3D Membrane Research Articles

Lamellar structured GO-Melamine nanocomposite membranes with varying d-spacing for efficient organic solvent nanofiltration (OSN)

There is a lot of research being done on GO lamellar 2D membranes for separating organic solvents and dyes. These membranes are highly sought-after due to their exceptional characteristics. However, existing challenges include inadequate solvent permeability and limited dye rejection capacity due to swelling of membranes. In this study, we proposed a novel technique that employs low-pressure assisted filtration to fabricate nanocomposite membranes using GO and melamine. Remarkably, these composite membranes exhibited outstanding separation performance for dyes (≥99.06 %) in organic solvents, regardless of their positive or negative charges or when present in mixtures. The optimum GO-M0.02 nanocomposite membrane exhibits impressive organic solvent flux (J), attaining a value as high as 50.8 L/m2h (acetone), which is 6.57 times greater than that of the pure GO membrane. Furthermore, these GO-Melamine nanocomposite membranes showed excellent durability against both common and harsh organic solvents, and the flux of solvents through the GO-M0.02 nanocomposite membrane remained almost unchanged even after being immersed in methanol for up to one week. Additionally, the membrane exhibited consistent solvent flux and rejection rates for methyl green during continuous filtration. These results highlight the exceptional stability and immense potential of GO-melamine nanocomposite membranes for real organic solvent nanofiltration.

Two-Dimensional Sulfonate-Functionalized Metal-Organic Framework Membranes for Efficient Lithium-Ion Sieving.

Two-dimensional (2D) membranes have shown promising potential for ion-selective separation but often suffer from the trade-off between permeability and selectivity. Herein, we report an ultrathin 2D sulfonate-functionalized metal-organic framework (MOF) membrane for efficient lithium-ion sieving. The narrow pores with angstrom precision in the MOF assist hydrated ions to partially remove the hydration shell, according to different hydration energies. The abundant sulfonate groups in the MOF channels serve as hopping sites for fast lithium-ion transport, contributing to a high Li-ion permeability. Then, the difference in affinity of the Li+, Na+, K+, and Mg2+ ions to the terminal sulfonate groups further enhances the Li-ion selectivity. The reported ultrathin MOF membrane overcomes the trade-off between permeability and selectivity and opens up a new avenue for highly permselective membranes.

Plasma‐oxidized 2D MXenes subnanochannel membrane for high‐performance osmotic energy conversion

AbstractNanofluidic channels inspired by electric eels open a new era of efficient harvesting of clean blue osmotic energy from salinity gradients. Limited by less charge and weak ion selectivity of the raw material itself, energy conversion through nanofluidic channels is still facing considerable challenges. Here, a facile and efficient strategy to enhance osmotic energy harvesting based on drastically increasing surface charge density of MXenes subnanochannels via oxygen plasma is proposed. This plasma could break Ti–C bonds in the MXenes subnanochannels and effectively facilitate the formation of more Ti–O, C═O, O–OH, and rutile with a stronger negative charge and work function, which leads the surface potential of MXenes membrane to increase from 205 to 430 mV. This significant rise of surface charge endows the MXenes membrane with high cation selectivity, which could make the output power density of the MXenes membrane increase by 248.2%, reaching a high value of 5.92 W m−2 in the artificial sea‐river water system. Furthermore, with the assistance of low‐quality heat at 50°C, the osmotic power is enhanced to an ultrahigh value of 9.68 W m−2, which outperforms those of the state‐of‐the‐art two‐dimensional (2D) nanochannel membranes. This exciting breakthrough demonstrates the enormous potential of the facile plasma‐treated 2D membranes for osmotic energy harvesting.

High performance mixed-dimensional assembled MXene composite membranes for molecular sieving

