1. Introduction
Filled single-walled carbon nanotubes (SWCNTs) are attracting ever-increasing attention of the research community due to their extraordinary physical and chemical properties. Tuning the electronic properties of SWCNTs by filling with electron donor and acceptor compounds opens the way for applications of filled nanotubes in various fields, such as nanoelectronics, energy storage, sensors and nanomedicine [
1,
2,
3]. The filled SWCNTs have homogenous properties, including a defined metallic or semiconducting conductivity type and electronic properties [
4]. It was demonstrated that the SWCNTs can be filled with elementary substances, chemical compounds and molecules [
4].
In our work, we chose an electron acceptor (cobalt iodide (CoI2)) and electron donor (nickel carbide (Ni3C)) for encapsulation inside SWCNTs and investigated the modification of the electronic properties of SWCNTs. The properties of filled SWCNTs were analyzed by high-resolution transmission electron microscopy (HRTEM), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS).
2. Materials and Methods
The filling of SWCNTs with CoI2 was performed by the melt method. The 1.4 nm-diameter mixed metallicity SWCNTs and CoI2 were sealed inside a quartz ampoule under high vacuum, and it was heated in a tube furnace up to atemperature that exceeded the melting point of salt by 100 °C (615 °C) and kept at this temperature for 10 h. Then, the ampoule was slowly cooled down to room temperature to obtain homogeneous crystallization of the salt. The filling of SWCNTs with Ni3C was performed by the two-step method. The 1.7 nm diameter mixed metallicity SWCNTs and nickelocene powder were sealed inside a quartz ampoule under high vacuum, and it was heated up to 50 °C and kept at this temperature for 5 days. Then, the ampoule was heated up to 250 °C and kept at this temperature for 2 h to convert nickelocene to nickel carbide.
3. Results
The HRTEM data prove the filling of internal channels of SWCNTs with both compounds. In the case of CoI
2, one-dimensional nanocrystals of the salt were formed. For nickel carbide, the formation of ~1–2 nm nanoclusters was observed. The Raman spectroscopy data of the CoI
2-filled SWCNTs show the modifications of the radial breathing mode (RBM) and G-bands of SWCNTs. The RBM and G-bands of Raman spectra of the pristine and filled SWCNTs were fitted with individual components. The data show the shifts and changes in peak intensities in the RBM-band of the filled SWCNTs as compared to the pristine SWCNTs. This demonstrates changes in the electronic properties of SWCNTs due to doping accompanied by the charge transfer between the nanotubes and salt [
5]. The Raman spectroscopy data of nickel carbide-filled SWCNTs do not show noticeable differences as compared to the pristine nanotubes. The XPS data of the CoI
2- and nickel carbide-filled SWCNTs show the down- and upshift of the C 1s XPS peak, respectively, as well as its broadening as compared to the pristine nanotubes. This was attributed to the down- and upshift of the Fermi level of SWCNTs, respectively [
6]. By combining the Raman spectroscopy and XPS data, it was shown that the encapsulated CoI
2 and nickel carbide lead to
p- and
n-doping of SWCNTs, respectively.
4. Conclusions
The mixed metallicity SWCNTs were filled with CoI2 and nickel carbide (Ni3C). The electronic properties of the filled SWCNTs were investigated in detail by Raman spectroscopy and XPS. It was shown that the embedded CoI2 causes p-doping of SWCNTs with downshifting of the Fermi level of nanotubes. Ni3C results in n-doping of SWCNTs with upshifting of the Fermi level of nanotubes. These results allow for implementation of the filled SWCNTs in devices for various applications, such as nanoelectronics, energy storage, sensors, catalysis and biomedicine.
Author Contributions
M.V.K. performed the synthesis, characterization of the filled SWCNTs and data analysis. C.K. assisted in the Raman spectroscopy investigations. D.E. supervised the research work. All authors have read and agreed to the published version of the manuscript.
Funding
M.V.K. acknowledges funding for postdocs with experience of international work inleading research centers for conducting research in leading laboratories of the Moscow Institute of Physics and Technology.
Acknowledgments
We thank T. Saito (Nanotube Research Center, AIST, Tokyo, Japan) for providing SWCNTs; M. Sauer, T. Pichler (University of Vienna, Vienna, Austria) and L. Yashina (Lomonosov Moscow State University, Moscow, Russia) for assisting in the XPS spectroscopy investigations; H. Shiozawa (University of Vienna, Austria) for assisting in the Raman spectroscopy measurements; Y. Sato, K. Suenaga (Nanotube Research Center, AIST, Japan) and N. Kiselev (Institute of Crystallography of the RAS, Russia) for the HRTEM measurements.
Conflicts of Interest
The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.
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