A kind of preparation method of high specific capacity lithium battery negative electrode material
A negative electrode material, high specific capacity technology, applied in battery electrodes, secondary batteries, circuits, etc., can solve the problems of poor conductivity, large volume change, large irreversible capacity, etc., to achieve the effect of improved stability and simple method
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specific Embodiment 1
[0036] (1) Organic ligand H 3 Synthesis of BTPCA
[0037] Such as figure 1 Organic ligand H in the present invention 3 The schematic diagram of the synthetic reaction steps of BTPCA is shown, and the specific experimental steps are as follows:
[0038]4-piperidinecarboxylic acid (1 g, 10 mmol) was added into the flask, and then 3 ml of a 2 mol / L sodium hydroxide solution was added to the flask. And sodium bicarbonate (0.92 g, 11 mmol) and 0.6 g of cyanuric chloride were added thereto. The flask was stirred at normal temperature for ten minutes, and 5 ml of 1,4-dioxane was dropped thereinto during stirring. The flask was heated to a temperature ranging from 80-130°C for 12 hours. After the reaction, the flask was cooled to room temperature and diluted to pH=1 with dilute hydrochloric acid. Filtrate at room temperature and wash with water to obtain the ligand.
[0039] (2) Synthesis of metal-organic framework complexes (MOFs)
[0040] Such as figure 2 As shown in the s...
specific Embodiment 2
[0042] (1) Organic ligand H 3 Synthesis of BTPCA
[0043] Such as figure 1 Organic ligand H in the present invention 3 The schematic diagram of the synthetic reaction steps of BTPCA is shown, and the specific experimental steps are as follows:
[0044] 4-piperidinecarboxylic acid (2 g, 15 mmol) was added into the flask, and then 3 ml of a 2 mol / L sodium hydroxide solution was added to the flask. And sodium bicarbonate (0.92 g, 11 mmol) and 0.6 g of cyanuric chloride were added thereto. The flask was stirred at normal temperature for ten minutes, and 5 ml of 1,4-dioxane was dropped thereinto during stirring. The flask was heated to a temperature ranging from 80-130°C for 12 hours. After the reaction, the flask was cooled to room temperature and diluted to pH=1 with dilute hydrochloric acid. Filtrate at room temperature and wash with water to obtain the ligand.
[0045] (2) Synthesis of metal-organic framework complexes (MOFs)
[0046] Such as figure 2 As shown in the ...
specific Embodiment 3
[0048] (1) Organic ligand H 3 Synthesis of BTPCA
[0049] Such as figure 1 Organic ligand H in the present invention 3 The schematic diagram of the synthetic reaction steps of BTPCA is shown, and the specific experimental steps are as follows:
[0050] 4-piperidinecarboxylic acid (1.4 g, 13 mmol) was added into the flask, and then 3 ml of a 2 mol / L sodium hydroxide solution was added to the flask. And sodium bicarbonate (0.92 g, 11 mmol) and 0.6 g of cyanuric chloride were added thereto. The flask was stirred at normal temperature for ten minutes, and 5 ml of 1,4-dioxane was dropped thereinto during stirring. The flask was heated to a temperature ranging from 80-130°C for 12 hours. After the reaction, the flask was cooled to room temperature and diluted to pH=1 with dilute hydrochloric acid. Filtrate at room temperature and wash with water to obtain the ligand.
[0051] (2) Synthesis of metal-organic framework complexes (MOFs)
[0052] Such as figure 2 As shown in th...
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