Temperature Dependence of G<sup>−</sup> Mode in Raman Spectra of Metallic Single-Walled Carbon Nanotubes

Wu, Qianru; Wen, Zhijie; Zhang, Xiuyun; Tian, Lei; He, Maoshuai

doi:https://doi.org/10.1155/2018/3410306

Journal of Nanomaterials

On this page

Abstract Introduction Results and Discussion Data Availability Conflicts of Interest Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2018 | Article ID 3410306 | https://doi.org/10.1155/2018/3410306

Temperature Dependence of G⁻ Mode in Raman Spectra of Metallic Single-Walled Carbon Nanotubes

Qianru Wu,¹Zhijie Wen,^2,3Xiuyun Zhang,⁴Lei Tian,²and Maoshuai He^1,5

Academic Editor: Bhanu P. Singh

Received22 Feb 2018

Accepted28 May 2018

Published17 Jul 2018

Abstract

The temperature evolution of G mode in the Raman spectra of surface grown single-walled carbon nanotubes (SWNTs) is investigated. It is revealed that the intensity of G⁻ mode in Raman spectra varies with the measurement temperature. The intensity variation of the G⁻ mode is synchronized to that of the radial breathing mode, which is sensitive to the resonance condition (). Such an intensity evolution is associated with the temperature-induced change of . That is, the intensity of G⁻, an indication of electron-phonon coupling in metallic SWNTs, can be greatly enhanced only when the laser energy well matches the transition energy of nanotubes (). In other words, the window for observing asymmetric and broad G⁻ mode is very narrow. This work further confirms that the G⁻ mode in the Raman spectrum mainly arises from metallic SWNTs, and caution should be paid when using the intensity ratio of G⁻/G⁺ to estimate the percentage of metallic SWNTs in products.

1. Introduction

Single-walled carbon nanotubes (SWNTs) have been the subject of intensive research because of their fascinating optical, electronic, and chemical properties [1–4]. An SWNT exhibits either metallic or semiconducting characteristics depending on its chiral indices () [3]. SWNTs with different conductivities function differently when they are incorporated into nanodevices [5, 6]. For example, semiconducting SWNTs can be the core component in field effect transistors [5] and metallic SWNTs may be well applied in highly conductive transparent thin films [6]. However, most produced SWNTs consist of both semiconducting and metallic species [7, 8]. To facilitate the separation and practical application of the metallic SWNTs, it is necessary to characterize them based on their intrinsic electrical properties. Among different optical characterization techniques, Raman spectroscopy is particularly sensitive to metallic SWNTs and is a facile technique to analyze as-produced SWNTs. The sensitivity to metallic species is partly due to the possible emergence of a broad, softened G⁻ peak, sometimes referred as a Breit-Wigner-Fano (BWF) line shape [9] in the Raman spectrum, which can unambiguously identify as a metallic nanotube [10–13]. Furthermore, the intensity/area ratio of the G⁺ to the G⁻ band has been widely adopted to evaluate the relative concentration of semiconducting and metallic SWNTs in bulk products [14–16].

The G⁻ peak is the longitudinal mode of the metallic tube, and its broadening arises from coupling between the phonon and the electronic excitations, as predicated by theoretical calculations and verified experimentally [10, 11, 17–20]. However, the broadening G⁻ mode from metallic SWNTs is not necessarily observed by Raman spectroscopy. This is because the strength of electron-phonon coupling, reflected by the intensity and the full-width at half-maximum (FWHM) of G⁻ mode, is sensitive to many factors, like the position of Fermi energy () [11]. When the metallic SWNT is sufficiently biased at either positive or negative potential through electrostatic gating, the is moved far from the Dirac point, thus blocking the low-energy vertical electronic transitions [11]. Besides, shift is also realized by doping and chemical functionalization of SWNTs [21], causing a high degree of variation in the broadening of G⁻ mode.

