Graphene oxide is highly desired for printing electronics, catalysis, energy storage, separation membranes, biomedicine, and composites. However, the present synthesis methods depend on the reactions of graphite with mixed strong oxidants, which suffer from explosion risk, serious environmental pollution, and long-reaction time up to hundreds of hours. Here, we report a scalable, safe and green method to synthesize graphene oxide with a high yield based on water electrolytic oxidation of graphite. The graphite lattice is fully oxidized within a few seconds in our electrochemical oxidation reaction, and the graphene oxide obtained is similar to those achieved by the present methods. We also discuss the synthesis mechanism and demonstrate continuous and controlled synthesis of graphene oxide and its use for transparent conductive films, strong papers, and ultra-light elastic aerogels.
Graphene oxide (GO), which were usually used as a precursor for the synthesis of graphene, but is attracting increasing interest because of many unique properties and promising applications that are different from graphene1,2,3,4. In GO, a great number of oxygen-containing functional groups such as hydroxyl, epoxy, and carboxyl are covalently bonded to graphene basal plane and edges with a C/O atomic ratio of around 2.01,2,3, which makes GO sheets strongly hydrophilic and can be well dispersed in water1,2,3,4,5,6. The stable and homogeneous GO suspensions allow easy assembly of various graphene macrostructures with tunable fascinating properties such as transparent conductive films7, 8, strong and stiff papers9, multifunctional separation membranes10, 11, conductive and strong fibers12 and ultralight super-elastic aerogels13, 14. Moreover, the oxygen-containing functional groups enable GO to be easily functionalized and strongly interacted with other materials, which endures GO a chemically tunable platform and a wide range of technological applications such as supercapacitors and lithium batteries15, 16, fuel cells17, biomedicine18, and polymer composites19, 20.
Generally, GO is synthesized by exfoliation of graphite oxide1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21. Since the first preparation by Brodie in 185922, the Brodie and the subsequently developed Staudenmaier23 and Hummers24 methods have been the three primary routes for synthesizing graphite oxide, which all depend on the homogeneous reactions of graphite with mixed strong oxidants (Supplementary Table 1). Both Brodie and Staudenmaier methods use KClO3 and nitric acid (most commonly fuming [higher than 90% purity]), and suffers from explosion risk, as well as production of hazardous gases (e.g., NOx and ClO2) and carcinogenic ClO-. The most commonly used Hummers methods1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21, 24, 25 use a large amount of concentrated H2SO4 and KMnO4 to ensure sufficient oxidation. The highly reactive Mn2O7 intermediates can cause severe explosion at elevated temperatures as well. Inevitably, all these three methods produce serious environmental pollution and metal ion impurities on GO sheets. For instance, in Hummers method, around 1000 times more water than graphite has to be used to remove the excessive H2SO4 and KMnO4 after oxidation reaction (Supplementary Table 1), producing a huge amount of waste water containing mixed acids and heavy metal ions, and Mn2+ are usually detected on GO sheets. Moreover, they are all time-consuming, which need a few to hundreds of hours for oxidation (Supplementary Table 1). Although the oxidation time can be reduced to about 1 h by using strong oxidant K2FeO4 and concentrated H2SO426, more oxidizing mixtures are used (Supplementary Table 1), leading to more pollution.
Recently, electrochemical (EC) processes have been developed and widely used to synthesize graphene sheets because of the environmental-friendliness, high efficiency and relatively low cost27 (Supplementary Table 2). It has been shown that nearly pristine graphene with a C/O of 25.3 and mobility of 405 cm2·V−1s−1 could be synthesized within seconds by EC exfoliation of graphite foil28. Inspired by these successes, researchers also tried to synthesize GO by EC oxidation of various graphitic materials such as pencile core29, graphite rode30 and graphite flakes31, 32. Unfortunately, the accompanied water/solvent electrolysis process aggravates the expansion and delamination of graphitic materials, which lead to ineffective current supply or broken circuit before the desired EC oxidation process can be achieved27, 28. Therefore, the products suffer from low oxidation and exfoliation degree29,30,31,32,33,34,35 (Supplementary Table 3), which are much different from the GO synthesized by traditional chemical oxidation methods mentioned above. Although the products synthesized by EC oxidation of graphite rode show a low C/O atomic ratio of 2.2, they are mainly oxidized at edges and electrically conductive30. Recently, an EC Tee-cell setup has been used to try to ensure the electrical current to all graphitic flakes, however, the product shows a maximum C/O atomic ratio of 3.0 even after about 48 h reaction34.