Two-dimensional (2D) separation membranes have proved their superiorities in addressing global water scarcity and recycling resources. However, current 2D membranes usually suffer from swelling and irregular stacking issues, which result in poor separation performance. Herein, we developed novel mix-dimensional assembled MXene composite membranes with high permeability and selectivity by intercalating 1D carboxylated cellulose nanofibers (CNFs) into 2D lamellar MXene nanosheets. The effects of chain length of CNFs and MXene/CNFs mass ratios on the morphologies, physicochemical properties, and separation performances of composite membranes were systematically investigated. The optimized MXC-3-L membrane exhibited superior rejection to Congo red (CR, >99%) and remarkable separation efficiency of dye/salt. The separation factors for the CR/NaCl and CR/Na2SO4 mixtures were 512.0 and 517.2, respectively. Moreover, the MXC-3-L membrane showed distinct rejections to perfluoroalkyl substances (PFAS) (>95%) with a nearly 8-fold increase of permeance in comparison with the commercial polyamide membrane. The 2D X-ray diffraction analysis verified that the intercalation of 1D CNFs into 2D MXene nanosheets via strong hydrogen bonding can regulate the nanochannel into more stable and regularly stacking lamellar structures, which plays a key role in high permeance and excellent molecular separation efficiency. In addition, 1D CNFs play an essential role as “threading” and “stitching”, shielding the defects between adjacent MXene nanosheets and improving the separation efficiencies. Our work provides new insights into design of defect-free and highly selective 2D materials-based membranes for enhanced wastewater treatment and molecular sieving.

Bioinspired cell membrane-based nanofiltration membranes with hierarchical pore channels for fast molecular separation

Owing to intrinsic perm-selectivity, cell membranes have attracted considerable attention in the field of biomimetic membranes. Herein, largest possible cell membranes of E.coli were prepared and then used as two-dimensional (2D) materials to fabricate high-performance nanofiltration (NF) membranes. The structure parameters of the selective layer of the E.coli-NF membrane could be finely tailored through the loading mass of cell membranes and the applied pressure during vacuum filtration. The E.coli-NF membrane exhibited a high rejection towards dyes (98.5%, brilliant blue R), antibiotics (91.1%, erythromycin), and divalent ions (64.8%, sodium sulfate). The membrane effective pore size was found to be significantly smaller than the interlayer spacing because of the small intrinsic nanochannels inside the E.coli cell membranes, which is distinct from GO and MXene-based 2D membranes. Moreover, the membrane water permeance was 52.6 L m−2 h−1 bar−1, higher than that of most of the reported 2D materials-based NF membranes. The E.coli-NF membrane exhibited the typical separation behavior of the negatively charged NF membranes governed by Donnan effect and size exclusion. This work gives some insights into the fabrication of the selective membranes using cell membranes as 2D materials with intrinsic nanochannels and fruitful choices in nature.

Two-dimensional metal–organic framework nanocomposite membranes with shortened ion pathways for enhanced salinity gradient power harvesting

Harnessing energy through the reverse electrodialysis-based salinity gradient power conversion is an exciting and promising technological endeavor. The key to its success lies in developing the advanced ion-selective membrane capable of enhancing ion flux and accelerating ion transport at confined nanospaces. Traditional two-dimensional (2D) membranes typically employ a layer-by-layer arrangement of nanosheets with an extremely narrow layer separation, limiting ion flux and creating elongated 2D ion pathways. In response to this limitation, our study introduces an innovative design of the 2D metal–organic framework (MOF)-based nanocomposite membrane (named as Cu-TCPP@SNF), which is composed of the 2D Cu-TCPP and natural-based silk nanofibers (SNFs). We show that the introduction of the space-charged SNFs can significantly enhance the stability of the 2D MOF nanocomposite membrane in electrolyte solutions, and this unique framework facilitates a multitude of abundant one-dimensional ion pathways across the membrane while maintaining the advantage of minimal layer separation. Our results demonstrate that the Cu-TCPP@SNF exhibits low resistance, thus facilitating ion transport. Furthermore, numerical simulations elucidate the impacts of the SNF content and membrane thickness on power performance. Remarkably, our membrane achieves a notable power density of ∼6.48 W/m2 by mixing artificial seawater and river water. Impressively, an ultrahigh performance of ∼29.5 W/m2 can be achieved under a 5 M/0.01 M NaCl gradient, surpassing the existing advanced membranes. These findings hold significant promise for the future of composite 2D membrane development, paving the way for scalable applications in salinity-based energy harvesting.

Computational Assessment of the Biocompatibility of Two-Dimensional g-C3N3 Toward Lipid Membranes.

