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FePO4-coated Li[Li0.2Ni0.13Co0.13Mn0.54]O2 with improved cycling performance as cathode material for Li-ion batteries 被引量:4

FePO_4-coated Li[Li_(0.2)Ni_(0.13)Co_(0.13)Mn_(0.54)]O_2 with improved cycling performance as cathode material for Li-ion batteries
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摘要 Li[Li0.2Ni0.13Coo.13Mn0.54]O2 cathode materials were synthesized by carbonate-based co-precipitation method, and then, its surface was coated by thin layers of FePO4. The prepared samples were characterized by X-ray diffraction (XRD), field emission scanning electron micro- scope (FESEM), energy-dispersive spectroscopy (EDS), and transmission electron microscopy (TEM). The XRD and TEM results suggest that both the pristine and the coated materials have a hexagonal layered structure, and the FePO4 coating layer does not make any major change in the crystal structure. The FePO4-coated sample exhibits both improved initial discharge capacity and columbic efficiency compared to the pristine one. More significantly, the FePO4 coating layer has a much positive influence on the cycling perfor- mance. The FePO4-coated sample exhibits capacity reten- tion of 82 % after 100 cycles at 0.5℃ between 2.0 and 4.8 V, while only 28 % for the pristine one at the same charge-discharge condition. The electrochemical impe- dance spectroscopy (EIS) results indicate that this improved cycling performance could be ascribed to the presence of FePO4 on the surface of Li[Li0.2Ni0.13Co0.13Mno.54102 par- ticle, which helps to protect the cathode from chemical attacks by HF and thus suppresses the large increase in charge transfer resistance. Li[Li0.2Ni0.13Coo.13Mn0.54]O2 cathode materials were synthesized by carbonate-based co-precipitation method, and then, its surface was coated by thin layers of FePO4. The prepared samples were characterized by X-ray diffraction (XRD), field emission scanning electron micro- scope (FESEM), energy-dispersive spectroscopy (EDS), and transmission electron microscopy (TEM). The XRD and TEM results suggest that both the pristine and the coated materials have a hexagonal layered structure, and the FePO4 coating layer does not make any major change in the crystal structure. The FePO4-coated sample exhibits both improved initial discharge capacity and columbic efficiency compared to the pristine one. More significantly, the FePO4 coating layer has a much positive influence on the cycling perfor- mance. The FePO4-coated sample exhibits capacity reten- tion of 82 % after 100 cycles at 0.5℃ between 2.0 and 4.8 V, while only 28 % for the pristine one at the same charge-discharge condition. The electrochemical impe- dance spectroscopy (EIS) results indicate that this improved cycling performance could be ascribed to the presence of FePO4 on the surface of Li[Li0.2Ni0.13Co0.13Mno.54102 par- ticle, which helps to protect the cathode from chemical attacks by HF and thus suppresses the large increase in charge transfer resistance.
出处 《Rare Metals》 SCIE EI CAS CSCD 2017年第11期899-904,共6页 稀有金属(英文版)
基金 financially supported by the National Nature Science Foundation of China (No.51302017) the National High Technology Research and Development Program of China (No.2012AA110102) the fund from the Science and Technology Commission of Beijing (No.2121100006712002)
关键词 Cathodes Charge transfer Coated materials Coatings Crystal structure Electric batteries Electrochemical impedance spectroscopy Electrodes Energy dispersive spectroscopy Field emission cathodes High resolution transmission electron microscopy Lithium Lithium alloys Lithium compounds Manganese Nickel Precipitation (chemical) Scanning electron microscopy Secondary batteries Transmission electron microscopy X ray diffraction Cathodes Charge transfer Coated materials Coatings Crystal structure Electric batteries Electrochemical impedance spectroscopy Electrodes Energy dispersive spectroscopy Field emission cathodes High resolution transmission electron microscopy Lithium Lithium alloys Lithium compounds Manganese Nickel Precipitation (chemical) Scanning electron microscopy Secondary batteries Transmission electron microscopy X ray diffraction
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