Efficient
bifunctional catalysts are highly desirable for Li–O2 batteries to accerlerate the oxygen reduction and oxygen
evolution reactions. Surface/interface regulation or doping has been
used to enhance the activity of the catalysts. Herein, we propose
a facile synchronous reduction strategy to fabricate a yolk–shell
Co3O4@Co3O4/Ag hybrid
which integrates the advantages of surface, interface, and doping
engineering as a highly active catalyst for Li-O2 batteries.
The Co3O4@Co3O4/Ag-based
cathode shows a high initial capacity (12000 mAh g–1@200 mA g–1), high rate capability (4700 mAh g–1@800 mA g–1), low overpotential,
and long cycle life due to the synergetic interactions of surface,
interface, and doping engineering. The underling synergetic mechanism
has been uncovered by X-ray diffraction, X-ray photoelectron spectroscopy,
X-ray absorption near-edge structure spectra, aberration-corrected
scanning transmission electron microscopy, electrochemical impedance
spectra, and ex situ scanning electron microscopy. For Co3O4@Co3O4/Ag, part of Ag has formed
on the surface of Co3O4 shell as single atoms
or clusters and a fraction of Ag has been doped into the crystal lattice
of Co3O4 at the same time, which not only strengthens
the Ag–Co3O4 interface binding but also
tailors the valence electronic structure of Ag and Co species as well
as improves the electronic conductivity. This particular architecture
provides more active sites for the ORR/OER and also enhances the catalytic
activity. In addition, flowerlike Li2O2 forms
on the Co3O4@Co3O4/Ag
cathode, which is more feasible to decompose in comparison to toroidal-like
Li2O2. This study offers some insights into
designing efficient cathode catalysts through a synergetic surface/interface/doping
engineering strategy.