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Cobalt Titanate–Phosphorous-Doped g-C3N4 Heterostructure with Impressive Electrocatalytic Activity for Oxygen Evolution Reaction.
- Source :
- Journal of Electronic Materials; Aug2024, Vol. 53 Issue 8, p4740-4750, 11p
- Publication Year :
- 2024
-
Abstract
- Hydrogen (H<subscript>2</subscript>) is a viable alternative to the finite fossil fuels to meet the escalating energy demands. Water splitting is a cleaner way of producing H<subscript>2</subscript>, which can effectively generate electricity via fuel cells. The slower oxygen evolution reaction (OER) with large overpotential hinders the practicality of the electrocatalytic water-splitting process to generate H<subscript>2</subscript>. Cobalt titanate (CoTiO<subscript>3</subscript>) and graphitic carbon nitride (g-C<subscript>3</subscript>N<subscript>4</subscript>) are promising candidates for OER catalysts. The composite of CoTiO<subscript>3</subscript> supported on phosphorous doped g-C<subscript>3</subscript>N<subscript>4</subscript> substrate (CoTiO<subscript>3</subscript>/P-C<subscript>3</subscript>N<subscript>4</subscript>) has been synthesized and demonstrated as an excellent electrocatalyst with enhanced charge transport properties exhibiting a lower overpotential of 310.0 mV, a lower charge transfer resistance (R<subscript>ct</subscript>) and faster OER kinetics. The synergistic interaction of CoTiO<subscript>3</subscript> and P-C<subscript>3</subscript>N<subscript>4</subscript> at the hetero-interface has resulted in enhancing the conductivity and the accessible active sites. The composite also exhibited appreciable operational stability and Faradaic efficiency. CoTiO<subscript>3</subscript>/P-C<subscript>3</subscript>N<subscript>4</subscript> was thus proved to be competent to substitute the unstable and expensive benchmark catalysts in terms of cost, activity, and stability. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03615235
- Volume :
- 53
- Issue :
- 8
- Database :
- Complementary Index
- Journal :
- Journal of Electronic Materials
- Publication Type :
- Academic Journal
- Accession number :
- 178208865
- Full Text :
- https://doi.org/10.1007/s11664-024-11148-z