Crystal structure analysis of Li3PO4 powder prepared by wet chemical reaction and solid-state reaction by using X-ray diffraction (XRD)

被引:50
作者
Ayu, Nur I. P. [1 ]
Kartini, Evvy [2 ]
Prayogi, Lugas D. [1 ]
Faisal, Muhamad [1 ]
Supardi [2 ]
机构
[1] Inst Teknol Sepuluh Nopember, Engn Phys, ITS Campus, Sukolilo 60111, Surabaya, Indonesia
[2] PUSPIPTEK, BATAN, Sci & Technol Ctr Adv Mat, Tangerang Selatan 15314, Banten, Indonesia
关键词
Lithium phosphate; Li3PO4; X-ray diffraction; Crystal structure; ELECTROLYTE; CONDUCTIVITY;
D O I
10.1007/s11581-016-1643-z
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Lithium phosphate (Li3PO4) is one of the promising solid electrolyte materials for lithium-ion battery because of its high ionic conductivity. A crystalline form of Li3PO4 had been prepared by two different methods. The first method was wet chemical reaction between LiOH and H3PO4, and the second method was solid-state reaction between Li2O and P2O5. Crystal structure of Li3PO4 white powder had been investigated by using an X-ray diffraction (XRD) analysis. The results show that Li3PO4 prepared by wet chemical reaction belongs to orthorhombic unit cell of beta-Li3PO4 with space group Pmn2(1). Meanwhile, Li3PO4 powder prepared by solidstate reaction belongs to orthorhombic unit cell of gamma-Li3PO4 with space group Pmnb and another unknown phase of Li4P2O7. The impurity of Li4P2O7 was due to phase transformation in solid state reaction during quenching of molten mixture from high temperature. Ionic conductivity of Li3PO4 prepared by solid-state reaction was similar to 3.10(-7) S/cm, which was higher than Li3PO4 prepared by wet chemical reaction similar to 4.10(-8) S/cm. This increasing ionic conductivity may due to mixed crystal structures that increased Li-ion mobility in Li3PO4.
引用
收藏
页码:1051 / 1057
页数:7
相关论文
共 25 条
  • [1] Transport pathways for mobile ions in disordered solids from the analysis of energy-scaled bond-valence mismatch landscapes
    Adams, Stefan
    Rao, R. Prasada
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2009, 11 (17) : 3210 - 3216
  • [2] AR W, 1972, J SOLID STATE CHEM, V28, P20, DOI [10.1016/0022-4596(72)90127.2, DOI 10.1016/0022-4596(72)90127.2]
  • [3] Avdeev M., 2009, Solid State Electrochemistry I ed, P227, DOI [10.1002/9783527627868.ch7, DOI 10.1002/9783527627868.CH7]
  • [4] Li ion diffusion mechanisms in the crystalline electrolyte γ-Li3PO4
    Du, Yaojun A.
    Holzwarth, N. A. W.
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2007, 154 (11) : A999 - A1004
  • [5] A CORRECTION FOR POWDER DIFFRACTION PEAK ASYMMETRY DUE TO AXIAL DIVERGENCE
    FINGER, LW
    COX, DE
    JEPHCOAT, AP
    [J]. JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1994, 27 : 892 - 900
  • [6] Computer modeling of lithium phosphate and thiophosphate electrolyte materials
    Holzwarth, N. A. W.
    Lepley, N. D.
    Du, Yaojun A.
    [J]. JOURNAL OF POWER SOURCES, 2011, 196 (16) : 6870 - 6876
  • [7] CONTINUOUS, MARTENSITIC NATURE OF THE TRANSITION BETA-]GAMMA LI3PO4
    IBARRARAMIREZ, C
    VILLAFUERTECASTREJON, ME
    WEST, AR
    [J]. JOURNAL OF MATERIALS SCIENCE, 1985, 20 (03) : 812 - 816
  • [8] Mixed cation effect on silver-lithium solid electrolyte (AgI)0.5(LiPO3)0.5
    Kartini, E.
    Sakuma, T.
    Basar, K.
    Ihsan, M.
    [J]. SOLID STATE IONICS, 2008, 179 (19-20) : 706 - 711
  • [9] Structure and dynamics of solid electrolyte (LiI)0.3(LiPO3)0.7
    Kartini, E.
    Nakamura, M.
    Arai, M.
    Inamura, Y.
    Nakajima, K.
    Maksum, T.
    Honggowiranto, W.
    Putra, T. Y. S. P.
    [J]. SOLID STATE IONICS, 2014, 262 : 833 - 836
  • [10] Anion effect on the structure of Ag2S-AgPO3 superionic glasses
    Kartini, E
    Kennedy, SJ
    Itoh, K
    Kamiyama, T
    Collins, MF
    Suminta, S
    [J]. SOLID STATE IONICS, 2004, 167 (1-2) : 65 - 71