One of the most recent additions to the family of two-dimensional (2D) materials, graphitic C3N3 (g-C3N3), has been considered a viable contender for biomedical applications, although its potential toxicity remains elusive. We perform all-atom molecular dynamics simulations to decipher the interactions between model lipid membranes and g-C3N3 as a first step toward exploring the cytotoxicity induced at the nanoscale. We show that g-C3N3 can easily insert into the cellular membranes following a multistage mechanism consisting of simultaneous desolvation of the 2D material along with enrichment of nanomaterial-lipid interactions. Free energy calculations indicate that g-C3N3 is more stable in a membrane-bound state compared to an aqueous solution; however, the insertion of the material does not disturb the structural integrity of lipid membranes. After being inserted into a membrane, g-C3N3 is unlikely to be released into the cellular environment and is incapable of extracting lipid molecules from the membrane. The nature of interaction between the 2D material and membranes is found to be independent of the nanomaterial size. Also, the performance of g-C3N3 toward biomolecular delivery is shown to be significantly improved compared to the state-of-the-art 2D materials graphene and hexagonal boron nitride (h-BN). It is revealed that, the affinity of g-C3N3 toward lipid membranes is weaker compared to the nanotoxic graphene and h-BN, while being marginally higher than h2D-C2N, which in turn, increases the biocompatibility of the material, thereby brightening its future as a noncytotoxic material for forthcoming biomedical applications.

Nanomaterials Based Micro/Nanoelectromechanical System (MEMS and NEMS) Devices.

The micro- and nanoelectromechanical system (MEMS and NEMS) devices based on two-dimensional (2D) materials reveal novel functionalities and higher sensitivity compared to their silicon-base counterparts. Unique properties of 2D materials boost the demand for 2D material-based nanoelectromechanical devices and sensing. During the last decades, using suspended 2D membranes integrated with MEMS and NEMS emerged high-performance sensitivities in mass and gas sensors, accelerometers, pressure sensors, and microphones. Actively sensing minute changes in the surrounding environment is provided by means of MEMS/NEMS sensors, such as sensing in passive modes of small changes in momentum, temperature, and strain. In this review, we discuss the materials preparation methods, electronic, optical, and mechanical properties of 2D materials used in NEMS and MEMS devices, fabrication routes besides device operation principles.

Memristive Response and Capacitive Spiking in Aqueous Ion Transport through Two-Dimensional Nanopore Arrays.

In living organisms, information is processed in interconnected symphonies of ionic currents spiking through protein ion channels. As a result of dynamic switching of their conductive states, ion channels exhibit a variety of current-voltage nonlinearities and memory effects. Fueled by the promise of computing architectures entirely different from von Neumann, recent attempts to identify and harness similar phenomena in artificial nanofluidic environments focused on demonstrating analogue circuit elements with memory. Here we explore aqueous ionic transport through two-dimensional (2D) membranes featuring arrays of ion-trapping crown-ether-like pores. We demonstrate that for aqueous salts featuring ions with different ion-pore binding affinities, memristive effects emerge through coupling between the time-delayed state of the system and its transport properties. We also demonstrate a nanopore array that behaves as a capacitor with a strain-tunable built-in barrier, yielding behaviors ranging from current spiking to an ohmic response. By focusing on the illustrative underlying mechanisms, we demonstrate that realistically observable memory effects may be achieved in nanofluidic systems featuring crown-porous 2D membranes.

Promising sensors for pharmaceutical pollutant adsorption using Clar’s goblet-based 2D membranes

This study focuses on the design of new 2D membranes from connected Clar’s Goblet as a potential sensor for pharmaceutical pollutants, specifically the painkiller drugs aspirin, paracetamol, ibuprofen, and diclofenac. The electronic, optical, and interaction properties are investigated using density functional theory calculations. The Clar’s Goblet membranes (CGMs) that were chosen are semiconductors with an energy gap of around 1.5 eV, according to energy gap calculations and density of states. Molecular electrostatic potential (ESP) analysis shows that CGMs have electrophilic and nucleophilic sites, suggesting their suitability for interacting with pharmaceutical pollutants. The adsorption energies confirm the chemical adsorption of pharmaceutical pollutants with diclofenac showing the strongest adsorption. The UV–Vis absorption spectra of CGMs-drug complexes are analyzed, revealing a redshift compared to the absorption spectrum of CGMs alone, confirming the adsorption of these drugs. Further analysis using hole/electron examinations indicates that the type of excitation is local excitation rather than charge transfer excitation. This study quantitatively characterized hole and electron distribution in excited states using various indices. The analysis revealed local excitation transitions and significant charge transfer between the CGMs molecule and pharmaceutical pollutants. Additionally, non-covalent interaction analysis indicates the presence of van der Waals interactions, highlighting the adsorption behavior of the drugs. These results demonstrate the potential of CGMs as a highly sensitive sensor for pharmaceutical pollutants.