Here, we report a scalable, safe, ultrafast, and green method to synthesize clean GO sheets by water electrolytic oxidation of graphite. It is found that the pre-intercalation of graphite efficiently inhibit the anodic electrocatalytic oxygen evolution reaction of water at high voltage to enable the ultrafast oxidation of graphene lattice within a few seconds, which is over 100 times faster than the present methods. The GO obtained shows similar chemical composition, structure, and properties to those achieved by traditional Hummers method. As examples, we demonstrate its use for high-performance transparent conductive films, strong papers and ultra-light elastic aerogels. Moreover, this method enables continuous production and easy control on the oxidation degree, number of layers and lateral size of GO sheets.
Synthesis and characterization of GO sheets by EC method
The synthesis of GO contains two sequential EC processes at room temperature with commercial flexible graphite paper (FGP) as raw material (Fig. 1a and Supplementary Figs. 1, 2). The commercial FGP has similar structure with graphite, high tensile strength (4 to 5 MPa), excellent electrical conductivity comparable with HOPG, and good flexibility (Fig. 1b, Supplementary Note 1, and Supplementary Figs. 3, 4). It usually has a thickness from micrometers to millimeters, width up to meters, and length up to kilometers. First, the FGP is subjected to EC intercalation in concentrated H2SO4 to form stage-I graphite intercalation compound paper36 (GICP, Fig. 1c and Supplementary Movie 1). Then, the GICP is used as anode for EC reaction in diluted H2SO4 (50 wt.%). Very surprisingly, the blue-colored GICP dipped in diluted H2SO4 is oxidized quickly to yellow-colored graphite oxide24 within a few seconds along with exfoliation (Fig. 1d, Supplementary Movies 2, 3, and Supplementary Fig. 5). After vacuum filtration and cleaning with water, the filter cake is exfoliated in water by sonication to form electrochemically synthesized GO (EGO) dispersion (Fig. 1e).
It is worth noting that the total amount of water used for cleaning graphite oxide in our method (mass ratio to raw FGP, around 150, Supplementary Note 2 and Supplementary Fig. 6) is significantly lower than those used in the Hummers methods (typically around 1000). Similar to the GO synthesized by traditional Hummers method (HGO)5, our EGO shows highly stable solubility in water. It retains a homogeneous dispersion, without any precipitates and color change, after storage for 6 months at a concentration of 1 mg·mL−1 in water (Fig. 2a). After freezing drying, the yield of EGO is estimated to be around 96 wt.% of raw FGP. In addition, this method is very easy to scale up. EGO can be continuously produced by continuously introducing the GICP slice into dilute H2SO4 solution with a specific rate (Supplementary Movie 2). For example, using two 250 mL beakers as reactors and a 0.5 mm-thick, 40 mm-wide FGP as raw material, EGO was continuously produced with a productivity of about 12 g·h−1, showing the great potential of this method for mass production of GO sheets. It is needed to point out that FGP is an ideal raw material for continuous production of GO sheets by our method because of its combined excellent properties mentioned above and the good tolerance to the volume expansion caused by intercalation shown below, although it is relatively difficult being oxidized by traditional Hummers method comparing with natural graphite flakes (Supplementary Note 1 and Supplementary Table 4). Graphite powders cannot be used directly in our method because of the very small size and have to be fabricated into macroscopic electrode to ensure voltage supply. Graphite rods are also not suitable for our method since they are easily broken into small pieces even after short time intercalation and cannot be used for further oxidation.
The chemical composition of the continuously produced EGO was analyzed by combustion elemental analyzer (EA), X-ray photoelectron spectrometer (XPS), Fourier transform infrared spectrometer (FTIR), and inductively coupled plasma atomic emission spectrometer (ICP-AES). The EA analysis shows that EGO has a typical composition (at. %) of C (50.2), O (29.2), H (19.7), and S (0.9). This gives C/O atomic ratio of around 1.7, which is lower than the typical value for HGO (about 2.0)7, 24, 26, indicating a higher oxidation degree of EGO. XPS C1s spectra show strong C=C peak (284.6 eV), prominent epoxy/hydroxyl peak (C–O, 287.0 eV), and weak carbonyl (C=O, 288.0 eV) and carboxyl (O–C=O, 289.2 eV) peaks (Fig. 2b). FTIR spectra show O–H stretching vibration (in the range of 3000 to 3700 cm−1), C=O vibration (1740 cm−1), C=C vibration from sp2 bonds (1645 cm−1) and C–O vibration (1402, 1087, and 1042 cm−1) (Fig. 2c). These XPS and FTIR features are similar to those of HGO, suggesting that EGO has the same oxygen-containing functional groups as HGO. The abundant functional groups enables EGO a high zeta potential of −56.8 mV (pH = 6.8), leading to excellent solubility in water, as shown in Fig. 2a. Consistent with the fact that no metal-containing chemicals are used, ICP-AES measurements confirm the absence (less than 50 ppb) of typical metal impurities (Fe, Co, Ni, Mn, Cu, Zn) in EGO.
