Graphene oxide (GO) was synthesized via a simple electrochemical exfoliation of graphite in a surfactant-containing aqueous solution. A novel custom-made surfactant, 1,4-bis (neopentyloxy)-3-(neopentyloxycarbonyl)-1,4-dioxobutane-2-sulfonate (TC14) was used to assist the exfoliation process. The structural and magnetic properties of prepared GO were examined using electron microscopies, micro-Raman, and Fourier transform infrared spectroscopies, and vibrating sample magnetometer (VSM). Room temperature VSM measurement showed a diamagnetic response of pristine GO under a high magnetic field. This indicated the low defect and the absence of any impurities in the synthesized GO. Simple mixing of GO and carbon nanotubes (CNTs) was also done to study their magnetic properties. CNTs were initially synthesized from waste engine oil using thermal chemical vapour deposition. It was found that the addition of magnetic CNTs has successfully induced the ferromagnetism in the GO sample. The saturation magnetization and average coercivity of GO/CNTs were observed to be 6.13 memu and 345.12 G, respectively. This study offers a low cost and simple method to induced magnetism in GO as compared to the common chemical modifications of GO.
Graphene has been known with its outstanding properties and wide range applications. A derivative of graphene namely graphene oxide (GO) also has received enormous attention because it is easily synthesized, modified or chemically reduced for mass production of graphene and offers many practical applications. Graphene and its derivatives also show potential in spintronic applications due to their excellent carrier mobility and long spin diffusion length arise from the weak spin–orbit coupling of carbon atom [1, 2]. However, it is known that perfect graphene is intrinsically diamagnetic [1, 3]. The presence of defects such as vacancies, impurity, dislocations and grain boundaries in graphene can induce the spin polarization and increase its magnetism [4, 5]. Hence, several studies have been done to enhance the magnetic properties of GO such as nanocomposite with metallic or magnetic materials [6, 7] and chemical activation . Meanwhile, GO produced from the Hummers method and chemically reduced GO (RGO) was reported [8, 9] to show ferromagnetism response without any further treatments. It was believed that nature uses of acids during the synthesis process using Hummers method has contributed to the magnetic properties of GO.
Modification of another carbon material namely carbon nanotubes (CNTs) is also seen can improve their properties and expand their applications. Pistone et al.  reported the synthesis of CNTs from isobutene using Fe/Al2O3 based catalyst decorated with Fe3O4 magnetite nanoparticle. They use of metal-based catalyst and the addition of magnetite nanoparticle has successfully induced the magnetization in CNTs sample. Magnetic carbon materials offer many potential applications such as magnetic data storage, nanoprobe in magnetic force microscopy , adsorbent  and biosensor .
Moreover, the use of surfactant in stabilizing the carbon nanostructures also gained much attention due to its natural role of surfactant [13, 14]. Previous works have implemented the triple-tails surfactant, TC14 in various nanocomposites applications including CNTs/natural rubber latex and graphene-based rubber [15,16,17]. However, so far, there is no work reported on the use of triple-tails surfactant, TC14 in the magnetic properties study of GO incorporated with CNTs.
Therefore, in this study, GO synthesized via an electrochemical exfoliation process was directly mixed with magnetic CNTs synthesized from waste engine oil (WEO) in the presence of ferrocene (C10H10Fe). A novel custom-made surfactant, 1,4-bis (neopentyloxy)-3-(neopentyloxycarbonyl)-1,4-dioxobutane-2-sulfonate (TC14)  was used to assist the exfoliation process during the synthesis of GO. The use of ferrocene catalyst did contribute to the magnetic properties of CNTs. As compared to the conventional routes to induce the magnetic properties of GO, we offered a simpler, greener and cheaper process by avoiding the use of hazardous chemicals such as acid treatment. Moreover, the mixing of GO and CNTs which were both carbon-based materials did not give additional contaminations or impurities to the nanocomposite sample.
