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Strict molecular sieving over electrodeposited 2D-interspacing-narrowed graphene oxide membranes


To separate small molecules/species, it’s crucial but still challenging to narrow the 2D-interspacing of graphene oxide (GO) membranes without damaging the membrane. Here the fast deposition of ultrathin, defect-free and robust GO layers is realized on porous stainless steel hollow fibers (PSSHFs) by a facile and practical electrophoresis deposition (ED) method. In this approach, oxygen-containing groups of GO are selectively reduced, leading to a controlled decrease of the 2D channels of stacked GO layers. The resultant ED-GO@PSSHF composite membranes featured a sharp cutoff between C2 (ethane and ethene) and C3 (propane and propene) hydrocarbons and exhibited nearly complete rejections for the smallest alcohol and ion in aqueous solutions. This demonstrates the versatility of GO based membranes for the precise separation of various types of mixtures. At the same time, a robust mechanical strength of the ED-GO@PSSHF membrane is also achieved due to the enhanced interaction at GO/support and GO/GO interfaces.


Graphene oxide (GO), an atomically thin 2D structure encompassing oxygen-containing groups, has been widely considered for membrane separation applications because the 2D channels of stacked GO provide molecular sieving capabilities1,2,3,4. Benefiting from water preferential adsorption and fast capillary diffusion1, GO membranes have exhibited excellent water permselectivity for various aqueous mixtures like water/solvents5,6,7,8,9, dyed water10, and saline water11,12,13. Moreover, high selectivities for the separation of organics were also obtained through the exclusion of large molecules8, 9, 14. In the case of gas separation, exciting selectivities of H2/N2, H2/CO2 and CO2/N2 have been achieved through elaborate controls of GO membrane preparation3, 4, 15. Actually, GO is a collective name for exfoliated graphitic oxygenates with diverse oxidation degrees16. Thus, GO membranes can be tailored for these various separations because the oxidation degree determines the size of 2D channels of stacked GO. To cater to the specific separations, therefore, it’s crucial but still challenging to control the 2D channel size of GO membranes.

The channel could be somewhat enlarged by inserting hetero-species8, 10, 17, which endow GO membranes with large-size species separation capacity. On the contrary, narrowing the 2D interspacing of GO-based membranes is more attractive as the tighter GO membranes are actually desired for small molecule sieving13, 17,18,19. Theoretically, the 2D channel of stacked GO could be narrowed near to zero through different reduction levels20. Various reduction methods, like chemical reduction and thermal deoxygenation, have been purposed for the preparation of reduced graphene oxide (rGO)20, 21. In the case of supported membrane preparation, however, GO reduction either before or after membrane formation is always incompatible with achieving perfect membranes22. The pre-reduction of GO weakens its dispersibility and increases disorder in the membrane, while the post-reduction of supported GO membranes normally leads to significant deformations and defects. As an alternative, in situ GO reduction during membrane formation is greatly expected to narrow GO 2D channels without damaging the membranes.

Electrophoresis deposition (ED) is a well-developed and economical technology where charged colloids in suspension migrate and deposit onto the surface of an electrode. For thin-film fabrication, it can offer advantages of high deposition rate, thickness controllability, good uniformity, strong adhesion and facile scale-up23, 24. The ED method is well suited for preparation of GO thin films because the highly hydrophilic and easily deprotonated functional groups endow GO hydrosol with uniform dispersibility and negative charges25. In this way, GO thin films have been prepared for electrochemistry, anti-corrosion, and optics applications24, 26, 27. Importantly, GO could be partially deoxygenated in the ED process25, 26, 28. Therefore, ED is a promising method to prepare uniform GO membranes with narrower 2D channels. To address the issues of mechanical strength and practicality of soft GO membranes29, moreover, porous stainless steel hollow fiber (PSSHF) is a superior GO support owing to its rigidity, high surface-to-volume ratio and packing density, facile scale-up and affordability. In addition, PSSHF can be directly used as a working electrode for membrane deposition due to its conductivity.

Here the deposition of ultrathin and defect-free GO layers was realized on PSSHFs through an ED process. The 2D channels of the resultant GO membranes are well narrowed and controlled. The obtained ED-GO@PSSHF composite membranes exhibit excellent separation performance for C2/C3 hydrocarbons, alcohol dehydration and desalination as well as enhanced stability.


Electrophoresis deposition of GO@PSSHF membranes

Figure 1a illustrates the anodic ED process employed for the fabrication of the GO@PSSHF membrane. A circular electric field was formed between the two concentric electrodes of PSSHF (anode/working electrode, WE) and stainless steel tubular container for the GO suspension (cathode/counter electrode, CE), which insured a uniform driving force from every direction (Supplementary Figs. 1 and 2). Applying a DC voltage, the negative GO colloids were partially reduced by the cathode, and then driven by the electrostatic force to stack onto the surface of the PSSHF30. To optimize the ED conditions, the effects of voltage V WEV CE, electrode spacing and working time on membrane thickness and GO composition were investigated. At constant V WEV CE, the current density reflects the migration and deposition rate of GO colloids. As shown in Fig. 1b, the current density depends on V WEV CE, which remained first stable on a plateau and then declined with time. In the range of 4.0–4.8 V, the It curves show clear and relative long plateaus of current density. It’s worth noting that low current density leads to slow deposition and inhomogeneous coverage whereas high current density results in fast deposition but disorder of GO on the support. In addition, fine bubbles, probably consisting of oxygen from water electrolysis and/or CO2 from deoxidization of functional groups28, are generated on the PSSHF at high V WEV CE, which could damage the membrane quality. As shown in Fig. 1c, the cyclic voltammogram (CV) at the initial scan yields a reduction signal (peak III) at −0.77 V which can be assigned to the irreversible reduction of GO, indicating that GO could be reduced if V CE is more negative than that value. On the other hand, the stable oxidation peak I and reduction peak II in the successive scans are ascribed to the redox pair of some active oxygen-containing groups of GO that cannot be reduced by the CV tests, suggesting a selective and partial reduction of GO in the ED process26. In a three-electrode system, V CE was more negative than −0.77 V when V WEV CE was varied in the range of 4.3–5.3 V (Fig. 1d). It indicates that GO reduction will occur when the DC voltage of V WE -V CE was set higher than 4.3 V. However, the ED-GO layer quality was difficult to control under high V WEV CE due to the very fast deposition rate and impact of bubbles (Supplementary Fig. 3). Thus the V WEV CE was normally set around 4.5 V. In this ED conditions, the thickness of ED-GO@PSSHF exhibits nearly linear dependent on the ED time within 90 s (Supplementary Fig. 4). The C/O ratio of ED-GO layer increased fast from 2.2 to 2.6 in the beginning and then sluggishly grew to around 2.7 in the following. At the same time, a depth profile analysis of the ED-GO membrane reveals that the C/O ratio increased from the GO/PSSHF interface but remained relatively stable in/on the membrane bulk and top surface (Supplementary Fig. 5). In addition, the deposition rate was evidently impacted by the electrode gap (Supplementary Fig. 6). Therefore, taking GO reduction, bubble impact, thickness and defects control into account, the ED-GO@PSSHF membranes described in the following were fabricated in a 1 mg mL−1 GO suspension with 9 mm electrode spacing and 4.5 V V WEV CE during 35 s.

