Rational synthesis and electrochemical performance of LiVOPO4 polymorphs. Issue 14 (20th March 2019)

• Record Type: Journal Article
• Authors: Hidalgo, Marc Francis V.; Lin, Yuh-Chieh; Grenier, Antonin; Xiao, Dongdong; Rana, Jatinkumar; Tran, Richard; Xin, Huolin; Zuba, Mateusz; Donohue, Jennifer; Omenya, Fredrick O.; Chu, Iek-Heng; Wang, Zhenbin; Li, XiangGuo; Chernova, Natasha A.; Chapman, Karena W.; Zhou, Guangwen; Piper, Louis; Ong, Shyue Ping; Whittingham, M. Stanley
• Is Part Of: Journal of materials chemistry. Volume 7:Issue 14(2019)
• Page Start: 8423
• Page End: 8432
• Publication Date: 2019-03-20
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c8ta12531g
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : A thorough study on the stability of LiVOPO4 polymorphs to determine which is the most promising for Li-ion batteries. Abstract : LiVOPO4 is a promising cathode material for Li-ion batteries due to its ability to intercalate up to two electrons per vanadium redox center. However, LiVOPO4 exhibits polymorphism, forming either the αI, β, or ε phase. A thorough comparison between the properties of these phases is difficult because they usually differ in synthesis methods. In this study, we synthesize all three polymorphs by annealing a single precursor, LiVOPO4 ·2H2 O, thereby reducing the effect of synthesis on the properties of the materials. We show through in situ XRD with heating and DFT calculations that, in terms of stability, αI -LiVOPO4 ⋘ ε-LiVOPO4 ≤ β-LiVOPO4 . We also show experimentally and through DFT calculations that the tolerance to O-interstitials and O-vacancies can explain the differences in stability, morphology, and electrochemical performance between β- and ε-LiVOPO4 . β-LiVOPO4 is more stable in the presence of O-interstitials while ε-LiVOPO4 is favored in the presence of O-vacancies. These defects affect the surface energies and morphology of the products formed, which are confirmed in the Wulff shape calculations and transmission electron microscopy images. These imply that β-LiVOPO4 has an improved rate performance under an oxidizing atmosphere due to the increased presence of facets with superior ion diffusion at the surface. This improved performance is seen by the improved rate capability and capacity of β-LiVOPO4 in the high-voltage region. In contrast, synthesis conditions have little effect on improving the rate performance of ε-LiVOPO4 .