High-efficiency water-transport channels using the synergistic effect of superhydrophilic PA layer and robust BU cross-linked GO laminates

Graphene oxide (GO) membranes show immense promise in nanofiltration separation for water purification and recycling of water resources. However, pristine GO membranes often suffer from insufficient membrane stability due to swelling and low water permeance under high operation pressure, which severely limits the real-world utilization of GO membranes. Herein, a strategy involving surface modification of GO membrane with superhydrophilic polyamide (PA) layer combined with cross-linking with biurea (BU) amine, is proposed to fabricate highly permeable and robust GO membranes for dye removal from aqueous solution. The PA layer is prepared onto BU cross-linked GO membrane by in-situ interfacial polymerization, which results in superhydrophilic and negative-charged membrane surface. Moreover, the low reactivity of 2,5-diaminobenzenesulfonic acid (DBS) monomer contributes to low cross-linking degree and loose network of PA layer. The BU cross-linked GO laminates possess multi-level interlayer spacings and sufficient covalent interaction between GO interlayer due to crosslinking with BU, which offer large and robust transport channels for water molecules. PA@BU/GO hybrid membrane shows the optimum pure water permeability of 140.2 L·m−2·h−1·bar−1, with water permeance and TB rejection rate of 67.4 L·m−2·h−1·bar−1 and 99.9 %, respectively. Moreover, the membrane exhibits impressive dye/salt selectivity (the dye/NaCl separation factor is up to 873), long-term operation stability and good anti-fouling property, which makes it a potential candidate for the fractionation of dye/salts in textile wastewater. This work provides a promising idea for the development of high-performance 2D membranes with high-efficiency water transport channels using the synergistic effect of superhydrophilic PA Layer and robust BU cross-linked GO laminates.

Mechanistic insights into microwave-accelerated permeation through graphene-based membranes

Two-dimensional (2D) membranes, composed of stacked 2D nanomaterials, are increasingly utilized in separation fields due to their structured interlayer channels and ease of modification. The application of microwave technology to 2D membrane separation enhances permeability, but the unclear strengthening mechanism limits the further applications of this technique. This study aims to elucidate the fundamental principle behind microwave-accelerated permeability by investigating the performance of two distinct 2D membranes in response to microwaves: a microwave-transparent graphene oxide (GO) membrane and a microwave-absorbing GO-based membrane doped with molybdenum disulfide (MoS2-GO). Experimental results demonstrate that compared to conventional heating, microwave irradiation amplifies water and ethanol permeation flux through the GO membrane by 122% and 154%, respectively, without observed changes in membrane structure via SEM, XRD, and Raman analyses. In addition, the microwave accelerated permeation also occurs (by 110%) when Rhodamine B - aqueous solution was used as feed liquid, while the rejection rate was remained at above 99%, indicating the promising applications of microwave technology in sewage treatment. Further experiments show that the microwave-induced augmentation of water/ethanol permeation through the GO membrane was primarily governed by the dielectric loss values of the feed liquid. In contrast, this dependence vanished in the MoS2-GO membrane, indicating that accelerated permeation was mainly determined by the interaction between microwaves and diffusing molecules in the 2D channels, disrupted by microwave absorbing MoS2 in the latter case. These findings offer comprehensive insights into the enhancement of membrane permeation induced by microwave irradiation.

Designing biomimetic two-dimensional channels for uranium separation from seawater.

Efficient separation of uranium from seawater stands as a pivotal challenge. This study unveils an approach focusing on the ingenious design of biomimetic two-dimensional (2D) membranes tailored explicitly for this purpose. Leveraging the unique interplay of DNA strands housing U aptamers, pH-responsive i-motifs, and poly A(10) segments ingeniously embedded within graphene oxide membranes, a distinctive biomimetic 2D channel is engineered. The strategic integration of these bio-inspired elements enables dynamic adjustment of interlayer spacing, augmenting both the permeability of the membrane and the selectivity of the aptamer for uranyl ions. During the separation process, the encounter between uranyl ions and the enhanced aptamer within the interlayers initiates a crucial interaction, triggering a specific concentration polarization mechanism. This mechanism stands as the cornerstone for achieving a highly selective separation of uranyl ions from the vast and complex matrix of seawater. The membrane exhibits excellent performance in real seawater, with a rejection rate of uranyl ions of ≈100% and sustained selectivity of uranyl ions over ten cycles. Importantly, the selectivity of uranium and vanadium can reach 14.66. The significance of this research lies not only in the effective separation of uranyl ions but also in showcasing the broader applicability of 2D membrane design in chemical engineering.

