Synthesis and characterization of LiFe0.5Mn0.3Co0.2PO4/C composite material for high-voltage Li-ion battery application
Creators
- 1. Department of Chemical and Materials Engineering, Green Technology Research Center, Chang Gung University, Taoyuan City 333, Taiwan (China)
- 2. Department of Chemical Engineering, Ming Chi University of Technology, New Taipei City 24301, Taiwan (China)
- 3. Battery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan (China)
- 4. Department of Safety, Health and Environmental Engineering, Ming Chi University of Technology, New Taipei City 243, Taiwan (China)
- 5. Department of Radiation Oncology, Chang Gung Memorial Hospital, Taoyuan City 333, Taiwan (China)
Description
Highlights: • The work reports the preparation of LiFe0.5Mn0.3Co0.2PO4/C by a solid-state method. • Flower-like nano-sized Co3O4 is prepared by a hydrothermal process. • The capacity of LFMCP/C with 1%TMB shows 150 mAh g−1 at 0.1C and 120 mAh g−1 at 1C. • XPS and SIMS were used to study the properties of CEI with and without 1%TMB. • We propose a dual layer structure CEI model for LFMCP. A LiFe0.5Mn0.3Co0.2PO4/C composite cathode material was prepared using a solid-state ball-milling method. The flower-like Co3O4 precursor was prepared by hydrothermal method and used to improve the electrochemical properties of composite material. The galvanostatic charge–discharge profile is performed in the potential range of 2–5 V by using different electrolyte compositions with/without 1 wt% trimethyl boroxane (TMB) additive at various C rates. The highest discharge capacities of the composite material were 150.42 mAh g−1 at 0.1C and 120 mAh g−1 at 1C in LiPF6+1 wt%TMB in EC:EMC (1:2, v/v). In addition, the excellent cycle-life was observed at 0.1C and 1C rate for 30 and 100 cycles with the charge retention of 97.7% and 73%, respectively. These appreciable results were obtained due to the carbon coating layer and highly active composite material. The thickness of cathode electrolyte interphase layer on composite electrode is ca. 3 nm which was measured by secondary ion mass spectroscopy. And also, we found that the B element on interphase layer that acts as F-scavenger to reduce the amount of LiF formation over cathode interphase layer. As a result, it can markedly reduce the charge transfer resistance and improve the electrochemical performance for long-term cycling.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jallcom.2018.04.098Additional details
Identifiers
- DOI
- 10.1016/j.jallcom.2018.04.098;
- PII
- S0925838818313938;
Publishing Information
- Journal Title
- Journal of Alloys and Compounds
- Journal Volume
- 750
- Journal Page Range
- p. 945-958
- ISSN
- 0925-8388
- CODEN
- JALCEU
INIS
- Country of Publication
- Switzerland
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 53077618
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CATHODES; COBALT OXIDES; COMPOSITE MATERIALS; ELECTRIC POTENTIAL; ELECTROLYTES; HYDROTHERMAL SYNTHESIS; ION MICROPROBE ANALYSIS; LAYERS; LITHIUM ION BATTERIES; MASS SPECTROSCOPY; NANOSTRUCTURES; SOLIDS; THICKNESS; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- CHALCOGENIDES; CHEMICAL ANALYSIS; COBALT COMPOUNDS; DIMENSIONS; ELECTRIC BATTERIES; ELECTROCHEMICAL CELLS; ELECTRODES; ELECTRON SPECTROSCOPY; ENERGY STORAGE SYSTEMS; ENERGY SYSTEMS; MATERIALS; MICROANALYSIS; NONDESTRUCTIVE ANALYSIS; OXIDES; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; SPECTROSCOPY; SYNTHESIS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2018 Elsevier B.V. All rights reserved.