Besides the position of Fermi energy, the measurement temperature is also reported to affect the profile of Raman spectra [22–27]. With the increase of temperature, the peak position shifts to lower frequency due to the softening of the C-C bond [25–27]. Based on the frequency downshift, the temperature coefficient, which reflects the thermal stability of SWNTs, can be deduced [25–27]. However, the temperature evolution of G⁻ mode, which is an indication of the strength of electron-phonon coupling, has rarely been reported [23]. Uchida et al. [23] studied the G band in Raman spectra of bundled SWNTs and found that the line width of the BWF mode decreases with increasing temperature. They attributed the temperature-dependent behavior of BWF line to the bundling effect, which affects the formation of plasmon band. However, as phonon energies of G mode (~0.2 eV) and RBM (~0.02 eV) are different, in the case of scattering resonance, the Raman responses of G mode and RBM are not necessarily from the same SWNTs, ruling out the possibility of establishing an evolution correlation between them. To circumvent the problem, temperature-dependent Raman spectra of SWNTs grown either on the surface or across trenches are investigated [24, 28]. In such a case, incident resonance where both the RBM and G mode arising from the same SWNT occurs. The temperature coefficients () for the different peaks, including RBM, G⁻, G⁺, and G, are therefore unambiguously determined. For example, Zhang et al. [28] measured the temperature coefficients of 13 SWNTs and found that depends on both SWNT diameter and chirality. Despite overall progress, investigation on the temperature-evolution correlation between SWNT RBM and G⁻ mode remains lacking.

In the work reported here, we present a systematic study on the temperature-dependent Raman spectra of surface-grown metallic SWNTs. By following the evolution of Raman spectra acquired at different temperatures, a correlation between the intensities of RBM and G⁻ mode is established, where a simultaneous change in the RBM and G⁻ intensities is observed. Such a result could be explained based on the temperature-induced shift of optical transition energy ( for the metallic SWNTs in our experiment) and resonance effect.

1.1. Experimental

SWNTs were synthesized in a vertical chemical vapor deposition system using a CO catalyst, which had been sputtered onto a SiO₂ substrate using an agar sputter coater. After being heated to the desired temperature, CO was introduced as the carbon source and the reaction lasted for 30 min. Detailed procedure for SWNT synthesis is described elsewhere [29].

Raman measurements on the SWNTs were carried out with a JY LabRAM HR 300 using 1.96 eV (633 nm) Ar ion laser excitation source. Temperature-dependent Raman spectra were recorded in a Linkam CCR1000 heating stage with a controlled environment sample chamber. Samples were heated or cooled to the desired temperature at a rate of 20°C/min under a continuous Ar flow (50 cm³/min). After reaching the desired temperature, the hot stage was stabilized for more than 10 min to ensure that the temperature of the hot stage was the same as the sample. Prior to Raman measurements, the SWNTs were annealed in Ar at 450°C for 60 min to minimize gas absorption from the ambient environment. Laser power was kept at ~10 μW to avoid the heating effect of the laser.

2. Results and Discussion

Figure 1(a) presents a scanning electron microscope image of SWNTs grown on a SiO₂ substrate. SWNTs with lengths of several μm and a density of 3–8 tube/μm² were synthesized. Figure 1(b) shows a typical Raman spectrum of as-produced SWNTs. A characteristic RBM peak of SWNT centered at 192 cm⁻¹ is observed. According to Kataura et al.’s plot [9], such a SWNT can be assigned as a metallic one. However, high-energy modes around 1600 cm⁻¹ (G⁻ and G⁺) exhibit typical Lorentzian line shapes without the appearance of a broad and soft G⁻ peak. Such a result is in agreement with many previous reports where BWF lines were not necessarily observed in the Raman spectra of individual metallic SWNTs [3]. In our sample, most of the observed RBMs are located in the range of 150 cm⁻¹ to 265 cm⁻¹, corresponding to SWNT diameters ranging from 0.9 to ~1.7 nm.