It is well accepted that GO has a structure of small sp2 C–C domains isolated within the sp3 C–O matrix1,2,3. Raman spectroscopy provides a powerful tool to obtain the detailed structural information of graphene-based materials. The G peak is attributed to bond stretching of sp2 carbon pairs, and the D peak is attributed to the breathing mode of sp2 carbon rings and activated by defects37. As shown in Fig. 2d, both EGO and HGO show prominent D peak (1323 cm−1) and G peak (1580 cm−1), and very weak 2D peak (2650 cm−1) and D + G peak (2903 cm−1). It is worth noting that the intensity ratio of D peak to G peak in EGO is higher than that in HGO, suggesting that the sp2 domains in EGO are smaller than those in HGO. This is consistent with the higher oxidation degree of EGO shown above.
We then used an atomic force microscope (AFM), scanning electron microscope (SEM), high resolution transmission electron microscope (HRTEM) to characterize the number of layers and lateral size of EGO (Fig. 2e–j). Similar to HGO, the monolayer EGO sheets show a thickness of about 1.0 nm (Fig. 2e) because of the presence of functional groups and adsorbed water. AFM and SEM measurements indicate that the lateral size of EGO sheets is mostly in the range of 1 μm to 10 μm (about 61%), with about 7% larger than 10 μm and about 32% smaller than 1 μm (Fig. 2i). HRTEM images of the folded edges give direct evidence on the number of layers (Fig. 2h). Extensive HRTEM observations on 150 EGO sheets show that about 46% of them are monolayer and about 86% are no more than three layers (Fig. 2j), which are consistent with the AFM measurement results (Supplementary Fig. 7). Figure 2k shows the mass-produced EGO aqueous solution (5 mg·mL−1). Note that there are also some multilayers in the GO samples exfoliated from the graphite oxide made by Hummers method without centrifugation25, 38. In our method, extending the sonication time greatly reduces the percentage of multilayers and the lateral size of the EGO sheets (Fig. 2i, j and Supplementary Fig. 7). For instance, the samples obtained by 30 min sonication contain about 95% monolayers and about 5% bilayers, and the lateral size is mostly smaller than 1 μm.
Synthesis mechanism and controlled synthesis of GO sheets by EC method
To understand the synthesis mechanism of EGO, we used in-situ Raman spectroscopy (Fig. 3a, e), ex-situ XRD (Fig. 3b, f) and XPS (Fig. 3c, g), and optical microscopy (Fig. 3d) to monitor the structure and chemical composition changes of a FGP slice with reaction time in the two-step EC process. As shown in Figs. 1b, 3a and 3b, after 20 min reaction in concentrated H2SO4, the FGP slice changes color from lustering-grey to blue, the Raman G peak shifts from 1580 to 1631 cm−1 and the XRD (002) peak shifts from 26.5° to 23.2°, which give clear evidence for stage-I intercalation of graphite36, 39. It is worth noting that there are no defects or oxidation-containing functional groups in the obtained GICP (Fig. 3a, c, Supplementary Note 3, and Supplementary Fig. 8). Moreover, the GICP remains nearly the same fracture force and flexibility with FGP, and the surface resistance greatly decreases because of the doping of sulfuric acid (Supplementary Table 5). Although no oxidation occurs after a long-reaction time (2 h) in concentrated H2SO4, the GICP suffers severe swelling (about 7 times increase in thickness compared to FGP, Supplementary Table 5), which leads to dramatic decrease in mechanical strength and conductivity, and therefore cannot be used in the following EC process.
To show the structure and composition change of GICP clearly during the second EC process, we fixed a GICP slice in the electrolyte (initial dipping length: 1 cm) without moving. During EC process, once the graphite was oxidized, it became insulating, and consequently its EC oxidation reaction stopped immediately although it was still kept in the electrolyte. Very surprisingly, as shown in Fig. 3d, Supplementary Movie 3 and Supplementary Fig. 5, only after a few seconds, some areas of the GICP surface change from blue to yellow, evidence of the oxidation of graphite24. With extending the reaction time, the yellow areas quickly expand and the whole surface becomes yellow after about 60 s. Then, the color becomes darker and darker with the oxidation of the interior part, and no color changes any more after 3 min. The evolutions of Raman spectra, XRD pattern and XPS C1s spectra confirm the full oxidation of GICP from the surface to the interior (Fig. 3e–g). During the continuous production process of EGO, a GICP slice was continuously introduced into the electrolyte at a speed of around 5 mm·min−1 but the GICP dipped in the electrolyte remained almost a constant length of around 1 mm, as shown in Supplementary Movie 2. All these results suggest that the EC oxidation of graphite lattice finishes within a few seconds. JM Tour and co-workers studied the formation mechanism of graphene oxide by a modified Hummers method using a single graphite flake, and found that the conversion of the graphite intercalation compound into graphite oxide, a key step in the formation of GO, takes a few hours even days40. Therefore, the EC oxidation rate in our method is over 100 times faster than the oxidation rate of the Hummers methods.
