Thermal and structural instability of sodium-iron carbonophosphate ball milled with carbon
- 1. Institute of Solid State Chemistry and Mechanochemistry, Siberian Branch of the Russian Academy of Sciences, 18 Kutateladze, 630128, Novosibirsk (Russian Federation)
- 2. Institute of Chemistry, Far-East Branch of the Russian Academy of Sciences, 159 pr. Stoletiya Vladivostoka, 690022, Vladivostok (Russian Federation)
- 3. Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences, 91 Pervomaiskaya, 620990, Yekaterinburg (Russian Federation)
Description
Highlights: • NFPC/C composites were prepared by ball milling NFPC with carbon using SPEX 8000. • Structural disordering and partial decomposition of NFPC occurs upon ball milling. • NFPC/C composites show better high-rate performance due to improved conductivity. • A single-phase mechanism of sodium (de)intercalation is established. -- Abstract: Pristine Na3FePO4CO3 (NFPC) with the monoclinic structure and the P21/m space group was prepared by hydrothermal synthesis at 120 °C. To increase the conductivity of NFPC, it was ball milled with carbon using a SPEX 8000 mill. Crystal and local structure, morphology, thermal stability, conductivity and electrochemical properties of NFPC and NFPC/C composites were studied by XRD, DSC/TG, FTIR, Mӧssbauer spectroscopy, 23NMR spectroscopy, magnetic measurements, SEM, EIS and galvanostatic cycling. It has been shown that the as-prepared NFPC is stable below 500 °C and then decomposes to Fe3O4 and Na3PO4. Ball milling of NFPC with and without carbon leads to its partial decomposition with the formation of nanosized superparamagnetic Fe3O4 particles and a significant structural disordering, though the crystal symmetry maintains unchanged. Due to high sensitivity of NFPC to air, pristine sample contains some portion of the Fe3+ ions; it increases after ball milling. As a result, all samples are able to cycle starting both with charge and discharge. NFPC shows high stability upon cycling with the specific discharge capacity close to the theoretical one (96 mA·h·g−1 for one-electron reaction). Though the capacity of the NFPC/C composites is slightly lower at low cycling rate than that of pristine NFPC, they show better high-rate performance due to improved conductivity via the formation of the highly conductive carbon matrix. As-established low lattice volume variation upon (de)intercalation of the sodium ions along with realization of a single-phase mechanism is responsible for a long cycle life of the NFPC/C cathode material.
Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2019.02.001;
- PII
- S0013468619302269;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 302
- Journal Page Range
- p. 119-129
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55102818
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CARBON; DECOMPOSITION; ELECTROCHEMISTRY; HYDROTHERMAL SYNTHESIS; INFRARED SPECTRA; MILLING; MONOCLINIC LATTICES; NANOSTRUCTURES; SCANNING ELECTRON MICROSCOPY; SODIUM; SPACE GROUPS; SPECTROSCOPY; THERMAL CONDUCTIVITY; X-RAY DIFFRACTION
- Descriptors DEC
- ALKALI METALS; CHEMICAL REACTIONS; CHEMISTRY; COHERENT SCATTERING; CRYSTAL LATTICES; CRYSTAL STRUCTURE; DIFFRACTION; ELECTRON MICROSCOPY; ELEMENTS; MACHINING; METALS; MICROSCOPY; NONMETALS; PHYSICAL PROPERTIES; SCATTERING; SPECTRA; SYMMETRY GROUPS; SYNTHESIS; THERMODYNAMIC PROPERTIES; THREE-DIMENSIONAL LATTICES
Optional Information
- Copyright
- Copyright (c) 2019 Elsevier Ltd. All rights reserved.