Bioinspired 2D nanofluidic membranes for energy applications.

Bioinspired two-dimensional (2D) nanofluidic membranes have been explored for the creation of high-performance ion transport systems that can mimic the delicate transport functions of living organisms. Advanced energy devices made from these membranes show excellent energy storage and conversion capabilities. Further research and development in this area are essential to unlock the full potential of energy devices and facilitate the development of high-performance equipment toward real-world applications and a sustainable future. However, there has been minimal review and summarization of 2D nanofluidic membranes in recent years. Thus, it is necessary to carry out an extensive review to provide a survey library for researchers in related fields. In this review, the classification and the raw materials that are used to construct 2D nanofluidic membranes are first presented. Second, the top-down and bottom-up methods for constructing 2D membranes are introduced. Next, the applications of bioinspired 2D membranes in osmotic energy, hydraulic energy, mechanical energy, photoelectric conversion, lithium batteries, and flow batteries are discussed in detail. Finally, the opportunities and challenges that 2D nanofluidic membranes are likely to face in the future are envisioned. This review aims to provide a broad knowledge base for constructing high-performance bioinspired 2D nanofluidic membranes for advanced energy applications.

Separation of oxygen from nitrogen using a graphdiyne membrane: a quantum-mechanical study.

Efficient separation of oxygen and nitrogen from air is a process of great importance for many industrial and medical applications. Two-dimensional (2D) membranes are very promising materials for separation of gases, as they offer enhanced mass transport due to their smallest atomic thickness. In this work, we examine the capacity of graphdiyne (GDY), a new 2D carbon allotrope with regular subnanometric pores, for separating oxygen (16O2) from nitrogen (14N2). A quantum-mechanical model has been applied to the calculation of the transmission probabilities and permeances of these molecules through GDY using force fields based on accurate electronic structure computations. It is found that the 16O2/14N2 selectivity (ratio of permeances) is quite high (e.g., about 106 and 102 at 100 and 300 K, respectively), indicating that GDY can be useful for separation of these species, even at room temperature. This is mainly due to the N2 transmission barrier (∼0.37 eV) which is considerably higher than the O2 one (∼0.25 eV). It is also found that molecular motions are quite confined inside the GDY pores and that, as a consequence, quantum effects (zero-point energy) are significant in the studied processes. Finally, we explore the possibility of 18O2/16O2 isotopologue separation due to these mass-dependent quantum effects, but it is found that the process is not practical since reasonable selectivities are concomitant with extremely small permeances.

Ultrathin two-dimensional membranes by assembling graphene and MXene nanosheets for high-performance precise separation

Ultrathin 2D membranes were assembled by graphene and MXene nanosheets for separation to overcome the “trade-off” limitation between permeability and selectivity.

Functionalized 2D membranes for separations at the 1-nm scale.

The ongoing evolution of two-dimensional (2D) material-based membranes has prompted the realization of mass separations at the 1-nm scale due to their well-defined selective nano- and subnanochannels. Strategic membrane functionalization is further found to be key to augmenting channel accuracy and efficiency in distinguishing ions, gases and molecules within this range and is thus trending as a research focus in energy-, resource-, environment- and pharmaceutical-related applications. In this review, we present the fundamentals underpinning functionalized 2D membranes in various separations, elucidating the critical "method-interaction-property" relationship. Starting with an introduction to various functionalization strategies, we focus our discussion on functionalization-induced channel-species interactions and reveal how they shape the transport- and operation-related features of the membrane in different scenarios. We also highlight the limitations and challenges of current functionalized 2D membranes and outline the necessary breakthroughs needed to apply them as reliable and high-performance separation units across industries in the future.

