Abstract
Two-dimensional graphitic carbon nitride (g-C3N4) nanosheets are ideal candidates for membranes because of their intrinsic in-plane nanopores. However, non-selective defects formed by traditional top-down preparation and the unfavorable re-stacking hinder the application of these nanosheets in gas separation. Herein, we report lamellar g-C3N4 nanosheets as gas separation membranes with a disordered layer-stacking structure based on high quality g-C3N4 nanosheets through bottom-up synthesis. Thanks to fast and highly selective transport through the high-density sieving channels and the interlayer paths, the membranes, superior to state-of-the-art ones, exhibit high H2 permeance of 1.3 × 10−6 mol m−2 s−1 Pa−1 with excellent selectivity for multiple gas mixtures. Notably, these membranes show excellent stability under harsh practice-relevant environments, such as temperature swings, wet atmosphere and long-term operation of more than 200 days. Therefore, such lamellar membranes with high quality g-C3N4 nanosheets hold great promise for gas separation applications.
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Find the latest articles, discoveries, and news in related topics.Introduction
Carbon dioxide (CO2) concentrations in the atmosphere have rapidly increased in the last decades due to the consumption of fossil fuels, which have caused various global climate issues1,2,3. Therefore, the Paris Agreement was reached to stipulate that carbon neutrality should be achieved in the second half of the 21st century4. As a carbon-free energy carrier, hydrogen is now widely considered the next generation energy to reduce CO2 emissions5. However, most produced hydrogen is mixed with larger molecules like CO2, N2, CH4, which needs further purification before practical applications6. Nowadays, traditional industrial separation methods such as distillation and pressure swing adsorption are energy-intensive. As an emerging technology, membranes separation offers an efficient energy-saving alternative for H2 purification7,8. However, the development of traditional polymer membranes is limited by the trade-off relationship between permeability and selectivity (known as Robeson’s upper bounds)9. Recently, two-dimensional (2D) nanosheets have offered a superb building platform for membrane construction owing to their nanometer-thin thickness10,11,12,13. Graphitic carbon nitride (g-C3N4) nanosheets, hosting high-density molecular-sized pores composed of tri-s-triazine units in the entire 2D plane14,15, are considered ideal building blocks for molecular sieving membrane. Benefits to the nanometer-thin thickness and high-density nanopores, g-C3N4 nanosheet membranes should be a superior candidate for H2 separation16,17, which was already proved by theoretical investigations. For instance, Li et al.18 found that H2 had the lowest diffusion barrier to go through the g-C3N4 nanosheets by density functional theory (DFT) calculations, which resulted in a superior selectivity between H2 and other larger gases. Moreover, Guo et al.19 predicted a high H2 permeance (13 mol m−2 s−1 Pa−1) across a bilayer g-C3N4 nanosheets membrane by molecular dynamics (MD) simulation. Therefore, the prospect of developing g-C3N4 nanosheets membrane is highly attractive.
Nevertheless, only a few g-C3N4 nanosheet membranes have been reported for gas separation. One reason for this is the difficulty of obtaining high-quality g-C3N4 nanosheets. Similar to other 2D materials, most g-C3N4 nanosheets are usually exfoliated from bulk materials by top-down methods20,21. During the top-down exfoliation processes, harsh environments (oxidative atmosphere or acid solution) were applied to destroy the interlayer interactions in bulk g-C3N4, and thereby obtaining single or few-layer nanosheets22,23. However, the structural deterioration may occur simultaneously during this exfoliation process, leading to the formation of larger defects in g-C3N4 nanosheets. For example, Wang et al.24 fabricated g-C3N4 nanosheet membranes containing 1.5–3 nm artificial nanopores through the top-down method using concentrated hydrochloric acid. These membranes exhibited excellent performance in nanofiltration, while the artificial nanopores were too large for H2 purification. On the other hand, it was reported that g-C3N4 nanosheets tended to re-stack to form tight films due to strong π–π interaction25, leading to the blockage of intrinsic in-plane nanopores. By adding polybenzimidazole chains as spaces in g-C3N4 nanosheets to prevent the re-stacking, Villalobos et al.26 developed a g-C3N4 nanosheets-based mixed matrix membrane with considerable separation performance. However, the merits of g-C3N4 nanosheets can not be exploited in the mixed matrix membranes.
