4.7 Article

Hierarchical self-supported NiSe2/TiN@Ni12P5 on nickel foam for the urea oxidation reaction

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 47, Issue 87, Pages 36814-36822

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.08.182

Keywords

Urea oxidation reaction; Integrated electrode; Dispersion strengthening; Ultra-low potential

Funding

  1. National Natural Science Foundation of China [51874154, 22109034, 22109035, 52164028, 62105083]
  2. Kunming University of Science and Technology
  3. Natural Science Foundation of Hainan Province [221RC1018]
  4. Foundation of State Key Laboratory of Marine Resource Utilization in South China Sea (Hainan University) [MRUKF2021029]
  5. Postdoctoral Science Foundation of Hainan Province [RZ2100007123]
  6. Start-up Reuter Foundation of Hainan University [KYQD(ZR)-20008, 20082, 20083, 20084, 21065, 21124, 21125]

Ask authors/readers for more resources

In this study, NiSe2/TiN@Ni12P5/NF catalysts with a stalactite structure were prepared by chemical vapor deposition for urea oxidation reaction, showing excellent activity and stability.
The development of high-performance, low-cost, and non-noble metal catalysts for the urea oxidation reaction (UOR) as an alternative to oxygen evolution reaction (OER) has received much attention but remains a huge challenge. In this work, NiSe2/TiN@Ni12P5/NF catalysts with a stalactite structure were prepared by chemical vapor deposition to obtain the integrated electrode Ni12P5/NF on the nickel foam (NF), and subsequently NiSe2/TiN was formed on the Ni12P5/NF surface by the hydrothermal method. The designed catalyst delivers an ultra-low potential of 1.270 Vat 10 mA cm-2, and a Tafel slope of 33.3 mV dec-1 for UOR. Furthermore, the catalyst only shows a 1.7% decrease in potential after an 80-h stability test, which demonstrates its excellent stability. The prepared NiSe2/TiN@Ni12P5/ NF shows a high specific surface area, and the strengthening effect between TiN and NiSe2, endowing the catalyst a high activity and durability. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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