Method for preparing lithium-sulfur battery positive electrode material of composite metal organic framework
An organic framework and lithium-sulfur battery technology, applied in the field of material chemistry, can solve the problems of poor cycle performance of lithium-sulfur batteries, corrosion of metal lithium, loss of active materials, loss of active materials, etc., to improve redox reaction kinetics, excellent cycle Stability, the effect of inhibiting the shuttle effect
Image
Examples
Embodiment example 1
[0029] Step 1: Synthesize ZIF67 material:
[0030] 1.145g Co(NO 3 ) 2 ·6H 2 O was dissolved in 125ml of methanol, stirred until completely dissolved to obtain Co(NO 3 ) 2 ·6H 2 O solution. 1.640 g of 2-methylimidazole (Hmim) was dissolved in 125 mL of methanol, and stirred until completely dissolved to obtain a 2-methylimidazole solution. Pour the 2-methylimidazole solution slowly into Co(NO 3 ) 2 ·6H 2 In the O solution, stir for 30 min. After the purple clear liquid turns into a purple turbid liquid, leave it to stand and age for 24 hours, and centrifuge to collect the precipitate. Subsequently, it was washed 5 times with methanol, 2 times with ethanol, and dried in vacuum at 60° C. for 24 hours to obtain ZIF67 material.
[0031] Step 2: Synthesize ZIF67 / ZnO material:
[0032] 0.3864g Zn(CH 3 COO) 2 ·H 2 O was added to 50ml methanol, put on the heating plate at 65℃ and stirred until completely dissolved to obtain Zn(CH 3 COO) 2 ·H 2 O solution. Put 0.2384g of KOH into 40ml of me...
Embodiment example 2
[0038] Step 1: Synthesize ZIF67 material:
[0039] 1.145g Co(NO 3 ) 2 ·6H 2 O was dissolved in 125ml of methanol, stirred until completely dissolved to obtain Co(NO 3 ) 2 ·6H 2 O solution. 1.640 g of 2-methylimidazole (Hmim) was dissolved in 125 mL of methanol, and stirred until completely dissolved to obtain a 2-methylimidazole solution. Pour the 2-methylimidazole solution slowly into Co(NO 3 ) 2 ·6H 2 In the O solution, stir for 30 min. After the purple clear liquid turns into a purple turbid liquid, leave it to stand and age for 24 hours, and centrifuge to collect the precipitate. Then it was washed with methanol for 5 times by centrifugation, and washed with ethanol for 2 times, and dried in vacuum at 60° C. for 24 hours to obtain the ZIF67 material.
[0040] Step 2: Synthesis of ZIF67 / ZnO:
[0041] 0.3864g Zn(CH 3 COO) 2 ·H 2 O was added to 50ml methanol, put on the heating plate at 65℃ and stirred until completely dissolved to obtain Zn(CH 3 COO) 2 ·H 2 O solution. Put 0.238...
PUM
Login to View More Abstract
Description
Claims
Application Information
- IPC
- C08G83/00; H01M4/62; H01M10/052
- CPC
- C08G83/008; H01M4/624; H01M4/628; H01M10/052; Y02E60/10
- Inventors
- 钊妍; 邱伟龙


