Anchoring Polydopamine on ZnCo 2 O 4 Nanowire To Facilitate Urea Water Electrolysis
To overcome the sluggishness of the oxygen evolution reaction (OER), the urea oxidation reaction was developed. In the case of OER application studies ZnCo 2 O 4 is an excellent electrocatalyst, towards the UOR has been performed with surface‐grown polydopamine (PDA) with surface‐grown polydopamine...
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Veröffentlicht in: | Chemistry : a European journal 2023-09, Vol.29 (54) |
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Sprache: | eng |
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Zusammenfassung: | To overcome the sluggishness of the oxygen evolution reaction (OER), the urea oxidation reaction was developed. In the case of OER application studies ZnCo
2
O
4
is an excellent electrocatalyst, towards the UOR has been performed with surface‐grown polydopamine (PDA) with surface‐grown polydopamine (PDA). ZnCo
2
O
4
@PDA is produced over the surface of nickel foam by a hydrothermal method followed by self‐polymerization of dopamine hydrochloride. Dopamine hydrochloride was varied in solution to study the optimal growth of PDA necessary to enhance the electrochemical activity. Prepared ZnCo
2
O
4
@PDA was characterized by X‐ray diffraction, electronic structural, and morphology/microstructure studies. With successful confirmation, the developed electrode material was applied to UOR and ZnCo
2
O
4
@PDA‐1.5, delivering an excellent low overpotential of 80 mV at 20 mA cm
−2
in the electrolyte mixture of 1 M potassium hydroxide+0.33 M urea. To support the excellent UOR activity, other electrochemical properties such as the Tafel slope, electrochemical surface active sites, and electrochemical impedance spectroscopy were also studied. Furthermore, a schematic illustration explaining the UOR mechanism is shown to allow a clear understanding of the obtained electrochemical activity. Finally, urea water electrolysis was carried out in a two‐electrode symmetrical cell and compared with water electrolysis. This clearly showed the potential of the developed material for efficient electrochemical hydrogen production. |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.202301872 |