Ensuring or even optimizing the activity and stability
of iridium
oxide-coated titanium anodes while reducing the amount of iridium
is still practically significant. In this work, IrO
x
-Ti electrodes are prepared by galvanostatic deposition at
different deposition current densities and times. The iridium loading
level, morphology, microstructure, and element composition distribution
of these obtained electrodes are characterized, and their cyclic voltammetry
and accelerated life tests were carried out in 0.5 M H2SO4 to investigate their electrochemical performance for
the acidic oxygen evolution reaction (OER). For a better understanding
of the anodic electrodeposition mechanism, a competing mechanistic
hypothesis was proposed to describe the reactions and their relationship
involved in this process. The results show that the IrO
x
electrodes electrodeposited at 0.1 mA cm–2 exhibited a superior performance for the OER in terms of stability.
Especially, the electrode electrodeposited for 5 h (0.1 mA cm–2) demonstrated a long-term durability for 73.14 h
(equivalent to at least 14,642 h, i.e., 610 days, in actual lifetime)
with 1.0 mg cm–2 iridium loading. Simultaneously,
a mathematical model was used to fit the relationship between accelerated
lifetime and deposition current and iridium loading. This research
provides some valuable insights into how to optimally use Ir as an
OER electrocatalyst.