Fig. 1

Electrophoresis deposition of graphene oxide on PSSHF. a Schematic of GO electrophoresis deposition on PSSHF with a circular electric field, b current variation with fixed DC voltages of V WEV CE in the GO electrophoresis deposition, c CV curves of GO on the glass-carbon electrode at room temperature and d time dependence of voltages V WEV CE and V CE in the three-electrode system for GO deposition with a V WE of 3.2 V

Morphology and structure of ED-GO@PSSHF membranes

The scanning electron microscope (SEM) image of the membrane cross-section shows a uniform thickness of 95 nm with a highly ordered and well-packed 2D lamellar structure, indicating that GO flakes are tightly stacked in the in-plane direction (Fig. 2a). The ED-GO@PSSHF membrane had a homogenously brown color (Fig. 2b), slightly darker than the typical GO membranes shown in Supplementary Fig. 7 and literature1, 7. The surface view of the membrane further reveals a dense coverage without visible defects, with large defects of the PSSHF (dash lines) even being completely covered (Fig. 2c). It also shows typical wrinkles, which were probably caused by the stacked GO boundaries, in SEM and AFM images (Figs. 2c and d). These wrinkles are helpful for the membrane’s permeability and the mechanical stability because wrinkles can act not only as entrances but also buffering spaces upon the intercalation of permeation species3.

Fig. 2

Morphology of ED-GO@PSSHF membrane. SEM images of a cross-section and c surface of ED-GO@PSSHF membrane, b optical image of PSSHFs and ED-GO@PSSHF, d atomic force microscopy (AFM) measurement of ED-GO surface, scale bars a 200 nm and c 2 μm

The structures of pristine GO and ED-GO were analyzed by XRD (Fig. 3a). The pristine GO exhibited the intense peak of graphite oxide (001) at 2Θ =11.1° (d-value = 0.80 nm) without any signal of a graphitic structure. However, the peak of ED-GO (001) was slightly up-shifted to 12.1°, translating to a smaller d-value of 0.73 nm. Deducting the single layer thickness of graphite or well-reduced GO (ca. 0.34–0.40 nm)1, 2, the average 2D channel size of ED-GO is estimated at 0.36 ± 0.03 nm. In contrast, the channel size of pristine GO was 0.43 ± 0.03 nm. In addition, a weak signal of graphite (002) was observed at 25.5°23. It reveals that the ED-GO layer was slightly reduced, which indicated a successful narrowing of the 2D channel. In comparison with the broadened (001) peak of pristine GO, ED-GO exhibits a sharp and symmetrical (001) peak, indicating that the ED-GO possesses a uniform orientation and stacking structure. The high resolution transmission electron microscope (HRTEM) cross-section view of the ED-GO fragment depicts a highly ordered GO morphology (Fig. 3b). From the fast Fourier transform (FFT) of Fig. 3b, the interplanar spacing of the stacked ED-GO was derived as 0.70 ± 0.02 nm by a reciprocal translating with 2/d nm−1, where d nm−1 is the diffraction spots distance (Fig. 3b inset). It is fairly close to the d-value determined by XRD. From the AFM analyses of GO bilayers, the thickness of pristine GO monolayer is averaged at 1.02 nm, in line with the literature18, while the ED-GO monolayer thickness is ~0.76 nm (Figs. 3c–e). Deducting the graphite or rGO monolayer, the 2D channel size between the ED-GO bilayer is 0.39 ± 0.03 nm, a little bit larger but very close to that estimated from the diffraction result. Thus the narrowed 2D channel of ED-GO is further confirmed by the bilayer measurements. The height profile of ED-GO layer exhibits a smooth surface with reasonable roughness as well as a continuous surface texture without visible defects, implying that the ED process has no appreciable impact on the surface structure of GO (Fig. 3e). Therefore, the quantitative XRD analysis with support of the semi-quantitative results from TEM and AFM leads to the conclusion that the 2D channels of ED-GO were narrowed during the ED process.

Fig. 3

Structure analysis of ED-GO layers. a X-ray diffraction (XRD) patterns of pristine and ED-GO, b HRTEM cross-section image of ED-GO fragment (inset: fast Fourier transform of TEM image), AFM measurements of c pristine GO and d ED-GO bilayers and e layer height profiles of the GO bilayers (offsets made for clarity), scale bars b 10 nm, inset b 5 nm−1 and c, d 100 nm

Chemical properties of ED-GO@PSSHF membranes

To identify the chemical states of ED-GO, Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy were employed to analyze the pristine GO and ED-GO layers. In the FTIR spectrum of pristine GO (Fig. 4a), the broad peak centered at 3250 cm−1 is attributed to the stretching vibrations of C-OH and the intercalated H2O. The H-bonds between hydroxyl and carboxyl groups probably lead to peak broadening. The adsorption bands at 1730, 1620, 1370, 1220, and 1040 cm−1 are assigned to C = O stretching, sp2-hybridized C = C and O-H bending, C-OH stretching, C-O-C stretching and C-O vibrations of epoxy/alkoxy groups, respectively31. In contrast, the C-OH peak of ED-GO was shifted to 3480 cm−1, indicating the decrease of intercalated H2O24. In addition, the intensity of carboxyl groups at 1730 cm−1 was significantly decreased and the band of epoxy groups at 1220 cm−1 became weaker, which proves that GO was partially reduced through preferential consumption of carboxyl and epoxy groups in the ED process. In agreement with that, the intensity of sp2 carbon at 1620 cm−1 was slightly increased for the ED-GO, implying the repair of the C = C network structure of GO25.

