The
photoassisted electrochemical reactions are considered an effective
method to reduce the overpotential of Li–O2 batteries.
However, achieving long-term cell cycling stability remains a challenge.
Here, we report a solid-phase interfacial reaction (SPIR) strategy
that introduces both oxygen vacancies (OV) and metal centers
(Ru) into the MoO2 to synthesize the surface plasmon (i.e.,
Ru/OV-MoO2). Then, Ru/OV-MoO2 can be uniformly loaded on the TiO2 nanowires
by the hydrothermal method. The plasma effect of Ru/OV-MoO2 demonstrates the effective reduction of the photoexcited
electron and hole recombination to improve visible light-harvesting
ability. The lifetime of electrons and holes can be extended by Ru
nanoparticles, which is beneficial for promoting the formation and
decomposition of Li2O2. In addition, the generated
OV further enhanced the migration of electrons and Li+, thus improving the ORR performance. The Ru/OV-MT/CC cathode corroborates excellent stability and catalytic performance
in the photoassisted Li–O2 battery, with an overpotential
value of 0.47 V, achieving the highest energy efficiency of 93.94%,
retaining at 89.13% after 800 h. This work offers a platform for preparing
a stable, bifunctional catalyst with the high total activity of a
photoassisted Li–O2 battery.