Fe-N-C
catalyst is one of most promising candidates for oxygen
electrocatalysis reaction in zinc–air batteries (ZABs), but
achieving sustained high activity is still a challenging issue. Herein,
we demonstrate that introducing Mn single atoms into Fe-N-C (Mn1@Fe-N-C/CNTs) enables the realization of highly efficient
and durable oxygen electrocatalysis performance and application in
ZABs. Multiple characterizations confirm that Mn1@Fe-N-C/CNTs
is equipped with Mn-N2O2 and Fe-N4 sites and Fe nanoparticles. The Mn-N2O2 sites
not only tune the electron structure of Fe-N
x
sites to enhance intrinsic activity, but also scavenge the
attack of radicals from Fe-N
x
sites for
improvement in ORR durability. As a result, Mn1@Fe-N-C/CNTs
exhibits enhanced ORR performance to traditional Fe-N-C catalysts
with high E
1/2 of 0.89 V vs reversible
hydrogen electrode (RHE) and maintains ORR activity after 15 000
CV. Impressively, Mn1@Fe-N-C/CNTs also presents excellent
OER activity and the difference (ΔE) between E
1/2 of ORR and OER potential at 10 mA cm–2 (E
j10) is only 0.59 V,
outperforming most reported catalysts. In addition, the maintainable
bifunctional activity of Mn1@Fe-N-C/CNTs is demonstrated
in ZABs with almost unchanged cycle voltage efficiency up to 200 h.
This work highlights the critical role of Mn single atoms in enhancing
ORR activity and stability, promoting the development of advanced
catalysts.