Freestanding (Ni<sub>4</sub>Zn)<sub>0.8</sub> Intermetallic Nanosheets as Bifunctional Electrocatalysts for Urea-Assisted Hydrogen Production
The electrochemical oxidation of urea provides an efficient and energy-saving method for the treatment of wastewater containing urea along with hydrogen production. However, it is crucial to develop electrocatalysts possessing both high electrocatalytic activity and long-term stability. In this study, a (Ni4Zn)0.8 intermetallic catalyst is deposited on nickel foam (labeled as (Ni4Zn)0.8/NF) by a rapid one-step electrodeposition technique. The as-deposited intermetallic catalyst can facilitate the hydrogen evolution reaction (HER) and urea oxidation reaction (UOR) simultaneously, displaying obvious bifunctional characteristics. Benefiting from metal–metal electronic modulation, the (Ni4Zn)0.8/NF integral electrode exhibits a low overpotential of 45 mV at −10 mA cm–2 with a small Tafel slope of 54.35 mV dec–1 in 1 M KOH solution for the HER; meanwhile, the as-obtained electrode requires only 1.40 V voltage to achieve the current density of 100 mA cm–2 in 1 M KOH with 0.5 M urea. Employing the as-prepared (Ni4Zn)0.8/NF electrode as the anode and cathode simultaneously, the urea-assisted water electrolysis device (HER||UOR system) exhibits a voltage reduction of 258 mV against the conventional water electrolysis device (HER||OER system), which offers a catalyst selection for the HER||UOR in practical application.
Authors
- Yonghong Ni (ORCID: https://orcid.org/0000-0002-4979-9867)
- Shaoxia Wang (ORCID: https://orcid.org/0000-0002-1762-8684)
- Huihui Li (ORCID: https://orcid.org/0000-0002-1579-323X)
- Shifeng Li (ORCID: https://orcid.org/0000-0002-4668-8758)
- Qianqian Zhu (ORCID: https://orcid.org/0009-0001-2948-0381)
Institutions
- Anhui Normal University (CN)
Publication Details
- Journal
- ACS Applied Nano Materials
- Published
- 2024-08-09
- DOI
- https://doi.org/10.1021/acsanm.4c02488
- Citations
- 2
- Primary Topic
- Electrocatalysts for Energy Conversion
- Type
- article
- Field-Weighted Citation Impact
- 0.20