Hence, in this work, high-quality g-C3N4 nanosheets are prepared by a bottom-up method where the produced g-C3N4 has been delaminated into nanosheets along with the thermal polycondensation, skipping the exfoliation step, thus significantly avoiding the structural deterioration of g-C3N4 nanosheets. Then the isopropanol is used as a dispersant for membrane preparation to weaken the π–π interaction between g-C3N4 nanosheets. As a result, laminar g-C3N4 membranes with disordered stacking structures assembled by high-quality g-C3N4 nanosheets are obtained. The lamellar g-C3N4 nanosheet membranes exhibit excellent H2 permeance of 1.3 × 10−6 mol m−2 s−1 Pa−1 with high selectivity in mixed-gas separation. Furthermore, the gas separation mechanism through the g-C3N4 membrane is revealed by DFT and MD simulations, which is based on the synergistic influence of size exclusion and the interactions between gas molecules and g-C3N4 nanosheets. Therefore, this work not only prepares a lamellar g-C3N4 nanosheets membrane for efficiently H2 purification but also provides a strategy for constructing other 2D nanosheets membranes for gas separation.
Results
Fabrication of high-quality g-C3N4 nanosheets
The detailed steps of the bottom-up method are shown in Fig. 1a. First, melamine (Mel) and cyanuric acid (Cya) are self-assembled into layered supramolecular precursors (Supplementary Fig. 1). Then, the ethanol (EtOH)/glycerol (Glyc) mixture are intercalated into the layered precursors. During subsequent calcination in an inert gas, the g-C3N4 is formed through thermal polycondensation. At the same time, the released gases (such as EtOH, Glyc, NOx, and H2O) produced by evaporation and decomposition of the intercalated molecules lead to the exfoliation of the layered precursors. Different from the top-down method (Supplementary Fig. 2), no further exfoliation is required, hence the structural deterioration of the g-C3N4 nanosheets can be greatly avoided. The obtained g-C3N4 nanosheets by the bottom-up method were first examined using 13C solid-state nuclear magnetic resonance (NMR). The spectrum of the g-C3N4 nanosheets exhibits two signal groups at 163 and 155 ppm, corresponding to the CN2(NHx) carbon atoms (C1) and CN3 carbon atoms (C2), respectively27, indicating the successful synthesis of g-C3N4 (Supplementary Fig. 3). The Fourier transform infrared spectroscopy (FTIR) of both types of nanosheets (Supplementary Fig. 4a) shows the typical molecular structure of g-C3N414. The signal located at 810 cm−1 is originated from the characteristic tri-s-triazine breathing mode. The wide bands at 1690–1150 cm−1 and 3680–2970 cm−1 can be assigned to the stretching vibrations of C–N heterocycles and the N–H stretching vibrations of the terminal -NH2/NH of g-C3N4, respectively. In the X-ray diffraction (XRD) patterns, the (100) peak at 12.9° stems from the lattice planes along c-axis due to the 2D planer disorder28 (Supplementary Figs. 4b and 5). It was reported that the disordered g-C3N4 structure was formed by the incompletely condensed tri-s-triazine units connected by hydrogen bonds through -NH2/NH at their edges29. However, this is not detected in the g-C3N4 nanosheets prepared using the top-down method, indicating that the in-planar atomic structure is destroyed. The differences between the two nanosheets were confirmed by scanning electron microscopy (SEM) and atomic force microscopy (AFM) images. As shown in Fig. 1b, c, g-C3N4 nanosheets with a thickness of approximately 0.5 nm are almost transparent to electron beams. In the case of the 0.326 nm g-C3N4 single layer30, the obtained g-C3N4 nanosheet with a thickness less than double layers can be regarded as a single-layer nanostructure. The increased thickness is likely due to a “dead layer” caused by the adsorbed water between the sample and the substrate or the presence of surface adsorbates such as water molecules31. More importantly, no apparent nanopore defects are observed in the g-C3N4 nanosheets fabricated via this bottom-up technology (Fig. 1b, c and Supplementary Fig. 6), which is desirable for molecular sieving of gases. In contrast, large defects are inevitable in nanosheets prepared by traditional top-down thermal oxidation processes due to structural degradation. As shown in Fig. 1d, e, the g-C3N4 nanosheets obtained by the classical top-down technique contain distinct randomly distributed artificial defect pores (10–100 nm).
a The fabrication process of g-C3N4 nanosheets. Step 1: The melamine (Mel) and cyanuric acid (Cya) were self-assembled into layered supramolecular precursors under hydrothermal conditions. Step 2: Through intercalation of an ethanol (EtOH)/glycerol (Glyc) mixture (3:1), the layers were expanded. Step 3: The g-C3N4 nanosheets were obtained via a calcination process under nitrogen. C, N, O, and H atoms are colored in gray, blue, red, and white, respectively. Morphology of bottom-up g-C3N4 nanosheets: b SEM image and c AFM image with relative height profile. Morphology of top-down g-C3N4 nanosheets: d SEM image and e AFM image with relative height profile. f Room-temperature EPR spectra and g N 1s XPS spectra of bottom-up and top-down g-C3N4 nanosheets. Source data are provided as a Source data file.