Fig. 4

Chemical and surface properties of pristine GO and ED-GO. The pristine GO and ED-GO samples measured by a FTIR spectroscopy, b XPS and c Raman spectroscopy; the static WCA of d GO membrane prepared by filtration, e ED-GO membrane and f graphene membrane prepared by filtration

XPS analyses suggest that the C/O ratio in ED-GO was increased to 2.7 from 2.3 of pristine GO due to the loss of oxygen groups (Supplementary Fig. 8), which agrees with the results of XRD and FTIR. The C1s spectra of both samples can be deconvoluted into five Gaussian peaks at 284.4 ± 0.1 eV (-C = C-/-C-C-), 285.0 ± 0.2 eV (-C-OH), 286.4 ± 0.2 eV (-C-O-C-), 287.2 ± 0.2 eV (-C = O), and 288.5 ± 0.2 eV (-O-C = O) (Fig. 4b)32. The -O-C = O and -C-O-C fractions were decreased from 12.2 and 12.9 at.% for pristine GO to 6.4 and 6.5 at.% for ED-GO, respectively (Supplementary Table 1), which further confirms that epoxy and carboxyl groups were partially removed.

The structural regularity of GO was analyzed by Raman spectroscopy (Fig. 4c). The spectrum of pristine GO contains a G band at 1616 cm−1, arising from the first-order scattering of sp2 carbon atoms in a 2D hexagonal lattice, and a D band at 1360 cm−1, ascribed to the vibrations of carbon atoms in plane terminations of disordered graphite33. Compared to the pristine GO, the D band intensity of ED-GO is increased slightly while that of the G band is almost unchanged. The enhanced D-band suggests an imperfect repairing of the sp2 bonding during reduction. On the other hand, it is known that the G band intensity will increase with the reduction of GO due to the recovery of the hexagonal carbon network23. Thus the unchanged G band intensity of ED-GO indicates that the reduction degree is low. The intensity ratio of the D and G band (I D /I G), which is sensitive to the level of disorder on the basal plane of GO and defects on the carbon backbone, was slightly increased from 0.95 of pristine GO to 0.99 of ED-GO. It indicates that defects may be generated during the repair of the ordered sp2 carbon network structure25. Yet, the small difference of I D /I G between pristine and ED-GO also suggests a relatively low number of new defects generated during the ED process. Furthermore, the D- and G band positions of ED-GO were slightly shifted to 1367 and 1614 cm−1 because the partial loss of epoxy and carboxyl groups weakens the electron withdrawing ability34.

The surface wettability of ED-GO, pristine GO and graphene membranes was determined by the water contact angle (WCA). Due to the highly hydrophilic nature, the static WCA of the pristine GO membrane is 46.7 ± 1.1° (Fig. 4d). For lack of hydrophilic groups, as comparison, the WCA of the graphene membrane is 140.1 ± 1.1° (Fig. 4f). The ED-GO membrane yields a higher WCA, 71.7 ± 1.4°, than that of pristine GO, suggesting that the ED-GO membrane was still somewhat hydrophilic owing to the weak reduction (Fig. 4e). The dynamic WCA of these samples further indicate that water molecules can slightly access the bulk of pristine GO and ED-GO membranes (Supplementary Fig. 9). The surface charge of pristine and ED-GO was measured by zeta potential analysis (Supplementary Fig. 10). It reveals that both samples are negatively charged and the electronegativity is gradually enhanced in the range of pH 3–11, which is mainly contributed by the deprotonation of the carboxyl group at the edges of GO flakes35. But the ED-GO is less negative owing to the partial consumption of carboxyl groups during the reduction of GO, in line with the results of IR and XPS results in Fig. 4.

Gas separation with the ED-GO@PSSHF membrane

The permeation performance of the ED-GO@PSSHF membrane for small gas molecules and light hydrocarbons was firstly measured using a single gas feeding method (Supplementary Fig. 11). As shown in Fig. 5a, generally, the permeances of gases with small kinetic molecular diameters (from 0.29 to 0.39 nm) are close, leading to a low ideal selectivity follows in the range of 0.6 to 10.1 for any couple comprised of H2, CO2, N2, CH4, C2H4 and C2H6 (Table 1). Neglecting the impact of membrane defects, it suggests that these gases can pass through the membrane easily and the gas permeation is dominated by Knudsen diffusion rather than molecular sieving. However, a sharp decrease of permeation rate is observed when switching from ethane to propene, which leads to a clear cutoff boundary between C2 and C3. Except for C3 hydrocarbons, the permeances are around the order of 10−7 mol m−2 s−1 Pa−1, whereas propene and propane have much lower permeances on the order of 10−10 mol m−2 s−1 Pa−1. Therefore, the ideal selectivity of C2/C3 hydrocarbons amounted to C2H4/C3H8 = 551, C2H4/C3H6 = 319, C2H6/C3H8 = 332 and C2H6/C3H6 = 192, respectively (Table 1), which are two orders of magnitude higher than their Knudsen selectivities (~1.2). The high ideal selectivity of C2/C3 first implies that the ED-GO@PSSHF membrane is nearly perfect-stacked with almost no defects. Importantly, it demonstrates a precise molecular sieving effect by excluding gas molecules larger than ethane (0.39 nm). It is worth noting that the 2D channel of the ED-GO layer determined by XRD, 0.36 ± 0.03 nm, is slightly smaller than the molecular cutoff point presented in Fig. 5a. It is reasoned that gases with the molecular size a little bit larger than the GO 2D channel also can intercalate into the bulk of the membrane due to the flexibility of GO membranes. Such expansion of GO channels would be limited to a certain range by the uniform π−π interaction force between carbon layers. Therefore, methane (0.38 nm) and ethene/ethane (0.39 nm), which are slightly larger than the ED-GO channel, can pass through the membrane rapidly. It reveals that the flexibility of GO leads to an up-shift of the cutoff point but doesn’t hinder the ED-GO@PSSHF membrane from achieving high selectivity.

Fig. 5

Gas permeation performance of ED-GO@PSSHF composite membrane. a Single-gas measurements of small gas molecules and light hydrocarbons permeation through ED-GO@PSSHF membrane (ΔP = 2 bar and room temperature) and b separation performance of ED-GO@PSSHF membrane for binary gas mixtures (The volume ratio of mixture is 1:1, ΔP = 2 bar and room temperature); error bars derived from SD

Table 1 The ideal selectivity and separation factors of small gas molecules and light hydrocarbons over the ED-GO@PSSHF membrane (ΔP = 2 bar, room temperature)

The separation performance of the ED-GO@PSSHF membrane was further investigated using binary gas mixtures (50 : 50 v.%) that are composed of one small gas (H2, CH4, or C2 hydrocarbon) and a C3 hydrocarbon. As shown in Fig. 5b, the permeance of H2, CH4, C2H4, and C2H6 in the mixed-gas systems are similar to that of single gas within 15% variations. On the other hand, the permeance of C3 hydrocarbons from the binary mixtures was increased in comparison with those following from single-gas measurements. For example, the permeances of propene and propane from H2-C3 mixtures were increased several times to 12.0 and10.8×10−10 mol m−2 s−1 Pa−1, respectively. In gas separation with membrane, concentration polarization (CP) results in the increase of the slower-permeating gas when the preferentially permeating gas is rapidly depleted and the slower-permeating gas is enriched near the membrane surface36. But the CP has been minimized here by using a high feed flux (100 mL min−1). In addition, the permeances of H2 and CH4 from the mixtures were also slightly increased, which are opposite to the CP effect on faster-permeating components. Thus the CP effect could be neglected here. It’s logical that the 2D channel size of ED-GO was expanded to some extent by the faster-permeating gas due to the flexibility and weak interaction between GO flakes, facilitating the access of larger molecules. As shown in Fig. 5b and Table 1, the separation factors (SFs, α) of these binary mixtures exhibit the impressive molecular sieving effect for the mixture separation.

