METHOD FOR GROWING VERTICALLY ORIENTED SINGLE-WALLED CARBON NANOTUBES WITH THE SAME ELECTRONIC PROPERTIES AND FOR REPRODUCING SINGLE-WALLED CARBON NANOTUBES WITH THE SAME ELECTRONIC PROPERTIES

Abstract

The present invention relates to a method of reproducing at least one single-walled carbon nanotube (3) having predefined electronic properties or a plurality of single-walled carbon nanotube (3) having the same electronic properties. A dispersion (2) is produced for this purpose and carbon nanotubes (3) contained in the dispersion are processed into fragments (6) by energy input. These fragments (6) are applied to and oriented on a carrier (7). The fragments (6) are subsequently extended by chemical vapor deposition and the originally present carbon nanotubes (3) are thus reproduced.

Claims

1. A method of reproducing at least one single-walled carbon nanotube (3) having predefined electronic properties or a plurality of single-walled carbon nanotubes (3) having the same electronic properties, the method comprising the steps: a) preparing a dispersion (2) from a liquid and from the at least one single-walled carbon nanotube (3) having predefined electronic properties or from the plurality of single-walled carbon nanotubes (3) having the same electronic properties; b) forming fragments (6) of the at least one single-walled carbon nanotube (3) or of the plurality of single-walled carbon nanotubes (3) by an energy input into the dispersion (2); c) applying the fragments (6) of the at least one single-walled carbon nanotube (3) or of the plurality of single-walled carbon nanotubes (3) from the dispersion (2) onto a surface (8) of a carrier (7) as a starting layer for reproducing and orienting the fragments (6) on the surface (8) during the application from the dispersion (2) so that the surface (8) is intersected by a longitudinal axis of the fragments (6) and the fragments (6) are not oriented in parallel in a plane with respect to the surface (8) of the carrier (7); and d) introducing the fragments (6) applied to and oriented on the carrier (7) into an apparatus for chemical vapor deposition (9), with single-walled carbon nanotubes (3) having the same electronic properties being extended in the apparatus for chemical vapor deposition (9), starting from the fragments (6) serving as the starting layer, in a gas atmosphere containing carbon by means of chemical vapor deposition.

2. A method in accordance with claim 1, characterized in that the fragments (6) are formed by introduction of ultrasound into the dispersion (2), with fragments (6) having a length between 30 nm and 100 nm preferably being obtained.

3. A method in accordance with claim 2, characterized in that ultrasound is used having a power of 30 W to 100 W at a frequency between 20 kHz and 40 kHz.

4. A method in accordance with claim 1, characterized in that the fragments (6) are oriented on the surface (8) by application of an electrical field.

5. A method in accordance with claim 1, characterized in that the fragments (6) are oriented by self-organization on a gold layer applied to the surface (8) of the carrier (7), with SH(CH.sub.2).sub.nNH.sub.2 molecules preferably being used for the orientation.

6. A method in accordance claim 1, characterized in that the longitudinal axis of the applied fragments (6) has an angle with respect to the surface between 60 and 120, preferably between 75 and 105, particularly preferably between 80 and 100, with the carrier (7) preferably being a silicon oxide substrate.

7. A method in accordance with claim 1, characterized in that plasma-assisted chemical vapor deposition is used to extend the carbon nanotubes (6).

8. A method in accordance with claim 1, characterized in that the carbon nanotubes (3) used for reproduction have the same diameter and the same chirality.

9. A method in accordance with claim 1, characterized in that the dispersion (2) is prepared from water, preferably from distilled water, and from a surface-active substance, preferably a surfactant, for producing a homogeneous dispersion.

10. A method in accordance with claim 1, characterized in that the produced carbon nanotubes (3) having the same electronic properties are removed from the carrier (7) and the method is carried out again using these removed carbon nanotubes (3) for a further reproduction of the carbon nanotubes (3).

11. A method in accordance with claim 1, characterized in that the single-walled carbon nanotubes are formed with a diameter between 0.6 nm and 2 nm.

12. A method in accordance with claim 1, characterized in that the reproduced carbon nanotubes (3) are preferably measured with respect to their properties by optical absorption spectroscopy, Raman spectroscopy and/or a photoluminescence measurement after the growing by chemical vapor deposition and carbon nanotubes (3) differing from the desired properties are separated.

13. A method in accordance with claim 1, characterized in that the carbon nanotubes (3) are manufactured with a packing density of up to 10,000 carbon nanotubes per m.sup.2, preferably of up to 20,000 carbon nanotubes per m.sup.2, and particularly preferably of up to 40,000 carbon nanotubes per m.sup.2.

14. A method in accordance with claim 1, characterized in that the carbon nanotubes (3) and/or the fragments (6) of the carbon nanotubes (3) are arranged on the carrier (7) with a spacing from one another of less than 0.5 m.

15. A carrier (7) having a surface (8) on which single-walled carbon nanotubes (3) having the same electronic properties are applied such that a longitudinal axis of the carbon nanotubes (3) intersects the surface (8) and the carbon nanotubes (3) are not oriented in parallel in a plane with respect to the surface (8) of the carrier (7).

