The development of potassium-ion batteries (PIBs) has
been impeded
by the lack of an appropriate carbon anode material that could accommodate
K+ with a large ionic radius. Hard carbon with low cost
and larger interlayer spacing is a promising anode material for PIBs.
However, the impact of oxygen-containing functional groups in hard
carbon (HC) is less reported. Herein, a hypercrosslinked polymer (HCLP)
is prepared and used for the synthesis of microporous hard carbons
with superior structural stability and abundant oxygen-containing
functional groups and defects, in which the crosslinking agent provided
copious oxygen atoms. It is found that a large number of CO
groups and micropores provide more storage sites for K+. The surface-controlled process is dominated by the reversible reaction
of CO + K+ + e– ↔ C–O–K,
which directly increases the capacity contribution. The HCs obtained
at 600 °C exhibit good cycling and rate performance with an initial
specific capacity of about 254.3 mAh g–1 and the
capacity retention of 83.2% after 200 cycles at 50 mA g–1. The capacity reached up to 121 mAh g–1 at 2 A
g–1. A possible capacitive-adsorption mechanism
is proposed by kinetic analysis. The redox reaction mechanism between
CO and K+ at the HC is clearly also revealed.