Another very important feature of our method is that the oxidation degree of the graphite oxide obtained can be easily tuned by simply changing the concentration of H2SO4 in electrolyte, as shown in Fig. 3h (also see Supplementary Note 5, Supplementary Fig. 10, and Supplementary Table 6). Highly oxidized GO (C/O < 2) is achieved only when the H2SO4 concentration is in the range of 40 wt.% to 60 wt.%, and the highest oxidation degree with C/O atomic ratio of 1.5–1.8 is achieved at a H2SO4 concentration of 50 wt.%. Below and above this concentration range, only partially oxidized products (C/O > 2) are obtained. Moreover, mass spectrometry analysis of the gaseous products of the EC oxidation process shows no sulfur-containing byproduct (Supplementary Note 6, Supplementary Fig. 11a–d, and Supplementary Table 7), indicating that H2SO4 is not decomposed. These results suggest that the water in electrolyte plays a key role in the EC synthesis of graphite oxide. Further 18O isotropic tracing experiments clearly reveal that the oxygen functional groups in EGO dominantly originate from water (Fig. 3i, Supplementary Note 7 and Supplementary Fig. 12).
We also studied the EC reaction of FGP directly in dilute H2SO4 aqueous solution. However, only weakly oxidized graphene sheets with a C/O atomic ratio larger than 7 or thin graphite flakes were obtained (Fig. 3j, Supplementary Fig. 10 and Supplementary Table 6). This is similar to the reported EC methods27, 28, 34, which directly use pristine graphitic materials for EC reaction in acid or salt aqueous solution and can only produce pristine or weakly oxidized graphene sheets with a C/O atomic ratio mostly larger than 3.0 even after a very long reaction time of 48 h (Supplementary Tables 2 and 3). Therefore, the pre-intercalation of graphite by H2SO4 plays a key role in ultrafast EC synthesis of highly oxidized GO sheets in our method.
It is well established that the anodic electrocatalytic oxygen evolution reaction of water occurs under an applied voltage, and it contains four elementary reactions as following41:
Where * stands for an active site on electrode surface, *OH, *O, and *OOH represent the radical intermediates adsorbed on the active site, and E refers to the driving voltage. In the case of graphitic anode, the adsorbed reactive *OH, *O, and *OOH can react with the carbon lattice that is highly positively charged to form covalently bonded oxygen-containing functional groups34, 42. However, the rapid formation of a great number of O2 gas will exacerbate the exfoliation of the graphitic anode, leading to ineffective current supply or broken circuit and consequently stopping the electrochemical oxidation reaction27, 28.
We then studied the gaseous products of the EC reactions with GICP, FGP, or Pt as anode and Pt as cathode in 50 wt.% H2SO4 aqueous solution at 5 V (Supplementary Note 6 and Supplementary Fig. 11e). It was found that the mole ratio of O2 to H2 is only 1:8.36 for GICP as anode, which is significantly smaller than that produced by water electrolysis with Pt as both anode and cathode (1:2.05). In contrast, the mole ratio of O2 to H2 is about 1:3.4 for FGP as anode. As a result, the exfoliation rate of GICP is about one order of magnitude slower than that of FGP (Fig. 3h, j and Supplementary Movies 3, 4). These results indicate that the use of GICP efficiently inhibits the formation of O2 at a high voltage. The sufficient adsorbed reactive *OH, *O, and *OOH together with the high voltage enable the ultrafast synthesis of fully oxidized graphite oxide and GO (Fig. 3d–g). For FGP as anode, because of the absence of sufficient reactive *OH, *O, and *OOH and exfoliation induced broken circuit, only graphene sheets or graphite flakes with a low oxidation degree are obtained (Fig. 3j). It has been reported that 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) can efficiently suppress the formation of oxygen radicals from water electrolysis28. When adding 4‰ and 10‰ of TEMPO in 50 wt.% H2SO4 aqueous solution during the optimized EC oxidation process of GICP, the C/O ratio of the products increases from 1.8 to 2.2 and 2.6, respectively (Supplementary Note 8, Supplementary Fig. 13 and Supplementary Table 8). This gives evidence of the existing of oxygen radicals and their key role in the synthesis of GO during our EC oxidation process.
