Negative electrode composite material for sodium ion battery and preparation method thereof
A sodium-ion battery and negative electrode material technology, applied in battery electrodes, secondary batteries, carbon preparation/purification, etc., can solve poor electronic conductivity, limit the rate performance of sodium-ion batteries, cycle stability, volume expansion, etc. problems, achieve good industrialization prospects, improve charge specific capacity and rate performance, and stabilize crystal structure
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Embodiment 1
[0035] A method for preparing a carbon-coated bimetallic sulfide composite material for a negative electrode of a sodium ion battery, comprising the following steps:
[0036] 2.48g tungsten disulfide (WS 2 ) powder material and 4g polyvinylpyrrolidone (PVP) were uniformly mixed and dissolved in 1L methanol solution, and then 8.93g zinc nitrate hexahydrate (Zn(NO 3 ) 2 ·6H 2 O), stirred at 30°C for 48h at a stirring speed of 300rpm to WS 2 with Zn(NO 3 ) 2 ·6H 2 O was uniformly dispersed in methanol solution to form solution A.
[0037] Solution B was formed by dissolving 24.62 g of dimethylimidazole in 1 L of methanol solution. Solution B was slowly added to solution A, and the stirring was continued for 60 min until the reaction was complete. Centrifuge and wash three times under the condition of rotating speed of 6000 rpm, and place the obtained product in a vacuum drying oven to dry at 80° C. for 12 hours.
[0038]The dried material was heated to 800°C at a rate of...
Embodiment 2
[0044] A method for preparing a carbon-coated bimetallic sulfide composite material for a negative electrode of a sodium ion battery, comprising the following steps:
[0045] 2.48g tungsten disulfide (WS 2 ) powder material and 4g polyvinylpyrrolidone (PVP) were uniformly mixed and dissolved in 1L methanol solution, and then 2.97g zinc nitrate hexahydrate (Zn(NO 3 ) 2 ·6H 2 O), stirred at 30°C for 48h at a stirring speed of 300rpm to WS 2 with Zn(NO 3 ) 2 ·6H 2 O was uniformly dispersed in methanol solution to form solution A.
[0046] Solution B was formed by dissolving 8.21 g of dimethylimidazole in 1 L of methanol solution. Solution B was slowly added to solution A, and the stirring was continued for 60 min until the reaction was complete. Centrifuge and wash three times under the condition of rotating speed of 6000 rpm, and place the obtained product in a vacuum drying oven to dry at 80° C. for 12 hours.
[0047] The dried material was heated to 800°C at a rate of...
Embodiment 3
[0049] A method for preparing a carbon-coated bimetallic sulfide composite material for a negative electrode of a sodium ion battery, comprising the following steps:
[0050] 2.48g tungsten disulfide (WS 2 ) powder material and 4g polyvinylpyrrolidone (PVP) were uniformly mixed and dissolved in 1L methanol solution, and then 14.89g zinc nitrate hexahydrate (Zn(NO 3 ) 2 ·6H 2 O), stirred at 30°C for 48h at a stirring speed of 300rpm to WS 2 with Zn(NO 3 ) 2 ·6H 2 O was uniformly dispersed in methanol solution to form solution A.
[0051] Solution B was formed by dissolving 41.05 g of dimethylimidazole in 1 L of methanol solution. Solution B was slowly added to solution A, and the stirring was continued for 60 min until the reaction was complete. Centrifuge and wash three times under the condition of rotating speed of 6000 rpm, and place the obtained product in a vacuum drying oven to dry at 80° C. for 12 hours.
[0052] The dried material was heated to 800°C at a rate ...
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