4.5 Article

Enhanced oxygen evolution reaction on polyethyleneimine functionalized graphene oxide in alkaline medium

Journal

MOLECULAR CATALYSIS
Volume 516, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.mcat.2021.111960

Keywords

Graphene Oxide; Polymeric Amine, Monomeric Amine, Cross-linking; OER

Funding

  1. Qatar National Research Fund under National Priorities Research Program [NPRP12S-0131-190024]
  2. Qatar Shell Research and Technology Center (QSRTC)
  3. Ministry of Higher Education through Universiti Teknologi Malaysia [Q.K130000.21A6.00P22]

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Synthesis and functionalization of graphene oxide via a modified Tour's method result in excellent catalytic performance and stability, providing a valuable route for the development and practical application of metal-free catalytic materials for water oxidation reaction.
Practical applications of metal free catalysts are hindered by their innate poor stability for electrocatalytic application. Accordingly, in this study, synthesis and functionalization of graphene oxide via a modified Tour's method (GOT) with different amine containing molecules results in excellent catalytic performance and stability toward OER in alkaline medium. The as-synthesized polyethyleneimine GOT electrode (P-GOT), produced current densities of 10, 50 and 100 mA/cm(2) at overpotentials of 240, 350 and 420 mV, respectively, with small Tafel slope of 47 mV/dec. The X-ray diffraction analysis (XRD), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) analysis confirms the successful functionalization of GOT by ethylenediamine (E) and polyethyleneimine (P) molecules, respectively. Morphological studies based on field emission scanning electron microscopy (FESEM) confirm that the modification via covalent bonding preserved the original wrinkled and layered structure of GOT. The P-GOT with cross-linked amine can expose more active sites and is not easy to peel off, which corresponds to attaining lower charge transfer resistance (1.01 Omega cm(2)) and remarkable current stability in 1.0 M KOH solution, compared to the pristine GOT and E-GOT electrodes. From this perspective, our results therefore provide a valuable route for development and practical application of metal free catalytic materials for water oxidation reaction.

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