TY - JOUR
T1 - Wet-chemical coordination synthesized Li3V2(PO4)3/C for Li-ion battery cathodes
AU - Ni, Qiao
AU - Bai, Ying
AU - Yang, Zhi
AU - Li, Yu
AU - Chen, Guanghai
AU - Ling, Liming
AU - Ren, Haixia
AU - Chen, Shi
AU - Wu, Feng
AU - Wu, Chuan
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017
Y1 - 2017
N2 - Lithium vanadium phosphate (Li3V2(PO4)3) is one of the most promising cathode materials for developing practical Li-ion batteries due to its advantages of structural stability, low cost, relatively high energy density. For this purpose, a wet-chemical coordination approach has been applied to synthesis of the Li3V2(PO4)3/C (LVP/C) cathode materials for Li-ion batteries. The structure, morphology, and electrochemical and kinetic behaviors of LVP/C samples calcined at different temperatures are studied. The optimized Li3V2(PO4)3 sample calculated at 850 °C (denoted as LVP-850) exhibits excellent rate performance: at high rate of 0.5, 1, 5, 10 and 20 C, impressive specific capacity of 110.9, 106, 91.2, 83 and 43.6 mAh g−1 can still be attainted, respectively. Even through it recovers back to 0.1 C, the cell can still deliver a capacity of 114.4 mAh g−1 (about 97.9% of the initial capacity). Combined with cyclic voltammetry technique and ex-situ X-ray photoemission spectroscopy (XPS), the Li+ insertion/extraction reaction mechanisms are also confirmed. Such an efficient method plays a critical role in improving rate performance and cyclic reversibility of Li3V2(PO4)3 particles, and should also be appropriate for other functional electrode materials.
AB - Lithium vanadium phosphate (Li3V2(PO4)3) is one of the most promising cathode materials for developing practical Li-ion batteries due to its advantages of structural stability, low cost, relatively high energy density. For this purpose, a wet-chemical coordination approach has been applied to synthesis of the Li3V2(PO4)3/C (LVP/C) cathode materials for Li-ion batteries. The structure, morphology, and electrochemical and kinetic behaviors of LVP/C samples calcined at different temperatures are studied. The optimized Li3V2(PO4)3 sample calculated at 850 °C (denoted as LVP-850) exhibits excellent rate performance: at high rate of 0.5, 1, 5, 10 and 20 C, impressive specific capacity of 110.9, 106, 91.2, 83 and 43.6 mAh g−1 can still be attainted, respectively. Even through it recovers back to 0.1 C, the cell can still deliver a capacity of 114.4 mAh g−1 (about 97.9% of the initial capacity). Combined with cyclic voltammetry technique and ex-situ X-ray photoemission spectroscopy (XPS), the Li+ insertion/extraction reaction mechanisms are also confirmed. Such an efficient method plays a critical role in improving rate performance and cyclic reversibility of Li3V2(PO4)3 particles, and should also be appropriate for other functional electrode materials.
KW - Cathode
KW - Li-ion batteries
KW - LiV(PO)
KW - Wet-chemical coordination approach
UR - http://www.scopus.com/inward/record.url?scp=85029493879&partnerID=8YFLogxK
U2 - 10.1016/j.jallcom.2017.09.106
DO - 10.1016/j.jallcom.2017.09.106
M3 - Article
AN - SCOPUS:85029493879
SN - 0925-8388
VL - 729
SP - 49
EP - 56
JO - Journal of Alloys and Compounds
JF - Journal of Alloys and Compounds
ER -