Furthermore, the Electron paramagnetic resonance (EPR), X-ray photoelectron spectroscopy (XPS), and element analysis (EA) of the two types of g-C3N4 nanosheets were investigated to identify defect concentrations in nanosheets. As presented in Fig. 1f, a lower EPR peak intensity in bottom-up nanosheets is observed, which can be assignable to unpaired electrons, indicating fewer defects in bottom-up g-C3N4 nanosheets32. The N 1s XPS spectra (Fig. 1g) shows three peaks at 398.7, 399.6, and 400.9 eV, which can be attributed to C–N = C, N–(C)3, and C–NH, respectively33. The C–N=C to N–(C)3 ratio drastically decreases from 2.32 (bottom-up method) to 0.73 (top-down approach), which also suggests a lower defect concentration in the bottom-up g-C3N4 nanosheets34. In the EA results, the C/N atom ratio decreases from 0.68 (bottom-up method) to 0.65 (top-down approach), further confirming fewer defects in the bottom-up nanosheets (Supplementary Table 1)32. In addition, all g-C3N4 nanosheets obtained via the bottom-up and top-down methods are homogenously dispersed with apparent Tyndall effects (Supplementary Fig. 7). The g-C3N4 nanosheet suspensions show a clear linear relationship between UV/Vis spectroscopic absorbance and nanosheet concentration, which can be applied to determine the nanosheet concentration for membrane fabrication (Supplementary Fig. 8).
Fabrication of lamellar g-C3N4 membranes
It has been reported that the guest solvent can tune the stacking modes of nanosheets according to host-guest noncovalent interactions, such as steric hindrance or van der Waals interactions35. Therefore, in this work, using isopropanol as a guest molecule to weaken the π-π interaction between g-C3N4 nanosheets to prevent undesired re-stacking, the lamellar g-C3N4 membranes were prepared on porous anodic aluminum oxide (AAO) substrates (Supplementary Fig. 9). All the prepared g-C3N4 membranes are intact with no detectable pinholes or cracks and have homogeneous elemental distributions, as seen in the SEM images (Fig. 2a, b and Supplementary Figs. 10–12). The cross-sectional transmission electron microscopy (TEM) image of the g-C3N4 membrane (Fig. 2c) reveals the turbostratic arrangement of the bottom-up nanosheets, which can be attributed to the stronger repulsive interactions weakening the π-π interactions between adjacent nanosheets (Supplementary Fig. 13). Such structures have also been reported in GO membranes36. While it is shown in Fig. 2d that the top-down g-C3N4 nanosheets form a compact membrane structure. Besides, considering that the aligned and unaligned stacking between adjacent layers will affect the separation applications of the membrane37, the stacking modes of g-C3N4 nanosheets were calculated by DFT. As shown in Fig. 2e, the calculated total energy of bilayer bottom-up g-C3N4 shows that its AA stacking has minimum energy configuration, indicating that the bottom-up g-C3N4 nanosheets tend to the aligned AA stacking in the g-C3N4 membrane, forming conceivable gas-permeable interlayer pathways (Fig. 2f). In contrast, the top-down g-C3N4 nanosheets tend to be nonaligned AB stacking (Supplementary Fig. 14), which greatly reduces the effective sieving channel of g-C3N4 membrane and thus blocks the transmission of gas. Moreover, the corrugated surfaces of the g-C3N4 membrane (Supplementary Fig. 15) suggest disordered stacked nanosheets, which is consistent with the TEM results. From the 1D and corresponding 2D XRD patterns of the g-C3N4 nanosheets and membrane (Fig. 2g), the (002) diffraction peak of the g-C3N4 membrane becomes broader than that of the nanosheets, further indicating the disordered stacking of the bottom-up nanosheets in the g-C3N4 membrane38. Grazing incidence angle X-ray diffraction could provide more accurate XRD information of the membrane by eliminating the interference of the substrates, which also shows a broad (002) diffraction peak with a disordered turbostratic arrangement in the g-C3N4 membrane (Supplementary Fig. 16). Indeed, such lamellar disordered structure may provide additional gas transport pathways and plays a dominant role in constructing ultra-permeable membranes. For example, Yang et al.39 reported that the performance of 2D MOF nanosheet membranes was correlated with the stacking order of the nanosheets, where the membrane with disordered stacking showed increased permeance and selectivity by 255% and 449% compared with that of ordered re-stacking, respectively. The XPS spectra of the g-C3N4 membrane confirms the preservation of the g-C3N4 structure in the membrane (Supplementary Fig. 17), where the characteristic peak of g-C3N4 membrane is similar to that of the prepared nanosheets. In addition, the g-C3N4 membrane exhibits the Young’s modulus up to 159 MPa, revealing its excellent mechanical property (Supplementary Fig. 18 and Supplementary Table 2).