(a)

(b)

To study the temperature-dependent behavior of G⁻ mode in metallic SWNTs, we performed the Raman characterizations on SWNTs at different temperatures. As O₂ adsorption on a SWNT surface could shift the position of Fermi energy [30] and complicate the analysis, the sample was preannealed in Ar to eliminate possible molecular adsorption [13]. Figure 2 depicts the Raman spectra acquired at three different temperatures from two spots of the sample surface. In both cases, only one RBM correlated with metallic SWNT is observed and the high-energy mode displays one G⁻ peak and one G⁺ peak. As the resonance window of the G mode is wider than that of the RBM mode [2], besides the RBM-correlated metallic SWNTs, other SWNT species, including semiconducting SWNTs, could contribute to the G mode. As revealed by Fouquet et al. [10], the G⁺ peak is assigned to the longitudinal mode of the semiconducting tube and the G⁻ peak is assigned to the longitudinal mode of the metallic tube.

(a)

(b)

(c)

From the temperature-dependent profiles of G mode (Figure 2), we can clearly see that, with increased temperature, the profile of G⁺ mode shows negligible change except for the frequency downshift arising from temperature-induced C-C bond softening [24, 28]. In contrast, the relative intensity and profile of G⁻ show striking differences at different temperatures. Figure 2(a) shows that the broadening and softening of G⁻ peak are not significant for the Raman spectrum acquired at 70°C. When the temperature reaches 90°C, a broad G⁻ peak with a high intensity appears, suggesting a strong electron-phonon coupling. Further increasing the temperature to 110°C diminishes the broadening characteristic of G⁻ peak. A similar trend is observed for the Raman spectra displayed in Figure 2(b). Only at a fixed temperature (225°C) can a soft G⁻ mode with a high intensity be observed. Interestingly, the intensity of G⁻ peak is synchronized with the RBM intensity, which reaches the maximum at 90°C for SWNT as depicted in Figure 2(a) and at 225°C for SWNT as depicted in Figure 2(b). The variation of the RBM intensity is correlated with the temperature-induced change of . Generally, is downshifted with increasing temperature [31, 32]. At a low temperature, the transitional energy of the metallic SWNT is slightly larger than the excitation laser energy (), and the RBM shows modest intensity. When raising temperature, the decreases towards , resulting in a strong RBM peak. Excessively increasing temperature separates from again, causing a decrease in RBM intensity. Schematic illustration of the change of resonance conditions as a function of temperature is shown in Figure 2(c). Such a resonance condition change can also explain the simultaneous intensity change of G⁻ mode, which originated from the longitudinal mode of metallic SWNT. More importantly, the results suggest that under weak resonance condition, the intensity and broadening of G⁻ peak are not significant. Such a finding could partially account for the lack of a broad and soft G⁻ mode in the Raman spectra of some metallic SWNTs reported previously [33].

Figure 3(a) shows the Raman spectra of SWNTs acquired at temperatures ranging from 500°C to 650°C on one sample spot. Although two RBM peaks (182 cm⁻¹ and 190 cm⁻¹) are observed at a low temperature range, the one centered at 190 cm⁻¹ diminishes with increasing temperature and contributes little to the G⁻ mode. Consequently, we only discuss temperature evolution of the RBM centered at 182 cm⁻¹ and the G mode here. The RBM is almost invisible at 500°C, indicating that the tube is out of resonance and of the metallic nanotube is much larger than . Increasing temperature decreases the of the tube, which falls into the resonance window and accounts for the appearance of RBM. When increasing the temperature from 500°C to 550°C, becomes smaller and the difference between and decreases. As a result, the scattering cross-section of Raman signal is getting larger, an intensity maximum is achieved at 550°C where matches well. However, further decreases of with increasing temperature leads to a gradual decrease in the intensity of RBM peak (550–650°C). At a temperature of 650°C, the tube is out of resonance with and the RBM vanishes. Assuming the incident resonance window for the isolated SWNT is ~10 meV [3], the appearance of the RBM in the temperature window of 500°C~650°C gives a downshift coefficient of on the order of 67 μeV/K, well within the range calculated by Capaz et al. [31]. In addition, the resonance window for observing a soft G⁻ is estimated to be less than 5 meV (from 530°C to 600°C).