The above results suggest that EGO is synthesized by water electrolytic oxidation of graphite, which is conceptually different from the present methods. In this EC method, H2SO4 mainly acts as a control agent to tune the anodic electrocatalytic oxygen evolution reaction of water to enable the ultrafast oxidation of graphene lattice, and no other oxidants are used. Therefore, there is no explosive risk and metal ion contaminations, and H2SO4 can be fully recycled (Supplementary Note 9). Second, the EC oxidation rate is over 100 times faster than the oxidation rate of Hummers and K2FeO4 methods. Third, the obtained graphite oxide is mixed with dilute H2SO4 solution (50 wt.%). In the Hummers method, however, the graphite oxide is homogeneously mixed with concentrated H2SO4 and other oxidants, forming very viscous slurry. Therefore, the cleaning of graphite oxide in our method is much easier, which needs ten times less of water. Fourth, this method has a good controllability. The oxidation degree of GO sheets can be easily tuned by changing the concentration of H2SO4 solution in the EC oxidation process, and the number of layers and lateral size can be tuned by sonication time. Fifth, continuous production of GO sheets can be realized easily by continuously introducing GICP into dilute H2SO4, as shown in Supplementary Movie 2. Therefore, our EC oxidation method combines the advantages of safety, ultrafast synthesis, easy control, environmentally friendliness, no metal ion contaminations and easiness to scale up, which paves the way for industrial production and applications of GO sheets at a low cost.
As examples, we demonstrated the use of EGO for transparent conductive films (TCFs) (Fig. 4a–c), flexible and strong papers (Fig. 4d–f) and ultra-light elastic aerogels (Fig. 4g–i), which are typical applications of HGO. After reduction by hydroiodic (HI) acid, the EGO-based TCF shows a surface resistance of about 1.5 kΩ·□−1 with a transparency of 80% at 550 nm, which is comparable to those of the TCFs made by HGO with a similar lateral size7. The EGO paper shows a well-aligned layered structure and a mechanical strength of 175 MPa, which is stronger than the papers made by HGO (120 MPa)9 and K2FeO4-GO with larger lateral size (140 MPa)26. The EGO aerogel has a highly porous structure with a density of about 3 mg·cm−3, but is highly elastic. As shown in Fig. 4i, it can sustain their structural integrity under a load of more than 1000 times their own weight and can rapidly recover from more than 80% compression.
FGP and natural graphite flakes (80 mesh, mean particle size of about 150 μm) were purchased from Shenyang RuiYu Chemical Co. Ltd, and fully dried in an oven at 80 °C for 24 h before use. Concentrated sulfuric acid (98 wt.%, H2SO4), phosphorus pentoxide (Analytical reagent [AR], P2O5), ethylenediamine (AR, C2H8N2), potassium permanganate (AR, KMnO4), and sodium nitrate (AR, NaNO3) were purchased from Sinopharm Chemical Reagent Co., Ltd. and used as received. Distilled water was used as solvent and reagent. Platinum (Pt) wire with a diameter of 0.4 mm (99.99%, Shenyang RuiYu Chemical Co. Ltd.) was used as cathode in EC intercalation and oxidation processes. Heavy-oxygen water (97 atom%, H218O) and TEMPO (98%) were purchased from Shanghai Aladdin Biochemical Technology Co., Ltd. and used as received. SO3 gas was first synthesized by the reaction of 98 wt.% H2SO4 and excessive P2O5, and then excessive SO3 was absorbed by H218O to form the concentrated 18O-containing sulfuric acid (H2S16O318O).
The fully dried FGP slice was first cut into slices with a dimension of 10 × 4 cm2, and then dipped into a beaker (250 mL) containing 200 mL concentrated H2SO4 (98 wt.%) for EC intercalation, in which the FGP slice was used as anode and Pt wire as cathode with a DC power supply (Bio Logic, VSP-300 multichannel electrochemical workstation) of 1.6 V. After 20 min reaction, the GICP obtained was taken out and pressed to remove the absorbed H2SO4. Then the GICP was subjected to EC oxidation. In this process, the GICP was used as anode and Pt wire as cathode with a DC power supply of 5 V, and a diluted H2SO4 solution (50 wt.%) worked as the electrolyte. In order to keep a balance between the dipping and exfoliation, the GICP slice gradually dipped into a beaker (250 mL) containing 200 mL electrolyte at a speed of 5 mm·min−1 controlled by a programmed automated lifting platform. The exfoliated graphite oxide was collected by vacuum filtration. The filter cake obtained was washed several times with distilled water to remove absorbed acid, and then dispersed in water by short time sonication to form EGO solution. All the unproductive H2SO4 involved in the synthesis process of EGO, including the absorbed concentrated H2SO4 on GICP and the very dilute H2SO4 solution obtained after distilled water washing, were collected and recycled (Supplementary Note 9).