Cross-sectional SEM images of the a bottom-up g-C3N4 and b top-down g-C3N4 membranes. Cross-sectional TEM images of the c bottom-up g-C3N4 and d top-down g-C3N4 membranes. e The DFT calculations about stacking states of bottom-up g-C3N4 nanosheets in g-C3N4 membranes. The front represents the first layer of nanosheet in a two-layer system of g-C3N4 and the rear represents another layer of nanosheet below the first layer of nanosheet. f The AA stacking of bottom-up g-C3N4 nanosheets. C, N, and H atoms are colored in gray, blue, and white, respectively. g 1D and corresponding 2D wide-angle XRD patterns of bottom-up g-C3N4 nanosheets and g-C3N4 membrane. Source data are provided as a Source data file.
Gas separation performance of g-C3N4 membranes
The gas separation performance of the g-C3N4 membranes were measured systematically using Wicke-Kallenbach permeation cells (Supplementary Fig. 19). The H2 flux through a 1 μm-thick g-C3N4 membrane reaches high permeance of 3.3 × 10−7 mol m−2 s−1 Pa−1 (Fig. 3a, b and Supplementary Fig. 20). As the kinetic diameter of the molecules increases, the gas permeance decreases sharply, indicating a clear cut-off between H2 and the other tested gases. The H2 to CO2, N2, CH4, C3H6, and C3H8 selectivity are 41, 23, 21, 83, and 113, respectively, which far exceeds the Knudsen selectivity (Supplementary Table 3). However, the 1-μm-thick g-C3N4 membranes assembled by the top-down g-C3N4 nanosheets exhibit similar selectivity to the Knudsen diffusion (Supplementary Fig. 21). Considering the same material and thickness of the two types of membranes, their performance differences are attributed to membrane defects. The g-C3N4 membrane assembled by the bottom-up g-C3N4 nanosheets exhibits noticeable separation performance while the one using the top-down nanosheets does not, indicating that the defects have a significant adverse effect on membrane performance. Recently, Li et al.40 developed a strategy of vapor linker exchange inducing partial amorphization to conglutinate grain boundary/crack defects of membranes, where the ZIF-8 composite membrane showed competitive H2/CO2 selectivity up to 2400, which also indicated the great significance of restraining membrane defects, further illustrating the advantages of the bottom-up method for the synthesis of g-C3N4. Gas permeation through the g-C3N4 membrane is different from Knudsen diffusion and is mainly governed by the kinetic gas diameter rather than its molecular weight, known as the size exclusion or molecular sieving mechanism41 (Supplementary Fig. 22). Besides, the g-C3N4 membranes with different thicknesses were fabricated (Supplementary Fig. 23 and Supplementary Table 4). As the membrane thickness increases, the H2 permeance of the g-C3N4 membrane decreases and the H2/CO2 selectivity increases, which is characteristic of molecular separation membranes. The 300-nm-thick g-C3N4 membranes exhibit an H2 flux of 1.3 × 10−6 mol m−2 s−1 Pa−1 with an H2/CO2 separation factor of 16. The results are promising for industrial applications as enhancing permeance is more important than improving selectivity to reduce separation costs42. Indeed, the g-C3N4 membranes show ultra-high H2 flux with considerable selectivity compared to the other membranes reported in the literatures (see Supplementary Table 5), which breaks the conventional upper bound, as shown in Fig. 3c. Moreover, the g-C3N4 membrane exhibits excellent stability during a 1000 h continuous operation. After being stored in an ambient environment without the introduction of any protective gas at room temperature for 200 days, the membrane was examined again, whose H2/CO2 separation performance was still stable and as high as the fresh one as shown in Fig. 3d. Furthermore, the gas performance of the g-C3N4 membranes were further investigated in harsh environments, including water vapor, elevated temperatures and pressures (Supplementary Fig. 24)43. When exposed to a 3 vol% water vapor environment, the membrane can operate stably for 100 h at room temperature (Supplementary Fig. 25). After three temperature cycles between 25 and 150 °C, the separation performance of the g-C3N4 membrane is recovered (Supplementary Figs. 26–28), which can be attributed to the excellent thermostability of the g-C3N4 material22 (Supplementary Fig. 29). Additionally, the g-C3N4 membrane was also evaluated by durability testing with an equimolar H2/CO2 mixture feed at 120 °C in the presence of water vapor (water activity of 0.353, Supplementary Note 1). It can be seen that the g-C3N4 membrane performs well for 100 h even under wet gas mixture conditions at elevated temperatures (Supplementary Fig. 30), indicating the good hydrothermal stability of the g-C3N4 membrane. The stability of g-C3N4 system can also be confirmed by MD simulation. It can be seen that g-C3N4 system shows very small energy fluctuations in the long-term MD simulations (Supplementary Fig. 31). This is consistent with the substantially unchanged schematic diagrams of the g-C3N4 layer before and after MD simulations, also reflecting its good structural stability44 (Supplementary Fig. 32). Moreover, when the feed pressure increases to 2 bar (transmembrane pressure: 1 bar), the g-C3N4 membrane exhibits a decreased H2/C3H8 separation factor of 17, which can be recovered to the initial value basically after releasing the pressure, as shown in Fig. 3e. However, the H2 and CO2 permeances increase rapidly while the H2/CO2 selectivity decreases with the increased feed pressure (Fig. 3f). The possible reason behind the decrease in selectivity at high pressure might be the existence of the parallel non-selective transport pathways where viscous diffusion is prevalent and which dominates the membrane performance when the transmembrane pressure difference is greater than zero45,46.
