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)
Hauptverfasser: Bhanuse, Gita B., Kumar, Sanath, Fu, Yen‐Pei
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Kumar, Sanath
Fu, Yen‐Pei
description 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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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. 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