Characterization of EGO
The microstructure was characterized by SEM (FEI Nova NanoSEM 430), HRTEM (FEI Tecnai G2 20), AFM (Bruker, Dimension FastScan with ScanAsystTM, operating in the tapping mode), and Raman spectroscopy (JY Labram HR 800,632.8 nm laser). The chemical composition was evaluated by a combustion elemental analyzer (Elementar, vario MICRO cube), XPS (ESCALAB 250 using Al Kα radiation source), FTIR (Bruker Tensor 27), and ICP-AES (IRIS Intrepid, THERMO ELEMENTAL). XPS spectra were fitted using the XPS peak 4.1 software in which a Shirley background was assumed. For comparison, the Raman, XPS and FTIR spectra of HGO sheets were also measured using the same instruments and same conditions. Zeta-potential was measured with Malvern Zetasizer Nano-ZS90.
In-situ Raman spectroscopy and ex-situ XRD and XPS measurements
The structure and composition evolution of FGP with reaction time in the two EC processes were monitored by in-situ Raman and ex-situ XRD and XPS measurements. The Raman spectra were measured in-situ with a home-made sample holder. The integral time was 40 s, and 20 s was used for re-focusing of laser beam on the expanded sample surface. For XRD measurements, the samples were first filtered to remove liquid phase without washing, and then measured on D/Max-2400 with Cu Kα radiation (k = 1.5418 Å). For XPS measurements, the samples were collected, washed and exfoliated with water to remove absorbed sulfuric acid and form suspensions. Then a small amount of suspension was subjected to vacuum filtration, and finally the thin film obtained was dried at 40 °C for 24 h for XPS measurements.
Isotopic tracing experiments
The oxygen-containing reagents used for EGO synthesis can be divided into three types: concentrated H2SO4 used for EC intercalation (Acid-Int), water (Aq-OX), and H2SO4 (Acid-OX) in electrolyte for EC oxidation. To trace the transfer path of oxygen, we replaced these three reagents by their isotopic homologs (H218O or H2S16O318O) for EGO synthesis. Four different EGO samples were synthesized with different combinations of reagents: Normal sample, which was synthesized with normal reagents with no 18O addition; 18O Aq-OX sample, which was synthesized with normal H2SO4 for intercalation but electrolyte containing H218O (97 atom%) and normal H2SO4 for oxidation; 18O Acid-Int sample, which was synthesized with H2S16O318O (98 wt.%) for intercalation and normal reagents for oxidation; 18O Acid-OX sample, which was synthesized with normal H2SO4 for intercalation but electrolyte containing H2S16O318O and normal H2O for oxidation. After freezing drying, the 18O content in each EGO sample was measured by thermogravimetric mass spectrometry (TG-MS) with Netzsch STA 449C Jupiter/QMS 403C.
Fabrication and measurements of GO macrostructures
A TCF was fabricated by rod-coating of EGO aqueous solution on a PET substrate followed by chemical reduction. Typically, EGO aqueous solution (0.5 mg·mL−1) was first coated with a Mayer rod (type: 150 μm) on the surface of a PET substrate, which had been treated to be hydrophilic by short time oxygen plasma treatment. The resulting wet coating was then dried at 50 °C for 2 h to form an EGO film on the PET substrate. Then the EGO coating was reduced by immersing into the hot HI acid (40 wt.%, 80 °C) and held for 15 min. After reduction, the PET slice with reduced EGO coating was washed in ethanol and water in sequence, and finally blow dried with nitrogen gas followed by thermal treatment at 80 °C for 1 h. The coating thickness was controlled by changing the concentration of EGO solution used for rod-coating. The transparency of the TCF (transmittance at 550 nm wavelength) was measured by a UV-vis-NIR spectrometer (Varain Cary 5000) with a pure PET substrate as reference. The surface resistance of the TCF was measured by a 4-point probe resistivity measurement system (RTS-9, Guangzhou, China).
EGO paper was fabricated by vacuum filtration of the solution containing mildly reduced EGO sheets. Typically, 0.5 g of 40 wt.% HI acid was first added into 100 mL of EGO aqueous solution (0.5 mg·mL−1), then the solution was heated to 60 °C and mildly stirred for 30 min. During this process, the solution gradually changed color from pale-yellow to black, but was still well dispersed without obvious aggregation. After that, the dispersion was subjected to vacuum filtration for about 30 min to obtain a film on the surface of a filter membrane (CMC membrane, pore size 0.45 μm). After drying at 80 °C for 30 min, the film was peeled off from the filter membrane surface to get a free-standing EGO paper. For tensile strength measurements, the EGO paper was cut into narrow strips with a dimension of 10 × 2 mm2, and measured with a Hounsfield H5K-S materials tester. The thickness of the strip was measured with a spiral micrometer.