(a)

(b)

(c)

Unlike the RBM intensity evolution with temperature, the intensity of G⁺ peak, mainly arising from the contribution of semiconducting SWNTs [10], does not exhibit dramatic change when modulating the temperature. To normalize the RBM peak and analyze its intensity change with temperature, we plotted the intensity ratio () as a function of temperature (Figure 3(b)). Clearly, a maximum ratio of 1.01 is observed at 550°C. In both sides of the point, the intensity ratio gradually decreases. A similar behavior is detected for the G⁻ mode. It is noted that the change trend of full-width at half-maximum (FWHM) is similar to the change of the intensity. For simplicity, only the intensity of G⁻ is discussed here. Figure 3(a) shows that the intensity of G⁻ peak demonstrates striking differences when raising temperature. The normalized intensity ratio () is also plotted against the temperature (Figure 3(c)). Obviously, the change of intensity ratio is related to the resonance conditions, which occurs simultaneously with the resonance scattering process of RBM. As the intensity and width of G⁻ mode are indications of the strength of electron-phonon coupling [11, 12], when the of the metallic tube matches , an increase in electron-phonon coupling is well suggested.

Based on the observations, the intensities of both RBM and G⁻ mode show similar trends when changing temperature, which modifies the of the tubes. Such observations have three immediate implications. The first is related to the use of peak intensity ratios (RBMs or high-energy mode from metallic and semiconducting SWNTs) to evaluate the selectivity of semiconducting or metallic SWNTs in bulk products. Caution should be paid when using the intensity (or area) ratio to determine the selectivity of SWNTs with different conductivities. Independent verification from other approaches, like electrical property measurement or electron microscopy technique, is necessary to make reliable conclusions. Second, it is possible to tune by changing temperature, thus offering more opportunity to detect different SWNT species with only one available fixed Raman laser wavelength. Third, changing the Raman characterization temperature provides an alternative solution for recovering the broad and soft G⁻ mode in individual metallic SWNTs.

In conclusion, in agreement with theoretical predications, of metallic SWNTs is observed to decrease with increasing temperature. Taking the resonance window for isolated SWNT of ~10 meV into account, the change of with temperature is estimated to be several tens of μeV/K. More importantly, both RBM intensity and G⁻ mode intensity are demonstrated to depend on the resonance conditions, that is, the match between and . Only when well matches with can a strong G⁻ with a large FWHM be observed. This work not only confirms that the G⁻ mode mainly arises from metallic SWNTs but also establishes a correlation between the intensities of RBM and G⁻ mode, which would help gain more insights in understanding the Raman spectra of metallic SWNTs.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

The work is supported by the Natural Science Foundation of Shandong Province of China (no. ZR2016EMM10); the Scientific Research Foundation of Shandong University of Science and Technology for Recruited Talents (no. 2016RCJJ001); the National Natural Science Foundation of China (no. 51304126); the State Key Research Development Program of China (no. 2016YFC0600708); and the State Key Laboratory of Open Funds (nos. MDPC201703, MDPC201601, and SKLGDUEK1520). The authors thank Dr. P. R. Mudimela for preparing the carbon nanotube samples.

