Transition
metal sulfides (TMS) exhibit proliferated edge sites,
facile electrode kinetics, and improved intrinsic electrical conductivity,
which demand low potential requirements for total water splitting
application. Here, we have propounded copper sulfide-coupled cobalt
sulfide nanosheets grown on 3D nickel as an electrocatalyst for hydrogen
(HER) and oxygen evolution (OER) reactions. The formation of djurleite
copper sulfide with a Cu vacancy enables faster H+ ion
transport and shows improved HER activity with a remarkably lower
overpotential of 164 mV at 10 mA/cm2, whereas cobalt-incorporated
copper sulfide undergoes cation exchange during synthesis and shows
elevated OER activity with a lower overpotential of 240 mV at 10 mA/cm2 for the OER. Moreover, Cu2–x
S/Co is said to have a hybrid CoS–CoS2 interface
and provide Co2+ active sites on the surface and enable
the fast adsorption of intermediate species (OH*, O*, and OOH*), which
lowers the potential requirement. The copper vacancy and cation exchange
with a hybrid CoS–CoS2 structure are helpful in
supplying more surface reactive species and faster ion transport for
the HER and OER, respectively. The full-cell electrolyzer requires
a very low potential of 1.58 V to attain a current density of 10 mA/cm2, and it shows excellent stability for 50 h at 100 mA/cm2 as confirmed by the chronopotentiometry test.