Graphene-like
molybdenum disulfide (MoS2) with unique
catalytic features and chemical/electrochemical stability holds great
potential as an oxygen reduction reaction (ORR) catalyst, but the
overall weak oxygen adsorption and low electron conductivity limit
its catalytic activity. Herein, MoS2 strongly coupled with
an oxophilic SnS heterostructure embedded in nitrogen-doped porous
carbon sheets (MoS2-SnS/NPC) was developed. The coupled
SnS can not only tune the electronic structure but also promote the
oxygen molecule adsorption and activation. Moreover, NPC can enhance
the electron transfer as well as the structural stability of the MoS2-SnS heterostructure without agglomeration. As expected, MoS2-SnS/NPC exhibited enhanced catalytic activity that is superior
to those of MoS2/NPC and SnS/NPC along with good catalytic
stability for ORR. As a cathode catalyst, a homemade zinc–air
battery driven by MoS2-SnS/NPC showed considerable discharging
performance superior to the one driven by a commercial Pt/C catalyst
in terms of open-circuit voltage, peak power density, and specific
capacity. Furthermore, a MoS2-SnS/NPC-based zinc–air
battery displayed a stable charging and discharging voltage gap for
48 h without an expanding trend, suggesting a robust cycling performance
and heralding promising application prospects. The rotating ring-disk
electrode and in situ electrochemical Raman tests revealed that the
ORR underwent a combined 2-electron and 4-electron associative mechanism
on MoS2-SnS/NPC, and the improved catalytic activity came
from the synergistic effect of MoS2, SnS, S vacancy, and
porous carbon sheets. This study provided a heterojunction strategy
by coupling oxophilic SnS for boosting ORR electrocatalysis, which
can be extended to other cheap transition-metal catalysts for efficient
energy conversion.