16. A carrier (7) having a surface (8) on which fragments (6) of the at least one single-walled carbon nanotube (3) are applied and are oriented such that a longitudinal axis of the fragments (6) of the at least one carbon nanotube (3) intersects the surface (8) and the fragments (6) of the at least one carbon nanotube (3) are not oriented in parallel in a plane with respect to the surface (8) of the carrier (7).

17. A carrier (7) in accordance with claim 16, characterized in that a surfactant layer (9) is applied to the surface (8) and the fragments (6) of the at least one single-walled carbon nanotube (3) are applied to and oriented on it.

18. A carrier (7) in accordance with claim 17, characterized in that the surfactant layer (9) has a thickness that is less than a length of the fragments (6).

19. A carrier (7) in accordance with claim 15, characterized in that the surface (8) of the carrier (7) is provided with a gold layer on which the fragments (6) of the at least one single-walled carbon nanotube (3) are applied and oriented, with the surface (8) preferably being provided with a layer of SH(CH.sub.2).sub.nNH.sub.2 molecules for the orientation.

Description

[0030] Embodiments of the invention are shown in the drawings and will be explained in the following with reference to FIGS. 1 to 8.

[0031] There are shown:

[0032] FIG. 1 a dispersion of a liquid and single-walled carbon nanotubes contained in a vessel shown in a perspective view;

[0033] FIG. 2 an ultrasound treatment of the dispersion shown in FIG. 1 in a view corresponding to FIG. 1;

[0034] FIG. 3 the fragments of the carbon nanotubes obtained in the ultrasound treatment shown in FIG. 2 in a view corresponding to FIG. 1;

[0035] FIG. 4 the fragments deposited from the dispersion on a surface of a carrier in a perspective view;

[0036] FIG. 5 a reactor for chemical vapor deposition in a perspective view in which reactor the carrier shown in FIG. 4 has been introduced,

[0037] FIG. 6 a view of the carrier corresponding to FIG. 4 with the extended, vertically oriented carbon nanotubes;

[0038] FIG. 7 a plurality of the carriers shown in FIG. 6 with carbon nanotubes arranged thereon, and

[0039] FIG. 8 a view of the carrier corresponding to FIG. 4 with a surfactant layer and with carbon nanotubes applied thereto.

[0040] A vessel 1 is shown in FIG. 1 in which a homogeneous dispersion 2 of a liquid having a surfactant and a plurality of carbon nanotubes 3 is contained. In further embodiments, only a single carbon nanotube having predefined electronic properties can also be taken as the starting material for the method. The liquid in the embodiment shown is distilled water; deionized water can, however, also generally be used. The surfactant, sodium dodecyl sulfate, SDS, in the embodiment shown, is present in the dispersion in a concentration of 0.1 wt. %. In addition, isopropanol has been admixed in the dispersion, but this can also be dispensed with in further embodiments. One of the carbon nanotubes 3 is shown in an enlarged representation by way of example. At least 90% of the carbon nanotubes 3 contained in the dispersion 2 have the same electronic properties, are therefore semiconductive in the embodiment shown, and preferably have a diameter of the same size and an identical chirality. In addition, the carbon nanotubes 3 are all single-walled. In further embodiments, the carbon nanotubes 3 can, however, also be metallic. It is avoided by the addition of surfactants that the carbon nanotubes 3 are attached to one another and form bundles, but are rather present evenly distributed in the dispersion 2. In further embodiments, the carbon nanotubes 3 can also be oxidized by an acid and can thus be hydrophilic instead of hydrophobic; or organic solutions such as dimethylformamide (DMF) are used for producing a homogeneous dispersion. The carbon nanotubes 3 having identical physical properties were produced using a method known from the prior art in the example shown and were subsequently sorted. In the embodiment shown, 99% of the carbon nanotubes 3 used for the dispersion 2 have identical properties.

[0041] To reproduce the carbon nanotubes 3 contained in the dispersion 2, a breaking of the carbon nanotubes 3 into smaller fragments is effected by the effect of ultrasound in the vessel 1 having the dispersion 2 of the carbon nanotubes 3. Repeating elements are provided with identical reference numerals in this Figure and also in the following Figures. To produce the fragments, a tip 4 of an ultrasound sonicator is introduced into the dispersion 2 and ultrasound of a frequency of 30 kHz and at a power of 30 W to 100 W is introduced into the dispersion 2 via the ultrasound device 5.

[0042] The vessel 1 with the dispersion 2 and the produced fragments 6 is shown in FIG. 3. The fragments 6 have a length of 30 nm to 100 nm with a diameter of approximately 1 nm. Since further particles such as bundles of carbon nanotubes 3, amorphous carbon or residues of catalysts can also have formed due to the ultrasound input, these particles can be removed from the dispersion 2 in a further method step by centrifugation; for example, the dispersion 2 is centrifuged for 8 hours at 20,000 times gravitational acceleration, that is at 20,000 g.

