Chemical sensors containing carbon nanotubes, method for making same, and uses therof

Patent metadata

Field	Value
Publication number	US-10106403-B2
Application number	US-200913121377-A
Country	US
Kind code	B2
Filing date	Sep 28, 2009
Priority date	Sep 29, 2008
Publication date	Oct 23, 2018
Grant date	Oct 23, 2018

Abstract

A device is disclosed for detecting at least one chemical compound comprising at least one carbon nanotube with several graphene layers, on which is grafted at least one molecule bearing group G1 capable of reacting with the chemical compound or a precursor of such a group G1. The uses and the method of making such a device is also disclosed.

First claim

The invention claimed is:

1. A device for detecting at least one chemical compound, the device comprising at least one carbon nanotube with several graphene layers, wherein at least one molecule bearing a group G 1 capable of reacting with the chemical compound or a precursor of the group G 1 is grafted on the carbon nanotube with several graphene layers, wherein the carbon nanotube with several graphene layers is annealed under an inert atmosphere in a temperature above 1500° C. after being prepared, and before being grafted.

2. The device according to claim 1 , wherein the carbon nanotube has a length of between about 1 μm and about 1 mm.

3. The device according to claim 1 , wherein the molecule to be grafted is a cleavable aryl salt selected from the group consisting of aryl diazonium salts, aryl ammonium salts, aryl phosphonium salts and aryl sulfonium salts, the aryl group bearing a group G 1 capable of reacting with the chemical compound or a precursor of the group G 1 .

4. The device according to claim 1 , wherein the molecule to be grafted is a cleavable aryl salt of the following formula (I):
R—N 2 + ,A −   (I)

wherein:
A represents a monovalent anion and
R represents an aryl group R bearing a group G 1 capable of reacting with the chemical compound or a precursor of the group G 1 .

5. The device according to claim 3 , wherein the aryl group is selected from the group consisting of aromatic or heteroaromatic carbon structures, consisting of one or more aromatic or heteroaromatic rings each including 3 to 8 atoms, the heteroatom(s) including N, O, P or S.

6. The device according to claim 4 , wherein A is selected from the group consisting of halides, haloborates, perchlorates, sulfonates, alcohoholates and carboxylates.

7. The device according to claim 1 , wherein the molecule grafted on the carbon nanotube is a polymer or copolymer mainly derived from several identical and/or different monomer units, said polymer or copolymer bearing at least one group G 1 capable of reacting with said chemical compound or a precursor of the group G 1 .

8. The device according to claim 7 , wherein the monomer units are monomers which are polymerizable via a radical route.

9. The device according to claim 8 , wherein the monomers are selected from monomers of the following formula (II):

and wherein the groups R 1 to R 4 , either identical or different, represent a non-metal monovalent atom selected from the group consisting of a halogen atom, a hydrogen atom, a saturated or unsaturated chemical group such as an alkyl, aryl group, a nitrile, a carbonyl, an amine, an amide or a —COOR 5 group wherein R 5 represents a hydrogen atom or a C 1 -C 12 , or a C 1 -C 6 alkyl group.

10. The device according to claim 1 , wherein the group G 1 capable of reacting with the chemical compound is selected from the group consisting of hydroxyl, thiol, azide, epoxide, azyridine, amine, nitrile, isocyanate, thiocyanate, nitro, amide, halide notably alkyl halide, carboxylic acid and ester functions.

11. The device according to claim 1 , further comprising
a support; and
two electrodes positioned on the support,
wherein the carbon nanotube is configured to ensure electric contact between the two electrodes.

12. The device according to claim 11 , wherein the electrodes have an interdigitated comb configuration.

13. The device according to claim 1 , wherein the nanotube has an orientation substantially perpendicular with respect to the two electrodes.

14. A system comprising at least two devices according to claim 1 .

15. A method of using at least one device according to claim 1 for detecting and optionally quantifying one or more gaseous chemical compounds.

16. The method according to claim 15 , wherein the gaseous chemical compound is selected from the group consisting of volatile organic compounds, hydrogen, carbon monoxide, carbon dioxide, chlorine and chlorinated compounds, ammonia, organo-phosphorus gases, hydrocyanic acid, thionyl chloride, phosphene, tetrahydrofurane, methane and dimethyl methyphosphonate.

17. A method for preparing a device for detecting at least one chemical compound according to claim 1 , wherein the method comprises depositing on two electrodes, at least one carbon nanotube with several graphene layers, wherein at least one molecule bearing a group G 1 capable of reacting with the chemical compound or a precursor of the group G 1 is grafted on the carbon nanotube with several graphene layers, and wherein the carbon nanotube ensures electric contact between the electrodes, wherein the carbon nanotube with several graphene layers is annealed in a temperature above 1500° C. in an inert atmosphere after being prepared, and before being grafted.

18. The method according to claim 17 , wherein deposition is carried out by dielectrophoresis.

19. The method according to claim 17 , wherein the method comprises grafting on the carbon nanotube the molecule bearing a group G 1 capable of reacting with the chemical compound or a precursor of the group G 1 .

20. The method according to claim 17 , wherein the method comprises:
annealing the carbon nanotube with several graphene layers,
placing the annealed nanotube in contact with a solution S 2 containing at least one molecule bearing a group G 1 capable of reacting with the chemical compound or a precursor of the group G 1 or at least one precursor of the latter to form a mixture;
submitting the mixture to non-electrochemical conditions so as to graft on the nanotube, the molecule or the precursor;
recovering the grafted nanotube obtained and depositing the grafted nanotube on two electrodes, notably by dielectrophoresis.

21. The device according to claim 5 , wherein the aryl group is mono-substituted or poly-substituted, and wherein the substituent(s) contain one or more hetero-atoms or C 1 -C 6 alkyl groups.

22. The device according to claim 8 , wherein the monomer units comprise molecules of the ethylene type.

Assignees

• Mayne Lhermite Martine
• Palacin Serge
• Chenevier Pascale
• Chancolon Jer Hacek Over O Me
• Gohier Aurelien
• Commissariat Energie Atomique

Inventors

• Mayne-L'Hermite Martine
• Palacin Serge
• Chenevier Pascale
• Chancolon Jér{Hacek Over (O)}Me
• Gohier Aurélien

Classifications

• Y10T436/18

  Sulfur containing · CPC title

• Y10T436/214

  Acyclic [e.g., methane, octane, isoparaffin, etc.] · CPC title

• Y10T436/22

  Hydrogen, per se · CPC title

• Y10T436/175383

  Ammonia · CPC title

• Y10T436/142222

  Hetero-O [e.g., ascorbic acid, etc.] · CPC title