Materials and methods
GO was initially synthesized via an electrochemical exfoliation method as similarly reported in [19, 20]. A custom-made surfactant, 1,4-bis (neopentyloxy)-3-(neopentyloxycarbonyl)-1,4-dioxobutane-2-sulfonate (TC14) with concentration of 0.1 M was used to assist the GO dispersion in deionized (DI) water. The graphite electrodes were connected to the voltage source of 7.0 V for 24 h synthesis process. CNTs were separately synthesized using thermal CVD method from waste engine oil as carbon source with a ferrocene catalyst of 17.99 wt% . For the preparation of GO/CNTs sample, 0.05 g CNTs and 0.5 wt% TC14 was dispersed in 10 ml deionized water and stirred for 30 min. GO solution was then simultaneously mixed into CNTs dispersion with volume ratio of 1:1 and sonicated for 30 min in an ultrasonic bath. The mixture was further stirred in a water bath system at 85 °C for 1 h. The prepared dispersion was then repeatedly centrifuged at 5000 rpm and the precipitation was further dried in an oven to form a fine GO/CNTs powder. The samples were characterized using field emission scanning electron microscopy (FESEM-Hitachi SU 8020), high-resolution transmission electron microscopy (HRTEM- FEI Tecnai F30 200 kV), micro-Raman spectroscopy (Renishaw InVia Raman Microscope), Fourier transform infrared spectroscopy (FTIR-Thermo scientific Nicolet 6700 FTIR spectrometer), and vibrating sample magnetometer (VSM-LakeShore 7404).
Result and discussion
FESEM analysis was performed to observe the morphology of pristine GO, pure CNTs and GO/CNTs nanocomposites as seen in Fig. 1. Pristine GO (Fig. 1a) presented a lateral surface area, crumple, and typical wrinkle structure. The edges part exhibited a highly roll-up structure due to the intra-planar interaction between the layers of GO sheets . Meanwhile, a dense quasi aligned CNTs from WEO precursor with a diameter at around 31–33 nm was presented in Fig. 1b. Hollow tube CNTs were observed to be covered between the crumple GO sheets in the GO/CNTs nanocomposite sample (Fig. 1c–d). The diameter of the CNTs in the GO/CNTs sample was consistent with pristine CNTs. The formed nanocomposites between GO and CNTs shows a thick flake-like shape with wrinkles and hollow tube structure similar to the reported of GO/CNTs composites . However, both GO and CNTs structures were slightly deformed after the mixing process due to the stirring and sonication processes to produce a uniform GO/CNTs dispersion. This might be due to the π–π bonding in-between CNTs and GO, thus altered the size of the nanostructures [22, 23].
The morphology of pristine GO and GO/CNTs nanocomposites was further investigated by high-resolution transmission electron microscopy (HRTEM) as shown in Fig. 2. Figure 2a shows a pristine GO consisted of multi-layers of graphene sheets (< 10 layers) due to its natural wavy and stacked characteristics. Meanwhile, GO/CNTs nanocomposites image in Fig. 2b revealed the CNTs structure was distributed over the GO surfaces. It is clearly shown in all regions that the end-tubes of CNTs were pulled out from the GO structures, thus confirmed the nanocomposites are well-attached due to the higher compatibility of GO led by the stabilization of triple-tails surfactant within the nanocomposite.
Micro-Raman spectroscopy was used to investigate the carbon structure ordering of the sample (Fig. 3a). A typical micro-Raman spectrum of GO was observed with strong D (disorder) and G (graphitic) peaks at ~ 1359 and 1597 cm−1, respectively and ID/IG ratio of 0.91. A slightly broad and intense peak at 1361 cm−1 was due to the defects contributed by the oxygenesis group at GO edges, indicating a successful oxidation and intercalation process . Meanwhile, for CNTs synthesized from WEO, the ID/IG ratio showed a slightly lower (0.90) than the GO sheets, which is consistent with the typical crystallinity of CNTs in previous work . After the incorporation of GO and CNTs, the ratio was slightly increased up to 1.09. The distortion at G peak indicates the successful interactions between the GO and CNTs . Higher disorder as also observed in FESEM analysis showed that the mixing process did affect the structure of the nanocomposite sample.
