Regulating nitrogen/sulfur terminals on 3D porous TiC MXene with enhanced reaction kinetics toward high-performance alkali metal ion storage.

In this paper, we have developed a simple and efficient sulfur-amine chemistry strategy to prepare a three-dimensional (3D) porous TiCT composite with large amounts of N and S terminal groups. The well-designed 3D macroporous architecture presents enlarged interlayer spacing, large specific surface area, and unique porous structure, which successfully solves the re-stacking issue of MXene during storage and electrode fabrication. It is the amount of concentrated hydrochloric acid added to the S-EDA (ethylenediamine)/MXene colloidal suspension that is critical to the formation of 3D morphology. In addition, N and S terminals on MXene could improve the adsorption ability of K. Owing to the synergistic effect of the structure design and terminal modification, the N, S codoped three-dimensional porous TiCT (3D-NSPM) material shows a high surface capacitive contribution and rapid diffusion kinetics for K and Na. As a result, the as-prepared 3D-NSPM delivers high reversible capacity (237 and 273 mAh g at 0.1 A g for PIBs and SIBs, respectively), superb cycling stability (84.9% capacity retention after 10,000 cycles at 1 A g in PIBs and 74.0% capacity retention after 2200 cycles at 1 A g in SIBs), and excellent rate capability (111 and 196 mAh g at 5 A g for PIBs and SIBs, respectively), which are superior to other MXene-based anodes for PIBs and SIBs. Moreover, the described strategy provides a new insight for constructing the 3D porous structure from 2D building blocks beyond MXene.