4.7 Article

Facile fabrication of hierarchically porous Ni foam@Ag-Ni catalyst for efficient hydrazine oxidation in alkaline medium

出版社

ELSEVIER
DOI: 10.1016/j.jtice.2019.09.022

关键词

Silver; Templated electrodeposition; Hierarchical structure; Hydrazine oxidation

资金

  1. National Natural Science Foundation of China [21706198]
  2. Natural Science Foundation of Hubei Province [2018CFB214]
  3. Open Foundation from Key Laboratory of Hubei Province for Coal Conversion and New Carbon Materials [WKDM201710, WKDM201712]
  4. Key Laboratory of Hubei Province Efficient Utilization and Agglomeration of Metallurgic Mineral Resources [2017zy007]

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With the procedure of H-2 gas templated electrodeposition and subsequent galvanic replacement reaction, we successfully fabricate the Ni foam@Ag-Ni (Ni foam coated with Ag-Ni bimetals) electrode. Results show the electrodeposition time of 1.5 min produces Ni foam@Ni (Ni foam coated with Ni) with the largest mass specific surface area, and the galvanic replacement time of 8 min yields Ni foam@Ag-Ni with the most favorable catalytic activity toward hydrazine oxidation reaction (HzOR). Materials characterizations reveal the formation of Ag-Ni alloy, the presence of hierarchical pore-structure, the large superficial metallic Ni content and the low amount of Ag mass loading (0.0765 mg cm(-2)) in Ni foam@Ag-Ni. Electrochemical evaluations show the optimized Ni foam@Ag-Ni electrode delivers the significantly lowest onset potential toward HzOR, with a negative shift of similar to 260 mV than Ni foam, similar to 220 mV than Ni foam@Ni and similar to 60 mV than Ni foam@Ag. Furthermore, it exerts the highest current density in 1.0 mol L-1 KOH and 25 mmol L-1 N2H4, more than 2 fold that of the Ni foam, Ni foam@Ni and Ni foam@Ag at -0.05 V versus Ag/AgCl. The superiority in micro-scale construction and surface composition also endows Ni foam@Ag-Ni electrode with the remarkable durability and considerable whole-cell performance. (C) 2019 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.

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