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Engineered CoS/Ni 3 S 2 Heterointerface Catalysts Grown Directly on Carbon Paper as an Efficient Electrocatalyst for Urea Oxidation.
- Source :
- Catalysts (2073-4344); Sep2024, Vol. 14 Issue 9, p570, 16p
- Publication Year :
- 2024
-
Abstract
- Developing highly efficient and stable electrocatalysts for urea electro-oxidation reactions (UORs) will improve wastewater treatment and energy conversion. A low-cost cobalt sulfide-anchored nickel sulfide electrode (CoS/Ni<subscript>3</subscript>S<subscript>2</subscript>@CP) was synthesized by electrodeposition in DMSO solutions and found to be highly effective and long-lasting. The morphology and composition of catalyst surfaces were examined using comprehensive physicochemical and electrochemical characterization. Specifically, CoS/Ni<subscript>3</subscript>S<subscript>2</subscript>@CP electrodes require a potential of 1.52 volts for a 50 mA/cm<superscript>2</superscript> current, confirming CoS in the heterointerface CoS/Ni<subscript>3</subscript>S<subscript>2</subscript>@CP catalyst. Further, the optimized CoS/Ni<subscript>3</subscript>S<subscript>2</subscript>@CP catalyst shows a decrease of 100 mV in the onset potential (1.32 V<subscript>RHE</subscript>) for UORs compared to bare Ni<subscript>3</subscript>S<subscript>2</subscript>@CP catalysts (1.42 V<subscript>RHE</subscript>), demonstrating much greater performance of UORs. As compared to Ni<subscript>3</subscript>S<subscript>2</subscript>@CP, CoS/Ni<subscript>3</subscript>S<subscript>2</subscript>@CP exhibits twofold greater UOR efficiency as a result of a larger electroactive surface area. The results obtained indicate that the synthetic CoS/Ni<subscript>3</subscript>S<subscript>2</subscript>@CP catalyst may be a favorable electrode material for managing urea-rich wastewater and generating H<subscript>2</subscript>. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 20734344
- Volume :
- 14
- Issue :
- 9
- Database :
- Complementary Index
- Journal :
- Catalysts (2073-4344)
- Publication Type :
- Academic Journal
- Accession number :
- 180009707
- Full Text :
- https://doi.org/10.3390/catal14090570