Membrane separation of C2/C3 hydrocarbons with superior performance has been reported for a ZIF-8 membrane, for which a αethane/propane of 80 and a ethane permeance on the order of 10−7 mol m−2 s−1 Pa−1 were achieved from the separation of equimolar binary mixture37. By comparison, the ED-GO@PSSHF membrane exhibited 50% higher αethane/propane and a comparable permeability on the same order. It suggests that the stacked ED-GO membrane with narrowed 2D channels is able to achieve a comparable sieving performance as the regular microporous membranes. A GO@PSSHF membrane with high selectivity for C2/C3 hydrocarbon separation has a high potential to meet the emergent separation requirements in many industrial processes. For instance, the products of methanol-to-olefins (MTO) contain ~90% C2-C4 light-olefins, for which an efficient method is needed to take the main product ethylene out38. Similar demands also exist for the separation of Fischer-Tropsch-to-olefins (FTO) products or natural gas purification39. In addition, the ED-GO@PSSHF membrane further provides high separation factors of several hundred for the separation of the small gases from C3 molecules, indicating an even larger potential for separation of such mixtures (Table 1).

Alcohol dehydration with the ED-GO@PSSHF membrane

The ED-GO@PSSHF membrane was tested in alcohol dehydration via pervaporation using alcohol (C1–C4)—water binary mixtures (50 : 50 wt.%) at 70 °C (Supplementary Fig. 12). For large-size alcohols like iso-propanol (IPA) and iso-butanol (IBA), as shown in Fig. 6a, the alcohol concentrations on the permeate side were below the detection limit of our GC (0.01%), revealing ultrahigh selectivity towards water. In the case of ethanol–H2O binary mixture separation, the purity of H2O on the permeate side was as high as 99.94%, translating to a separation factor \({\alpha}_{{{\rm H}_2{\rm O}}/{\rm E}{t}{\rm O}{\rm H}}\) of 1665, which is one order magnitude higher than that of the typical filtration-prepared GO membranes5, 7 and even comparable with that of NaA zeolite membranes40. Interestingly, very high water purity, 99.89%, was also achieved for the methanol-water mixture, yielding a \({\alpha}_{{{\rm H}_2{\rm O}}/{\rm M}{\rm e}{\rm O}{\rm H}}\) of 908.

Fig. 6

Alcohol dehydration performance and comparison with literature. a 50 : 50 wt.% alcohol/water binary mixture separations by pervaporation with ED-GO@PSSHF membrane at 70 °C (error bars derived from SD); b comparison of ED-GO@PSSHF membrane with polymeric and inorganic membranes for the separation of methanol-water mixtures (squares, cycles, and triangles represent polymeric, silica, and zeolite membranes, respectively, open and solid stars indicate the reported GO based membranes and ED-GO@PSSHF membrane, respectively)

It is known that a water molecular layer is easily intercalated into the GO lamellas and connected with GO through hydrogen bonding in humid environments due to the inherent hydrophilicity of GO, which results in an increase of the distance between GO lamellas41. Thus the GO based membranes assume different states in the “dry” gas separation and “wet” aqueous phase permeation. The XRD patterns of pristine GO implies that the d-value increased from 0.80 nm in the dry state to 1.15 nm following water adsorption (Fig. 3a and Supplementary Fig. 13), in line with the literature2, 42. Similarly, the ED-GO also exhibits a d-value growth from 0.73 to 0.96 nm upon water incorporation. The loss of oxygen-containing groups in the ED-GO may weaken the capacity for water capture, leading to a smaller expansion of the d-value (Δ = 0.23 nm) than that of pristine GO (Δ = 0.35 nm) after water uptake. Considering the thickness of graphite/rGO (0.34–0.40 nm), therefore, the 2D channels of the ED-GO and pristine GO in water are estimated at 0.59 ± 0.03 and 0.78 ± 0.03 nm, respectively.

On the other hand, the effective size of methanol, ethanol and propanol in water are ~0.57, ~0.68, and ~0.90 nm, respectively, based on their hydrated radii2, 43. Obviously, it can be readily understood that C2 or larger alcohols could be rejected by the ED-GO@PSSHF membrane because these hydrated alcohols are much bigger than the 2D channel of wet ED-GO@PSSHF membranes. In the case of methanol-water mixture, the size of hydrated methanol is very close to the 2D channel of ED-GO. Therefore, the steric hindrance effect caused by membrane channels became serious, which impacts the access and diffusion of hydrated methanol. In contrast, the water component possesses both higher solubility and diffusivity because the hydrophilic membrane trends to capture and hold more water and, moreover, the larger ratio of channel size to water molecular size means lower diffusion resistance. Based on the solution-diffusion model, both diffusivity and solubility contribute to the permeability of a species. Thus the high separation factor between water and methanol results from the good solubility and diffusivity of water in ED-GO layers. The water fluxes of the ED-GO@PSSHF membrane ranged from 0.90 to 1.05 kg m−2 h−1, which are on the same order as the GO membranes prepared by filtration5, 6.

As methanol is the smallest alcohol, the methanol dehydration performance of ED-GO@PSSHF membrane was compared with those of polymeric, inorganic and GO based membranes (Fig. 6b)8, 44, 45. For polymeric membranes, the separation factors decrease as the liquid fluxes increase, forming an upper bound depends on the flux and separation factor. Our ED-GO@PSSHF membrane resides far above the upper bound for polymeric membranes and also shows superior performance compared with silica membranes. The ED-GO@PSSHF membrane is even comparable with A-type and T-type zeolite membranes, which demonstrates the extraordinary molecular sieving effect. Solvent dehydration is a common purification process in industry, which is normally costly and energy intensive, especially for the (near-) azeotropic systems. The ED-GO@PSSHF membrane can sieve the smallest alcohol out, providing a versatile method for solvent dehydration.