[0043] The dispersion 2 shown in FIG. 3 is applied to a planar carrier 7 by a pipette, for example, and the liquid is removed, for example by heating. The planar carrier 7 is a silicon wafer that is introduced into an electrical field during or after the drying for the removal of liquid components of the dispersion 2 and also withstands a subsequent further treatment without damage due to its temperature resistance up to 1200 C. Field lines of the electrical field in this respect stand perpendicular on a planar surface 8 of the carrier 7 so that the fragments 6 are oriented in parallel with the field lines on the surface 8, that is a longitudinal axis of the fragments 6 is likewise at a right angle to the surface 8. A layer is thus produced of fragments 6 oriented vertically on the carrier 7. It may, however, also occur that only a certain percentage of the fragments 6 have the same orientation. For example, in the embodiment shown, 80% of the fragments 6 are oriented in parallel with a surface normal, whereas the remainder has an angular offset of up to 20 from the surface normal.

[0044] In a further embodiment, a gold layer is applied areally to the surface 8 and the fragments 6 are oriented on said gold layer by self-organization assisted by cysteamines, namely SH(CH.sub.2).sub.2NH.sub.2, such that the longitudinal axis intersects the surface 8, that is the fragments 6 stand at a right angle on the surface 8. The application of the dispersion 2 onto the carrier takes place by dipping the carrier 7 into the dispersion. The cysteamines used are in this respect contained in the dispersion 2 or are applied to the gold layer in a preceding method step, for example by dipping into a liquid mixed with the cysteamines.

[0045] The carrier 7 prepared in this manner having the fragments 6 of the single-walled carbon nanotubes having the same electronic properties oriented on the surface 8 can be temporarily stored in this form and can only subsequently be further processed in a further step.

[0046] The carrier 7 shown in FIG. 4 having fragments 6 of the single-walled carbon nanotubes 3 having the same electronic properties oriented on the surface 8 is introduced, as shown in FIG. 5, into a reactor 9 that is suitable for chemical vapor deposition (CVD). In this reactor 9, tips of the fragments 6 are first chemically activated in an atmosphere containing hydrogen and carbon nanotubes 3 having the same electronic properties and, provided that carbon nanotubes 3 having the same diameter and the same chirality were used as the starting material, also having the same diameter and the same chirality, are then grown epitaxially by chemical vapor deposition, starting from the fragments 6, in an atmosphere containing carbon until the desired length is reached. In further embodiments, plasma-assisted chemical gas vapor deposition can also be used for this purpose. The atomic structure of the fragments 6, that is in particular their diameter and their chirality, is not changed by the epitaxial growth. In addition, doped carbon nanotubes, boron nitride nanotubes, boron nanotubes or silicon nanotubes can also be grown in a corresponding atmosphere.

[0047] After the end of the chemical vapor deposition, the carbon nanotubes 3 are grown on the surface 8 of the carrier 7, starting from the fragments 6 used as the starting layer, as shown in FIG. 6. These carbon nanotubes in the embodiment shown are single-walled, semiconductive, and typically have the same respective diameter and the same chirality when carbon nanotubes having the same diameter and the same chirality were used as the starting material. In addition, they are all arranged vertically to the surface 8, i.e. are grown along a longitudinal axis of the fragments 6 and form a layer of vertically arranged carbon nanotubes 3. A packing density amounts in the embodiment shown to 10,000 carbon nanotubes per m.sup.2, while a spacing of the carbon nanotubes from one another is smaller than 0.5 m.

[0048] Provision can be made in further embodiments that the grown carbon nanotubes 3 are measured by Raman spectroscopy or by another measuring process with respect to their electrical and optical properties. Carbon nanotubes 3 whose physical properties differ from the majority can subsequently be removed from the bundle of obtained carbon nanotubes 3, for example by ultracentrifugation, chromatography or a process based on gels or polymers.

[0049] The carbon nanotubes 3 can be removed from the carrier 7 and can be installed in applications, for example in transistors, for example field effect transistors, or in other components such as sensors, photon detectors, optical modulators, light sources, solar cells or thermoelectric components.

[0050] Alternatively, the carbon nanotubes 3 can be removed from the carrier 7 and a further dispersion 2 can be formed, as shown in FIG. 1. The method can then be repeated for the cascading reproduction of the carbon nanotubes 3, that is fragments 6 can likewise be produced by ultrasound and these fragments 6 can be deposited and extended on a further carrier 7. The configuration shown in FIG. 7 hereby results of a plurality of carriers 7 on which respective carbon nanotubes 3 having defined physical properties are deposited.

[0051] FIG. 8 shows in a view corresponding to FIG. 4 the carrier 7 having a surfactant layer 9 of SDS that is deposited on, that is shown hatched, that has a thickness of 200 nm and that, as an intermediate layer, covers a surface 8 of the carrier 7 on which the fragments 6 are deposited completely, that is without cut-outs or holes. The fragments 6 have a length that is larger than the thickness of the surfactant layer 9 so that the fragments 6 are deposited and are oriented on the surfactant layer 9 and are stabilized in their orientation by the dried surfactant layer 9.

[0052] Features of the different embodiment only disclosed in the embodiment examples can be combined with one another and claimed individually.