posted on 2021-06-14, 13:34authored byHehe Zhang, Yong Cheng, Qiaobao Zhang, Weibin Ye, Xiaohua Yu, Ming-Sheng Wang
Transition
metal dichalcogenides are regarded as promising anode
materials for potassium-ion batteries (PIBs) because of their high
theoretical capacities. However, due to the large atomic radius of
K+, the structural damage caused by the huge volume expansion
upon potassiation is much more severe than that of their lithium counterparts.
In this research, a stress-dispersed structure with Co3Se4 nanocrystallites orderly anchored on graphene sheets
is achieved through a two-step hydrothermal treatment to alleviate
the structural deterioration. The ability to reduce the contact stress
by the well-dispersed Co3Se4 nanocrystallites
during K+ intercalation, together with the highly conductive
graphene matrix, provides a more reliable and efficient anode architecture
than its two agminated counterparts. Given these advantages, the optimized
electrode delivers excellent cycling stability (301.8 mA h g–1 after 500 cycles at 1 A g–1), as well as an outstanding
rate capacity (203.8 mA h g–1 at 5 A g–1). Further in situ and ex situ characterizations
and density functional theory calculations elucidate the potassium
storage mechanism of Co3Se4 during the conversion
reaction and reveal the fast electrochemical kinetics of the rationally
designed electrode. This work provides a practical approach for constructing
stable metal-selenide anodes with long cycle life and high-rate performance
for PIBs.