関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Lithium Carbonate | HCID 11125 | — |
| 反応物 | Cobalt | HCID 104730 | — |
| 反応物 | Lithium | HCID 3028194 | — |
| 反応物 | Cobalt oxide | HCID 6432046 | — |
| 反応物 | HCID 178528048 | HCID 178528048 | — |
| 生成物 | Vanadium | HCID 23990 | — |
| 生成物 | Cobalt | HCID 104730 | — |
| 生成物 | Cobalt oxide | HCID 6432046 | — |
反応手順
For the starting material, lithium carbonate (Li2CO3) was used as a lithium source, and (Cu0.999V0 001)3O4 which was a composite of tricobalt tetraoxide and vanadium (V) was used as a cobalt source. The composite of tricobalt tetraoxide and vanadium was obtained such that cobalt dissolved in an acid solution and vanadium were precipitated as a composite hydroxide and then were calcined at 300° C. Next, the lithium carbonate and the composite of tricobalt tetraoxide and vanadium were weighed out such that the molar ratio of Li to (Co+V) was 1, and there was then added MgF2 such that the fluorine content in the total amount of positive electrode active material was 0.01 mass %, and then the mixture was mixed. Subsequently, the mixture was calcined in an air atmosphere to obtain a calcined product of LiCo0.999V0 001O2 of a hexagonal crystal system containing fluorine and magnesium, and then the calcined product was ground in a mortar to an average particle size of 10 μm, thereby obtaining a positive electrode active material.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06919144B2 |
|---|
| 出典データセット | uspto-grants-2005_07 |
|---|
| ORD ID | ord-824df667e5044fb4b5461148b5c49453 |
|---|
| 出典メモ | uspto-grants-2005_07 |
|---|