Highlights of this article
Key point 1: Reveal the growth mechanism of sodium niobate cubes by controlling the different hydrothermal time of f-Nb2CTx MXene nanosheets to reveal the nucleation-growth mechanism of S-P-NNO NCs. In the hydrothermal reaction, the highly active sites on the surface of the f-Nb2CTx MXene nanosheets are easily gradually oxidized to nanoscale Na7(H2O)Nb6O19(H2O)14. As the reaction progressed, the nanosheets were further broken under the attack of NaOH, and more active sites were exposed, forming more and more Na7(H2O)Nb6O19(H2O)14. These formed mesophases use f-Nb2CTx MXene nanosheets as the growth substrate and niobium source, and follow the Oswald maturation growth model to further grow into nanocubes. Finally, all nanosheets are completely converted into S-P-NNO NCs.
Key point 2: The electrochemical characterization of S-P-NNO/f-Nb2CTx composites benefited from the synergistic effect of S-P-NNO NCs and f-Nb2CTx NSs. The composites exhibit ultra-high reversible capacity and excellent rate performance. On the one hand, the existence of MXene nanosheets builds an interconnected conductive network for S-P-NNO NCs, facilitates the insertion of lithium ions, and shortens the diffusion path. On the other hand, the inclusion of S-P-NNO NCs between the MXene sheets can reduce the aggregation and self-accumulation of MXene, which is beneficial to the transport of ions in the electrolyte.
Point 3: Revealing the energy storage mechanism of SP-NNO/f-Nb2CTx composites. In-situ XRD test results show that SP-NNO NCs electrodes have continuous ion insertion/extraction behaviors during charging and discharging. However, it should be noted that in 2 After sub-charge and discharge, part of the diffraction peaks (such as 141 crystal plane) compared with the original state, not only the diffraction angle is slightly shifted, but also the diffraction intensity has not completely recovered to the original state. This is actually because when Li+ was first embedded in NaNbO3 crystals, it exchanged with Na+ in NaNbO3 and transformed into Li0.025Na0.975NbO3 phase. Subsequent ex-situ XRD and EELSs spectra further confirmed this lithium-sodium exchange phenomenon. That is, the lithium storage mechanism of S-P-NNO/f-Nb2CTx is a lithium-sodium double-ion co-intercalation mechanism caused by special ion exchange. This fundamentally explains the real reason why the S-P-NNO NCs electrode cannot be restored to its original state after the lithium ion is released.
Key point four: SP-NNO/f-Nb2CTx//AC lithium ion capacitor characterization SP-NNO/f-Nb2CTx composite as the negative electrode, commercial activated carbon (AC) as the positive electrode, constructed SP-NNO/f-Nb2CTx//AC Lithium ion capacitors. Thanks to the synergistic effect of the intercalation pseudocapacitance characteristics of SP-NNO NCs and the 3D conductive network constructed by MXene, electrons and ions can achieve rapid migration in the electrode, which better overcomes the innate dynamics between the positive and negative electrodes unbalanced. The device can provide an ultra-high energy density of 241 Wh kg1 at 125 W kg1 and a high power density of 13 kW kg1 at an energy density of 55.6 Wh kg1, and a capacity retention rate of 75% after 4000 cycles.
Article link
Formation and Operating Mechanisms of Single-Crystalline Perovskite NaNbO3 Nanocubes/Few-Layered Nb2CTx MXene Hybrids towards Li-Ion Capacitors https://pubs.rsc.org/en/content/articlehtml/2021/ta/d1ta03684j
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