Lithium iron phosphate (LiFePO4) is prepared by hydrothermal process using Fe(III) as precursor and pyrrole as an efficient reducing agent. The Fe(III) precursor in the system reacts with pyrrole to generate polypyrrole (PPy) and reduce Fe(III) to Fe(II). The different molar ratio Fe(III) polymerize different content of PPy and PPy can also be a carbon source for further calcination. The structural and morphological properties of LiFePO4 powder were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and a transmission electron microscope (TEM). The XRD and TEM results demonstrate that LiFePO4 powder has an orthorhombic olivine-type structure with a space group of Pnma. The SEM and TEM results show that the particle size of LiFePO4 is around 200 nm and a layer of carbon coats on LiFePO4. The chemical composition of the LiFePO4 powder was characterized by elemental analysis (EA) and inductively coupled plasma/mass spectroscopy (ICP/MS). Raman and X-ray photoelectron spectroscopy (XPS) results indicate that pyrrole as a reducing agent reduces and prevents the formation of Fe(III) impurity and the resulting PPy plays a role as carbon source. Among the synthesized cathode materials, LiFePO4 synthesized using 5% molar ratio of Fe(III) and subsequent calcinations of 600 ¢XC shows the best electrochemical property with an discharge capacity of 160 mAhg−1 close to its theoretical capacity 170 mAh g−1 at 0.2 C rate. Using 10% molar ratio of Fe(III), and the discharge capacity of LiFePO4 at 10 C rate reaches 106 mAhg−1.
Identifer | oai:union.ndltd.org:NSYSU/oai:NSYSU:etd-0803112-150151 |
Date | 03 August 2012 |
Creators | Chen, Wen-jing |
Contributors | Chi-wi Ong, Jyh-tsung Lee, Mao-sung Wu |
Publisher | NSYSU |
Source Sets | NSYSU Electronic Thesis and Dissertation Archive |
Language | Cholon |
Detected Language | English |
Type | text |
Format | application/pdf |
Source | http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0803112-150151 |
Rights | user_define, Copyright information available at source archive |
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