a Single gas permeation of the 1-μm-thick g-C3N4 membrane at room temperature and 1 bar. The inset shows the gas selectivity for H2 over other gases. b Permeance and separation factors of the 1-μm-thick g-C3N4 membranes in the equimolar mixed-gas permeation at room temperature and 1 bar. Inset shows the kinetic diameters of various gas molecules. Errors bars indicate the standard deviation of three measurements. c Comparison of H2/CO2 separation performance of g-C3N4 membranes with state-of-the-art membranes at room temperature. d Long-term stability of the g-C3N4 membrane for equimolar H2/CO2 mixture. The gray areas represent the membrane was stored in an ambient environment without the introduction of any protective gas at room temperature for 200 days. e Gas permeances and H2/C3H8 separation factor of the g-C3N4 membrane as a function of the feed pressure at room temperature. The gray areas show the performance of g-C3N4 membrane after releasing the pressure. f Gas permeances and H2/CO2 separation factor of the g-C3N4 membrane as a function of the feed pressure at room temperature. The gray areas show the performance of g-C3N4 membrane after releasing the pressure. Source data are provided as a Source data file.
Discussion
The permeances of H2, CO2, N2, and CH4 do not completely follow the order of kinetic diameters of gas molecules, indicating gas transport behaviors are not only affected by molecular size. Therefore, the behaviors of gas molecules passing through the g-C3N4 layer were investigated using DFT. Considering the universality, we still used the most typical g-C3N4 structure to perform the simulation process. It is found that when H2, CO2, N2, and CH4 molecules pass through the g-C3N4 layer, the electron clouds of gas molecules partially overlap with the atoms around the g-C3N4, as shown in the partial density of states (PDOS)47 results (Supplementary Fig. 33). As a result, H2, CO2, N2, and CH4 molecules can pass through g-C3N4 layer after the partial overlap of electron clouds of the gas molecules and the g-C3N4. However, in virtue of a large number of negatively polarized N atoms in the g-C3N4 nanosheets (red reflects negatively polarized sites, blue represents the opposite), g-C3N4 nanosheets show stronger electrostatic interactions with CO2 molecules with the deepest blue48, which increases the resistance to CO2 diffusion and results in a high separation factor of H2/CO2 (Fig. 4a). While CH4 with light blue possesses relatively weak interactions with g-C3N4 nanosheets, resulting in relatively fast CH4 diffusion. This is consistent with N-functionalized graphene membranes reported previously49. When the carbon atoms were substituted by nitrogen in the porous graphene membrane, the properties of the nanosheets changed and influenced the gas permeability. Consequently, the calculated energy barriers (Eb)18 for gas molecules across the nanosheets are 0.132, 0.969, 0.782, and 0.791 eV for H2, CO2, N2, and CH4, respectively (Fig. 4b and Supplementary Table 6), which suggests that g-C3N4 is promising for sieving H2 from these larger molecules, especially CO2. The adsorption isotherms of H2, CO2, N2, and CH4 on the g-C3N4 membranes at room temperature also indicate that the g-C3N4 membranes tend to preferentially adsorb CO2 compared to other gases, such as H2, N2, CH4 (Supplementary Fig. 34), delaying the CO2 transport50. However, the permeation of CH4 is slightly higher than that of N2 in the experiment, which is different from the simulation results. This may be because the deviation in the experimental measurement or CH4 as a spherical molecule51 is easier to pass through. It should be noted that the g-C3N4 membranes exhibit a sharp separation of H2/C3 with higher gas selectivity for H2/C3H6 and H2/C3H8 (exceeding 80), which can be attributed to the size sieving effect due to the larger size of C3H6 (4.0 Å) and C3H8 (4.2 Å) molecules52. These results show that the gas separation mechanism of the g-C3N4 membrane is based on the synergistic effect of size exclusion and the interactions between gas molecules and g-C3N4 nanosheets.
a Schematic illustrations of gas molecules with electrostatic potentials distribution through the g-C3N4 layer. b Potential energy surfaces for H2, CO2, N2, and CH4 on the g-C3N4 layer. Inset is the energy barrier for gas molecules across the monolayer g-C3N4. The number of gas molecules of c H2/CO2 mixtures and d H2/C3H6 mixtures through the g-C3N4 layer in molecular dynamics (MD) simulations as a function of simulation time. Simulation snapshots at 0, 1, and 100 ns for H2/CO2 mixtures and H2/C3H6 mixtures are given. C, O, and H atoms are colored in red, yellow, and blue, respectively. Source data are provided as a Source data file.
