2017
DOI: 10.1149/2.1121707jes
|View full text |Cite
|
Sign up to set email alerts
|

Enhanced Electrochemical Performance of Li3V2(PO4)3/C Coated with Li Fast Ion Conductive Li7La3Zr2O12

Abstract: Li7La3Zr2O12-coated Li3V2(PO4)3/C (LLZO-coated LVP/C) has been synthesized via a conventional sol-gel method, in which LLZO as the fast Li-ion conductor and carbon as the mixed coating with excellent electronic conductivity could enhance the transport of both electrons and Li-ions at the electrode's surface. X-ray diffraction (XRD) and transmission electron microscopy (TEM) with energy dispersive spectrometer (EDS) have been performed to prove the existence of LLZO on the surface of LVP. The valence states of … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
3
0

Year Published

2018
2018
2024
2024

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 18 publications
(3 citation statements)
references
References 53 publications
0
3
0
Order By: Relevance
“…24 It is due to the fact that the electrochemical reaction is primarily a surface reaction, and the surface state of the cathode material largely determines its properties. [25][26][27][28][29] Therefore, in this study, a thin CoS 2 layer was successfully coated on FeS 2 via the hydrothermal method and a subsequent heat-treatment. The CoS 2 coating improved the thermal stability and electrochemical performance of FeS 2 .…”
mentioning
confidence: 99%
“…24 It is due to the fact that the electrochemical reaction is primarily a surface reaction, and the surface state of the cathode material largely determines its properties. [25][26][27][28][29] Therefore, in this study, a thin CoS 2 layer was successfully coated on FeS 2 via the hydrothermal method and a subsequent heat-treatment. The CoS 2 coating improved the thermal stability and electrochemical performance of FeS 2 .…”
mentioning
confidence: 99%
“…Figure 4c shows the CV curves of LVPNCHG and LVPNC in 3.0–4.8 V at 0.2 mV s −1 , and the observed oxidation/reduction peaks correspond to plateaus during charge/discharge processes. Obviously, the peaks difference during oxidation/reduction for LVPNCHG is smaller than LVPNC, indicating LVPNCHG has less polarization behavior and is more favorable than LVPNC in the electrochemical process [40,41] …”
Section: Resultsmentioning
confidence: 99%
“…Obviously, the peaks difference during oxidation/reduction for LVPNCHG is smaller than LVPNC, indicating LVPNCHG has less polarization behavior and is more favorable than LVPNC in the electrochemical process. [40,41] Figure 4d shows the long-term cycling performance of LVPNCHG and LVPNC at 10 C at 3.0-4.8 V. The first 3 cycles at 0.2 C were conducted to activate the electrodes. LVPNCHG delivered about 140 mAh g À 1 in the initial several cycles, keeping 101 mAh g À 1 after 2000 cycles (70.2 % capacity retention) and 92 mAh g À 1 after 4000 cycles (63.9 % capacity retention), which was higher than LVPNC with 57 mAh g À 1 after 2000 cycles (43.3 % capacity retention).…”
Section: Chemsuschemmentioning
confidence: 99%