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Journal of Nanomaterials
Volume 2018, Article ID 3457263, 11 pages
Research Article

Graphene Synthesis Using a CVD Reactor and a Discontinuous Feed of Gas Precursor at Atmospheric Pressure

1Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Real de Juriquilla, 76230 Santiago de Querétaro, QRO, Mexico
2Laboratorio de Nanotecnología Ambiental, Tecnológico de Monterrey, Escuela de Ingeniería y Ciencias, Ave. Eugenio Garza Sada 2501, 64849 Monterrey, NL, Mexico
3Instituto Tecnológico de Cd. Victoria, Boulevard Emilio Portes Gil No. 1301, Pte. A.P. 175, 87010 Ciudad Victoria, TAMPS, Mexico
4Laboratorio de Síntesis y Modificación de Nanoestructuras y Materiales Bidimensionales, Centro de Investigación en Materiales Avanzados S.C., Alianza Norte No. 202, Parque PIIT, 66628 Apodaca, NL, Mexico

Correspondence should be addressed to A. G. García; xm.ude.vamic@aicrag.ardnajela

Received 18 October 2017; Revised 26 January 2018; Accepted 30 January 2018; Published 18 March 2018

Academic Editor: Victor M. Castaño

Copyright © 2018 A. Moreno-Bárcenas 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.


The present work shows a new method in order to cost-effectively achieve the synthesis of graphene by Chemical Vapor Deposition (CVD). Unlike most usual processes, where precursors such as argon, H2, CH4, and high purity copper foil are used, the proposed method has replaced the previous ones by N2, N2 (90%) : H2 (10%), C2H2, and electrolytic copper (technical grade) since the use of industrialized precursors helps reduce production costs. On the other hand, the process was modified from a continuous flow system with vacuum to a discontinuous one at atmospheric pressure, eliminating the use of vacuum pump. In addition, this modification optimized the consumption of gases, which reduced the waste and the emission of pollutant gases into the atmosphere. Graphene films were grown under different gas flowrates and temperatures. Then, the obtained material was characterized by TEM, Raman spectroscopy, and AFM, confirming the presence of few graphene layers. In brief, the growth time was reduced to six minutes with acetylene as a carbon precursor at 1000°C and at atmospheric pressure, with a flow rate of 30 sccm. Finally, the reported conditions can be used for the synthesis of good quality graphene films in industrial applications.

1. Introduction

Graphene is a two-dimensional material with sp2 hybridization and carbon atoms in a honeycomb arrangement [1, 2]. Nevertheless, it was not until 2004, after its isolation by mechanical exfoliation, that electric properties of a monolayer were published [3], followed by many other studies that showed extremely interesting properties, such as electronic mobility in room temperature higher than 2.105 cm2 V−1S−1, Young’s Modulus of 1 TPa, thermal conductivity above 3000 WmK−1, 2.3% of optical absorption, and the capacity to be functionalized by a wide range of organic groups [46]. Hence, graphene is a material with a broad range of applications from mechanical, electrical, and optical applications to medical ones [5, 7]. Several methods have been used to prepare graphene, including graphite micromechanical exfoliation, epitaxial growth over SiC, graphite oxide reduction, and CVD [8] with the unique purpose to obtain large areas and more production [9, 10].

Therefore considering its high productivity, CVD is one of the most promising processes to grow high quality graphene in large areas [1113]. Accordingly, in recent years a considerable effort has been done to optimize the process, improve the kind of substrate, and control graphene growth [12, 14].

In initial experiments to form graphene, CVD systems with methane as the carbon precursor and hydrogen as a balancing gas were used and are still commonly used today. Thereafter, atmospheric pressure CVD (AP-CVD) or other carbon feedstocks have been explored (other gaseous hydrocarbons or carbon containing liquid or solid precursors) [15, 16]. Hydrogen is almost always used to achieve a better control in the synthesis of graphene on Cu. In industry, due to safety and cost issues, the use of pure hydrogen may not be preferred. Although processes using diluted hydrogen and methane have been developed, it should be noted that, in practice, these gases invariably contain trace amounts of oxidative impurities, which may have a significant effect on graphene growth [17].

