Sodium-ion batteries are regarded as one of the most promising energy storage systems, but the choice of anode material is still facing great challenges. Biomass carbon materials were explored for their low cost and wide range of sources. Here, a hard carbon material with a "honeycomb" structure using pine pollen (PP) as a precursor was successfully prepared and applied as an anode. The initial discharge capacity can reach 370 mA h g −1 at a current density of 0.1 A g −1 . After cycling 200 times, the reversible capacity also stabled at 203.3 mA h g −1 with the retention rate of 98%. We further studied the sodium storage mechanism by different methods, especially the Na + diffusivity coefficient (D Na + ) calculated by galvanostatic intermittent titration technique, which was more accurate. Interestingly, the trend of D Na + coincides with cyclic voltammetry curves. Carbonized PP exhibited excellent electrochemical properties because of its three-dimensional structure and larger layer spacing (∼0.41 nm), which reduces the resistance of sodium ions to intercalation and deintercalation.
Recycling
of spent lithium-ion batteries is extremely urgent with
their increasing decommission. In this work, eutectic molten salts
of LiOH–Li2CO3 used as lithium sources
for direct regeneration of LiNi0.5Co0.2Mn0.3O2 were developed. Based on the phase diagram
of LiOH and Li2CO3, the effects of different
lithium sources on material regeneration have been investigated. The
cathode materials regenerated with eutectic molten salts have high
capacity, good cycling performance, and rate performance. The discharge
capacities during the 1st and 200th cycles at 1 C are 146.3 and 130.3
mA h g–1, respectively, and the capacity retention
rate reaches 89.06%. Using the combined X-ray diffraction (XRD), high-resolution
transmission electron microscopy (HRTEM), and X-ray photoelectron
spectroscopy (XPS) analysis, the original layered structure of spent
cathode materials was restored. Therefore, the eutectic molten salt
of LiOH–Li2CO3 is feasible for direct
regeneration of spent cathode materials.
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