Electrooxidation of Hydrazine Utilizing High-Entropy Alloys: Assisting the Oxygen Evolution Reaction at the Thermodynamic Voltage

Journal article


Kumar, N., Dhakar, Shikha, Parui, Arko, Gakhad, Pooja, Singh, A., Biswas, K., Tiwary, C. and Sharma, S. (2021). Electrooxidation of Hydrazine Utilizing High-Entropy Alloys: Assisting the Oxygen Evolution Reaction at the Thermodynamic Voltage. ACS Catalysis. 11 (22), pp. 14000-14007. https://doi.org/10.1021/acscatal.1c03571
AuthorsKumar, N., Dhakar, Shikha, Parui, Arko, Gakhad, Pooja, Singh, A., Biswas, K., Tiwary, C. and Sharma, S.
Abstract

Hydrazine electrooxidation is an important reaction as it assists in decreasing the OER overvoltage. Herein, we report the utilization of high entropy nano-catalyst alloy for the electrooxidation of hydrazine. High entropy nano-catalyst comprising five elements (Ag, Au, Pt, Pd, Cu) shows profound activity towards this molecule at low overvoltage. An intriguingly high entropy nano-catalyst prepared by the casting-cum-cryomilling method is endowed with unique catalytic activity for HzOR. Detailed analysis of gaseous product points to the formation of nitrogen as well as oxygen as the oxidation product, a sign of accompanying oxygen evolution reaction (OER). Interestingly, significant oxygen is detected at 1.13 V (RHE) in a neutral buffered medium, confirming that OER is functional at a voltage near to the thermodynamic voltage of 1.23V (RHE). The quantitative contribution of each hydrazine and OER reaction is ascertained which explains a vital insight into this reaction. Density functional theory calculations showed that both HzOR and OER assist each other where the electron-donating effect of H2O to the surface can reduce the endothermicity of the HzOR. Whereas, the electron acceptance of *NHNH2 helps in the favorable overlap of the HEA Fermi level and vacant states with the HOMO of H2O.

KeywordsCatalysis; General Chemistry
Year2021
JournalACS Catalysis
Journal citation11 (22), pp. 14000-14007
PublisherAmerican Chemical Society (ACS)
ISSN2155-5435
Digital Object Identifier (DOI)https://doi.org/10.1021/acscatal.1c03571
Web address (URL)https://pubs.acs.org/doi/abs/10.1021/acscatal.1c03571
Funder/ClientDepartment of Scientific and Industrial Research, Ministry of Science and Technology, India
Science and Engineering Research Board
Air Force Office of Scientific Research
Ministry of Human Resource Development
Publication dates
Print19 Nov 2021
Online04 Nov 2021
Publication process dates
Accepted18 Oct 2021
Deposited20 Oct 2021
Accepted author manuscript
Page range14000-14007
Permalink -

https://openresearch.lsbu.ac.uk/item/8y23y

Download files


Accepted author manuscript
  • 16
    total views
  • 1
    total downloads
  • 0
    views this month
  • 0
    downloads this month

Export as