At the same time, a deeper understanding has been acquired for each role in the synthesis stages [10, 13, 18, 19]. And two main challenges have been identified concerning graphene quality. First, substrates can lose their catalytic activity during permanence time inside the reactor, a process known as “cooking.” The second factor is related to the high temperatures and long growth times needed when monocrystalline cooper (111) is used as a substrate. An important challenge in graphene synthesis is to obtain high production volumes with high structural quality and visualize a methodology for future application on an industrial scale. Even so, the reported experiments still contemplate long synthesis times of up to 27 hrs at continuous gas flowrates [20] and expensive substrates [21] (Table 1). When the above variables are not taken into account, the performance and commercial attractiveness of this material could be decreased or limited [22].

Table 1: Overview of CVD processes synthesis.

The improvement of each of these aspects enables the control of graphene properties to satisfy the application-oriented needs such as production specifications (e.g., cost, rate). Until now, the commercial use of graphene is still restricted by the lack of standardized techniques for production that guarantee high energy efficiency and high structural quality. The improvement of electronic devices depends strongly on the quality of the graphene obtained [23].

In this paper, a novel and fast CVD method for graphene synthesis is proposed in order to decrease dramatically the usage of gases in a batch process. In addition, Cu (technical grade) polycrystalline substrates are used instead of monocrystalline (111) or laboratory grade (reagent) decreasing the production costs about 80 percent when compared to traditional CVD processes. Finally, the proposed method allowed the production of graphene with a similar quality ( > 2) to that obtained by methods that require high vacuum and a continuous gas flowrate [24, 25].

2. Experimental

2.1. Materials

Polycrystalline copper foils of quality electrolytic industrial (C-1100) with a size of 15 × 30 cm and purity of 99.9% w/w were used as substrates. The copper was washed with plenty of acetone and cleaned with wipes to remove grease and dust. Acetylene gas was used as carbon precursor with 98% concentration. High purity nitrogen gas was used for getting a neutral atmosphere and a high purity 90 : 10 mixture of N2 : H2 gases were used to obtain reducing conditions inside the reactor and before the graphene deposition. A conventional CVD reactor provided with an inverted compressor was used in order to facilitate the gas expulsion.

2.2. Growth Process

The studied parameters were temperature and flow rate of carbon precursor. In brief, a flow of N2 gas was introduced into the reactor for 15 min to remove the present oxygen. Then 1 L/min of N2/H2 was introduced to reduce the copper oxides in the surface of the sheet. Afterwards, on the one hand, acetylene was injected to the reactor at constant flow rate for 1 min. The injection was stopped in order to start the graphene growth process with the gas trapped inside reactor at different temperatures (Table 2). The cooling down was carried out under nitrogen atmosphere with a ramp of 8°C/min.

Table 2: Evaluated temperatures for the growth process.
2.3. Characterization

Graphene layers were analyzed in a high-resolution transmission electron microscope (HRTEM) JEOL-JEM 2200FS equipped with a spherical aberration corrector in the condenser lens and operated at 200 kV. Images were acquired in STEM mode, with bright field (BF) and high angle annular dark field (HAADF) detectors. Also, atomic force microscopy (AFM) was used, Asylum, model MFP3D-SA, using the technique of noncontact mode or AC, with rectangular cantilever model AC240TS-R3 at 2 N/m and a scanning speed of 70 kHz. The Raman spectra of graphene layers on copper substrate were recorded using a Renishaw in Via Raman spectrometer with an electronically cooled (−70°C) CCD camera and a Leica microscope. The excitation source used was a He-Ne laser with emission at 633 nm; integration time was 10 seconds. A diffraction grating at 1200 lines/mm and objective of 50x magnification with numerical aperture of 0.75 were used.

3. Results and Discussion

3.1. Graphene Synthesis by CVD

Table 1 shows an overview of CVD processes used with different gas precursors and growth conditions. Unlike the conditions mentioned in Table 1, our process allows the graphene synthesis, in a maximum time of 66 min, without making use of vacuum pumps. Note that for similar times of synthesis, pressures of 3–9 × 10−2 torr are required in most of the processes reported in Table 1 while atmospheric pressure is used in ours. Also in our process N2 is used as carrier gas instead of using argon, which is more expensive.

The proposed synthesis method is compound by four stages (cleaning, precursor injection, reaction time, and cooling). The temperature and flowrate of carbon precursor were the studied parameters. In Figure 1(a) the traditional process and differences with our process are shown.

