Herein, the electrochemical properties and reaction mechanism of Li Ca V (PO ) /C (x = 0, 0.5, 1, and 1.5) as negative electrode materials for sodium-ion/potassium-ion batteries (SIBs/PIBs) are investigated. All samples undergo a mixed contribution of diffusion-controlled and pseudocapacitive-type processes in SIBs and PIBs via Trasatti Differentiation Method, while the latter increases with Ca content increase. Among them, Li V (PO ) /C exhibits the highest reversible capacity in SIBs and PIBs, while Ca V (PO ) /C shows the best rate performance with a capacity retention of 46% at 20 C in SIBs and 47% at 10 C in PIBs. This study demonstrates that the specific capacity of this type of material in SIBs and PIBs does not increase with the Ca-content as previously observed in lithium-ion system, but the stability and performance at a high C-rate can be improved by replacing Li with Ca . This indicates that the insertion of different monovalent cations (Na /K ) can strongly influence the redox reaction and structure evolution of the host materials, due to the larger ion size of Na and K and their different kinetic properties with respect to Li . Furthermore, the working mechanism of both LVP/C and Ca V (PO ) /C in SIBs are elucidated via in operando synchrotron diffraction and in operando X-ray absorption spectroscopy.
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http://dx.doi.org/10.1002/smll.202304102 | DOI Listing |
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