Moreover, MD simulations were conducted to study the gas transport through the g-C3N4 membrane. In H2/CO2 mixed gas simulations (Fig. 4c), it is found that all H2 molecules have moved quickly through the g-C3N4 layers at the very beginning, yielding a diffusivity ratio of 130:4 for H2:CO2 with the H2/CO2 selectivity of 32.5 at 1.0 ns. The predicted selectivity decreases with extended time because there is no H2 molecule on the feed side while CO2 continues to pass through in the subsequent simulation. Besides, the selectivity predicted by the DFT and MD simulations shows several orders of magnitude differences (see Supplementary Note 2), which may be that DFT calculations use different reference states for the energies (separate nucleus, electrons) while potential energy with classical MD simulation only includes the intra and intermolecular potential energies and not the piece due to internal part of the molecular partition function. There is a great difference between the two calculation methods. Therefore, in this work, there is not a strict one-to-one correspondence between the results by DFT calculations and MD simulations, as reported by Wang et al.53. Even so, the MD results qualitatively agree well with the DFT results. With respect to H2/C3H6 mixtures (Fig. 4d), H2 quickly passes through the g-C3N4 layer while C3H6 does not, exhibiting a sharpening sieving effect for H2/C3H6.
In this work, lamellar g-C3N4 nanosheet membranes with excellent gas separation performances are successfully constructed. The membranes are assembled using high-quality nanosheets obtained through a bottom-up method, allowing the exfoliation step to be skipped, thus maintaining structural integrity. Guest molecules are introduced during membrane preparation to prevent re-stacking of the g-C3N4 nanosheets. The fabricated laminar g-C3N4 nanosheet membranes exhibit H2 permeance of up to 1.3 × 10−6 mol m−2 s−1 Pa−1 due to the synergistic effect of the high-density sieving channels and disordered stacking structure. In addition, the gas separation mechanism of the g-C3N4 membrane is based on the integrated gating effects of size exclusion and the interactions between gas molecules and g-C3N4 nanosheets, as evidenced by both the experimental results and computational simulations. These membranes also show good stability even under harsh practice-relevant environments. The excellent separation performance with long-term stability enables the g-C3N4 membrane to serve as a promising candidate for H2 purification, offering an opportunity for the development of carbon neutrality.
Methods
Materials
Melamine (99%, Aladdin), phosphoric acid (≥85%, Guangzhou Chemical Reagent Factory), isopropanol (Guangzhou Chemical Reagent Factory), ethanol (Runjie Chemistry), glycerol (Runjie Chemistry), AAO substrate with a diameter of 15 mm (with a pore size of 160–200 nm, PuYuan Nanotechnology Limited Company). All of the materials were used as purchased without further purification.
Preparation of the g-C3N4 nanosheets
First, a bottom-up method was employed to fabricate the g-C3N4 nanosheets25, as follows. Melamine (1 g) and phosphoric acid (1.2 g) were dissolved in 100 mL of deionized water at 80 °C in a thermostatic water bath until the melamine dissolved completely. Then the solution was transferred into a hydrothermal reactor and heated at 180 °C for 10 h. After centrifugation at 2795 × g for 30 min, the obtained mixture was dried in an oven at 60 °C. The layered precursors were obtained and then refluxed for 3 hours at 90 °C with a 20 mL mixed solution of ethanol and glycerol (3:1, v-v). The powders were washed with ethanol several times, and then the layered precursors after intercalation were obtained after dried at 60 °C. Here, to keep the inherent nanoporous structures of g-C3N4, we chose N2 to achieve an inert operation condition. It has been reported that the gas atmosphere affects the nanoporous structures of g-C3N4, and more complete g-C3N4 nanoporous structures were obtained in an inert atmosphere.54 Aminabhavi et al.55 found that in the process of synthesizing g-C3N4, ammonia was obtained in melamine decomposition and made g-C3N4 produce N-defects. So the layered precursors after intercalation were heated to 520 °C under N2 condition with the heating rate of 2 °C min−1 and kept for 2 h. Then high-quality g-C3N4 nanosheets of 6–8 mg can be obtained. For comparison, a traditional top-down method was also employed to fabricate the g-C3N4 nanosheets56. 10 g melamine was heated to 520 °C for 6.5 h under an air atmosphere with a heating and cooling speed of 5 °C min−1. Then the obtained g-C3N4 powders (1 mg) were dispersed in the water (50 mL) to obtain the g-C3N4 suspension at the concentration of 0.02 mg mL−1. The g-C3N4 nanosheets suspension was obtained by ultrasonic treatment for 2 h.