Figure 1: Schematic representation of the graphene synthesis with (a) proposed method at atmosphere pressure using polycrystalline substrate and gas discontinuous flow and (b) traditional process at high vacuum using monocrystalline substrate and gas continuous flow.

In the first stage, the process temperatures 800, 900, and 1000°C were evaluated as shown in Table 2. The objective was to know the temperature at which amorphous carbon is formed and avoid it in the following tests. A flowrate at 100 sccm of acetylene was used as reference.

In the second stage, acetylene gas flowrate was tested at 100, 80, 30, and 10 sccm as shown in Table 3. The heating temperature was fixed after obtaining the results being 1000°C, the temperature which avoids the amorphous carbon deposition.

Table 3: Evaluated acetylene gas flow rates.
3.2. Proposed Reaction Mechanism

For graphene synthesis by CVD the use of both saturated and unsaturated hydrocarbons is essential [5, 8, 37, 38]. Saturated hydrocarbons are stable and less reactive than unsaturated hydrocarbons. C2H2 has a positive Gibbs free energy formation with a value of ΔG = 209 KJ/mol, indicating that reactants are favored in the following reaction: + = [39, 40]. According to thermodynamics data, C2H2 begins to decompose at 25°C and is highly reactive. Figure 2 shows a comparison of Δ between C2H2 and other hydrocarbons that have commonly been used in graphene synthesis [41]. As can be seen in Figure 2, as temperature increases, methane retains more stability when compared with acetylene (CH4 > C2H6 > C2H4 > C2H2). Thus, acetylene presents a positive Δ in a wide range of temperatures unlike methane which has a negative Δ in temperatures lower than 500°C.

Figure 2: Stability of hydrocarbon species.

Since acetylene is highly reactive, it might interact within the reactor with hydrogen, generating hydrogenation reactions. Thus other hydrocarbon species can be formed. To gain insight into the possible reactions occurring within the CVD furnace, the following acetylene reactions were analyzed: The variation of the standard Gibbs free energy change with temperature iswhere [42] and where is the equilibrium constant.

The constant allows knowing the behavior of a reaction by increasing the temperature; therefore, for , the reaction favors the products, while for the reaction favors the reagents [39]. Figure 3 shows the for acetylene hydrogenation reactions as well as its dehydrogenation reaction.

Figure 3: (a) for acetylene hydrogenation reactions and acetylene dehydrogenation. (b) Acetylene disintegration mechanism.

It is important to take into account that, within the experimental temperature range, for all reactions, the value of is greater than 1, for all reactions, and that the most favored reaction is the dehydrogenation of acetylene (solid line curve, Figure 3). Thus, acetylene is more susceptible to dehydrogenation rather than hydrogenation and releases carbon atoms for nucleation and graphene growth.

3.3. Transmission Electron Microscopy

Figure 4 shows typical micrographs obtained by electron transmission microscopy using dark and bright field illumination mode. By means of this technique, some highlights of the sample are visible which are difficult to observe in normal mode. Basically, transparent parts of the sample are shown in dark while the particles appear bright since they receive and scatter light in different directions. The results show sheets that were pulled up from Cu substrates during sonication. In Figure 4, images that appear at the top show the bright field and the corresponding dark field STEM images appear at the bottom. The acetylene flow was fixed at 100 sccm and images in the left, center and right side correspond to temperatures of 1000, 900, and 800°C, respectively (Table 2). Both images at 1000°C show the presence of few layers of graphene in contrast to the other temperatures (900 and 800°C). In samples obtained at 900°C the presence of graphene layers and carbon agglomerates as brighter areas (bottom) was observed. This effect can be attributed to the stacking of carbon atoms on the nucleation centers, which avoid the epitaxial growth of graphene sheets. Similarly, in process at 800°C, carbonaceous agglomerates are observed on a graphene sheet (top) confirming the agglomeration hypothesis using low temperatures. Initially, acetylene is decomposed on the copper surface facilitating the growth of a graphene sheet; nonetheless, under the growth conditions studied in this work, carbon precipitations were observed for process with temperatures below 900°C.

Figure 4: TEM bright (top) and dark field images (bottom) of graphene. Acetylene flow was fixed at 100 sccm. Samples obtained at different temperatures (1000, 900, and 800°C).

