posted on 2021-10-11, 04:33authored byJinchang Xu, Zilong Li, Di Chen, Sanxi Yang, Kaiwei Zheng, Jiaxi Ruan, Yinlong Wu, Hao Zhang, Jian Chen, Fangyan Xie, Yanshuo Jin, Nan Wang, Hui Meng
The
oxygen evolution reaction (OER) is crucial for hydrogen production
from water splitting and rechargeable metal–air batteries.
However, the four-electron mechanism results in slow reaction kinetics,
which needed to be accelerated by efficient catalysts. Herein, a hybrid
catalyst of novel nickel–iron layered double hydroxide (NiFe
LDH) on porous indium tin oxide (ITO) is presented to lower the overpotential
of the OER. The as-prepared NiFe LDH@ITO catalyst showed superior
catalytic activity toward the OER with an overpotential of only 240
mV at a current density of 10 mA/cm2. The catalyst also
offered high stability with almost no activity decay after more than
200 h of chronopotentiometry test. Furthermore, the applications of
NiFe LDH@ITO in (flexible) rechargeable zinc–air batteries
exhibited a better performance than commercial RuO2 and
can remain stable in cycling tests. It is supposed that the superior
catalytic behavior originates from the ITO conductive framework, which
prevents the agglomeration and facilitates the electron transfer during
the OER process.