One-pot synthesis of magnetite nanorods/graphene composites and its catalytic activity toward electrochemical detection of dopamine

  • J. Salamon
  • , Y. Sathishkumar
  • , K. Ramachandran
  • , Yang Soo Lee
  • , Dong Jin Yoo*
  • , Ae Rhan Kim
  • , G. GnanaKumar
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

Magnetite (Fe3O4) nanorods anchored over reduced graphene oxide (rGO) were synthesized through a one-pot synthesis method, where the reduction of GO and in-situ generation of Fe3O4 nanorods occurred concurrently. The average head and tail diameter of Fe3O4 nanorods anchored over the rGO matrix are found to be 32 and 11nm, respectively, and morphology, structure and diameter of bare Fe3O4 nanorods were not altered even after the composite formation with rGO. The increased structural disorders and decrement in the sp2 domains stimulated the high electrical conductivity and extended catalytic active sites for the prepared rGO/Fe3O4 nanocomposite. The constructed rGO/Fe3O4/GCE sensor exhibited excellent electrocatalytic activity toward the electrooxidation of dopamine (DA) with a quick response time of 6s, a wide linear range between 0.01 and 100.55μM, high sensitivity of 3.15μAμM-1cm-2 and a lower detection limit of 7nM. Furthermore, the fabricated sensor exhibited a practical applicability in the quantification of DA in urine samples with an excellent recovery rate. The excellent electroanalytical performances and straight-forward, surfactant and template free preparation method construct the rGO/Fe3O4 composite as an extremely promising material for the diagnosis of DA related diseases in biomedical applications.

Original languageEnglish
Pages (from-to)269-276
Number of pages8
JournalBiosensors and Bioelectronics
Volume64
DOIs
StatePublished - 2015.02.15

Keywords

  • Active sites
  • Electrooxidation
  • Magnetite nanorods
  • Restacking
  • Sensitivity

Quacquarelli Symonds(QS) Subject Topics

  • Chemistry
  • Biological Sciences

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