Preparation of the g-C3N4 membranes
For assembling nanosheets into membranes by vacuum filtration, the g-C3N4 nanosheets powders (1 mg) prepared by the bottom-up method need to be dispersed in isopropanol (50 mL) to obtain the nanosheets suspension. The nanosheets suspension was treated by ultrasonication for 5 min for better dispersion. Then the g-C3N4 membranes were fabricated on AAO substrates by filtering a certain amount of two different g-C3N4 nanosheets suspensions, respectively. Next, these g-C3N4 membranes were placed in a vacuum drying chamber at room temperature for more than 12 h to remove residual solvents in the membranes.
Gas permeation test
All the gas permeation tests were performed in a homemade Wicke-Kallenbach apparatus41. The gases with different kinetic diameters were used as the feed gas, while Ar was used as the sweep gas. The gas volumetric flow rate was constantly controlled at 50 mL min−1 for single and mixed gas tests. Gas chromatography (GC Agilent 7890) was employed to obtain the gas concentrations of permeate gas. The gas flow was controlled using mass flow controllers (MFCs) and corrected by a bubble flowmeter. The membrane module was packed with heating tape, and thermocouple and temperature controller devices were used to control the temperature and heating rate (2 °C min−1). Feed gas was saturated with water vapor before feeding to the membrane module. The partial pressure of water vapor in the feed gas was varied by controlling the temperature of the water tank. The permeate stream was chilled in an iced cold trap. The relative humidity (RH) of the feed stream was measured by a humidity transmitter.
At equilibrium conditions, the water activity (aw) is calculated by Eq. (1):
where \({P}_{{{{{{{\rm{H}}}}}}}_{2}{{{{{\rm{O}}}}}}}\) is the water vapor partial pressure, \({P}_{{{{{{\rm{sat}}}}}}}\) is the saturation water vapor pressure at the stream temperature and pressure57.
The following equations calculate the gas permeance (Pi, mol m−2 s−1 Pa−1) and ideal selectivity Si/j,
where Ni (mol s−1) is the permeate flow rate of the component gas i, ΔPi (Pa) is the transmembrane pressure difference of i, and A (m2) is the membrane area.
The mixed gas separation factor (αi/j) is calculated as follows:
where xi and xj are the volumetric fractions of component i and component j at the feed side, respectively; yi and yj are corresponding volumetric fractions at the permeate side.
DFT simulations
All the computational simulations were performed using the Materials Studio 7.0 package58. To determine the stable stacking status mode of nanosheets in g-C3N4 membranes, we constructed a two-layer system of g-C3N4 corresponding to both of them. One layer shifted to specific extents related to the other layer. The total energy of these two-layer systems is calculated in the Forcite module. The van der Waals (vdW) interactions between layers are described by Dreiding force field59, with cubic spline and a cutoff distance of 12.0 Å for vdW truncation. The electrostatic interactions are modeled by Ewald60 for the summation of atomic charges of g-C3N4 calculated using the QEq method, with the accuracy set to be 1 × 10−4 kcal/mol. The framework of g-C3N4 is assumed to be rigid in the calculations.
The PDOS analysis of g-C3N4 and gas molecules (H2, CO2, N2, and CH4) were computed by GGA/PBE level of functional under DNP basis set in Dmol3 module61, where DFT-D correction was considered with Grimme method62, and the core electrons were treated by an all-electron method. During the simulations, 1.0 × 10−6 Ha of self-consistent field (SCF) tolerance and 500 SCF cycles were used, and 0.05 Ha of thermal smearing were applied to orbital occupation to speed up convergence. The periodic boundary conditions were considered in DFT calculations.
With the same simulation level of PDOS, the electrostatic potential distributions of gas-free g-C3N4 and gas molecules (H2, CO2, N2, CH4, C3H6, and C3H8) were computed. In addition, the potential energy surfaces were obtained by calculating the interaction energies between gas molecules and g-C3N4 nanosheets at different distances from the nanosheets. Typically, a gas molecule was placed at several positions on the nanosheets, and the mass center of the gas was fixed in the z-direction (perpendicularly to the g-C3N4 layer). The interaction energy (Eint) of the gas molecules with g-C3N4 at the corresponding position is calculated by Eq. (5).
where \({E}_{{{{{{{\rm{g}}}}}}-{{{{{\rm{C}}}}}}}_{3}{{{{{{\rm{N}}}}}}}_{4}+{{{{{\rm{gas}}}}}}}\) is the total energy of the g-C3N4-gas configuration, and \(\,{E}_{{{{{{{\rm{g}}}}}}-{{{{{\rm{C}}}}}}}_{3}{{{{{{\rm{N}}}}}}}_{4}}\) and \({E}_{{{{{{\rm{gas}}}}}}}\) are the single point energy of g-C3N4 and the gas molecules, respectively.