Additionally, the effect of acetylene flowrate was studied (see Table 3) maintaining a fixed temperature at 1000°C as a direct consequence of the obtained results. The objective was reducing the amount the amount of graphene layers previously obtained with a flow of 100 sccm.

The presence of fairly thin sheets of graphene was achieved with a flow rate of 80 sccm (Figures 5(a) and 5(b)). In Figures 5(c), 5(d), and 5(e), samples where graphene was synthesized using 30 sccm can be seen. However, when acetylene flow rate of 10 sccm (data not shown) was tested, no graphene layers were observed, concluding that the flow rate of 10 sccm is not enough as carbon precursor.

Figure 5: TEM bright and dark field images for graphene growth with fixed temperature at 1000°C and acetylene flowrates of 80 (a, b) and 30 sccm (c, d, and e).
3.4. Raman Spectroscopy

Raman spectroscopy was carried out in order to evaluate the structure of the graphene film growth at different conditions. This spectroscopy technique has been used to probe structural and physical properties of graphitic materials, providing valuable information about the atomic structure of edges, presence of disorder, defects, charges, and strain [43].

Figure 6 shows the characteristic spectra of this kind of carbonaceous materials. The analysis of Raman is focused on the D, G, and 2D bands of the spectrum, which are expected to appear at ~1350 cm−1, ~1580 cm−1, and ~2680 cm−1, respectively [44]. D band corresponds to disordered structure in graphene, especially at the edges of the graphene sheets. The G peak originates from the first-order scattering process due to the double degenerate phonon mode vibrations at the center of Brillouin zone and is related to sp2 bonded carbon [45]. Measurement of ratio is a well-known method for characterization of disorder [46, 47]. Ferrari et al. [48] showed that it is possible to use the second-order 2D (or G′) band in the graphene Raman spectra to learn about the number of layers in a graphene sample by using the ratio [49].

Figure 6: Raman spectra for (a) graphene synthesized at different temperatures with a fixed C2H2 flowrate (100 sccm) and (b) with different C2H2 flow rates at 1000°C. Schematic representation for and ratios at (c) fixed flow rate and (d) fixed temperature.

On one hand, as can be seen in Figure 6(a) (black line), sample obtained at 800°C shows a spectrum with a lot of defects in the structure of the material. Peaks D and G are overlapped by a combination of sp2 and sp3 bonds, corresponding to the presence of structural disorder or defects [47]. Thus, these spectroscopic results and those obtained by using the microscopic technique indicate that 800°C is not an adequate temperature for the synthesis of graphene since different carbon species are obtained.

Samples obtained at 1000 and 900°C (Figure 6(a), blue and red lines, respectively) present spectra with the three principal graphene peaks, which are consistent with the results observed in micrographs from Figure 4. Therefore, both temperatures could be adequate for the synthesis of carbon laminar structures. Nonetheless, for some cases, the intensity ratio is high according to Malard et al., indicating that a greater intensity in the D band is attributed to defects such as incomplete carbon-carbon bonds at edges. On the other hand, as shown in Figure 6(c), a ratio value lower than two was obtained, which indicates that the synthesized graphene consists of multilayers [31]. At 1000°C an increase in this ratio () with respect to 800 and 900°C was observed. Thus, 1000°C was chosen as the synthesis temperature for further experiments.

As previously discussed, in order to reduce the number of layers and defects, different acetylene flowrates were tested in the synthesis of graphene. For this case, experiments were carried out by using 100, 80, 30, and 10 sccm of acetylene per minute of synthesis. The Raman spectra indicate that an acetylene flowrate of 30 sccm produces a 2D band two times more intense than the G band (Figure 6(b), blue line). An increase in the intensity of the 2D peak as well as a decrease of the D band may indicate a lower number of layers and fewer defects (Figure 6(d)).

The ratio obtained by using a gas flowrate of 80 sccm was of 1.3, while the ratio with a flowrate of 30 sccm was 2.5. In both cases, a reduction in the number of defects was observed (Figure 6(d)); however, its presence is expected due to polycrystallinity in the Cu substrate. It is important to take into account the fact that the Cu grain boundaries and the edges of the graphene domains promote defects in its structure [43]. However the honeycomb shaped arrangement predominates in the entire structure. A ratio of indicates the presence of graphene near to monolayer [21, 5052] which indicates the production of a film with high quality (Figure 6(d)) [53].