Desalination with the ED-GO@PSSHF membrane

Seawater desalination with membrane has been gaining more and more importance as a means of clean water supply. Simulations indicate that the pore size of membrane should be smaller than 1.0 nm to achieve high salt rejection46. Our ED-GO@PSSHF membrane readily meets this requirement due to the tight 2D channels. Therefore, desalination with the ED-GO@PSSHF membrane was tested using various saline solutions (0.1 mol salt L−1) by the vacuum membrane distillation (VMD) method at 60 °C. As shown in Fig. 7 and Supplementary Table 2, almost 100% salt rejections were achieved for the saline solutions of KCl (99.90%), NaCl (99.88%), Na2SO4 (99.98%), CaCl2 (99.99%), MgCl2 (99.97%), and MgSO4 (100%). In the desalination, cations and anions permeate through a membrane in stoichiometric amounts to maintain charge neutrality, which means that the permeation of ions is dominated by the larger ion of the cation-anion couple. On the basis of the hydrated ion radius, the effective size of ions increases in the order of 0.66 (K+), 0.66 (Cl), 0.72 (Na+), 0.76 (SO4 2−), 0.82 (Ca2+), and 0.86 nm (Mg2+)2, 47. According to the sieving mechanism, even the smallest K+ and Cl are much larger than the 2D channel size of the ED-GO membrane in water (0.59 ± 0.03 nm), in line with their nearly complete rejections. In contrast, the typical GO membranes without channel size control have incomplete ion rejections for small ions due to the larger 2D channels between 0.74 and 0.95 nm2, 11, 12.

Fig. 7

Desalination of saline water over ED-GO@PSSHF membrane. The concentration of saline aqueous solutions is 0.1 mol L−1 and the vacuum membrane distillation temperature is 60 °C; error bars derived from SD

Apart from the size sieving, the electrostatic interaction between ions and membrane fixed charges may also contribute to the ion rejection due to the electronegativity of the ED-GO membrane. This non-sieving mechanism is known as Donnan exclusion effect48. The charged membrane tends to reject co-ions for the repulsion and the requirement of a stoichiometric counter-ion balance to maintain electric neutrality of the solution results in the rejection of the whole salt. For the pristine GO@PSSHF membrane prepared by pressure-filtration, the rejection of the salt solutions follows the order of Na2SO4 > MgSO4 > NaCl ≈ MgCl2 (Supplementary Fig. 14), which is generally consistent with the Donnan exclusion dominated GO membranes18, 48. In contrast, the rejections of these four salts by the ED-GO@PSSHF membrane mainly depend on the effective ionic size rather than the charge ratio of salt (Fig. 7), which means the steric hindrance or sieving effect has become a governing factor in the desalination with the ED-GO@PSSHF membrane. But it is plausible that the electrostatic interaction between the ED-GO and co-ions is still contribute to the ion rejections since the repulsion enlarging the diffusion barrier for the salt at the surface of the ED-GO membrane.

The water fluxes for different solutions were 0.73–1.20 kg m−2 h−1, which is similar to that of alcohol dehydration. The fluxes of NaCl and KCl solutions are higher than those in the presence of the divalent ions since the divalent ions reduce the water flux more than monovalent ions49. On the other hand, the water fluxes depend on the thickness of the ED-GO@PSSHF membranes (Supplementary Fig. 15), in which higher water flux was observed from the thinner membrane owing to the lower mass transfer resistance in membrane. However, the salt rejection was significantly lower when the thickness of the ED-GO@PSSHF membrane was reduced to ~30 nm. This can be ascribed to two aspects. Defects may exist since the deposited layer being too thin to fully cover the pores of PSSHF. Furthermore, the relative lower reduction during the shorter ED process results in larger 2D channels, which is consistent with the time profile analysis of the C/O ratio in Supplementary Fig. 5.


Apart from selectivity and permeability, stability is another key property for practical membrane applications. The mechanical stability is a critical issue for the GO based membranes due to the weak interaction between stacked GO flakes. The ED-GO@PSSHF membrane exhibited an enhanced stability through tests in various mediums including gas mixtures, alcohol aqueous solutions and saline water with different temperature (up to 70 °C) and pressure (up to 2 bar). To further confirm the stability of ED-GO@PSSHF membrane, a long-term separation test was carried out using an ethanol-H2O binary mixture. The water flux of the membrane remained stable at 0.81 ± 0.05 kg m−2 h−1 with a 9% drop from start to the end, while the separation factor gradually increased from 1550 to 1750 simultaneously (Supplementary Fig. 16). It confirms that the membrane remained stable in water and ethanol without defect generation. The improved mechanical stability of the ED-GO@PSSHF membrane can be ascribed to the following aspects. Firstly, the rigid PSSHF substrate endows the soft GO layer with high mechanical strength. Furthermore, a stronger interaction was established between the interface of the GO layer and the substrate due to the formation of metal hydroxides on the PSSHF surface during the ED process50. For the bulk of the GO layer, the narrowed interspacing strengthens the π−π interaction force. Moreover, the decrease of oxygen-containing groups weakens the solubility of ED-GO in water and consequently improves the stability in aqueous media.

Based on the ED method, on the other hand, tighter ED-GO@PSSHF membranes could be obtained with deeper electro-reduction. Accordingly, the sieving points for gas molecules down-shifted to smaller scales. For example, the sieving span shifted from > 0.43 nm for a pristine GO@PSSHF membrane to 0.41 ± 0.02, 0.35 ± 0.02 and 0.31 ± 0.02 nm for ED-GO@PSSHF membranes (Supplementary Fig. 17). However, the deeply reduced ED-GO membrane also exhibits enhanced mass diffusion resistance. In this way, for example, the membrane with 0.31 ± 0.02 nm cutoff point is nearly gas tight because that the permeance of H2 was reduced by two orders of magnitude and the larger gases were even undetectable.

In conclusion, we have developed a facile and practicable ED method to realize the fast deposition of ultrathin, defect-free and robust GO layers with narrowed 2D channel on PSSHF. In this way, the oxygen-containing groups were selectively electrochemically reduced, which leads to the controlled decrease of the interspacing within stacked GO. The resultant ED-GO@PSSHF membranes feature a sharp cutoff point between C2 and C3 hydrocarbons and nearly complete rejections for the smallest alcohol and ions. This demonstrates a high versatility for the separation of various types of mixtures covering gases, solvent solutions and saline water. At the same time, robust mechanical strength of the ED-GO@PSSHF membranes were also achieved due to the enhanced interactions at GO/support and GO/GO interfaces.


Membrane preparation

GO powder was supplied by Cheaptubes Co. (US) and used without further purification. Homemade PSSHF with I.D./O.D. = ~1.0/1.8 mm were cut to ~65 mm and polished, washed and dried before GO deposition. The pH value and conductivity of GO suspensions (1 mg mL−1) were 3.0 and 245 μS cm−1, respectively.

