Efficient electrocatalytic performance of thermally exfoliated reduced graphene oxide-Pt hybrid. (October 2015)

• Record Type: Journal Article
• Authors: Antony, Rajini P.; Preethi, L.K.; Gupta, Bhavana; Mathews, Tom; Dash, S.; Tyagi, A.K.
• Is Part Of: Materials research bulletin. Volume 70(2015:Oct.)
• Page Start: 60
• Page End: 67
• Publication Date: 2015-10
• Subjects: A. Nanostructures -- C. Electrochemical measurements -- C. Elelctrochemical impedance spectroscopy -- D. Catalytic properties -- D. Electrochemical properties; Materials -- Periodicals; Crystal growth -- Periodicals; Matériaux -- Périodiques; Cristaux -- Croissance -- Périodiques; Crystal growth; Materials; Periodicals; 620.11
• DOI: 10.1016/j.materresbull.2015.04.015
• Languages: English
• ISSNs: 0025-5408

Abstract

Graphical abstract: Highlights: Synthesis of Pt–RGO nanohybrids of very high electrochemically active surface area. Electrocatalytic activity-cum-stability: ∼10 times that of commercial Pt-C catalyst. TEM confirms narrow size distribution and excellent dispersion of Pt nanoparticles. SAED and XRD indicate (1 1 1) orientation of Pt nanoparticles. Methanol oxidation EIS reveal decrease in charge transfer resistance with potential Abstract: High quality thermally exfoliated reduced graphene oxide (RGO) nanosheets decorated with platinum nanocrystals have been synthesized using a simple environmentally benign process. The electrocatalytic behaviour of the Pt–RGO nanohybrid for methanol oxidation was studied using cyclic voltammetry, chronoamperometry and electrochemical impedance spectroscopy. High resolution transmission electron microscopy shows uniform dispersion of Pt nanoparticles of ∼2–4 nm size. X-ray diffraction and selected area diffraction studies reveal (1 1 1) orientation of the platinum nanoparticles. The cyclic voltammetry and chronoamperometry results indicate higher catalytic activity and stability for Pt–RGO compared to commercial Pt-C. The electrochemical active surface area of Pt–RGO (52.16 m 2 /g) is found to be 1.5 times that of commercial Pt-C. Impedance spectroscopy shows different impedance behaviour at different potential regions, indicating change in methanol oxidation reaction mechanism with potential. The reversal of impedance pattern to the second quadrant, at potentials higher than ∼0.40 V, indicates change in the rate determining reaction.