Cu, Al,
and 316L stainless steel are the main components of the current collectors
and coin-type cells used in the characterization of potassium-ion
battery (KIB) materials and are expected to be electrochemically inactive.
Herein, their electrochemical stabilities in a nonaqueous potassium-bis(fluorosulfonyl)imide
(KFSI)-based electrolyte are investigated. In dynamic- and transient-mode
polarization, passivation of each metal is observed to occur below
3.9, 3.8, and 4.05 V versus K+/K for Cu, Al, and 316L stainless
steel, respectively, which are considered the threshold potentials.
The composition of the passive layers of each metal is determined
using time-of-flight secondary-ion mass spectrometry. The passive
layers of Cu and Al consist of Cu–O (CuO or Cu2O)
and Al–O (Al2O3), respectively, and 316L
stainless steel is passivated with an outermost Cr–F (CrF3) layer and an inner Cr–O (Cr2O3) layer. Above the threshold potentials, however, severe corrosion
of each metal occurs accompanied by the dissolution of metal ions,
which could affect the reliability of experimental results for KIBs
using KFSI-based electrolytes.