The reduction properties of GO in electro field was tested by cyclic voltammetry (CV) with an electrochemical station. 50 μL GO suspension (1 mg mL−1) was dropped on the glass-carbon electrode (GCE) and used as a working electrode after dried in vacuum. Pt wire, Ag/AgCl (saturated KCl) and GO suspension (1 mg mL−1) were employed as counter electrode, reference electrode and electrolyte, respectively. The CV test was carried out 100 cycles under a voltage of −1.1 to 0.7 V with a scan rate of 50 mV s−1.

The time dependence of voltage in the cyclic electric field electrodeposition of GO was tested by a three-electrode system. Tubular stainless steel GO container (I.D. = 20 mm), Ag/AgCl (saturated KCl) and PSSHF were employed as counter electrode, reference electrode and working electrode, respectively. The concentration of GO suspension is 1 mg mL−1. The voltage loaded on the working electrode was fixed on 3.2 V and the test time is 100 s.

For the ED-GO@PSSHF membrane preparation, the electrolytic setup consisted of an electrochemical station (Bio-Logic, VMP3), Teflon supported stainless steel tube and PSSHF (Fig. 1a and Supplementary Fig. 2). Typically, electrophoresis deposition of GO was conducted in a concentric two electrodes system, where PSSHF was used as working electrode and the stainless steel tube was set as counter electrode. The as-prepared membranes were dried overnight at 40 °C in vacuum and then stored in drying box before use. The deposition behaviors of GO on PSSHF were investigated with different V WEV CE (4.5–12.0 V), deposition time (3–150 s) and electrode spacing (4–15 mm).


For separation, the membrane was fixed into the module with two ends seals by epoxy glue. The feed was introduced from the shell side of module. To avoid the effect of moisture on membrane, the feed gas was dehydrated by passing through a molecular sieve column. In the single gas permeation, the feed flow rate of gas is 20 mL min−1 and the pressure of feed side is 2 bar. One end of permeate side was closed and the left end was connected to atmosphere without sweep gas. The permeate flux was measured by soap bubble flow meters (Supplementary Fig. 11). Before flux measurement, the system was kept at the desired pressure for ca. 5 min. The permeate flux of each gas is measured at least three times. For the binary mixture separation test, two types of gas are well mixed in the gas mixer and then fed into the membrane side with a constant flow rate of 50 mL min−1 for each gas and the total pressure of feed side is kept at 2 bar. In the permeate side, nitrogen was introduced from one end of membrane with a constant flow rate and used as sweep gas. The component concentration in the permeate gas was analyzed by a GC (Shimadzu GC-2014C). When the feed gas was changed, the shell side of module was purged with the corresponding feeding gas firstly and the flux measurements were carried out at least 10 min later. The membrane performance was evaluated by the permeance (J, mol m−2 s−1 Pa−1), ideal selectivity for single gas (IS) and separation factor (α) for gas mixture, as expressed in Eqs. (13):

$$\it {\rm{J}} = \frac{{PV}}{{RT}} \times \frac{1}{A} \times \frac{1}{t} \times \frac{1}{{\Delta P}}$$
$${\rm{IS}} = \frac{{{J_{{\rm{fast}}\,{\rm{gas}}}}}}{{{J_{{\rm{slow}}\,{\rm{gas}}}}}}$$
$$\alpha = \frac{{{C_{{\rm{fast}}\,{\rm{component}}}}}}{{{C_{{\rm{slow}}\,{\rm{component}}}}}} \times \frac{{{C_{{\rm{0}}\,{\rm{slow}}\,{\rm{component}}}}}}{{{C_{0\,{\rm{fast}}\,{\rm{component}}}}}}$$

Where P (Pa) and T (K) are the pressure and temperature of permeate side, R is gas constant, A is the membrane area (~2.5×10−4 m2), t (s) is the permeation time, ΔP (Pa) is the pressure difference and C i and C 0i are the component concentration in the permeate and feed side, respectively.

For the alcohol dehydration, pervaporation (PV) was carried out at 70 °C (Supplementary Fig. 12). The permeate side of module was connected in sequence with sample collector, which is immersed in liquid nitrogen cold trap, and vacuum pump, by which the pressure of permeate side was kept around 100 Pa. Permeation liquid was begun to collect after 1 h running of PV system. The flux was calculated from the weight difference. The composition of permeation liquid was analyzed by a GC. The membrane performance was evaluated by the separation factor (α) and flux (F, kg m−2 h−1) determined as Eqs. (3) and (4):

$${\rm{F}} = \frac{W}{{A \times t}}$$

Where W is the weight of permeation (kg), A is the membrane area (m2), t is the permeation time (h).

For the desalination, the vacuum membrane distillation (VMD) was conducted at 60 °C with C 0  = 0.1 mol L−1 salt solutions as feedstock using the same setup of alcohol pervaporation. The ion concentration (c i , mol L−1) was determined by inductively coupled plasma (ICP, PerkinElmer Optima 8000) and confirmed by ion chromatography (IC, Dionex ICS-3000) as needed. Therefore, the water flux (F, kg m−2 h−1) and ion rejection (R, %) are calculated by Eqs. (4) and (5):

$${\rm{R}} = \left( {1 - \frac{{{C_i}}}{{{C_0}}}} \right) \times 100{\rm{\% }}$$


The morphology and structure of membranes was characterized by SEM (Zeiss SUPRA 55 SAPPHIRE), TEM (JEM-2100), AFM (Oxford Instrument MFP-3Dinfinity and Bruker Co Dimension Icon) and XRD (Rigaku Ultima IV). The surface chemistry of the membranes was analyzed by XPS (Thermo Fisher, K-Alpha) and FTIR (Nicolet 6700). The carbon state was determined by Raman spectroscopy (Chameleon He–Ne laser generator with λ=531.6 nm). The water contact angle was measured by a contact angle tester (OCA20, Dataphysics). Surface charging behaviors in terms of zeta potential of GO materials were determined by an electrokinetic analyzer (SurPASS, Anton Paar GmbH, Austria).

Data availability

All data needed to evaluate the conclusions in the paper are present in the main text, the Supplementary Information and the Supplementary Data 1-13. Additional data are available from the authors on reasonable request.


  1. 1.

    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).

    ADS  CAS  Article  PubMed  Google Scholar 

  2. 2.

    Joshi, R. K. et al. Precise and ultrafast molecular sieving through graphene oxide. Science 343, 752–754 (2014).

    ADS  CAS  Article  PubMed  Google Scholar 

  3. 3.

    Kim, H. W. et al. Selective gas transport through few-layered graphene and graphene oxide membranes. Science 342, 91–95 (2013).

