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Bimetallic MnNi-hydroxide electrodeposited on Ni-foam for superior water-splitting and energy storage.

Authors :
Srivastava, Rishabh
Bhardwaj, Shiva
Kumar, Anuj
Robinson, Alexandra N.
Sultana, Jolaikha
Mishra, Sanjay R.
Perez, Felio
Gupta, Ram K.
Source :
International Journal of Hydrogen Energy. Jan2024:Part C, Vol. 49, p971-983. 13p.
Publication Year :
2024

Abstract

Electrochemical energy conversion (via water splitting) and storage (via supercapacitors) are emerging strategies for developing the renewable energy sector; nevertheless, the hunt for low-cost and effective electrode material is a bottleneck issue. Herein, a bimetallic manganese nickel hydroxide was electrodeposited on Ni-foam without polymeric binder, followed by calcination to reveal its oxide configuration. As prepared, manganese nickel hydroxide (MnNi-hydroxide) displayed low Oxygen evolution reaction (OER) and Hydrogen evolution reaction (HER) overpotentials of 231 mV and 327 mV at 10 mA/cm2 during electrochemical water splitting, along with a superior turnover frequency of 0.12 sec−1 and 0.056 sec−1, respectively. Theoretical investigations revealed an increase in MnNi-hydroxide activity due to synergistic electronic interaction between Mn and Ni. Further, the MnNi-hydroxide, having high specific capacitances of 1174 mF/cm2 at 2 mV/s and 308 mF/cm2 at 1 mA/cm2, demonstrated a retention capacity of 98.9% over 5000 cycles. [Display omitted] • A bimetallic Mn-Ni hydroxide was electrodeposited on Ni-foam without polymeric binder. • Mn-Ni hydroxide displayed low OER and HER overpotentials of 231 mV and 327 mV at 10 mA/cm2. • This material also showed high specific capacitances of 1174 mF/cm2 at 2 mV/s and 308 mF/cm2 at 1 mA/cm2. • The synergistic interaction between Mn and Ni is a crucial factor in the efficient bifunctional activity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03603199
Volume :
49
Database :
Academic Search Index
Journal :
International Journal of Hydrogen Energy
Publication Type :
Academic Journal
Accession number :
174104599
Full Text :
https://doi.org/10.1016/j.ijhydene.2023.10.208