3.5. Atomic Force Spectroscopy

AFM is one of the most important characterization techniques used to elucidate the amount of graphene layers present in a material. Figure 7 shows micrographs of graphene synthesized at 1000°C and with different acetylene flowrates. Synthesis carried out with 100 sccm (Figure 7(a)) renders plates with a thickness of 5.08 nm. Under these conditions, the 2D peak in Raman was small, but TEM micrographs showed hardly any laminar structures (data not shown). Assuming a distance between layers of approximately 0.34 nm [54], the number of layers could be set at 14. While, at flow rate of 80 sccm, plate thickness was 3.29 nm, corresponding to 8 graphene layers. Finally, injecting acetylene at 30 sccm generated plates of 1.65 nm, corresponding to approximately 4 layers of graphene.

Figure 7: AFM micrographs of graphene obtained at 1000°C and with different acetylene flow rates: (a) 100 sccm, (b) 80 sccm, and (c) 30 sccm.

4. Conclusions

The method described in this work offers important advantages such as (1) the number of parameters was simplified; (2) time of synthesis is shorter than those used in traditional methods; (3) it is a low-cost method when compared to those that using a continuous gas flowrates; (4) the proposed process in batch, besides using lower gas consumption, represents a significant reduction of emissions in the environment; (5) besides, the use of electrolytic technical grade copper instead of monocrystalline copper (reagent grade or high purity cooper foil) also contributes to reducing costs; (6) finally, the use of a mixture of N2/H2 (90 : 10) instead of pure H2, decreases the explosive risk by gas accumulation. In general, the synthesized graphene shows a good quality with spectral characteristics very near to the monolayer graphene; therefore, the obtained material with the proposed method represents an attractive option for industrial purposes or graphene mass production.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.


The financial support by CONACyT is acknowledged. The authors thank Oscar Eduardo Vega Becerra from CIMAV, Luz Maria Avilez from CINVESTAV QRO, and Iris Aguilar Hernández from ITESM Campus Monterrey for the technical support.


