Phase-Homogeneous LiFePO4 Powders with Crystallites Protected by Ferric-Graphite-Graphene Composite

Author:

Agafonov Dmitry1,Bobyl Aleksandr2,Kamzin Aleksandr2ORCID,Nashchekin Alexey2ORCID,Ershenko Evgeniy2,Ushakov Arseniy3ORCID,Kasatkin Igor4,Levitskii Vladimir5ORCID,Trenikhin Mikhail6,Terukov Evgeniy7

Affiliation:

1. Department of Electrochemical Production Technology, St. Petersburg State Institute of Technology, Moskovski Ave. 26, 190013 St. Petersburg, Russia

2. Division of Solid State Physics, Ioffe Institute, Politekhnicheskaya Str. 26, 194021 St. Petersburg, Russia

3. Institute of Chemistry, Saratov State University, Astrakhanskaya Str. 83, 410012 Saratov, Russia

4. Research Park, RC XRD, St. Petersburg State University, Universitetskaya nab. 7–9, 199034 St. Petersburg, Russia

5. RnD Center TFTE, Politekhnicheskaya Str. 26, 194021 St. Petersburg, Russia

6. Department “Chemistry and Chemical Technology”, Petrochemical Institute, Omsk State Technical University, Mira Ave. 11, 644050 Omsk, Russia

7. Department of Electronics, St. Petersburg State Electrotechnical Univeristy, ul. Professora Popova 5, 197022 St. Petersburg, Russia

Abstract

Phase-homogeneous LiFePO4 powders have been synthesized. The content of impurity crystalline phases was less than 0.1%, according to synchrotron diffractometry (SXRD) data. Anisotropic crystallite sizes L¯Vhkl were determined by XRD. A low resistance covering layer of mechanically strong ferric-graphite-graphene composite with impregnated ferric (Fe3+) particles < 10 nm in size increases the cycleability compared to industrial cathodes. In accordance with the corrosion model, the destruction of the Fe3+-containing protective layer of crystallites predominates at the first stage, and at the second stage Fe escapes into the electrolyte and to the anode. The crystallite size decreases due to amorphization that starts from the surface. The rate capability, Q(t), has been studied as a function of L¯Vhkl, of the correlation coefficients rik between crystallite sizes, of the Li diffusion coefficient, D, and of the electrical relaxation time, τel. For the test cathode with a thickness of 8 μm, the values of D = 0.12 nm2/s, τel = 8 s were obtained. To predict the dependence Q(t), it is theoretically studied in ranges closest to experimental values: D = 0.5 ÷ 0.03 nm2/s, τel = 8/1 s, average sizes along [010] L¯1 = 90/30 nm, averaged r¯ = 0/1.

Publisher

MDPI AG

Subject

Energy (miscellaneous),Energy Engineering and Power Technology,Renewable Energy, Sustainability and the Environment,Electrical and Electronic Engineering,Control and Optimization,Engineering (miscellaneous),Building and Construction

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