, Cuidad Universitaria, Ciudad de México, 20364, México
4 Cátedras CONACYT-Área Académica de Química, Universidad Autónoma del Estado de Hidalgo, carretera Pachuca-Tulancingo km 4.5, Mineral de la Reforma, Hidalgo, 42184, México
5 Departamento de Biociencias e Ingeniería, Centro Interdisciplinario de Investigaciones y Estudios sobre Medio Ambiente y Desarrollo (CIIEMAD), Instituto Politécnico Nacional, Cuidad de México, 07340, México
6 Unidad de Ciencias Químicas, Universidad Autónoma de Zacatecas, Campus UAZ Siglo XXI, Carr. a Guadalajara km 6, Ejido la escondida, Zacatecas, 98160, México