Aerogel compositions for high temperature applications
US-2024360363-A1 · Oct 31, 2024 · US
US2017040123A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017040123-A1 |
| Application number | US-201514820397-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 6, 2015 |
| Priority date | Aug 6, 2015 |
| Publication date | Feb 9, 2017 |
| Grant date | — |
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Disclosed here is a method for making a nitrogen-doped carbon aerogel, comprising: preparing a reaction mixture comprising formaldehyde, at least one nitrogen-containing resorcinol analog, at least one catalyst, and at least one solvent; curing the reaction mixture to produce a wet gel; drying the wet gel to produce a dry gel; and thermally annealing the dry gel to produce the nitrogen-doped carbon aerogel. Also disclosed is a nitrogen-doped carbon aerogel obtained according to the method and a supercapacitor comprising the nitrogen-doped carbon aerogel.
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What is claimed is: 1 . A method for making a nitrogen-doped carbon aerogel, comprising: preparing a reaction mixture comprising formaldehyde, at least one nitrogen-containing resorcinol analog, at least one catalyst, and at least one solvent; curing the reaction mixture to produce a wet gel; drying the wet gel to produce a dry gel; and thermally annealing the dry gel to produce the nitrogen-doped carbon aerogel. 2 . The method of claim 1 , wherein the resorcinol analog is selected from (a) an aromatic compound comprising a nitrogen-containing ring linked to at least two hydroxyl groups and (b) an aromatic compound comprising a benzene ring or nitrogen-containing ring linked to at least one hydroxyl group and at least one amine group, wherein the nitrogen-containing ring is selected from the group consisting of pyridine, pyrazine, pyrimidine, pyridazine, pyrrole, pyrazole and imidazole. 3 . The method of claim 1 , wherein the resorcinol analog is pyridinediol. 4 . The method of claim 1 , wherein the resorcinol analog is aminophenol. 5 . The method of claim 1 , wherein the solvent is water and/or an organic solvent. 6 . The method of claim 1 , wherein the catalyst is selected from the group consisting of acetic acid, nitric acid, ascorbic acid, hydrochloric acid, sulfuric acid, sodium carbonate, sodium hydroxide, ammonium hydroxide, and calcium sulfate. 7 . The method of claim 1 , wherein in the reaction mixture the molar ratio of the resorcinol analog to the catalyst ranges from about 10:1 to about 1000:1. 8 . The method of claim 1 , wherein the reaction mixture is substantially free of melamine. 9 . The method of claim 1 , wherein the reaction mixture is cured at a temperature of about 25° C. to about 100° C. 10 . The method of claim 1 , wherein the step of drying the wet gel comprises solvent exchange. 11 . The method of claim 1 , wherein the step of drying the wet gel comprises drying the wet gel with a supercritical fluid. 12 . The method of claim 1 , wherein the step of drying the wet gel comprises drying the wet gel with supercritical CO 2 . 13 . The method of claim 1 , wherein the dry gel is thermally annealed in an inert atmosphere at a temperature of about 600° C. or about 1200° C. 14 . A composition comprising a nitrogen-doped carbon aerogel obtained according to the method of claim 1 . 15 . The composition of claim 14 , wherein the nitrogen-doped carbon aerogel has a nitrogen content of about 4 wt. % or more. 16 . The composition of claim 14 , wherein the nitrogen-doped carbon aerogel has a surface area of about 100 m 2 /g or more. 17 . The composition of claim 14 , wherein the nitrogen-doped carbon aerogel has a density of about 0.5 g/ml or less. 18 . The composition of claim 14 , wherein the nitrogen-doped carbon aerogel has a specific capacitance of about 50 F/g or more. 19 . The composition of claim 14 , wherein the nitrogen-doped carbon aerogel has an areal capacitance of about 20 μF/cm 2 or more. 20 . A supercapacitor comprising the composition of claim 14 .
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