    ADS  CAS  Article  PubMed  Google Scholar 

  4. 4.

    Li, H. et al. Ultrathin, molecular-sieving graphene oxide membranes for selective hydrogen separation. Science 342, 95–98 (2013).

    ADS  CAS  Article  PubMed  Google Scholar 

  5. 5.

    Tang, Y. P., Paul, D. R. & Chung, T. S. Free-standing graphene oxide thin films assembled by a pressurized ultrafiltration method for dehydration of ethanol. J. Membrane Sci. 458, 199–208 (2014).

    CAS  Article  Google Scholar 

  6. 6.

    Hung, W. S. et al. Pressure-assisted self-assembly technique for fabricating composite membranes consisting of highly ordered selective laminate layers of amphiphilic graphene oxide. Carbon 68, 670–677 (2014).

    CAS  Article  Google Scholar 

  7. 7.

    Li, G., Shi, L., Zeng, G., Zhang, Y. & Sun, Y. Efficient dehydration of the organic solvents through graphene oxide (GO)/ceramic composite membranes. Rsc. Adv. 4, 52012–52015 (2014).

    CAS  Article  Google Scholar 

  8. 8.

    Li, G. et al. Sharp molecular-sieving of alcohol-water mixtures over phenyldiboronic acid pillared graphene oxide framework (GOF) hybrid membrane. Chem. Commun. 51, 7345–7348 (2015).

    CAS  Article  Google Scholar 

  9. 9.

    Huang, K. et al. A graphene oxide membrane with highly selective molecular separation of aqueous organic solution. Angew. Chem. Int. Ed. 53, 6929–6932 (2014).

    CAS  Article  Google Scholar 

  10. 10.

    Huang, H. et al. Ultrafast viscous water flow through nanostrand-channelled graphene oxide membranes. Nat. Commun. 4, 2979 (2013).

    PubMed  Google Scholar 

  11. 11.

    Sun, P. Z. et al. Selective ion penetration of graphene oxide membranes. ACS Nano 7, 428–437 (2013).

    CAS  Article  PubMed  Google Scholar 

  12. 12.

    Sun, P. Z. et al. Selective trans-membrane transport of alkali and alkaline earth cations through graphene oxide membranes based on cation-pi interactions. ACS Nano 8, 850–859 (2014).

    CAS  Article  PubMed  Google Scholar 

  13. 13.

    Liu, H. Y., Wang, H. T. & Zhang, X. W. Facile fabrication of freestanding ultrathin reduced graphene oxide membranes for water purification. Adv. Mater. 27, 249–254 (2015).

    Article  PubMed  Google Scholar 

  14. 14.

    Huang, L., Li, Y. R., Zhou, Q. Q., Yuan, W. J. & Shi, G. Q. Graphene oxide membranes with tunable semipermeability in organic solvents. Adv. Mater. 27, 3797–3802 (2015).

    CAS  Article  PubMed  Google Scholar 

  15. 15.

    Shen, J. et al. Membranes with fast and selective gas-transport channels of laminar graphene oxide for efficient CO2 capture. Angew. Chem. Int. Ed. 54, 578–582 (2015).

    Google Scholar 

  16. 16.

    Dreyer, D. R., Todd, A. D. & Bielawski, C. W. Harnessing the chemistry of graphene oxide. Chem. Soc. Rev. 43, 5288–5301 (2014).

    CAS  Article  PubMed  Google Scholar 

  17. 17.

    Xi, Y. H. et al. Graphene oxide membranes with strong stability in aqueous solutions and controllable lamellar spacing. ACS Appl. Mater. Interfaces 8, 15557–15566 (2016).

    CAS  Article  PubMed  Google Scholar 

  18. 18.

    Han, Y., Xu, Z. & Gao, C. Ultrathin graphene nanofiltration membrane for water purification. Adv. Funct. Mater. 23, 3693–3700 (2013).

    CAS  Article  Google Scholar 

  19. 19.

    Lin, L. C. & Grossman, J. C. Atomistic understandings of reduced graphene oxide as an ultrathin-film nanoporous membrane for separations. Nat. Commun. 6, 8335 (2015).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Dreyer, D. R., Park, S., Bielawski, C. W. & Ruoff, R. S. The chemistry of graphene oxide. Chem. Soc. Rev. 39, 228–240 (2010).

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Chua, C. K. & Pumera, M. Chemical reduction of graphene oxide: a synthetic chemistry viewpoint. Chem. Soc. Rev. 43, 291–312 (2014).

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Pei, S. F., Zhao, J. P., Du, J. H., Ren, W. C. & Cheng, H. M. Direct reduction of graphene oxide films into highly conductive and flexible graphene films by hydrohalic acids. Carbon 48, 4466–4474 (2010).

    CAS  Article  Google Scholar 

  23. 23.

    Wang, M. et al. Large-area, conductive and flexible reduced graphene oxide (RGO) membrane fabricated by electrophoretic deposition (EPD). ACS Appl. Mater. Interfaces 6, 1747–1753 (2014).

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    He, W. T. et al. Electrophoretic deposition of graphene oxide as a corrosion inhibitor for sintered NdFeB. Appl. Surf. Sci. 279, 416–423 (2013).

    ADS  CAS  Article  Google Scholar 

  25. 25.

    Toh, S. Y., Loh, K. S., Kamarudin, S. K. & Daud, W. R. W. Graphene production via electrochemical reduction of graphene oxide: synthesis and characterisation. Chem. Eng. J. 251, 422–434 (2014).

    CAS  Article  Google Scholar 

  26. 26.

    Chen, L. Y., Tang, Y. H., Wang, K., Liu, C. B. & Luo, S. L. Direct electrodeposition of reduced graphene oxide on glassy carbon electrode and its electrochemical application. Electrochem. Commun. 13, 133–137 (2011).

    CAS  Article  Google Scholar 

  27. 27.

    Koh, A. T. T., Foong, Y. M., Pan, L., Sun, Z. & Chua, D. H. C. Effective large-area free-standing graphene field emitters by electrophoretic deposition. Appl. Phys. Lett. 101, 183107 (2012).

    ADS  Article  Google Scholar 

  28. 28.

    An, S. J. et al. Thin film fabrication and simultaneous anodic reduction of deposited graphene oxide platelets by electrophoretic deposition. J. Phys. Chem. Lett. 1, 1259–1263 (2010).

    CAS  Article  Google Scholar 

  29. 29.

    Aba, N. F. D., Chong, J. Y., Wang, B., Mattevi, C. & Li, K. Graphene oxide membranes on ceramic hollow fibers-microstructural stability and nanofiltration performance. J. Membrane Sci. 484, 87–94 (2015).

