KVPO4F/carbon nanocomposite with highly accessible active sites and robust chemical bonds for advanced potassium-ion batteries

KVPO4F (KVPF) has been extensively investigated as the potential cathode material for potassium-ion batteries (PIBs) owing to its high theoretical capacity, superior operating voltage, and three-dimensional K+ conduction pathway. Nevertheless, the electrochemical behavior of KVPF is limited by the inherent poor electronic conductivity of the phosphate framework and unstable electrode/electrolyte interface. To address the above issues, this work proposes an infiltration-calcination method to confine the in-situ grown KVPF into the mesoporous carbon CMK-3 (denoted KVPF@CMK-3). The assembled KVPF@CMK-3 nanocomposite features three-dimensional interconnected carbon channels, which not only offer abundant active sites and significantly accelerate K+/electron transport, but also prevent the growth of KVPF nanoparticle agglomerates, hence stabilizing the structure of the material. Additionally, V-F-C bonds are created at the interface of KVPF and CMK-3, which reduce the loss of F and stabilize the electrode interface. Thus, when tested as a cathode material for PIBs, the KVPF@CMK-3 nanocomposite delivers superior reversible capacitiy (103.2 mAh g-1 at 0.2 C), outstanding rate performance (90.1 mAh g-1 at 20 C), and steady cycling performance (92.2 mAh g-1 at 10 C and with the retention of 88.2% after 500 cycles). Moreover, its potassium storage mechanism is further examined by ex-situ XRD and ex-situ XPS techniques. The above synthetic strategy demonstrates the potential of KVPF@CMK-3 to be applied as the cathode for PIBs. & COPY; 2022 Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).