Seeking highly efficient, stable,
and cost-effective
bifunctional
electrocatalysts of rechargeable Zn–air batteries (ZABs) is
the top-priority for developing new generation portable electronic
devices. For this, the rational and effective structural design, interface
engineering, and electron recombination on electrocatalysts should
be taken into account to reduce the reaction overpotential and expedite
the kinetics of oxygen reduction reaction (ORR) and oxygen evolution
reaction (OER). Herein, we construct a MnCo-based metal organic framework-derived
heterogeneous MnS–CoS nanocrystals, which are anchored on free-standing
porous N-doped carbon fibers (PNCFs) by the in situ growth method
and vulcanization process. Benefiting from the abundant vacancies
and active sites, strong interfacial coupling as well as favorable
conductivity, the MnS–CoS/PNCFs composite electrode delivers
a mentionable oxygen electrocatalytic activity and stability with
a half-wave potential of 0.81 V for ORR and an overpotential of 350
mV for OER in the alkaline medium. Of note, the flexible rechargeable
ZAB using MnS–CoS/PNCFs as binder-free air cathode offers high
power density of 86.7 mW cm–2, large specific capacity
of 563 mA h g–1, and adapts to different bending
degree of operation. In addition, the density functional theory calculation
clarifies that the heterogeneous MnS–CoS nanocrystals reduces
the reaction barrier and enhances the conductivity of the catalyst
and the adsorption capacity of the intermediates during the ORR and
OER process. This study opens up a new insight to the design of the
self-supported air cathode for flexible electronic devices.