Oxidation pressure leaching was proposed to selectively dissolve Li from spent LiFePO_(4) batteries in a stoichiometric sulfuric acid solution.Using O_(2) as an oxidant and stoichiometric sulfuric acid as leaching age...Oxidation pressure leaching was proposed to selectively dissolve Li from spent LiFePO_(4) batteries in a stoichiometric sulfuric acid solution.Using O_(2) as an oxidant and stoichiometric sulfuric acid as leaching agent,above 97% of Li was leached into the solution,whereas more than 99% of Fe remained in the leaching residue,enabling a relatively low cost for one-step separation of Li and Fe.And then,by adjusting the pH of leachate,above 95% of Li was recovered in the form of the Li_(3)PO_(4) product through iron removal and chemical precipitation of phosphate.展开更多
A supercritical hydrothermal method was employed to prepare sub-micrometer LiFePO4particles with high purity and crystallinity.The structure and morphology of LiFePO4particles were characterized by X-ray diffraction a...A supercritical hydrothermal method was employed to prepare sub-micrometer LiFePO4particles with high purity and crystallinity.The structure and morphology of LiFePO4particles were characterized by X-ray diffraction and scanning electron microscope.The electrochemical tests were carried out to determine the reversible capacity,rate and cycling performance of the LiFePO4particles as cathode material for lithium ion battery.Experimental results show that solvent and calcining time have significant effects on purity,size and morphology of LiFePO4particles.Mixed solvent contained deionized water and ethanol is conducive to synthesize smaller and more uniform particles.The size of LiFePO4particles as-prepared is about 100-300 nm.The specific discharge capacities of the LiFePO4particles are 151.3 and 128.0 mA·h·g?1 after first cycle at the rates of 0.1 and 1.0 C,respectively.It retains 95.0%of the initial capacity after 100 cycles at 1.0 C.展开更多
A facile and practical route was introduced to prepare LiFePO4/C cathode material with nano-sized primary particles and excellent electrochemical performance. LiH2PO4 was synthesized by using H3PO4 and LiOH as raw mat...A facile and practical route was introduced to prepare LiFePO4/C cathode material with nano-sized primary particles and excellent electrochemical performance. LiH2PO4 was synthesized by using H3PO4 and LiOH as raw materials. Then, as-prepared LiH2PO4, reduced iron powder andα-D-glucose were ball-milled, dried and sin-tered to prepare LiFePO4/C. X-ray diffractometry was used to characterize LiH2PO4, ball-milled product and LiFePO4/C. Differential scanning calorimeter-thermo gravimetric analysis was applied to investigate possible reac-tions in sintering and find suitable temperature for LiFePO4 formation. Scanning electron microscopy was em-ployed for the morphology of LiFePO4/C. As-prepared LiH2PO4 is characterized to be in P21cn（33） space group, which reacts with reduced iron powder to form Li3PO4, Fe3（PO4）2 and H2 in ball-milling and sintering. The appro-priate temperature for LiFePO4/C synthesis is 541.3-976.7 ℃. LiFePO4/C prepared at 700 ℃ presents nano-sized primary particles forming aggregates. Charge-discharge examination indicates that as-prepared LiFePO4/C displays appreciable discharge capacities of 145 and 131 mA·h·g^-1 at 0.1 and 1 C respectively and excellent discharge ca-pacity retention.展开更多
基金the financial supports from the National Natural Science Foundation of China(Nos.51804083,52104395,21906031)the Natural Science Foundation of Guangdong Province,China(No.2019A1515011628)+1 种基金the Science and Technology Planning Project of Guangdong Province,China(No.2017B090907026)the Special Program of Guangdong Academy of Sciences,China(Nos.2019GDASYL-0103069,2020GDASYL-0104027,2020GDASYL-0302004,2020GDASYL-0302009,2021GDASYL-0302004)。
文摘Oxidation pressure leaching was proposed to selectively dissolve Li from spent LiFePO_(4) batteries in a stoichiometric sulfuric acid solution.Using O_(2) as an oxidant and stoichiometric sulfuric acid as leaching agent,above 97% of Li was leached into the solution,whereas more than 99% of Fe remained in the leaching residue,enabling a relatively low cost for one-step separation of Li and Fe.And then,by adjusting the pH of leachate,above 95% of Li was recovered in the form of the Li_(3)PO_(4) product through iron removal and chemical precipitation of phosphate.
文摘A supercritical hydrothermal method was employed to prepare sub-micrometer LiFePO4particles with high purity and crystallinity.The structure and morphology of LiFePO4particles were characterized by X-ray diffraction and scanning electron microscope.The electrochemical tests were carried out to determine the reversible capacity,rate and cycling performance of the LiFePO4particles as cathode material for lithium ion battery.Experimental results show that solvent and calcining time have significant effects on purity,size and morphology of LiFePO4particles.Mixed solvent contained deionized water and ethanol is conducive to synthesize smaller and more uniform particles.The size of LiFePO4particles as-prepared is about 100-300 nm.The specific discharge capacities of the LiFePO4particles are 151.3 and 128.0 mA·h·g?1 after first cycle at the rates of 0.1 and 1.0 C,respectively.It retains 95.0%of the initial capacity after 100 cycles at 1.0 C.
基金Supported partially by the Natural Science Foundation of Yunnan Province(2010ZC051)Analysis and Testing Foundation(2009-041)Starting Research Fund(14118245) from Kunming University of Science and Technology
文摘A facile and practical route was introduced to prepare LiFePO4/C cathode material with nano-sized primary particles and excellent electrochemical performance. LiH2PO4 was synthesized by using H3PO4 and LiOH as raw materials. Then, as-prepared LiH2PO4, reduced iron powder andα-D-glucose were ball-milled, dried and sin-tered to prepare LiFePO4/C. X-ray diffractometry was used to characterize LiH2PO4, ball-milled product and LiFePO4/C. Differential scanning calorimeter-thermo gravimetric analysis was applied to investigate possible reac-tions in sintering and find suitable temperature for LiFePO4 formation. Scanning electron microscopy was em-ployed for the morphology of LiFePO4/C. As-prepared LiH2PO4 is characterized to be in P21cn（33） space group, which reacts with reduced iron powder to form Li3PO4, Fe3（PO4）2 and H2 in ball-milling and sintering. The appro-priate temperature for LiFePO4/C synthesis is 541.3-976.7 ℃. LiFePO4/C prepared at 700 ℃ presents nano-sized primary particles forming aggregates. Charge-discharge examination indicates that as-prepared LiFePO4/C displays appreciable discharge capacities of 145 and 131 mA·h·g^-1 at 0.1 and 1 C respectively and excellent discharge ca-pacity retention.
