Dysprosium-Catalyzed Growth of Single-Walled Carbon Nanotube Arrays on Substrates
© The Author(s) 2009
Received: 14 October 2009
Accepted: 20 November 2009
Published: 29 November 2009
In this letter, we report that dysprosium is an effective catalyst for single-walled carbon nanotubes (SWNTs) growth via a chemical vapor deposition (CVD) process for the first time. Horizontally superlong well-oriented SWNT arrays on SiO2/Si wafer can be fabricated by EtOH-CVD under suitable conditions. The structure and properties are characterized by scanning electron microscopy, transition electron microscopy, Raman spectroscopy and atomic force microscopy. The results show that the SWNTs from dysprosium have better structural uniformity and better conductivity with fewer defects. This rare earth metal provides not only an alternative catalyst for SWNTs growth, but also a possible method to generate high percentage of superlong semiconducting SWNT arrays for various applications of nanoelectronic device.
Single-walled carbon nanotubes (SWNTs) have attracted enormous attention due to their unique structures and excellent properties [1–4] since their discovery . Several approaches [5–8] have been developed for the production of SWNTs, among which the catalyst plays an important role in the chemical vapor deposition (CVD) process of SWNTs . It is generally accepted that the nanoscaled catalyst particles act as the initiating centers, and the SWNTs grow out from them via a vapor–liquid–solid (VLS) mechanism . The Fe-family elements are known to be the most common catalysts. Experimental  and theoretical [12, 13] studies all show their high catalytic activities. However, in the past 3 years, many other metals such as Ag, Pd, Au, Cu, Rh and Pb [14–19], semiconductors such as Si and Ge , carbides such as SiC , Fe3C  and more recently Mg, Mn, Cr, Sn and Al [21, 22] have been reported to be active for SWNTs growth. These materials were regarded as inactive catalysts for the growth of CNTs in the past. Therefore, these findings challenge the traditional thinking about the growth of CNTs and the role of the catalysts. Furthermore, different types of catalysts will provide more chance to understand the relationship between the catalyst and the structures of the SWNTs and thus may find out the approach for selective growth of semiconducting SWNTs (s-SWNTs) or metallic SWNTs (m-SWNTs).
In situ growth of horizontally well-aligned SWNT arrays up to a centimeter scale on suitable substrates is a critical step for large-scale, low-cost fabrication of the SWNT-based electronic devices, especially on commercial silicon wafer substrates [17, 23–25], which is more compatible with current silicon-based microelectronics technology. Compared with random networks of SWNT on substrates, the long parallel aligned SWNTs can avoid the overlap of the nanotubes and the resistance caused by the nanotube junctions; more importantly, they provide a controllable orientation for easy fabrication of multiple nanodevices with a possible consistent performance.
In this work, we firstly report that superlong well-oriented SWNT arrays can be generated by EtOH-CVD from rare earth metal Dy. The Raman spectroscopy with the combination of electrochemical deposition of Ag has been applied to evaluate the structure of the as-grown SWNTs. This new element provides not only an alternative catalyst for the growth of SWNTs, but also a possible high percentage of superlong s-SWNT arrays for various SWNT-based nanodevice fabrications and applications.
Superlong well-aligned SWNTs on SiO2/Si wafer were grown by EtOH-CVD using 1 mM ethanol solution of dysprosium chloride (DyCl3) that was purchased from Aldrich with purity higher than 99.99% as a catalyst precursor. The catalyst was loaded on one side of the substrate by dipping the wafer into catalyst-contained solution. The wafer was then placed in the middle of a 0.5-inch-diameter quartz tube within a 1-inch-diameter quartz tube in order to acquire laminar flow. After the furnace was heated to 900°C under the atmosphere of H2 and Ar, ethanol vapor was delivered by bubbling H2(200 sccm) into ethanol with 1–3% water at 25–35°C. The growth lasted for 10 min.
In a typical experiment, the samples were dipped into the solution containing 0.1 mM AgNO3 with 20 mM KNO3(analytical grade, Beijing reagents) as the supporting electrolyte. A saturated calomel electrode was used as the reference electrode, Pt gauze as counter electrode and long SWNT arrays connected by a conducting silver adhesive or Au layer by sputtering coating as a working electrode.
SEM images were taken from FEI NanoSEM at 1kv, spot 4,TEM images of SWNTs were taken from Si3N4 window where the nanotube grew in situ using a Philips CM200 TEM at 200 kV. AFM images were recorded at NanoScope III in tapping mode at room temperature, Raman spectra of SWNTs on silicon wafers were collected from JY-T64000 Raman spectroscopy under ambient conditions by using a laser excitation of 632.8 nm (1.96 eV, ~3 mw) or 514.5 nm (2.41 eV) from an air-cooled Ar+ laser. The beam size is 2 μm.
Results and Discussion
For superlong SWNTs from Dy and EtOH, we examined 93 individual, long nanotubes among which 85 nanotubes have Ag particles confirmed by Raman spectroscopy using 632.8 nm (Elaser = 1.96 eV) at 3 mw and found two different types of G band, type A and B, as shown in Fig. 4c and 4d. Nine nanotubes (9.7%) are type A that is typical m-SWNT with broad BWF and a Lorentzian peak around 1592 cm−1(small shift for different nanotubes), and 72 nanotubes (77.4%) are typical s-SWNTs having strong sharp peaks at around 1594 cm−1 with a small peak at 1571 cm−1(type B) that is typical s-SWNT. Eight nanotubes without Ag particles have possibly more defects along the nanotubes and behave as having an insulator character. In our recent article, we call them quasi-insulator nanotubes .
Since the Raman resonance of the SWNTs depends on both the excitation frequency and the diameter of the SWNT, it is necessary to use another laser line to identify the structures of the SWNTs. We further check the SWNTs by using Elaser 514.5 nm (Elaser = 2.41 eV) to collect the G band from 35 long tubes among which 32 nanotubes have Ag particles and find 4 m-SWNTs (11.4%) and 28 s-SWNTs (80%). The typical Raman spectra as shown in Fig. 4c and 4d. The percentage of the m-SWNTs measured from 514.4 nm excitation is similar to that from 632.8 nm excitation. Therefore, we could affirm that the well-aligned SWNTs from Dy catalyst with EtOH-CVD have a high percentage of s-SWNTs (∼80%). A high percentage of s-SWNTs both vertically and horizontally aligned SWNT arrays on substrate have been reported more recently [32–34]. The horizontally aligned SWNT arrays can grow on ST-cut single-crystal quartz; the enrichment of s-SWNT (up to 95%) is believed to be due to the induced growth by the substrate lattice and the optimized growth condition. The reason for the growth of vertically aligned SWNT arrays with s-SWNT (up to 96%) still remains unclear. Further, more experiments need to be carried out for the better understanding of the mechanism of the preferential growth of s-SWNTs and the catalytic properties.
In summary, for the first time we have demonstrated that rare earth metal Dy is an effective catalyst for SWNTs growth. By using ethanol as carbon source, superlong well-oriented SWNT arrays can be generated. The results show that the SWNTs from Dy and EtOH have better conductivity and better structural uniformity with less defects. This new element provides not only an alternative catalyst for SWNTs growth, but also a way to generate high percentage of superlong s-SWNTs arrays. The generation of such high percentage of s-SWNT arrays will represent a big step forward in controlled growth of s-SWNTs for electronic applications.
The authors would like to thank the MOST 973 project (2007CB616901) and NSFC (50772076) for their partial financial support.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
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