In order to affirm the attachment between CNTs and GO structures, the FTIR measurement was carried. From the FTIR analysis, the noticeable changes were observed at several points (Fig. 3b). As the previous report, there is no obvious peak presence in the CNTs spectrum . Meanwhile, the characteristics peaks around 3352, 2977, 1381, 1087, 1044 and 884 cm−1 were seen in the GO sample. The existence of the vibrational bands in the range of 1000–1400 cm−1 was due to the various oxygen functional groups attached at edges GO sheets [26, 27]. Meanwhile, the peak appeared at around 800 cm−1 was confirmed the stabilized GO sheets assisted surfactant . The presence of the intense and broad peaks at 2977 and 3352 cm−1, respectively, further supported that the GO solution is highly water- soluble . After the addition of CNTs in the GO solution, the FTIR spectrum of GO/CNTs exhibits all characteristics peaks for GO along with several peaks of CNTs. The peaks at below 1000 cm−1 (epoxy group) for GO and CNTs sample were disappeared in GO/CNTs nanocomposites meanwhile a broad and intense peak at 3440 cm−1 (hydroxyl group) was observed. This confirmed that the GO and CNTs are well-mixed during the mixing process. Meanwhile, the graphitic skeleton peak at 1582 and 1651 cm−1 further confirmed the functionalization between GO and CNTs [30, 31].
The magnetizations of the samples as the function of a magnetic field at room temperature are presented in Fig. 4. As reported in previous studies [4, 9], without any chemical modification and treatments, pristine GO was naturally diamagnetic. This is also consistent with our result (Fig. 4a) where the GO presented a diamagnetic response even under a high magnetic field up to 12,000 G. The addition of CNTs has successfully induced the magnetic properties of GO as seen in Fig. 4b. The ferromagnetic response was observed with the measured saturation magnetization and average coercivity of 6.13 memu and 345.12 G, respectively. Even though the results obtained is slightly lower but the magnetization value of GO composites is still comparable with other previous works [32, 33]. As previously reported, the CNTs exhibit ferromagnetic hysteresis with a saturation magnetization of ~ 30 \(\mu emu\) . The enhancement observed for the GO/CNTs nanocomposite sample was probably due to the presence of metallocene catalyst (ferrocene) in CNTs. On the other hand, as presented through micro-Raman analysis, the increase of GO/CNTs defect also led to the enhancement of their magnetic properties. It was known that the presence of defects in carbonaceous materials such as graphene can induce spin polarization which can enhance the magnetic properties of the materials [4, 35, 36].
Simple mixing of CNTs with GO has increased the magnetic properties of the GO-based nanocomposites. It was found that the addition of magnetic CNTs synthesized from wastes engine oil has successfully induced the ferromagnetism in the GO-assisted TC14 surfactant sample which suitably offers the nanocomposites in many sensors and photo-catalyst applications.
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The authors would like to acknowledge Short Term Grant, Universiti Sains Malaysia (USM) (304/PFIZIK/6315241) for financial support. The authors want to thank Nano-Optoelectronics Research and Technology Laboratory (USM), Nanotechnology Research Centre (UPSI) for their facilities support, and Department of Frontier Material, Nagoya Institute of Technology, Japan for the technical supports.
This study was funded by Short Term Grant, Universiti Sains Malaysia (USM) (Grant code: 304/PFIZIK/6315241).
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Nurhafizah, M.D. Magnetic properties of graphene oxide via a simple mixing with waste engine oil-based carbon nanotubes. SN Appl. Sci. 2, 534 (2020). https://doi.org/10.1007/s42452-020-2361-8
- Graphene oxide
- Electron microscopy
- Carbon nanotubes