A comparative study of LiTi2(P8/9V1/9O4)3 and LiTi2(PO4)3: Synthesis, structure and electrochemical properties

被引:9
作者
Pang, Jianyu [1 ]
Kuang, Quan [1 ]
Zhao, Yanming [1 ,2 ]
Han, Wei [2 ]
Fan, Qinghua [1 ]
机构
[1] South China Univ Technol, Sch Phys, Guangzhou 510641, Guangdong, Peoples R China
[2] South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
LiTi2(PO4)(3); LiTi2(P8/9V1/9O4)(3); Li-ion batteries; Anode material; Electrochemical performance; LITHIUM-ION BATTERY; ANODE MATERIAL; TITANIUM PHOSPHATE; CONDUCTIVITY; INTERCALATION; NANOCOMPOSITE; PERFORMANCE; IMPEDANCE; CATHODE;
D O I
10.1016/j.electacta.2017.12.073
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
NASICON-type LiTi2(PO4)(3) (LTP) is a representative solid-state electrolyte and promising anode for rechargeable Li batteries. However, the electronic conductivity and specific capacity of LTP anode are encumbered by its massy and sluggish phosphate groups. Herein, vanadium (V) substitution compound LiTi2(P8/9V1/9O4)(3) (LTPV) has been synthesized by using a selective vanadic source of Li3VO4 at an adjusted sintering temperature of 700 degrees C. The PO43- radicals partly replaced by VO43- radicals are confirmed via XRD refinement, SEM, Raman and infrared spectra. The electronic conductivity of LTPV is two orders of magnitude higher than that of the undoped one, and meanwhile the charge-transfer impedance observably decreases after V substitution. More importantly, the V5+ cations are electrochemical active in LTPV and contribute additional capacity during discharge and recharge processes. Benefitted from the increased electronic conductivity and the reduced charge-transfer impedance, the rate performance of LTPV is also distinctly improved when compared with the pristine LTP. (c) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:384 / 390
页数:7
相关论文
共 35 条
  • [1] On the structure of Li3Ti2(PO4)3
    Aatiq, A
    Ménétrier, M
    Croguennec, L
    Suard, E
    Delmas, C
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 2002, 12 (10) : 2971 - 2978
  • [2] Advances of aqueous rechargeable lithium-ion battery: A review
    Alias, Nurhaswani
    Mohamad, Ahmad Azmin
    [J]. JOURNAL OF POWER SOURCES, 2015, 274 : 237 - 251
  • [3] IONIC-CONDUCTIVITY OF THE LITHIUM TITANIUM PHOSPHATE (LI1+XALXTI2-X(PO4)3), (LI1+XSCXTI2-X(PO4)3), (LI1+XYXTI2-X(PO4)3), (LI1+XLAXTI2-X(PO4)3 SYSTEMS
    AONO, H
    SUGIMOTO, E
    SADAOKA, Y
    IMANAKA, N
    ADACHI, GY
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1989, 136 (02) : 590 - 591
  • [4] IONIC-CONDUCTIVITY OF SOLID ELECTROLYTES BASED ON LITHIUM TITANIUM PHOSPHATE
    AONO, H
    SUGIMOTO, E
    SADAOKA, Y
    IMANAKA, N
    ADACHI, G
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1990, 137 (04) : 1023 - 1027
  • [5] LiVOPO4 as a new cathode materials for Li-ion rechargeable battery
    Azmi, BM
    Ishihara, T
    Nishiguchi, H
    Takita, Y
    [J]. JOURNAL OF POWER SOURCES, 2005, 146 (1-2) : 525 - 528
  • [6] Vibrational spectroscopic study of lithium intercalation into LiTi2(PO4)3
    Burba, Christopher M.
    Frech, Roger
    [J]. SOLID STATE IONICS, 2006, 177 (17-18) : 1489 - 1494
  • [7] Self-assembled vanadium pentoxide (V2O5) hollow microspheres from nanorods and their application in lithium-ion batteries
    Cao, AM
    Hu, JS
    Liang, HP
    Wan, LJ
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (28) : 4391 - 4395
  • [8] Spark plasma sintering of LiTi2(PO4)3-based solid electrolytes
    Chang, CM
    Lee, YI
    Hong, SH
    Park, HM
    [J]. JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2005, 88 (07) : 1803 - 1807
  • [9] THE NASICON-TYPE TITANIUM PHOSPHATES LITI2(PO4)3, NATI2(PO4)3 AS ELECTRODE MATERIALS
    DELMAS, C
    NADIRI, A
    SOUBEYROUX, JL
    [J]. SOLID STATE IONICS, 1988, 28 : 419 - 423
  • [10] Modeling Ti/Ge Distribution in LiTi2-xGex(PO4)3 NASICON Series by 31p MAS NMR and First-Principles DFT Calculations
    Diez-Gomez, Virginia
    Arbi, Kamel
    Sanz, Jesus
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (30) : 9479 - 9486