4.8 Article

Hierarchical Structure of CuO Nanowires Decorated with Ni(OH)2 Supported on Cu Foam for Hydrogen Production via Urea Electrocatalysis

Journal

SMALL METHODS
Volume 6, Issue 1, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smtd.202101017

Keywords

electrocatalysis; hierarchical structures; hydrogen production; oxygen evolution reaction; urea oxidation reaction

Funding

  1. Ministry of Science, ICT [NRF2017M3A7B4049547, NRF-2019R1A2C2006006, 2021M3H4A1A01079300]
  2. Research Grant Council of Hong Kong [16201820, 16206019]
  3. Max Planck-POSTECH-Hsinchu Center for Complex Phase Materials
  4. Ministry of Science & ICT (MSIT), Republic of Korea [N10210012] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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By constructing a hierarchical structure of CuO nanowires decorated with nickel hydroxide on 3D Cu foam, this research achieved a significant reduction in the potential of urea oxidation reaction to 1.334 V, along with enhanced activity up to 100 mA cm(-2), and exceptional stability. Electrolysis of urea using this developed electrocatalyst as the anode showed promising results in terms of energy-saving hydrogen production.
Owing to the low theoretical potential of the urea oxidation reaction (UOR), urea electrolysis is an energy-saving technique for the generation of hydrogen. Herein, a hierarchical structure of CuO nanowires decorated with nickel hydroxide supported on 3D Cu foam is constructed. Combined theoretical and experimental analyses demonstrate the high reactivity and selectivity of CuO and Ni(OH)(2) toward the UOR instead of the oxygen evolution reaction. The hierarchical structure creates a synergistic effect between the two highly active sites, enabling an exceptional UOR activity with a record low potential of 1.334 V (vs the reversible hydrogen electrode) to reach 100 mA cm(-2) and a low Tafel slope of 14 mV dec(-1) in 1 m KOH and 0.5 m urea electrolyte. Assembling full urea electrolysis driven by this developed UOR electrocatalyst as the anode and a commercial Pt/C electrocatalyst as the cathode provides a current density of 20 mA cm(-2) at a cell voltage of approximate to 1.36 V with promising operational stability for at least 150 h. This work not only enriches the UOR material family but also significantly advances energy-saving hydrogen production.

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