References

R. H. Baughman, A. A. Zakhidov, and W. A. de Heer, “Carbon nanotubes--the route toward applications,” Science, vol. 297, no. 5582, pp. 787–792, 2002.
View at: Publisher Site | Google Scholar
M. S. Dresselhaus, G. Dresselhaus, R. Saito, and A. Jorio, “Raman spectroscopy of carbon nanotubes,” Physics Reports, vol. 409, no. 2, pp. 47–99, 2005.
View at: Publisher Site | Google Scholar
M. S. Dresselhaus, G. Dresselhaus, A. Jorio, A. G. Souza Filho, M. A. Pimenta, and R. Saito, “Single nanotube Raman spectroscopy,” Accounts of Chemical Research, vol. 35, no. 12, pp. 1070–1078, 2002.
View at: Publisher Site | Google Scholar
M. He, T. Yang, D. Shang et al., “High temperature growth of single-walled carbon nanotubes with a narrow chirality distribution by tip-growth mode,” Chemical Engineering Journal, vol. 341, pp. 344–350, 2018.
View at: Publisher Site | Google Scholar
S. J. Tans, A. R. M. Verschueren, and C. Dekker, “Room-temperature transistor based on a single carbon nanotube,” Nature, vol. 393, no. 6680, pp. 49–52, 1998.
View at: Publisher Site | Google Scholar
Z. Wu, Z. Chen, X. du et al., “Transparent, conductive carbon nanotube films,” Science, vol. 305, no. 5688, pp. 1273–1276, 2004.
View at: Publisher Site | Google Scholar
M. He, L. Zhang, H. Jiang et al., “Fe Ti O based catalyst for large-chiral-angle single-walled carbon nanotube growth,” Carbon, vol. 107, pp. 865–871, 2016.
View at: Publisher Site | Google Scholar
M. He, Y. Magnin, H. Jiang et al., “Growth modes and chiral selectivity of single-walled carbon nanotubes,” Nanoscale, vol. 10, no. 14, pp. 6744–6750, 2018.
View at: Publisher Site | Google Scholar
H. Kataura, Y. Kumazawa, Y. Maniwa et al., “Optical properties of single-wall carbon nanotubes,” Synthetic Metals, vol. 103, no. 1–3, pp. 2555–2558, 1999.
View at: Publisher Site | Google Scholar
M. Fouquet, H. Telg, J. Maultzsch et al., “Longitudinal optical phonons in metallic and semiconducting carbon nanotubes,” Physical Review Letters, vol. 102, no. 7, article 075501, 2009.
View at: Publisher Site | Google Scholar
Y. Wu, J. Maultzsch, E. Knoesel et al., “Variable electron-phonon coupling in isolated metallic carbon nanotubes observed by Raman scattering,” Physical Review Letters, vol. 99, no. 2, 2007.
View at: Publisher Site | Google Scholar
B. Hatting, S. Heeg, K. Ataka et al., “Fermi energy shift in deposited metallic nanotubes: a Raman scattering study,” Physical Review B, vol. 87, no. 16, 2013.
View at: Publisher Site | Google Scholar
M. He, E. Rikkinen, Z. Zhu et al., “Temperature dependent Raman spectra of carbon nanobuds,” The Journal of Physical Chemistry C, vol. 114, no. 32, pp. 13540–13545, 2010.
View at: Publisher Site | Google Scholar
R. Krupke, F. Hennrich, Löhneysen Hv, and M. M. Kappes, “Separation of metallic from semiconducting single-walled carbon nanotubes,” Science, vol. 301, no. 5631, pp. 344–347, 2003.
View at: Publisher Site | Google Scholar
L. Qu, F. du, and L. Dai, “Preferential syntheses of semiconducting vertically aligned single-walled carbon nanotubes for direct use in FETs,” Nano Letters, vol. 8, no. 9, pp. 2682–2687, 2008.
View at: Publisher Site | Google Scholar
D. Chattopadhyay, I. Galeska, and F. Papadimitrakopoulos, “A route for bulk separation of semiconducting from metallic single-wall carbon nanotubes,” Journal of the American Chemical Society, vol. 125, no. 11, pp. 3370–3375, 2003.
View at: Publisher Site | Google Scholar
S. D. M. Brown, A. Jorio, P. Corio et al., “Origin of the Breit-Wigner-Fano lineshape of the tangential G-band feature of metallic carbon nanotubes,” Physical Review B, vol. 63, no. 15, article 155414, 2001.
View at: Publisher Site | Google Scholar
M. A. Pimenta, A. Marucci, S. A. Empedocles et al., “Raman modes of metallic carbon nanotubes,” Physical Review B, vol. 58, no. 24, pp. R16016–R16019, 1998.
View at: Publisher Site | Google Scholar
