Modified carbon substrates for electrocatalytic oxidation of selected heterocyclic carbinols

Title

Modified carbon substrates for electrocatalytic oxidation of selected heterocyclic carbinols

Creator

Mathew, Agnus T.

Contributor

Varghese, Anitha.

Description

Electrochemically modified carbon electrodes are used as a substrate for electrocatalytic oxidation of different heterocyclic carbinols. Carbon fiber paper (CFP) is newlineused as the electrode substrate on which various modifications are employed. Modified newlineelectrodes were prepared by using different surface modification strategies such as newlineelectrodeposition of Pd nanoparticles or Pd-Pt bimetallic nanoparticles on a conducting newlinepolymer, polyaniline which is electropolymerized on to CFP. Biomass derived porous carbon nanoparticle coated CFP was also used for electrodeposition of Pd nanoparticles or MnO2-Pi nanoparticles. These modified electrodes were physicochemically characterized by X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM) with energy-dispersive X-ray spectroscopy (EDS), Transmission electron microscopy (TEM), Raman spectroscopy, Fourier transform infrared (FTIR) spectroscopy, Optical profilometry and X-ray photoelectron spectroscopy (XPS) and electrochemically characterized using Cyclic voltammetry (CV) and Electrochemical impedance spectroscopy (EIS). This modification methods have attracted a lot of attention due to their exceptional stability, high electronic conductivity, mechanical strength, and good adhesive property to the substrate and to the modified electrode. The modified electrodes show excellent electrochemical and newlinephysicochemical properties which are demonstrated using various analytical techniques. The organocatalytic reagent, TEMPO is used as a mediator throughout the studies which helps to carry out the oxidation of organic molecules in an aqueous acidic medium. The developed electrodes have been successfully applied for the oxidation of different heterocyclic alcohol such as 4-pyridinemethanol, 2-thiophene methanol, and 2-Furfuryl alcohol to corresponding 4-pyridinemethanal, 2-thiophene methanol and 2-Furfural.

Source

Author's Submission

Date

2022-01-01

Publisher

Christ(Deemed to be University)

Subject

Chemistry

Rights

Open Access

Relation

61000177

Format

PDF

Language

English

Type

PhD

Identifier

http://hdl.handle.net/10603/426627