The
design and development of bifunctional electrocatalysts that
can catalyze both the oxygen evolution reaction and oxygen reduction
reaction (OER/ORR) is a burning issue for energy conversion and storage
technologies. Herein, we demonstrate the bifunctional activity of
CeO2 nanospheres embedded in NiO nanoflakes. The CeO2/NiO nanocomposites are synthesized solvothermally by varying
their molar ratios. Among the synthesized nanocomposites, CeO2/NiO-2 exhibits an outstanding OER/ORR activity compared to
those of individual counterparts and other compositions and outperforms
the benchmark ORR catalyst Pt/C and the OER catalyst IrO2 in terms of stability. The CeO2/NiO-2 nanocomposite shows
the low onset potential of 1.47 and 0.8 V (vs reversible hydrogen
electrode) for OER and ORR, respectively. Moreover, a low potential
difference (i.e., ΔE) of 0.86 V between the
potential for 10 mA cm–2 OER current density and
the ORR half-wave potential for CeO2/NiO-2 makes it an
efficient bifunctional oxygen electrocatalyst. The excellent bifunctional
activity of the nanocomposite is ascribed to the electronic synergy
between CeO2 and NiO, which leads to the formation of an
increased number of oxygen vacancy defects as well as more accessible
active sites at an optimum molar ratio of CeO2 and NiO.
The unique morphology of CeO2 nanospheres embedded in NiO
nanoflakes facilitates the exposure of surface-active sites with the
bifunctional nature of the catalyst. The practical applicability of
the CeO2/NiO-2 nanocomposite is demonstrated with a Zn–air
battery, which delivers 1.41 V open-circuit voltage and 105.0 mW cm–2 peak power density. It has long-term cycling stability
for 22 h with negligible voltaic efficiency loss.