redox couples via X-ray absorption near-edge structure spectroscopy. The whole electrochemical reaction undergoes highly reversible single-phase and biphasic transitions with a moderate volume change of 7.7% through in situ X-ray diffraction and ex situ high-energy synchrotron X-ray diffraction. Combining density functional theory (DFT) calculations with the galvanostatic intermittent titration technique, the superior performance is ascribed to the low ionic-migration energy barrier and desirable Na-ion diffusion kinetics. The present work can offer a new insight into the design of multielectron-reaction cathode materials for SIBs.
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Zhang et al. (2020) studied this question.
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