In this section
@article{Duarte:2025:10.1039/d5ey00236b,
author = {Duarte, RPM and Rao, R and Ryan, MP and Dung, T and Celorrio, V and Sharman, J and Martinez-Bonastre, A and Stephens, IEL},
doi = {10.1039/d5ey00236b},
journal = {EES Catalysis},
title = {Beyond activity: a perspective on diagnosing instability of reversible O catalysts for metal-air batteries},
url = {http://dx.doi.org/10.1039/d5ey00236b},
year = {2025}
}
TY - JOUR
AB - Zinc–air redox flow batteries have high potential to penetrate the stationary energy storage market, due to the abundancy, and low cost of active species – oxygen and zinc. However, their technological fruition is limited by the development of reversible O2 electrodes operating at potentials between 0.6 VRHE to 1.7 VRHE, under which no catalyst material has been shown to be stable over long durations. Despite heavy research on the topic of reversible O2 catalysis, little is known about the parameters controlling the stability of the bifunctional catalyst. Several research accounts assess the activity of reversible O2 catalysts, but only a small portion cover degradation mechanism over such a large potential window. In this perspective, we summarize our current understanding of material challenges for Zn–air batteries, reversible O2 catalyst integration strategies, and electrochemical behaviour, with a particular focus on catalyst stability. Nickel cobalt oxide (NiCo2O4), a promising yet understudied system, is used as an example material for investigations at potentials of both the O2 reduction (ORR) and evolution (OER) reactions. We also report original data employing ex situ X-ray diffraction, electron energy loss spectroscopy, and X-ray photoelectron spectroscopy, as well as electrochemical measurements to study the activity of NiCo2O4. Furthermore, electrochemical accelerated stress tests are coupled with post-mortem transmission electron microscopy, inductively coupled plasma, and X-ray photoelectron spectroscopy to study the dissolution, compositional changes and amorphization of the top surface 5 nm of the catalyst surface. In situ X-ray absorption spectroscopy revealed irreversible oxidation of Co centres in NiCo2O4 during OER, which explains the reduction in activity of the ORR after the catalyst was exposed to anodic OER potentials. This methodology provides a broader method to screen reversible O2 catalyst stability and enables us to sum
AU - Duarte,RPM
AU - Rao,R
AU - Ryan,MP
AU - Dung,T
AU - Celorrio,V
AU - Sharman,J
AU - Martinez-Bonastre,A
AU - Stephens,IEL
DO - 10.1039/d5ey00236b
PY - 2025///
SN - 2753-801X
TI - Beyond activity: a perspective on diagnosing instability of reversible O catalysts for metal-air batteries
T2 - EES Catalysis
UR - http://dx.doi.org/10.1039/d5ey00236b
UR - https://doi.org/10.1039/d5ey00236b
ER -