Substituting
the energy-uphill water oxidation half-cell with readily
oxidizable urea-rich urine, a ground-breaking bridge is constructed,
combining the energy-efficient hydrogen generation and environmental
protection. Hence, designing a robust multifunctional electrocatalyst
is desirable for widespread implementation of this waste to fuel technology.
In this context, here, we report a simple tuning of the electrocatalytically
favorable characteristics of NiCo-layered double hydroxide by introducing
[MoS4]2– in its interlayer space. The
[MoS4]2– insertion as well as its effect
on the electronic structure tuning is thoroughly studied via X-ray
photoelectron spectroscopy in combination with electrochemical analysis.
This insertion induces overall electronic structure tuning of the
hydroxide layer in such a way that the designed catalyst exhibited
favorable kinetics toward all the required reactions of hydrogen generation.
This is why our homemade catalyst, when utilized both as a cathode
and anode to fabricate a urea electrolyzer, required a mere ∼1.37
V cell potential to generate sufficient H2 by reaching
the benchmark 10 mA cm–2 in 1 M KOH/0.33 M urea
along with long-lasting catalytic efficiency. Other indispensable
reason of selecting [MoS4]2– is its high-valent
nature making the catalyst highly selective and insensitive to common
catalyst-poisoning toxins of urine. This is experimentally supported
by performing the real urine electrolysis, where the nanospike-covered
Ni foam-based catalyst showed a performance similar to that of synthetic
urea, offering its industrial value. Other intuition of selecting
[MoS4]2– was to provide a ligand-based
mechanism for hydrogen evolution half-cell [hydrogen evolution reaction
(HER)] to preclude the HER-competing oxygen reduction. Another crucial
point of our work is its potential to avoid the mixing of two explosive
product gases, that is, H2 and O2.