  1. B. Wu, D. Geng, Y. Guo et al., “Equiangular hexagon-shape-controlled synthesis of graphene on copper surface,” Advanced Materials, vol. 23, no. 31, pp. 3522–3525, 2011. View at Publisher · View at Google Scholar · View at Scopus
  2. M. H. Rümmeli, S. Gorantla, A. Bachmatiuk et al., “On the role of vapor trapping for chemical vapor deposition (CVD) grown graphene over copper,” Chemistry of Materials, vol. 25, no. 24, pp. 4861–4866, 2013. View at Publisher · View at Google Scholar · View at Scopus
  3. J. W. Suk, A. Kitt, C. W. Magnuson et al., “Transfer of CVD-grown monolayer graphene onto arbitrary substrates,” ACS Nano, vol. 5, no. 9, pp. 6916–6924, 2011. View at Publisher · View at Google Scholar · View at Scopus
  4. L. S. Bernard, M. Spina, J. Jacimovic et al., “Functionalized graphene grown by oxidative dehydrogenation chemistry,” Carbon, vol. 71, pp. 11–19, 2014. View at Publisher · View at Google Scholar · View at Scopus
  5. G. Nandamuri, S. Roumimov, and R. Solanki, “Chemical vapor deposition of graphene films,” Nanotechnology, vol. 21, no. 14, Article ID 145604, 2010. View at Publisher · View at Google Scholar · View at Scopus
  6. Z.-S. Wu, G. Zhou, L.-C. Yin, W. Ren, F. Li, and H.-M. Cheng, “Graphene/metal oxide composite electrode materials for energy storage,” Nano Energy, vol. 1, no. 1, pp. 107–131, 2012. View at Publisher · View at Google Scholar · View at Scopus
  7. B. Wang, Y. Zhang, H. Zhang et al., “Wrinkle-dependent hydrogen etching of chemical vapor deposition-grown graphene domains,” Carbon, vol. 70, pp. 75–80, 2014. View at Publisher · View at Google Scholar · View at Scopus
  8. J. Kim, J. Seo, H. Kyung, S. H. Kim, and H. Woo, “The effect of various parameters for few-layered graphene synthesis using meth- ane and acetylene,” Journal of Ceramic Processing Research, vol. 13, no. 1, pp. 42–46, 2012. View at Google Scholar
  9. S. Bhaviripudi, X. Jia, M. S. Dresselhaus, and J. Kong, “Role of kinetic factors in chemical vapor deposition synthesis of uniform large area graphene using copper catalyst,” Nano Letters, vol. 10, no. 10, pp. 4128–4133, 2010. View at Publisher · View at Google Scholar · View at Scopus
  10. H. Kim, C. Mattevi, M. R. Calvo et al., “Activation energy paths for graphene nucleation and growth on Cu,” ACS Nano, vol. 6, no. 4, pp. 3614–3623, 2012. View at Publisher · View at Google Scholar · View at Scopus
  11. H. H. Kim, Y. Chung, E. Lee, S. K. Lee, and K. Cho, “Water-free transfer method for CVD-grown graphene and its application to flexible air-stable graphene transistors,” Advanced Materials, vol. 26, no. 20, pp. 3213–3217, 2014. View at Publisher · View at Google Scholar · View at Scopus
  12. C.-M. Seah, S.-P. Chai, and A. R. Mohamed, “Mechanisms of graphene growth by chemical vapour deposition on transition metals,” Carbon, vol. 70, pp. 1–21, 2014. View at Publisher · View at Google Scholar · View at Scopus
  13. J. Cho, L. Gao, J. Tian et al., “Atomic-scale investigation of graphene grown on Cu foil and the effects of thermal annealing,” ACS Nano, vol. 5, no. 5, pp. 3607–3613, 2011. View at Publisher · View at Google Scholar · View at Scopus
  14. M. Batzill, “The surface science of graphene: Metal interfaces, CVD synthesis, nanoribbons, chemical modifications, and defects,” Surface Science Reports, vol. 67, no. 3-4, pp. 83–115, 2012. View at Publisher · View at Google Scholar · View at Scopus
  15. C. Wang, B. Xiao, and Y.-H. Ding, “Theoretical investigation on the healing mechanism of divacancy defect in graphene growth by reaction with ethylene and acetylene,” New Journal of Chemistry, vol. 37, no. 3, pp. 640–645, 2013. View at Publisher · View at Google Scholar · View at Scopus
  16. A. Guermoune, T. Chari, F. Popescu et al., “Chemical vapor deposition synthesis of graphene on copper with methanol, ethanol, and propanol precursors,” Carbon, vol. 49, no. 13, pp. 4204–4210, 2011. View at Publisher · View at Google Scholar · View at Scopus
  17. S. M. Kim, A. Hsu, and Y. Lee, “Graphene growth with "no" feedstock,” 2D Materials, vol. 4, article 25089, 2017. View at Google Scholar
  18. I. Vlassiouk, M. Regmi, P. Fulvio et al., “Role of hydrogen in chemical vapor deposition growth of large single-crystal graphene,” ACS Nano, vol. 5, no. 7, pp. 6069–6076, 2011. View at Publisher · View at Google Scholar · View at Scopus
