Owing
to the expanding function of Li-ion transmission channels,
it is important to explore the doping effects of different compounds
into sulfide solid electrolytes to improve their electrochemical performances.
However, it is hard to characterize the doping behaviors within sulfide
solid electrolytes with low crystallinity and poor stability just
by conventional crystallography analytical methods. In this work,
the dielectric spectrum testing combined with other analytical methods,
such as 7Li solid-state nuclear magnetic resonance, X-ray
photoelectron spectroscopy, and the electrochemical method, have been
applied to investigate the dual-doping behaviors of WS2 and LiBr within Li7P3S11 glass-ceramic
electrolytes. This research method can not only evaluate the internal
acting effect between the skeleton of sulfide solid electrolytes and
the migrating kinetics of Li ions but also explore the capacitance
at the interfaces of LiCoO2/sulfide solid electrolytes.
The experimental results show that the number of Li ions with fast
transport velocity within Li2S-P2S5-based solid electrolytes has been increased. Meanwhile, the interfacial
capacitances between Li2S-P2S5-based
solid electrolytes and the LiCoO2 cathode have decreased
after dual-doping of WS2 and LiBr, indicating a synergetic
effect for the doped Li7P3S11 glass-ceramic
electrolytes in terms of the ionic conductivities and interfacial
compatibilities. This work may provide a novel analytical approach
to explore both the diffusion kinetics and interfacial behaviors for
the solid electrolytes of lithium batteries.