Exploring Enhanced Oxygen Reduction Reactions: A Study on Nanocellulose, Dopamine, and Cobalt Complex-Derived Non-Precious Electrocatalyst

Author:

Patwary Md Mohsin1,Haque Shanzida12,Szwedo Peter1,Hasan Ghada1,Kondrapolu Raja Shekhar1,Watanabe Fumiya3,KC Krishna1,Wang Daoyuan4,Ghosh Anindya1

Affiliation:

1. School of Physical Sciences, University of Arkansas at Little Rock, 2801 South University Avenue, Little Rock, AR 72204, USA

2. Department of Physics, Comilla University, Cumilla 3506, Bangladesh

3. Center for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, 2801 South University Avenue, Little Rock, AR 72204, USA

4. Department of Chemistry and Physics, University of Arkansas at Pine Bluff, 1200 North University Drive, Pine Bluff, AR 71601, USA

Abstract

Cobalt-based catalysts are recognized as promising electrocatalysts for oxygen reduction reactions (ORRs) in fuel cells that operate within acidic electrolytes. A synthesis process involving a cobalt complex, nanocellulose, and dopamine, followed by pyrolysis at 500 °C under a nitrogen atmosphere, was used to create a cobalt and nitrogen-doped carbonaceous material. Additionally, urea was incorporated to enhance nitrogen doping in the carbonaceous material. The morphology and structure of the material were examined using Scanning Electron Microscopy (SEM) and X-ray Diffraction (XRD), where SEM unveiled dispersed metal oxides within the carbonaceous framework. Energy Dispersive X-ray Spectroscopy (EDS) analysis showed an even distribution of elements across the cobalt-doped carbonaceous material. X-ray Photoelectron Spectroscopy (XPS) analysis further highlighted significant alterations in the elemental composition due to pyrolysis. The electrochemical behavior of the cobalt-doped carbonaceous material, with respect to the oxygen reduction reaction (ORR) in an acidic medium, was investigated via cyclic voltammetry (CV), revealing an ORR peak at 0.30 V against a reversible hydrogen reference electrode, accompanied by a notably high current density. The catalyst’s performance was evaluated across different pH levels and with various layers deposited, showing enhanced effectiveness in acidic conditions and a more pronounced reduction peak with uniformly applied electrode layers. Rotating disk electrode (RDE) studies corroborated the mechanism of a four-electron reduction of oxygen to water, emphasizing the catalyst’s efficiency.

Funder

National Science Foundation

Publisher

MDPI AG

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