(Digital Presentation) Present Status and Future Prospects of Large Area Growth and Devices of Two-Dimensional Materials

2D noble metal di- chalcogenides (NMDC or NMC) materials have attracted enormous research interests due to their novel physical and chemical properties with confined dimensions. Here we present two of our experimental works in investigating the growth of PtS and PtSx. (i) Platinum monosulfide as one of the most common platinum-group minerals has been less studied due to either the low purity in the natural product or the extremely high-pressure conditions for synthesis. Recently, platinum monosulfide (PtS) 2D membranes have emerged as rising-star materials for fundamental Raman and X-ray photoelectron spectral analysis as well as device exploration. However, a large-area homogeneous synthesis route has not yet been proposed and released. In this communication, we report a facile metal sulfurization strategy for the synthesis of a 4-inch wafer-scale PtS film. Enhanced characterization tools have been employed for thorough analysis of the crystal structure, chemical environment, vibrational modes, and atomic configuration. Furthermore, through theoretical calculations the phase diagram of the Pt–S compound has been plotted for showing the successful formation of PtS in our synthesis conditions. Eventually, a high-quality PtS film has been reflected in device demonstration by a photodetector. Our approach may shed light on the mass production of PtS films with precise control of their thickness and homogeneity as well as van der Waals heterostructures and related electronic devices. (ii) PtSx, as a more recent 2D material that aroused extensive research interests, has been applied in electronic and optoelectronic devices because of its excellent electronic characteristics and commendable stability. However, the synthesis of large-scale uniform PtSx remains a challenge. Here we studied a modified chemical vapor deposition (CVD) method to grow large-scale uniform PtSx films on SiO2/Si and c-plane sapphire substrates, which can avoid some disadvantages of the mechanical exfoliation method in the device fabrication. The large area uniform PtSx films are achieved through Pt sulfurization using H2S gas, replacing the sulfur powder in traditional methods, as the sulfur source. The material characterizations successfully proved that our modified CVD method is feasible and repeatable, and the PtSx film can be synthesized on different substrates. The PtSx photodevices show good photoresponse properties with a wide spectrum response range. The PtSx/sapphire device shows a better photoresponse in terms of the detectivity (9.17 × 109 Jones) and the responsivity (0.31 A W−1) than that of the PtSx/SiO2/Si device in our experiment, as well as one-year air stability, which may be caused by the different PtSx film quality due to a lattice mismatch difference between the PtSx and the different substrates. These results offer the design and synthesis technology for large-scale, uniform, and stable PtS and PtSx film, as well as an example of photoresponse-enhanced devices which could be generalizable to other transition metal dichalcogenides (TMDCs) and devices for future development and applications. Figure 1

From Sheep Track to Motorway: Supramolecular-Mediated 2D Nanofluidic Channels for Ultrafast Water Transport.

Atomic thick 2D materials hold great potential as building blocks to construct highly permeable membranes, yet the permeability of laminar 2D material membranes is still limited by their irregularity sheep track-like interlayer channels. Herein, a supramolecular-mediated strategy to induce the regular assembly of high-throughput 2D nanofluidic channels based on host-guest interactions is proposed. Inspired by the characteristics of motorways, supramolecular-mediated ultrathin 2D membranes with broad and continuous regular water transport channels are successfully constructed using graphene oxide (GO) as an example. The prepared membrane achieves an ultrahigh water permeability (369.94LMHbar-1) more than six times higher than that of the original membranes while maintaining dye rejection above 98.5%, which outperforms the reported 2D membranes. Characterization and simulation results show that the introduction of hyaluronate-grafted β-cyclodextrin not only expands the interlayer channels of GO membranes but also enables the membranes to operate stably under harsh conditions with the help of host-guest interactions. This universal supramolecular assembly strategy provides new opportunities for the preparation of 2D membranes with high separation performance and reliable and stable nanofluidic channels.

Two-dimensional graphene oxide/MXene lamellar membrane cross-linked by urea with adjustable interlayer spacing for efficient dye rejection and ion sieving

Two-dimensional (2D) membranes demonstrate good performance in molecular and ion separation due to their unique layer structure. However, the sieving performance of 2D membranes is severely limited by drawbacks such as poor stability and low mass transfer rates. Here, we propose a design strategy using urea as a cross-linking agent to construct stable and regular nanochannels inside the graphene oxide/MXene (GO/MXene) composite membranes. More importantly, by changing the composition, the effective interlayer spacing of the membrane can be easily adjusted within 4.47–8.92 Å with angstrom-level precision for tunable ion sieving. The composite membrane exhibits high water permeance (79.58 L m−2 h−1 bar−1) and excellent small molecule dye rejection (>99 %). Moreover, depending on the ionic valence state, the membrane exhibits significant ion sieving. The good Cl−/SO42− selectivity (11.64) makes it a promising alternative to conventional ion exchange membranes. This study demonstrates an innovative and facile way to construct 2D lamellar membranes with stable structures for efficient and precise separation.