Selective functionalization of carbon nanotubes
The present invention is directed toward methods of selectively functionalizing carbon nanotubes of a specific type or range of types, based on their electronic properties, using diazonium chemistry. The present invention is also directed toward methods of separating carbon nanotubes into populations of specific types or range(s) of types via selective functionalization and electrophoresis, and also to the novel compositions generated by such separations.
1. A method for selectively functionalizing carbon nanotubes, wherein the method comprises:
a) suspending a plurality of carbon nanotubes in a solvent to provide a plurality of suspended carbon nanotubes;
wherein the plurality of suspended carbon nanotubes comprise metallic carbon nanotubes, semimetallic carbon nanotubes and semiconducting carbon nanotubes; and
b) reacting a substoichiometric amount of a functionalizing species with respect to the amount of carbon of the carbon nanotubes, with the plurality of suspended carbon nanotubes;
wherein the substoichiometric amount of the functionalizing species is selected such that a reaction of the functionalizing species occurs only with metallic and semimetallic carbon nanotubes but not with semiconducting carbon nanotubes.
2. A method for selectively functionalizing carbon nanotubes, wherein the method comprises:
a) suspending a plurality of carbon nanotubes in a solvent to provide a plurality of suspended carbon nanotubes;
wherein the plurality of suspended carbon nanotubes comprise metallic carbon nanotubes, semimetallic carbon nanotubes and semiconducting carbon nanotubes; and
b) reacting a substoichiometric amount of a diazonium species, with respect to the amount of carbon of the carbon nanotubes, with the plurality of suspended carbon nanotubes;
wherein the substoichiometric amount of the diazonium species is selected such that a reaction of the diazonium species occurs only with metallic and semimetallic carbon nanotubes but not with semiconducting carbon nanotubes.
3. A method for selectively functionalizing carbon nanotubes, wherein the method comprises:
a) adding a plurality of carbon nanotubes to an aqueous surfactant solution and homogenizing to form a mixture of surfactant-suspended carbon nanotubes;
wherein the mixture of surfactant-suspended carbon nanotubes comprises metallic carbon nanotubes, semimetallic carbon nanotubes and semiconducting carbon nanotubes; and
b) reacting a substoichiometric amount of a diazonium species with respect to the amount of carbon of the carbon nanotubes with the mixture of surfactant-suspended carbon nanotubes;
wherein the substoichiometric amount of the diazonium species is selected such that a reaction of the diazonium species occurs only with metallic and semimetallic carbon nanotubes but not with semiconducting carbon nanotubes.
4. The method of any one of claims 1 - 3 , further comprising a step of thermal defunctionalization to regenerate separated, unfunctionalized carbon nanotubes.
5. The method of claims 1 , 2 or 3 , wherein the carbon nanotubes are selected from the group consisting of single-wall carbon nanotubes, multi-wall carbon nanotubes, double-wall carbon nanotubes, and combinations thereof.
6. The method of claims 1 , 2 or 3 , wherein the carbon nanotubes are single-wall carbon nanotubes.
7. The method of claim 3 , wherein the surfactant is selected from the group consisting of ionic surfactants, non-ionic surfactants, cationic surfactants, anionic surfactants, sodium dodecyl sulfate (SDS), sodium dodecylbenzene sulfonate (SDBS), sodium octylbenzene sulfonate, TRITON X-100, TRITON X-405, dodecyltrimethylammonium bromide (DTAB), and combinations thereof.
8. The method of claims 2 or 3 , wherein the diazonium species is an aryl diazonium salt.
9. The method of claim 8 , wherein the aryl diazonium salt comprises:
and wherein R is selected from the group consisting of halogen, nitro, cyano, alkyl, aryl, arylalkyl, OH, carboxylic ester, carboxylic acid, thiocarbonate, amide, alkoxy, polyether, polyalkyl, hydroxyl alkyl, and combinations thereof.
10. The method of claim 9 , wherein R is OH.
11. The method of claims 2 or 3 , wherein the diazonium species is generated in situ by reacting a substituted aniline species with an alkyl nitrite.
12. The method of claim 11 , wherein the substituted aniline species has a general formula
and wherein R is selected from the group consisting of halogen, nitro, cyano, alkyl, aryl, arylalkyl, OH, carboxylic ester, carboxylic acid, thiocarbonate, amide, alkoxy, polyether, polyalkyl, hydroxyl alkyl, and combinations thereof.
13. The method of claim 12 , wherein R is OH.