Next, the Eb (energy barrier) is defined as the difference between the interaction energies at the transition state (TS, z = 0) and the stable state (SS, the stable adsorption state when the attractive interaction is maximum and z ≠ 0) of the gas molecule on g-C3N426.
where ETS and ESS, respectively, stand for the TS energy and SS energy when a gas molecule permeates through the g-C3N4 nanosheet. This modeling method has been successfully used to explore the interaction mechanism between porous materials and small gas molecules26.
MD simulations
All the computational simulations were performed using the Materials Studio 7.0 package58. The gas permeation of H2/CO2 and H2/C3H6 mixtures through the g-C3N4 layer was modeled by MD simulations. For H2/CO2 mixtures, 260 gas molecules (130 for each gas species) were placed in the feed chamber in the simulation. For H2/C3H6 mixtures, 420 gas molecules (210 for each gas species) were placed in the feed chamber. Then gas mixtures were loaded into the two-layer system of g-C3N4 employing the Sorption module with the Metropolis method, where 1 × 106 kPa of pressure is fixed for each gas. The Dreiding force field and interaction settings were the same as the energy calculations of the gas-free g-C3N4 system. The loaded gas molecules were then optimized with a Forcite module for energy minimization of the adsorbent-adsorbate system, while the atom of g-C3N4 was kept rigid. Subsequently, MD simulations were performed with NVT ensemble in the Forcite module at 298 K, where 1 × 105 ps of total simulation time was used with a time step of 1.0 fs. The Berendsen method63 was applied to maintain the temperature. During the MD simulation, the Dreiding force field and Ewald summation describe the vdW and electrostatic interaction between the gas and g-C3N4. The periodic boundary conditions were considered in three dimensions. MD simulations were run for 10,000 ps to study the potential energy fluctuations of the g-C3N4 system with 298 K temperature to verify the stability of the g-C3N4 system.
Characterization
NMR measurements were recorded on an AVANCE III spectrometer (Bruker) operating at a proton frequency of 400 MHz. XRD patterns were recorded under ambient conditions with a Bruker D8 Advance diffractometer with Cu Kα radiation at 40 kV and 40 mA. The two-dimensional XRD patterns of the g-C3N4 membrane and g-C3N4 powder were obtained by XRD (Rigaku Smart Lab X-Ray Diffractometer) equipped with a 2D X-ray detector using Cu Kα radiation source from 5° to 40° under two-dimensional detection mode. The microstructure of the membranes was observed by the SEM using a HITACHI SU8200. The AFM images were obtained using a Bruker MultiMode 8 scanning probe microscope (SPM, VEECO) in the tapping mode. The room-temperature EPR spectra were measured with Bruker A300. The XPS analysis was performed using an ESCALAB 250 spectrometer (Thermo Fisher Scientific) with monochromated Al Kα radiation (1486.6 eV) under a 2 × 10−9 Torr pressure. The concentrations of the g-C3N4 nanosheets dispersions were measured by UV-vis spectrum (Shimadzu UV-2450). TEM images were obtained using a JEOL JEM-2100F microscope with an acceleration voltage of 200 kV. FTIR (Nicolet 5700 spectrometer) was used to detect the characteristic stretching vibration modes of the sample. Elemental analysis was measured on a Vario EL cube elementary. Thermogravimetric (TG) measurement was analyzed on a Netzsch STA 449F3 instrument under the flow of N2. The adsorption isotherms of H2, CO2, N2, and CH4 on the g-C3N4 membranes were measured using a Micromeritics (ASAP 2460) instrument. The mechanical properties were measured by using an Instron-5565 universal tensile testing machine (USA).
Data availability
Further data that support the findings of this study are available on request from the corresponding author. Source data are provided with this paper.
Change history
25 October 2022
A Correction to this paper has been published: https://doi.org/10.1038/s41467-022-34199-4
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Acknowledgements
J.X. acknowledges the funding from the National Key R&D Program of China (Grant No. 2020YFB1505603), the Natural Science Foundation of China (22075086), and the Guangdong Basic and Applied Basic Research Foundation (2022A1515010980). H.H.W. acknowledges the funding from the Natural Science Foundation of China (22138005, 22141001).
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Y.Z., J.X., and H.H.W. conceived the idea and designed the experiments. Y.Z. finished the experiments and performed the characterization of membrane performance with help of J.X., R.W., and L.D. Y.W. contributed to the computational simulations. Y.Z., H.Y.W., J.X., and H.H.W. wrote the manuscript.
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Zhou, Y., Wu, Y., Wu, H. et al. Fast hydrogen purification through graphitic carbon nitride nanosheet membranes. Nat Commun 13, 5852 (2022). https://doi.org/10.1038/s41467-022-33654-6
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DOI: https://doi.org/10.1038/s41467-022-33654-6
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