N. Caudal, A. M. Saitta, M. Lazzeri, and F. Mauri, “Kohn anomalies and nonadiabaticity in doped carbon nanotubes,” Physical Review B, vol. 75, no. 11, article 115423, 2007.
View at: Publisher Site | Google Scholar
J. S. Park, K. Sasaki, R. Saito et al., “Fermi energy dependence of the G-band resonance Raman spectra of single-wall carbon nanotubes,” Physical Review B, vol. 80, no. 8, article 081402, 2009.
View at: Publisher Site | Google Scholar
W. Zhou, J. Vavro, N. M. Nemes et al., “Charge transfer and Fermi level shift in p-doped single-walled carbon nanotubes,” Physical Review B, vol. 71, no. 20, article 205423, 2005.
View at: Publisher Site | Google Scholar
S. N. Bokova, V. I. Konov, E. D. Obraztsova, A. V. Osadchii, A. S. Pozharov, and S. V. Terekhov, “Laser-induced effects in Raman spectra of single-wall carbon nanotubes,” Quantum Electronics, vol. 33, no. 7, pp. 645–650, 2003.
View at: Publisher Site | Google Scholar
T. Uchida, M. Tachibana, S. Kurita, and K. Kojima, “Temperature dependence of the Breit-Wigner-Fano Raman line in single-wall carbon nanotube bundles,” Chemical Physics Letters, vol. 400, no. 4–6, pp. 341–346, 2004.
View at: Publisher Site | Google Scholar
X. Zhang, F. Yang, D. Zhao et al., “Temperature dependent Raman spectra of isolated suspended single-walled carbon nanotubes,” Nanoscale, vol. 6, no. 8, pp. 3949–3953, 2014.
View at: Publisher Site | Google Scholar
H. D. Li, K. T. Yue, Z. L. Lian et al., “Temperature dependence of the Raman spectra of single-wall carbon nanotubes,” Applied Physics Letters, vol. 76, no. 15, pp. 2053–2055, 2000.
View at: Publisher Site | Google Scholar
L. Song, W. Ma, Y. Ren et al., “Temperature dependence of Raman spectra in single-walled carbon nanotube rings,” Applied Physics Letters, vol. 92, no. 12, article 121905, 2008.
View at: Publisher Site | Google Scholar
Z. Zhou, X. Dou, L. Ci et al., “Temperature dependence of the Raman spectra of individual carbon nanotubes,” The Journal of Physical Chemistry B, vol. 110, no. 3, pp. 1206–1209, 2009.
View at: Publisher Site | Google Scholar
Y. Zhang, L. Xie, J. Zhang, Z. Wu, and Z. Liu, “Temperature coefficients of Raman frequency of individual single-walled carbon nanotubes,” Journal of Physical Chemistry C, vol. 111, no. 38, pp. 14031–14034, 2007.
View at: Publisher Site | Google Scholar
P. R. Mudimela, A. G. Nasibulin, H. Jiang, T. Susi, D. Chassaing, and E. I. Kauppinen, “Incremental variation in the number of carbon nanotube walls with growth temperature,” The Journal of Physical Chemistry C, vol. 113, no. 6, pp. 2212–2218, 2009.
View at: Publisher Site | Google Scholar
X. Cui, M. Freitag, R. Martel, L. Brus, and P. Avouris, “Controlling energy-level alignments at carbon nanotube/Au contacts,” Nano Letters, vol. 3, no. 6, pp. 783–787, 2003.
View at: Publisher Site | Google Scholar
R. B. Capaz, C. D. Spataru, P. Tangney, M. L. Cohen, and S. G. Louie, “Temperature dependence of the band gap of semiconducting carbon nanotubes,” Physical Review Letters, vol. 94, no. 3, article 036801, 2005.
View at: Publisher Site | Google Scholar
S. B. Cronin, Y. Yin, A. Walsh et al., “Temperature dependence of the optical transition energies of carbon nanotubes: the role of electron-phonon coupling and thermal expansion,” Physical Review Letters, vol. 96, no. 12, 2006.
View at: Publisher Site | Google Scholar
A. Jorio, A. G. Souza Filho, G. Dresselhaus et al., “G-band resonant Raman study of 62 isolated single-wall carbon nanotubes,” Physical Review B, vol. 65, no. 15, article 155412, 2002.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2018 Qianru Wu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

1577

Downloads

898

Citations

Journal of Nanomaterials

Temperature Dependence of G− Mode in Raman Spectra of Metallic Single-Walled Carbon Nanotubes

Abstract

1. Introduction

1.1. Experimental

2. Results and Discussion

Data Availability

Conflicts of Interest

Acknowledgments

References

Copyright

Temperature Dependence of G⁻ Mode in Raman Spectra of Metallic Single-Walled Carbon Nanotubes