    CAS  Article  Google Scholar 

  30. 30.

    Guo, H. L., Wang, X. F., Qian, Q. Y., Wang, F. B. & Xia, X. H. A green approach to the synthesis of graphene nanosheets. ACS Nano 3, 2653–2659 (2009).

    CAS  Article  PubMed  Google Scholar 

  31. 31.

    Golsheikh, A. M., Huang, N. M., Lim, H. N., Zakaria, R. & Yin, C. Y. One-step electrodeposition synthesis of silver-nanoparticle-decorated graphene on indium-tin-oxide for enzymeless hydrogen peroxide detection. Carbon 62, 405–412 (2013).

    Article  Google Scholar 

  32. 32.

    Wang, M. et al. All-Solid-State Reduced Graphene Oxide Supercapacitor with Large Volumetric Capacitance and Ultralong Stability Prepared by Electrophoretic Deposition Method. ACS Appl. Mater. Interfaces 7, 1348–1354 (2015).

    CAS  Article  PubMed  Google Scholar 

  33. 33.

    Marimuthu, M. et al. Sodium functionalized graphene oxide coated titanium plates for improved corrosion resistance and cell viability. Appl. Surf. Sci. 293, 124–131 (2014).

    ADS  CAS  Article  Google Scholar 

  34. 34.

    Mangadlao, J. D. et al. Grafted carbazole-assisted electrodeposition of graphene oxide. ACS Appl. Mater. Interfaces 7, 10266–10274 (2015).

    CAS  Article  PubMed  Google Scholar 

  35. 35.

    Hu, M. & Mi, B. X. Enabling graphene oxide nanosheets as water separation membranes. Environ. Sci. Technol. 47, 3715–3723 (2013).

    ADS  CAS  Article  PubMed  Google Scholar 

  36. 36.

    Avila, A. M., Funke, H. H., Zhang, Y. F., Falconer, J. L. & Noble, R. D. Concentration polarization in SAPO-34 membranes at high pressures. J. Membrane Sci. 335, 32–36 (2009).

    CAS  Article  Google Scholar 

  37. 37.

    Pan, Y. & Lai, Z. Sharp separation of C2/C3 hydrocarbon mixtures by zeolitic imidazolate framework-8 (ZIF-8) membranes synthesized in aqueous solutions. Chem. Commun. 47, 10275–10277 (2011).

    CAS  Article  Google Scholar 

  38. 38.

    Liu, X. et al. Coke suppression in MTO over hierarchical SAPO-34 zeolites. RSC Adv. 6, 28787–28791 (2016).

    CAS  Article  Google Scholar 

  39. 39.

    Zhong, L. et al. Cobalt carbide nanoprisms for direct production of lower olefins from syngas. Nature 538, 84–87 (2016).

    ADS  CAS  Article  PubMed  Google Scholar 

  40. 40.

    Uragami, T., Banno, M. & Miyata, T. Dehydration of an ethanol/water azeotrope through alginate-DNA membranes cross-linked with metal ions by pervaporation. Carbohyd. Polym. 134, 38–45 (2015).

    CAS  Article  Google Scholar 

  41. 41.

    You, S. J., Luzan, S. M., Szabo, T. & Talyzin, A. V. Effect of synthesis method on solvation and exfoliation of graphite oxide. Carbon 52, 171–180 (2013).

    CAS  Article  Google Scholar 

  42. 42.

    You, S. J., Sundqvist, B. & Talyzin, A. V. Enormous lattice expansion of hummers graphite oxide in alcohols at low temperatures. ACS Nano 7, 1395–1399 (2013).

    CAS  Article  PubMed  Google Scholar 

  43. 43.

    Van der Bruggen, B., Schaep, J., Wilms, D. & Vandecasteele, C. Influence of molecular size, polarity and charge on the retention of organic molecules by nanofiltration. J. Membrane Sci. 156, 29–41 (1999).

    Article  Google Scholar 

  44. 44.

    Tang, Y. et al. Development of flat-sheet membranes for C1–C4 alcohols dehydration via pervaporation from sulfonated polyphenylsulfone (sPPSU). J. Membrane Sci. 415–416, 686–695 (2012).

    CAS  Article  Google Scholar 

  45. 45.

    Villegas, M., Castro Vidaurre, E. F. & Gottifredi, J. C. Sorption and pervaporation of methanol/water mixtures with poly(3-hydroxybutyrate) membranes. Chem. Eng. Res. Design 94, 254–265 (2015).

    CAS  Article  Google Scholar 

  46. 46.

    Corry, B. Water and ion transport through functionalised carbon nanotubes: implications for desalination technology. Energy Environ. Sci. 4, 751–759 (2011).

    CAS  Article  Google Scholar 

  47. 47.

    Tansel, B. et al. Significance of hydrated radius and hydration shells on ionic permeability during nanofiltration in dead end and cross flow modes. Sep. Purif. Technol. 51, 40–47 (2006).

    CAS  Article  Google Scholar 

  48. 48.

    Han, Y., Jiang, Y. Q. & Gao, C. High-flux graphene oxide nanofiltration membrane intercalated by carbon nanotubes. ACS Appl. Mater. Interfaces 7, 8147–8155 (2015).

    CAS  Article  PubMed  Google Scholar 

  49. 49.

    Fornasiero, F. et al. Ion exclusion by sub-2-nm carbon nanotube pores. Proc. Natl Acad. Sci. USA 105, 17250–17255 (2008).

    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

  50. 50.

    Wu, Z.-S. et al. Field emission of single-layer graphene films prepared by electrophoretic deposition. Adv. Mater. 21, 1756–1760 (2009).

    CAS  Article  Google Scholar 

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We acknowledge supports from Natural Science Foundation of China (21506243) and the Youth Innovation Promotion Association of CAS (Y624211401). The authors thank Prof. Andreas Goldbach (DICP), Prof. Zhi Liu (ShanghaiTech), Dr. Xiaopeng Li (SARI) and Dr. Deng Hu (SARI) for fruitful discussions and Mrs Xinyan Wang (ShanghaiTech) for AFM assistance.

Author information




The original idea was conceived by G.Z.; the experimental design and data analysis were performed by B.Q., X.H., G.Z. and W.C.; G.H.L. and G.J.L. performed the XPS and SEM measurements. The manuscript was drafted by B.Q., X.H., G.Z., Y.P., Y.Z. and Y.S.; all authors have approved to the final version of the manuscript.

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Correspondence to Gaofeng Zeng or Yuhan Sun.

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Qi, B., He, X., Zeng, G. et al. Strict molecular sieving over electrodeposited 2D-interspacing-narrowed graphene oxide membranes. Nat Commun 8, 825 (2017).

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