Abstract
Ternary anodes have attracted more and more attention due to the characteristic advantages resulting from the effect integration of three different materials on the lithium storage mechanism with functional interfaces interaction. However, clarifying the distribution and interaction of carbon, MoS2 and TiO2 in the MoS2/C/TiO2 composite, which is helpful for the understanding of the formation and lithium storage mechanism of the ternary anodes, is a well-known challenge. Herein, a novel pore core-double shell nanostructure of P25@carbon network supported few-layer MoS2 nanosheet (P25@C@FL-MoS2) is successfully synthesized by a one-pot hydrothermal approach. The distribution and interaction of the carbon, MoS2 and TiO2 in the obtained P25@C@FL-MoS2 hybrid are systematically characterized by transmission electron microscopy, Raman spectra and X-ray photoelectron spectroscopy analysis et al. It is found that the carbon serves as binder, which supports few-layer MoS2 shell and coats the P25 core via TiOC bonds at the same time. Such multi-functional integration with smart structure and strong interfacial contact generates favorable structure stability and interfacial pseudocapacity-like storage mechanism. As a consequence, superior cycling and rate capacity of the muti-functional integration ternary P25@C@FL-MoS2 anode are achieved.
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