  19. W. Zhang, P. Wu, Z. Li, and J. Yang, “First-principles thermodynamics of graphene growth on Cu surfaces,” The Journal of Physical Chemistry C, vol. 115, no. 36, pp. 17782–17787, 2011. View at Publisher · View at Google Scholar · View at Scopus
  20. S. Dhingra, J.-F. Hsu, I. Vlassiouk, and B. D'Urso, “Chemical vapor deposition of graphene on large-domain ultra-flat copper,” Carbon, vol. 69, pp. 188–193, 2014. View at Publisher · View at Google Scholar · View at Scopus
  21. M. Ishihara, Y. Koga, J. Kim, K. Tsugawa, and M. Hasegawa, “Direct evidence of advantage of Cu(111) for graphene synthesis by using Raman mapping and electron backscatter diffraction,” Materials Letters, vol. 65, no. 19-20, pp. 2864–2867, 2011. View at Publisher · View at Google Scholar · View at Scopus
  22. Y.-P. Hsieh, M. Hofmann, and J. Kong, “Promoter-assisted chemical vapor deposition of grapheme,” Carbon, vol. 67, pp. 417–423, 2014. View at Publisher · View at Google Scholar · View at Scopus
  23. Z. Liu, L. Li, H. Ren, and X. Sun, “Thermal Transport in Carbon-Based Nanomaterials,” Copyright, 2017. View at Google Scholar
  24. A. V. Tyurnina, H. Okuno, P. Pochet, and J. Dijon, “CVD graphene recrystallization as a new route to tune graphene structure and properties,” Carbon, vol. 102, pp. 499–505, 2016. View at Publisher · View at Google Scholar · View at Scopus
  25. B. Tang, H. Gao, and G. Hu, “Growth mechanism and influences from kinetic factors on carbon materials with Cu and silica substrates during atmospheric pressure chemical vapor deposition,” The Journal of Physical Chemistry C, vol. 117, no. 47, pp. 25175–25184, 2013. View at Publisher · View at Google Scholar · View at Scopus
  26. L. Assaud, N. Massonnet, D. Evrard et al., “A new route for the integration of a graphene/diazonium/PEDOT electrode towards antioxidant biomarker detection,” Journal of Electroanalytical Chemistry, vol. 771, pp. 73–79, 2016. View at Publisher · View at Google Scholar · View at Scopus
  27. G. Deokar, J. Avila, I. Razado-Colambo et al., “Towards high quality CVD graphene growth and transfer,” Carbon, vol. 89, pp. 82–92, 2015. View at Publisher · View at Google Scholar · View at Scopus
  28. P. Trinsoutrot, C. Rabot, H. Vergnes, A. Delamoreanu, A. Zenasni, and B. Caussat, “High quality graphene synthesized by atmospheric pressure CVD on copper foil,” Surface and Coatings Technology, vol. 230, pp. 87–92, 2013. View at Publisher · View at Google Scholar · View at Scopus
  29. O. Frank, J. Vejpravova, V. Holy, L. Kavan, and M. Kalbac, “Interaction between graphene and copper substrate: The role of lattice orientation,” Carbon, vol. 68, pp. 440–451, 2014. View at Publisher · View at Google Scholar · View at Scopus
  30. J.-S. Yu, X. Jin, J. Park et al., “Structural analysis of graphene synthesized by chemical vapor deposition on copper foil using nematic liquid crystal texture,” Carbon, vol. 76, pp. 113–122, 2014. View at Publisher · View at Google Scholar · View at Scopus
  31. J. Tian, B. Hu, Z. Wei et al., “Surface structure deduced differences of copper foil and film for graphene CVD growth,” Applied Surface Science, vol. 300, pp. 73–79, 2014. View at Publisher · View at Google Scholar · View at Scopus
  32. R. Jaaniso, T. Kahro, J. Kozlova et al., “Temperature induced inversion of oxygen response in CVD graphene on SiO2,” Sensors and Actuators B: Chemical, vol. 190, pp. 1006–1013, 2014. View at Publisher · View at Google Scholar · View at Scopus
  33. C.-S. Chen and C.-K. Hsieh, “Effects of acetylene flow rate and processing temperature on graphene films grown by thermal chemical vapor deposition,” Thin Solid Films, vol. 584, pp. 265–269, 2015. View at Publisher · View at Google Scholar · View at Scopus
  34. M. Qi, Z. Ren, Y. Jiao et al., “Hydrogen kinetics on scalable graphene growth by atmospheric pressure chemical vapor deposition with acetylene,” The Journal of Physical Chemistry C, vol. 117, no. 27, pp. 14348–14353, 2013. View at Publisher · View at Google Scholar · View at Scopus
  35. J. Hwang, S. Sasaki, M. Ohnishi et al., “Electronic properties and strain sensitivity of CVD-grown graphene with acetylene signatures for the estimation of defect density electrodes,” Japanese Journal of Applied Physics, vol. 55, pp. 04EP05-1–04EP05-8, 2016. View at Google Scholar
