Insight into a pure spinel Co3O4 and boron, nitrogen, sulphur (BNS) tri-doped Co3O4-rGO nanocomposite for the electrocatalytic oxygen reduction reaction

The intricate problems concerning energy require innovative solutions. Herein, we propose a smart composite nano system that can be used in a sustainable and dichotomous manner to resolve energy crises. The current study describes a new way to synthesize a pure spinel cobalt oxide (Co3O4) and boron...

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Veröffentlicht in:RSC advances 2023-10, Vol.13 (41), p.28602-28612
Hauptverfasser: Afia Kanwal Bhatti, Jabeen, Naila, Bashir, Amna, Khan, Latif U, Bokhari, Syeda Wishal, Akhter, Zareen
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Sprache:eng
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Zusammenfassung:The intricate problems concerning energy require innovative solutions. Herein, we propose a smart composite nano system that can be used in a sustainable and dichotomous manner to resolve energy crises. The current study describes a new way to synthesize a pure spinel cobalt oxide (Co3O4) and boron (B), nitrogen (N), and sulfur (S) tri-doped Co3O4-reduced graphite oxide (rGO) nanocomposite (CBNS). A hydrothermal method has been used for the synthesis of these nanomaterials. The synthesized nanocomposite was characterized by UV-visible spectroscopy, X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), X-ray absorption spectroscopy (XAS), and transmission electron microscopy (TEM). The XRD results showed the formation of Co3O4 and B, N, S doped nanocomposite with high purity and crystallinity. XAS analysis elucidates the formation of spinel Co3O4 with tetrahedral and octahedral arrangement of cobalt ions. The peaks at 2.50 Å and 3.07 Å are due to the Co–Co bonding. The electrocatalytic oxygen reduction (ORR) was successfully implemented using these nanocomposites. The electrochemical study exhibits the better activity of the B, N, and S tri-doped Co3O4-rGO nanocomposite due to the mutual effect of B, N and S. The synthesized catalyst has maximum current density of 9.97 mA cm−2 with onset potential (Eonset) of 0.98 V in alkaline medium.
ISSN:2046-2069
DOI:10.1039/d3ra04600a