Copper-filled carbon nanotubes and synthesis methods thereof
Copper-filled carbon nanotubes and methods of synthesizing the same are provided. Plasma-enhanced chemical vapor deposition can be used to synthesize vertically aligned carbon nanotubes filled with copper nanowires. The copper filling can occur concurrently with the carbon nanotube growth, and the carbon nanotubes can be completely filled by copper. The filling of Cu inside the CNTs can be controlled by tuning the synthesis temperature.
1. A method of synthesizing copper (Cu)-filled carbon nanotubes (CNTs), the method comprising:
providing a Cu substrate in a reaction chamber;
heating the reaction chamber to a predetermined growth temperature;
providing a carbon precursor gas to the reaction chamber;
forming a carbon layer on the Cu substrate; and
performing a plasma-enhanced chemical vapor deposition (PECVD) technique for a predetermined amount of time to simultaneously grow CNTs directly on the Cu substrate and fill the CNTs with Cu, thereby synthesizing the Cu-filled CNTs on the Cu substrate, the Cu filling the CNTs and extending from tips thereof during the PECVD technique, and the Cu substrate becoming porous during the PECVD technique,
the CNTs having a filling rate of at least 70%, and
the Cu substrate being a Cu disk, a Cu foil, or a Cu plate.
2. The method according to claim 1 , the CNTs being grown vertically on the Cu substrate, such that the Cu-filled CNTs are Cu-filled vertically-aligned CNTs (VACNTs).
3. The method according to claim 1 , the CNTs having an average filling ratio of the Cu of at least 0.99.
4. The method according to claim 1 , the carbon precursor gas being acetylene, methane, ethylene, or ethanol.
5. The method according to claim 1 , the predetermined growth temperature being in a range of from 650° C. to 750° C.
6. The method according to claim 1 , the predetermined growth temperature being in a range of from 690° C. to 710° C.
7. The method according to claim 1 , the predetermined amount of time being in a range of from 15 minutes to 60 minutes.
8. The method according to claim 1 , further comprising providing a first gas to the reaction chamber prior to heating the reaction chamber to the predetermined growth temperature,
the first gas being ammonia gas or hydrogen gas.
9. The method according to claim 8 , further comprising evacuating the reaction chamber to a pressure of less than 0.1 Torr prior to providing the first gas to the reaction chamber,
the providing of the first gas to the reaction chamber resulting in a pressure of the reaction chamber increasing to at least 5 Torr.
10. The method according to claim 1 , further comprising polishing the Cu substrate prior to providing the Cu substrate in the reaction chamber,
the Cu substrate comprising an average surface roughness of less than 10 nanometers (nm) after the polishing.
11. The method according to claim 1 , further comprising cleaning the Cu substrate prior to providing the Cu substrate in the reaction chamber,
the cleaning of the Cu substrate comprising ultrasonically cleaning the Cu substrate in at least one solvent bath.
12. The method according to claim 1 , the plasma-enhanced chemical vapor deposition technique comprising applying a direct current (DC) plasma to the substrate once the predetermined growth temperature is reached.
13. The method according to claim 1 , further comprising allowing the Cu substrate with the Cu-filled CNTs thereon to naturally cool down to room temperature.
14. The method according to claim 1 , further comprising evacuating the reaction chamber to a pressure of less than 0.1 Torr prior to heating the reaction chamber to a predetermined growth temperature.
15. The method according to claim 1 , the CNTs having a filling rate of at least 80%.
16. The method according to claim 1 , the method being performed without addition of any catalyst.
17. A method of synthesizing copper (Cu)-filled carbon nanotubes (CNTs), the method comprising:
polishing a Cu substrate to provide a polished Cu substrate having an average surface roughness of less than 10 nanometers (nm);
ultrasonically cleaning the polished Cu substrate in at least one solvent bath to provide a cleaned Cu substrate;
providing the cleaned Cu substrate in a reaction chamber;
evacuating the reaction chamber to a pressure of less than 0.1 Torr;
providing a first gas to the reaction chamber, the providing of the first gas to the reaction chamber resulting in a pressure of the reaction chamber increasing to at least 5 Torr;
heating the reaction chamber to a predetermined growth temperature;
providing a carbon precursor gas to the reaction chamber;
forming a carbon layer on the Cu substrate;
performing a plasma-enhanced chemical vapor deposition (PECVD) technique for a predetermined amount of time to simultaneously grow CNTs directly on the Cu substrate and fill the CNTs with Cu, thereby synthesizing the Cu-filled CNTs on the Cu substrate, the Cu filling the CNTs and extending front tips thereof during the PECVD technique, and the Cu substrate becoming porous during the PECVD technique; and
allowing the Cu substrate with the Cu-filled CNTs thereon to naturally cool down to room temperature,
the CNTs having a filling rate of at least 80%,
the CNTs being grown vertically on the Cu substrate, such that the Cu-filled CNTs are Cu-filled vertically-aligned CNTs (VACNTs),
the CNTs having an average filling ratio of the Cu of at least 0.999,
the first gas being ammonia gas or hydrogen gas,
the carbon precursor gas being acetylene, methane, ethylene, or ethanol,
the predetermined growth temperature being in a range of from 690° C. to 710° C.,
the predetermined amount of time being in a range of from 15 minutes to 60 minutes,
the plasma-enhanced chemical vapor deposition technique comprising applying a direct current (DC) plasma to the substrate once the predetermined growth temperature is reached, and
the Cu substrate being a Cu disk, a Cu foil, or a Cu plate.
18. The method according to claim 17 , the method being performed without addition of any catalyst.