  36. N. S. Mueller, A. J. Morfa, D. Abou-Ras, V. Oddone, T. Ciuk, and M. Giersig, “Growing graphene on polycrystalline copper foils by ultra-high vacuum chemical vapor deposition,” Carbon, vol. 78, pp. 347–355, 2014. View at Publisher · View at Google Scholar · View at Scopus
  37. B. Xiao, X.-F. Yu, and Y.-H. Ding, “Theoretical investigation on the healing mechanism of divacancy defect in CNT growth by C2H2 and C2H4,” Journal of Molecular Modeling, vol. 20, no. 3, pp. 640–645, 2014. View at Publisher · View at Google Scholar · View at Scopus
  38. A. A. Puretzky, D. B. Geohegan, S. Pannala et al., “Real-time optical diagnostics of graphene growth induced by pulsed chemical vapor deposition,” Nanoscale, vol. 5, no. 14, pp. 6507–6517, 2013. View at Publisher · View at Google Scholar · View at Scopus
  39. P. Atkins and J. De Padua, Physical Chemistry, 8th edition, 2006.
  40. J. O. Maloney, Perry's Chemical Engineers' Handbook, United States of America: McGraw-Hill Companies, 8th edition, 2008.
  41. I. N. Levine, Physical Chemistry, 6th edition, 2002.
  42. R. D. Gaskell, Introducction to the Termodynamics of Materials, 5th edition, 2008.
  43. S. D. Costa, A. Righi, C. Fantini et al., “Resonant Raman spectroscopy of graphene grown on copper substrates,” Solid State Communications, vol. 152, no. 15, pp. 1317–1320, 2012. View at Publisher · View at Google Scholar · View at Scopus
  44. O. I. Aydin, T. Hallam, J. L. Thomassin, M. Mouis, and G. S. Duesberg, “Interface and strain effects on the fabrication of suspended CVD graphene devices,” Solid-State Electronics, vol. 108, pp. 75–83, 2015. View at Publisher · View at Google Scholar · View at Scopus
  45. C. Melios, A. Centeno, A. Zurutuza et al., “Effects of humidity on the electronic properties of graphene prepared by chemical vapour deposition,” Carbon, vol. 103, pp. 273–280, 2016. View at Publisher · View at Google Scholar · View at Scopus
  46. K. Gajewski, S. Goniszewski, A. Szumska et al., “Raman Spectroscopy and Kelvin Probe Force Microscopy characteristics of the CVD suspended graphene,” Diamond and Related Materials, vol. 64, pp. 27–33, 2016. View at Publisher · View at Google Scholar · View at Scopus
  47. S. Tian, Y. Yang, Z. Liu et al., “Temperature-dependent Raman investigation on suspended graphene: Contribution from thermal expansion coefficient mismatch between graphene and substrate,” Carbon, vol. 104, pp. 27–32, 2016. View at Publisher · View at Google Scholar · View at Scopus
  48. A. C. Ferrari, J. C. Meyer, V. Scardaci et al., “Raman spectrum of graphene and graphene layers,” Physical Review Letters, vol. 97, no. 18, pp. 1–4, 2006. View at Publisher · View at Google Scholar · View at Scopus
  49. L. M. Malard, M. A. Pimenta, G. Dresselhaus, and M. S. Dresselhaus, “Raman spectroscopy in graphene,” Physics Reports, vol. 473, pp. 51–87, 2009. View at Publisher · View at Google Scholar
  50. J. Han, J.-Y. Lee, and J.-S. Yeo, “Large-area layer-by-layer controlled and fully bernal stacked synthesis of graphene,” Carbon, vol. 105, pp. 205–213, 2016. View at Publisher · View at Google Scholar · View at Scopus
  51. R. K. de Castro, J. R. Araujo, R. Valaski et al., “New transfer method of CVD-grown graphene using a flexible, transparent and conductive polyaniline-rubber thin film for organic electronic applications,” Chemical Engineering Journal, vol. 273, pp. 509–518, 2015. View at Publisher · View at Google Scholar · View at Scopus
  52. M.-C. Chuang and W.-Y. Woon, “Nucleation and growth dynamics of graphene on oxygen exposed copper substrate,” Carbon, vol. 103, pp. 384–390, 2016. View at Publisher · View at Google Scholar · View at Scopus
  53. S. Chen, H. Ji, H. Chou et al., “Millimeter-size single-crystal graphene by suppressing evaporative loss of Cu during low pressure chemical vapor deposition,” Advanced Materials, vol. 25, no. 14, pp. 2062–2065, 2013. View at Publisher · View at Google Scholar · View at Scopus
  54. S. Kim, Y. Song, J. Wright, and M. J. Heller, “Graphene bi- and trilayers produced by a novel aqueous arc discharge process,” Carbon, vol. 102, pp. 339–345, 2016. View at Publisher · View at Google Scholar · View at Scopus