Poly(aniline-co-pyrrole) on the surface of reduced graphene oxide as high-performance electrode materials for supercapacitors
Creators
- 1. State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai 201620 (China)
- 2. College of Material Science and Engineering, Donghua University, Shanghai 201620 (China)
Description
Highlights: • Preparing PANi-co-PPy on the surface of the rGO sheets by in situ chemical oxidative polymerization. • Achieving high thermal stability and especially electrochemical performances. • Benifiting from its unique structure, intrinsic properties and synergistic effect among the three components. - ABSTRACT: Poly(aniline-co-pyrrole) was coated on the surface of reduced graphene oxide (rGO) through in situ chemical oxidative polymerization of aniline and pyrrole monomers. For comparison, rGO/polyaniline (PANi) and rGO/polypyrrole (PPy) were also prepared under the similar reaction condition, respectively. The resulting nanocomposites were characterized by field-emission scanning electron microscopy, atomic force microscopy, Fourier transform infrared and Raman spectrometry, and thermogravimetric analysis. Ultrathin layers of conducting polymers on the surface of rGO not only provide more electrochemically active sites but also shorten the distance for ion and electron transport, benefiting from the existence of strong interactions between polymeric chains and rGO. Besides, rGO in the composite can also provide an electron transfer path due to its excellent conductivity and high surface area. What is more, rGO/Copolymer exhibits the highest thermal stability and superior electrochemical stability among these composites, benefiting from its specific chemical structures, intrinsic electrochemical properties of three components, and more importantly, the synergistic effect in the composite. In 1 M Na2SO4 electrolyte, the specific capacitance of rGO/Copolymer was 541 F g−1 at the scan rate of 1 mV s−1, and 283 F g−1 at the scan rate of 20 mV s−1, respectively, which is larger than those for rGO/PANi and rGO/PPy. After 500 cycles, capacitance retention was 86% for rGO/Copolymer. These demonstrate that rGO/Copolymer can be applied as a high-performance electrode material for electrochemical supercapacitors
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2015.01.135Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2015.01.135;
- PII
- S0013-4686(15)00181-4;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 177
- Journal Page Range
- p. 335-342
- ISSN
- 0013-4686
- CODEN
- ELCAAV
Conference
- Title
- International conference on electrochemical energy science and technology
- Acronym
- EEST2014
- Dates
- 31 Oct - 4 Nov 2014
- Place
- Shanghai (China)
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47029684
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- ANILINE; ATOMIC FORCE MICROSCOPY; CAPACITIVE ENERGY STORAGE EQUIPMENT; COMPARATIVE EVALUATIONS; COPOLYMERS; ELECTROCHEMISTRY; ELECTRODES; FIELD EMISSION; FOURIER TRANSFORMATION; GRAPHENE; NANOCOMPOSITES; OXIDATION; OXIDES; POLYMERIZATION; PYRROLES; RAMAN SPECTROSCOPY; SCANNING ELECTRON MICROSCOPY; SODIUM SULFATES; SURFACES; THERMAL GRAVIMETRIC ANALYSIS
- Descriptors DEC
- ALKALI METAL COMPOUNDS; AMINES; AROMATICS; AZOLES; CARBON; CHALCOGENIDES; CHEMICAL ANALYSIS; CHEMICAL REACTIONS; CHEMISTRY; ELECTRON MICROSCOPY; ELEMENTS; EMISSION; EQUIPMENT; EVALUATION; GRAVIMETRIC ANALYSIS; HETEROCYCLIC COMPOUNDS; INTEGRAL TRANSFORMATIONS; LASER SPECTROSCOPY; MATERIALS; MICROSCOPY; NANOMATERIALS; NONMETALS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC POLYMERS; OXYGEN COMPOUNDS; POLYMERS; QUANTITATIVE CHEMICAL ANALYSIS; SODIUM COMPOUNDS; SPECTROSCOPY; SULFATES; SULFUR COMPOUNDS; THERMAL ANALYSIS; TRANSFORMATIONS
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.