Oxygen evolution catalyst ofnitrogen-sulfur-containing ordered mesoporous carbon coated nano Co3O4
A mesoporous carbon and catalyst technology, applied in the field of electrochemical energy, can solve problems such as slowness, limitation, high overpotential, and reduced catalytic efficiency of oxygen evolution reaction
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Embodiment 1
[0028] (1) 0.6g of phthalic anhydride and 0.5g of 2-(4-(thiophen-2-yl)phenyl)thiophene were dissolved in 20mL of dichloromethane, and 0.62g of catalyst was added in a nitrogen atmosphere Aluminum trichloride, heated to 25°C for reflux reaction for 12h, concentrated under reduced pressure after the reaction, and separated by column chromatography with petroleum ether: ethyl acetate = 3:1 eluent to obtain terephthalenedi(carboxyphenyl)thiophene compound.
[0029] (2) Dissolve 1g of p-di(carboxyphenyl)thiophene compound and 0.3g of pyrrole in 80mL of 1,2-dichloromethane, add 1.2g of dimethoxymethane and 1.1g of trichloride in a nitrogen atmosphere Iron, stirred evenly, heated to 70°C, reacted for 15 hours, cooled after reaction, distilled under reduced pressure, extracted with methanol, tetrahydrofuran and dichloromethane in sequence to obtain carboxyl-containing thiophene pyrrole hypercrosslinked polymer.
[0030] (3) Add 2 g of carboxyl-containing thiophene pyrrole hypercrossl...
Embodiment 2
[0033] (1) 0.65g of phthalic anhydride and 0.5g of 2-(4-(thiophen-2-yl)phenyl)thiophene were dissolved in 20mL of dichloromethane, and 0.7g of catalyst was added in a nitrogen atmosphere Aluminum trichloride, heated to 40°C for reflux reaction for 18h, concentrated under reduced pressure after the reaction, and separated by column chromatography with an eluent of petroleum ether:ethyl acetate=5:1 to obtain terephthalenedi(carboxyphenyl)thiophene compound.
[0034] (2) Dissolve 1g of p-di(carboxyphenyl)thiophene compound and 0.4g of pyrrole into 100mL of 1,2-dichloromethane, add 1.4g of dimethoxymethane and 1.25g of trichloride in a nitrogen atmosphere Iron, stirred evenly, heated to 70°C, reacted for 30h, cooled after reaction, distilled under reduced pressure, extracted with methanol, tetrahydrofuran and dichloromethane in sequence to obtain carboxyl-containing thiophene pyrrole hypercrosslinked polymer.
[0035] (3) Add 2g of carboxyl-containing thiophene pyrrole hypercross...
Embodiment 3
[0038] (1) 0.72g of phthalic anhydride and 0.5g of 2-(4-(thiophen-2-yl)phenyl)thiophene were dissolved in 30mL of dichloromethane, and 0.75g of catalyst was added in a nitrogen atmosphere Aluminum trichloride, heated to 40°C for reflux reaction for 18h, concentrated under reduced pressure after the reaction, and separated by column chromatography with petroleum ether: ethyl acetate = 15:1 eluent to obtain terephthalenedi(carboxyphenyl)thiophene compound.
[0039] (2) Dissolve 1g of p-phenylene di(carboxyphenyl)thiophene compound and 0.48g of pyrrole into 120mL of 1,2-dichloromethane, add 1.6g of dimethoxymethane and 1.5g of trichloride in a nitrogen atmosphere Iron, stirred evenly, heated to 75°C, reacted for 24 hours, cooled after reaction, distilled under reduced pressure, extracted with methanol, tetrahydrofuran and dichloromethane in sequence to obtain carboxyl-containing thiophene pyrrole hypercrosslinked polymer.
[0040] (3) Add 2g of carboxyl-containing thiophene pyrr...
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