EGO aerogel was fabricated by hydrothermal treatment followed by freezing drying. Typically, 20 μL of ethylenediamine was first mixed into 5 mL EGO aqueous solution (3 mg·mL−1). Then the solution was heated for 6 h at 95 °C in a sealed glass vial to form a hydrogel. After freezing drying, the obtained aerogel was heated at 150 °C overnight to fully eliminate the absorbed water. The compressive test was performed manually with a weight of 100 g.
The data that support the findings of this study are available from the corresponding author upon request.
Dreyer, D. R., Park, S., Bielawski, C. W. & Ruoff, R. S. The chemistry of graphene oxide. Chem. Soc. Rev. 39, 228–240 (2010).
Loh, K. P., Bao, Q., Eda, G. & Chhowalla, M. Graphene oxide as a chemically tunable platform for optical applications. Nat. Chem. 2, 1015–1024 (2010).
Kim, J., Cote, L. J. & Huang, J. Two dimensional soft material: New faces of graphene oxide. Acc. Chem. Res. 45, 1356–1364 (2012).
Huang, X., Qi, X., Boey, F. & Zhang, H. Graphene-based composites. Chem. Soc. Rev. 41, 666–686 (2012).
Paredes, J. I., Villar-Rodil, S., Martinez-Alonso, A. & Tascon, J. M. D. Graphene oxide dispersions in organic solvents. Langmuir 24, 10560–10564 (2008).
Li, D., Mueller, M. B., Gilje, S., Kaner, R. B. & Wallace, G. G. Processable aqueous dispersions of graphene nanosheets. Nat. Nanotechnol. 3, 101–105 (2008).
Zhao, J., Pei, S., Ren, W., Gao, L. & Cheng, H.-M. Efficient preparation of large-area graphene oxide sheets for transparent conductive films. ACS Nano 4, 5245–5252 (2010).
Eda, G., Fanchini, G. & Chhowalla, M. Large-area ultrathin films of reduced graphene oxide as a transparent and flexible electronic material. Nat. Nanotechnol. 3, 270–274 (2008).
Dikin, D. A. et al. Preparation and characterization of graphene oxide paper. Nature 448, 457–460 (2007).
Nair, R. R., Wu, H. A., Jayaram, P. N., Grigorieva, I. V. & Geim, A. K. Unimpeded permeation of water through helium-leak-tight graphene-based membranes. Science 335, 442–444 (2012).
Joshi, R. K. et al. Precise and ultrafast molecular sieving through graphene oxide membranes. Science 343, 752–754 (2014).
Xu, Z. & Gao, C. Graphene chiral liquid crystals and macroscopic assembled fibres. Nat. Commun. 2, 571 (2011).
Qiu, L., Liu, J. Z., Chang, S. L. Y., Wu, Y. Z. & Li, D. Biomimetic superelastic graphene-based cellular monoliths. Nat. Commun. 3, 1241 (2012).
Hu, H., Zhao, Z., Wan, W., Gogotsi, Y. & Qiu, J. Ultralight and highly compressible graphene aerogels. Adv. Mater. 25, 2219–2223 (2013).
Yang, X., Cheng, C., Wang, Y., Qiu, L. & Li, D. Liquid-mediated dense integration of graphene materials for compact capacitive energy storage. Science 341, 534–537 (2013).
Wang, H. et al. Graphene-wrapped sulfur particles as a rechargeable lithium-sulfur battery cathode material with high capacity and cycling stability. Nano. Lett. 11, 2644–2647 (2011).
Liang, Y. et al. Co3O4 nanocrystals on graphene as a synergistic catalyst for oxygen reduction reaction. Nat. Mater. 10, 780–786 (2011).
Yang, K., Feng, L., Shi, X. & Liu, Z. Nano-graphene in biomedicine: Theranostic applications. Chem. Soc. Rev. 42, 530–547 (2013).
Ramanathan, T. et al. Functionalized graphene sheets for polymer nanocomposites. Nat. Nanotechnol. 3, 327–331 (2008).
Stankovich, S. et al. Graphene-based composite materials. Nature 442, 282–286 (2006).
Park, S. & Ruoff, R. S. Chemical methods for the production of graphenes. Nat. Nanotechnol. 4, 217–224 (2009).
Brodie, B. C. On the atomic weight of graphite. Philos. Trans. R. Soc. Lond. 149, 249–259 (1859).
