کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1296996 | 1498315 | 2012 | 6 صفحه PDF | دانلود رایگان |
Fe0.5TiOPO4 oxyphosphate was prepared directly by solid state reaction. It crystallizes in the monoclinic system with P21/c space group and the use of Fe0.5TiOPO4 as an active material in lithium-ion batteries shows two potential plateaus and an irreversible discharge capacity of ~ 200 mAh/g. To understand the origin of this irreversibility, a series of LixFe0.5TiOPO4 (x = 0.06, 0.22, 0.76, 1.14) were chemically prepared and analyzed by X-ray diffraction. A structure amorphization of the LixFe0.5TiOPO4 phosphates takes place during the lithiation process. Magnetization and Mössbauer spectroscopy studies of the LixFe0.5TiOPO4 samples clearly show the formation of iron metal which induces a deterioration of the crystal structure of the studied electrode materials. The lithiation process leads thus to a conversion reaction which explains the irreversibility of the electrochemical process during the first discharge.
Mechanism of the first discharge of the Li//LixFe0.5TiOPO4.Figure optionsDownload as PowerPoint slideHighlights
► Fe0.5TiOPO4 exhibits a large capacity when used as active material for lithium-ion batteries.
► An irreversible discharge capacity of ~ 200 mAh/g is evidenced during the first discharge.
► Lithium insertion leads to an amorphization of the crystal structure of the studied phosphate.
► A conversion reaction occurs during the lithiation process inducing the formation of metallic Fe.
Journal: Solid State Ionics - Volume 224, 14 September 2012, Pages 15–20