Application of the High Electronic Conductivity Double Oxide to Cathode Active Material in Battery
Application of the High Electronic Conductivity Double Oxide to Cathode Active Material in Battery
批准号:
10650827
负责人:
ESAKA Takao
金额:
$1.73万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 1999
中文摘要
In order to check the application of high conductivity oxide ceramics to cathode active materials Inbatteries,cathodic behaviors were investigated as to the several types of substituted oxide ceramics basedon CaMnO D23-δ D2 in kaline solutions. As a result, it was found that some oxides,Ca-sites of which were substituted by rare earth elementshow high electronic conductivity of more than 10 - D11 - D1 S cm - D1-1 - D1 at room temperature evenin the sintered porous state and the ceramics work as the cathode active materials without anyconductive additives. The discharge performance changes depending on The kind of rare earth elementand alkaline solutionand the way of the substitution. the highest discharge capacity is 225mah g -1 -1 - D1 (810c)g -1 -1) for the x=0.1 sample of Ca - D21-x - D2La - D22x/3 - D2MnO - D23-δ D2 in 5% LiOHsolution.The sintered ceramic Ca d20 .9 D2La d20 .1 D2MnO D23-δ D2 also showed the cathodeactive material properties of batteries without conductive powder such as graphite in some salinesolutions including chloride ions. The discharge capacity changed depending on The kind and Theconcentration of saline solutions. The discharge能力obtained in 15%LiCl solution (670c)g -1 d -1 d),which corresponded to that manganese in the oxide was reduced partly from Mn D14+ D1 toMn - D12+ D1. This discharge capacity was almost comparable to that of electrolytic MnO - D22 - D2包含conductive material such as graphite.In the system Ca-Fe-O,CaFeO D23-δ D2 was not obtained by the ordinary sintering method. On the other hand,SrFeO D23-δ D2 was able to be prepared,which had a little lower discharge property than Ca d20 .9 D2La d20 .1 D2MnO D23-δ D2 but showedthe possibility to be employed as a cathode material in rechargeable battery
英文摘要
In order to check the application of high conductivity oxide ceramics to cathode active materials in batteries, the cathodic behaviors were investigated as to the several types of substituted oxide ceramics based on CaMnOィイD23-δィエD2 in alkaline solutions. As a result, it was found that some oxides, the Ca-sites of which were substituted by rare earth element, show high electronic conductivity of more than 10ィイD11ィエD1 S cmィイD1-1ィエD1 at room temperature even in the sintered porous state and the ceramics work as the cathode active materials without any conductive additives. The discharge performance changes depending on the kind of rare earth element and alkaline solution, and the way of the substitution. The highest discharge capacity is 225 mAh gィイD1-1ィエD1 (810 C gィイD1-1ィエD1) for the x=0.1 sample of CaィイD21-xィエD2LaィイD22x/3ィエD2MnOィイD23-δィエD2 in 5% LiOH solution.The sintered ceramic CaィイD20.9ィエD2LaィイD20.1ィエD2MnOィイD23-δィエD2 also showed the cathode active material properties of batteries without conductive powder such as graphite in some saline solutions including chloride ions. The discharge capacity changed depending on the kind and the concentration of saline solutions. The discharge capacity obtained in 15%LiCl solution (670 C gィイD1-1ィエD1), which corresponded to that manganese in the oxide was reduced partly from MnィイD14+ィエD1 to MnィイD12+ィエD1. This discharge capacity was almost comparable to that of electrolytic MnOィイD22ィエD2 including the conductive material such as graphite.In the system Ca-Fe-O, CaFeOィイD23-δィエD2 was not obtained by the ordinary sintering method. On the other hand, SrFeOィイD23-δィエD2 was able to be prepared, which had a little lower discharge property than CaィイD20.9ィエD2LaィイD20.1ィエD2MnOィイD23-δィエD2 but showed the possibility to be employed as a cathode material in rechargeable battery
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H.Sakaguchi, H.Honda, T.Esaka: "Synthesis and Anode Behavior of Lithium Storage Intermetallic Compounds with Various Crystallinities"Journal of Power Sources. Vol.81-82. 229-232 (1999)
H.Sakaguchi、H.Honda、T.Esaka:“具有不同结晶度的锂存储金属间化合物的合成和阳极行为”电源杂志。
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作者:
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通讯作者:
H.Sakaguchi, H.Honda, H.Maeta, T.Esaka: "Synthesis of Lithium Storage Intermetallic Compounds and Their Anode Behavior in Secondary Batteries"The Japan Institute of Metals, Proceedings. Vol.12. 1305-1308 (1999)
H.Sakaguchi、H.Honda、H.Maeta、T.Esaka:“锂存储金属间化合物的合成及其在二次电池中的阳极行为”日本金属学会会议录。
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通讯作者:
S.Takai: "Ionic Conduction Properties of Pb_<1-x>Ln_xWO_<4+δ>,(Ln=Prand Tb)"Material Research Bulletn. 34・2. 193-203 (1999)
S.Takai:“Pb_<1-x>Ln_xWO_<4+δ>,(Ln=Prand Tb)的离子传导性质”材料研究公报34・2 (1999)。
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H.sakaguchi, H.Honda, T.Esaka: "Synthesis of Lithium Storage Intermetallic Compounds as Anode Material"Denki Kagaku. Vol.66, No.12. 1291-1292 (1998)
H.sakaguchi、H.Honda、T.Esaka:“作为负极材料的锂储存金属间化合物的合成”Denki Kagaku。
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通讯作者:
S.Takai: "Mechanical Alloying of the Perovskite-type Structured Powder of La_<2/3-x>Li_<3x>TiO_3Showing Lithium Ion Conduction"Material Science Forum. 269. 93-97 (1998)
S.Takai:“显示锂离子传导的La_<2/3-x>Li_<3x>TiO_3钙钛矿型结构粉末的机械合金化”材料科学论坛。
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共 24 条
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