Staudenmaier, L. Verfahren zur darstellung der graphitsäure. Ber. Dtsch. Chem. Ges. 31, 1481–1487 (1898).
Hummers, W. S. & Offeman, R. E. Preparation of graphitic oxide. J. Am. Chem. Soc. 80, 1339–1339 (1958).
Marcano, D. C. et al. Improved synthesis of graphene oxide. ACS Nano 4, 4806–4814 (2010).
Peng, L. et al. An iron-based green approach to 1-h production of single-layer graphene oxide. Nat. Commun. 6, 5716 (2015).
Yang, S., Lohe, M. R., Muellen, K. & Feng, X. New-generation graphene from electrochemical approaches: Production and applications. Adv. Mater. 28, 6213–6221 (2016).
Yang, S. et al. Organic radical-assisted electrochemical exfoliation for the scalable production of high-quality graphene. J. Am. Chem. Soc. 137, 13927–13932 (2015).
Liu, J. et al. A green approach to the synthesis of high-quality graphene oxide flakes via electrochemical exfoliation of pencil core. RSC Adv. 3, 11745–11750 (2013).
Parvez, K., Rincon, R. A., Weber, N.-E., Cha, K. C. & Venkataraman, S. S. One-step electrochemical synthesis of nitrogen and sulfur co-doped, high-quality graphene oxide. Chem. Commun. 52, 5714–5717 (2016).
Gurzęda, B. et al. Synthesis of graphite oxide by electrochemical oxidation in aqueous perchloric acid. Carbon 100, 540–545 (2016).
Yu, P. et al. Mechanically-assisted electrochemical production of graphene oxide. Chem. Mater. 28, 8429–8438 (2016).
Wu, L. et al. Powder, paper and foam of few-layer graphene prepared in high yield by electrochemical intercalation exfoliation of expanded graphite. Small 10, 1421–1429 (2014).
Tian, Z. et al. Facile electrochemical approach for the production of graphite oxide with tunable chemistry. Carbon 112, 185–191 (2017).
Kakaei, K. & Hasanpour, K. Synthesis of graphene oxide nanosheets by electrochemical exfoliation of graphite in cetyltrimethylammonium bromide and its application for oxygen reduction. J. Mater. Chem. A 2, 15428–15436 (2014).
Dresselhaus, M. S. & Dresselhaus, G. Intercalation compounds of graphite. Adv. Phys. 30, 139–326 (1981).
Ferrari, A. C. & Robertson, J. Interpretation of raman spectra of disordered and amorphous carbon. Phys. Rev. B 61, 14095–14107 (2000).
Wu, Z. S. et al. Synthesis of high-quality graphene with a pre-determined number of layers. Carbon 47, 493–499 (2009).
Kang, F., Zhang, T. Y. & Leng, Y. Electrochemical behavior of graphite in electrolyte of sulfuric and acetic acid. Carbon 35, 1167–1173 (1997).
Dimiev, A. M. & Tour, J. M. Mechanism of graphene oxide formation. ACS Nano 8, 3060–3068 (2014).
Dau, H. et al. The mechanism of water oxidation: from electrolysis via homogeneous to biological catalysis. Chemcatchem 2, 724–761 (2010).
Beck, F., Jiang, J. & Krohn, H. Potential oscillations during galvanostatic overoxidation of graphite in aqueous sulfuric acids. J. Electroanal. Chem. 389, 161–165 (1995).
We thank Libo Gao and Long Chen for AFM measurements, Zhibo Liu for TEM measurements, Ying Li, Guodong Wen, Lichang Yin, Chenghua Sun, and Chao Zhen for helpful discussions. This work was financially supported by the National Key R&D Program of China (No. 2016YFA0200101), National Science Foundation of China (Nos. 51325205, 51290273, and 51521091), Chinese Academy of Sciences (Nos. KGZD-EW-303-1, KGZD-EW-T06, 174321KYSB20160011, and XDPB06), and the Youth Innovation Promotion Association of Chinese Academy of Sciences. All data are in the main paper and supplementary materials.
The authors declare no competing financial interests.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Pei, S., Wei, Q., Huang, K. et al. Green synthesis of graphene oxide by seconds timescale water electrolytic oxidation. Nat Commun 9, 145 (2018). https://doi.org/10.1038/s41467-017-02479-z
High-performance flexible resistive random access memory devices based on graphene oxidized with a perpendicular oxidation gradient
Regulating cations and solvents of the electrolyte for ultra-efficient electrochemical production of high-quality graphene
Water-endurable intercalated graphene oxide adsorbent with highly efficient uranium capture from acidic wastewater
Separation and Purification Technology (2021)
ACS Applied Bio Materials (2021)