摘要
Ti–O–C channels for ultrafast sodium storage were constructed in N/S-co-doped TiO2–C nanofibers, which deliver a high rate performance of 181.9 mAh g–1 at 5 A g–1 after 3000 cycles. The existence of Ti–O–C bonds at the interface of TiO2–C phases was revealed by synchrotron radiation X-ray absorption spectra. Based on this, first-principles calculations further verified the low energy barrier for Na+ insertion/extraction in the Ti–O–C channels formed by the intimately integrated graphite layer with TiO2 near the surface. In addition, surface defects induced by heteroatoms accelerate the Na+ mass transfer through the pathway from the carbon surface to the Ti–O–C channel.
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