Issue 25, 2018

Nickel sulfide anchored carbon nanotubes for all-solid-state lithium batteries with enhanced rate capability and cycling stability

Abstract

All-solid-state lithium batteries using nonflammable inorganic solid electrolytes can completely eliminate the safety issues, such as leakage and combustion. Moreover, energy densities can be improved significantly using transition metal sulfide electrodes and metallic lithium in all-solid-state lithium batteries owing to their high theoretical specific capacity and excellent interfacial compatibility with sulfide solid electrolytes. In this work, nickel sulfide anchored carbon nanotube (NiS–CNT) nanocomposites were successfully synthesized by a facile hydrothermal method. The very small NiS particle size with a distribution of 5–10 nm as well as the presence of multi-walled carbon nanotubes not only enhance the ionic/electronic conduction but also alleviate the volume changes, which endow the NiS–CNT based all-solid-state lithium batteries with superior rate capability and excellent cycling performances. Typically, Li/75% Li2S–24% P2S5–1% P2O5/Li10GeP2S12/NiS–CNT all-solid-state lithium batteries delivered a high reversible capacity of 515 mA h g−1 after 30 cycles at a current density of 0.1 A g−1. Even after increasing the current density to 1.0 A g−1, the all-solid-state lithium batteries still maintain a stable discharge capacity of 170 mA h g−1 after 150 cycles. Moreover, the conversion reaction mechanism of the NiS–CNT nanocomposites in all-solid-state lithium batteries was investigated by ex situ XRD measurements.

Graphical abstract: Nickel sulfide anchored carbon nanotubes for all-solid-state lithium batteries with enhanced rate capability and cycling stability

Supplementary files

Article information

Article type
Paper
Submitted
16 Apr 2018
Accepted
30 May 2018
First published
30 May 2018

J. Mater. Chem. A, 2018,6, 12098-12105

Nickel sulfide anchored carbon nanotubes for all-solid-state lithium batteries with enhanced rate capability and cycling stability

Q. Zhang, G. Peng, J. P. Mwizerwa, H. Wan, L. Cai, X. Xu and X. Yao, J. Mater. Chem. A, 2018, 6, 12098 DOI: 10.1039/C8TA03449D

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