4.6 Article

Synthesis of reduced graphene oxide by an ionothermal method and electrochemical performance

Journal

RSC ADVANCES
Volume 3, Issue 29, Pages 11807-11815

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3ra41485j

Keywords

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Funding

  1. National Natural Science Foundation of China [51001089, 51271169]
  2. Specialized Research Fund for the Doctoral Program of Higher Education of China [20100101120026]
  3. Key Science and Technology Innovation Team of Zhejiang Province [2010R50013]
  4. Natural Science Basic Research Open Foundation of the Key Lab of Automobile Materials, Ministry of Education, Jilin University [11-450060445349]

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An easy ionothermal method is proposed to deoxygenate graphene oxide (GO) for preparation of graphene by using a choline chloride (ChCl)/urea mixture-based ionic liquid. In the synthesis process, the urea portion in the ionic liquid breaks up to release NH3 at around 100 degrees C. This reacts with the oxygen functional groups of the GO sheets, leading to the formation of graphene. The ionothermal method is an environmentally-friendly and attractive strategy for reducing GO because both ChCl and urea are naturally biocompatible compounds. X-Ray photoelectron spectroscopy indicates that nitrogen atoms can be doped into the graphene skeleton accompanied by the reduction of GO. As an electrode for an electrochemical double layer capacitor in aqueous KOH, the ionothermally reduced GO exhibits a gravimetric capacitance of 155 F g(-1) at a current density of 0.2 A g(-1) and good cycling performance, which is comparable to the hydrazine reduced GO. We expect that the ionothermal method will have implications for the use of ionic liquids in the large-scale synthesis of graphene-based materials.

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