Journal
SMALL
Volume 17, Issue 19, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202008148
Keywords
hydrazine oxidation; hydrogen evolution; nanorod‐ confined‐ nanoflake array; superhydrophilic; waste battery
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Funding
- National Natural Science Foundation of China [52072359]
- Recruitment Program of Global Experts
- Fundamental Research Funds for the Central Universities [WK2060000016]
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In this study, superhydrophilic Ni-based multicomponent arrays were successfully designed and synthesized, allowing for hydrazine oxidation reaction and hydrogen evolution reaction to occur at very low working potentials with excellent bifunctional activity for overall hydrazine splitting.
The low thermodynamic potential (-0.33 V) and safe by-product of N-2/H2O, make utilizing hydrazine oxidation reaction (HzOR) to replace thermodynamically-unfavorable and kinetically-sluggish oxygen evolution reaction a promising tactic for energy-efficient hydrogen production. However, the complexity of bifunctionality increases difficulties for effective material design, thus hindering the large-scale hydrogen generation. Herein, we present the rationally designed synthesis of superhydrophilic Ni-based multicomponent arrays (Ni NCNAs) composed of 1D nanorod-confined-nanoflakes (2D), which only needs -26 mV of working potential and 47 mV of overpotential to reach 10 mA cm(-2) for HzOR and HER, respectively. Impressively, this Ni NCNA electrode exhibits the top-level bifunctional activity for overall hydrazine splitting (OHzS) with an ultralow voltage of 23 mV at 10 mA cm(-2) and a record-high current density of 892 mA cm(-2) at just 0.485 V, also achieves the high-speed hydrogen yield driven by a waste AAA battery for OHzS.
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