Fast Water Transport in UTSA-280 via a Knock-Off Mechanism.

Water and other small molecules frequently coordinate within metal-organic frameworks (MOFs). These coordinated molecules may actively engage in mass transfer, moving together with the transport molecules, but this phenomenon has yet to be examined. In this study, we explore a unique water transfer mechanism in UTSA-280, where an incoming water molecule can displace a coordinated molecule for mass transfer. We refer to this process as the "knock-off" mechanism. Despite UTSA-280 possessing one-dimensional channels, the knock-off transport enables water movement along the other two axes, effectively simulating a pseudo-three-dimensional mass transfer. Even with a relatively narrow pore width, the knock-off mechanism enables a high water flux in the UTSA-280 membrane. The knock-off mechanism also renders UTSA-280 superior water/ethanol diffusion selectivity for pervaporation. To validate this unique mechanism, we conducted 1 H and 2 H solid-state NMR on UTSA-280 after the adsorption of deuterated water. We also derived potential energy diagrams from the density functional theory to gain atomic-level insight into the knock-off and the direct-hopping mechanisms. The simulation findings reveal that the energy barrier of the knock-off mechanism is marginally lower than the direct-hopping pathway, implying its potential role in enhancing water diffusion in UTSA-280.

Vacuum-Assisted Self-Healing Amphiphilic Copolymer Membranes for Gas Separation.

Membrane gas separation provides a multitude of benefits over alternative separation techniques, especially in terms of energy efficiency and environmental sustainability. While polymeric membranes have been extensively investigated for gas separations, their self-healing capabilities have often been neglected. In this work, we have developed innovative self-healing amphiphilic copolymers by strategically incorporating three functional segments: n-butyl acrylate (BA), N-(hydroxymethyl)acrylamide (NMA), and methacrylic acid (MAA). Utilizing these three functional components, we have synthesized two distinct amphiphilic copolymers, namely, APNMA (PBAx-co-PNMAy) and APMAA (PBAx-co-PMAAy). These copolymers have been meticulously designed for gas separation applications. During the creation of these amphiphilic copolymers, BA and NMA segments were selected due to their vital role in the ease of tuning mechanical and self-healing properties. The functional groups (-OH and -NH) present on the NMA segment interact with CO2 through hydrogen bonding, thereby boosting CO2/N2 separation and achieving superior selectivity. We assessed the self-healing potential of these amphiphilic copolymer membranes using two distinct strategies: conventional and vacuum-assisted self-healing. In the vacuum-assisted approach, a robust vacuum pump generates a suction force, leading to the formation of a cone-like shape in the membrane. This formation allows common fracture sites to adhere and trigger the self-healing process. As a result, APNMA maintains its high gas permeability and CO2/N2 selectivity even after the vacuum-assisted self-healing operation. The ideal CO2/N2 selectivity of the APNMA membrane aligns closely with the commercially available PEBAX-1657 membrane (17.54 vs 20.09). Notably, the gas selectivity of the APNMA membrane can be readily restored after damage, in contrast to the PEBAX-1657 membrane, which loses its selectivity upon damage.

Mixed-linker strategy for suppressing structural flexibility of metal-organic framework membranes for gas separation.

Structural flexibility is a critical issue that limits the application of metal-organic framework (MOF) membranes for gas separation. Herein we propose a mixed-linker approach to suppress the structural flexibility of the CAU-10-based (CAU = Christian-Albrechts-University) membranes. Specifically, pure CAU-10-PDC membranes display high separation performance but at the same time are highly unstable for the separation of CO2/CH4. A partial substitution (30 mol.%) of the linker PDC with BDC significantly improves its stability. Such an approach also allows for decreasing the aperture size of MOFs. The optimized CAU-10-PDC-H (70/30) membrane possesses a high separation performance for CO2/CH4 (separation factor of 74.2 and CO2 permeability of 1,111.1 Barrer under 2 bar of feed pressure at 35°C). A combination of in situ characterization with X-ray diffraction (XRD) and diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy, as well as periodic density functional theory (DFT) calculations, unveils the origin of the mixed-linker approach to enhancing the structural stability of the mixed-linker CAU-10-based membranes during the gas permeation tests.

Challenges in Developing MOF-Based Membranes for Gas Separation.

Metal-organic frameworks (MOFs) are promising candidates for membrane gas separation. MOF-based membranes include pure MOF membranes and MOF-based mixed matrix membranes (MMMs). This Perspective discusses the challenges for the next stage of the development of MOF-based membranes based on research conducted in the past decade. We focused on three major issues associated with pure MOF membranes. First, some MOF compounds have been overstudied, despite the availability of numerous MOFs. Second, gas adsorption and diffusion in MOFs are often independently investigated. The correlation between adsorption and diffusion has seldom been discussed. Third, we identify the importance of characterizing the gas distribution in MOFs to understand the structure-property relationships for gas adsorption and diffusion in MOF membranes. For MOF-based MMMs, engineering the MOF-polymer interface is essential for achieving the desired separation performance. Various approaches to modify the MOF surface or polymer molecular structure have been proposed to improve the MOF-polymer interface. Herein, we present defect engineering as a facile and efficient approach for engineering the MOF-polymer interfacial morphology and its extended application for various gas separations.

X-ray Diffraction and Molecular Simulations in the Study of Metal-Organic Frameworks for Membrane Gas Separation.

For more than a decade, researchers have been developing metal-organic frameworks (MOFs) in the form of pure MOF membranes as well as MOF-containing mixed-matrix membranes. MOF membranes have been used for H2/CO2 or C3H6/C3H8 separation, but relatively few MOF membranes enable the high-performance separation of CO2/N2, CO2/CH4, or N2/CH4. This article describes the use of in situ XRD analysis and molecular simulation to elucidate gas transport within MOFs and derivative membranes at the molecular level. In a review of recent studies by the authors and other research groups, this article examines the flexibility of MOFs initiated by activation, gas adsorption, and aging effects during gas permeation. This article also discusses the application of XRD analysis in conjunction with computational methods to investigate the CO2-MOF Coulombic interaction and its effects on CO2 separation. Note that this combined analysis approach is also useful in studying the effects of linker rotation on N2/CH4 separation. This article also examines the use of computational tools in identifying new MOFs for gas separation and, more importantly, in elaborating the relationship between the structure of MOFs and their corresponding gas transport properties.

Thin Film Growth of 3D Sr-based Metal-Organic Framework on Conductive Glass via Electrochemical Deposition.

Integration of metal-organic frameworks (MOFs) as components of advanced electronic devices is at a very early phase of development and the fundamental issues related to their crystal growth on conductive substrate need to be addressed. Herein, we report on the structural characterization of a newly synthesized Sr-based MOF {[Sr(2,5-Pzdc)(H2 O)2 ] ⋅ 3 H2 O}n (1) and the uniform crystal growth of compound 1 on a conducting glass (fluorine doped tin oxide (FTO)) substrate using electrochemical deposition techniques. The Sr-based MOF 1 was synthesized by the reaction of Sr(NO3 )2 with 2,5-pyrazinedicarboxylic acid dihydrate (2,5-Pzdc) under solvothermal conditions. A single-crystal X-ray diffraction analysis revealed that 1 has a 3D structure and crystallizes in the triclinic P 1 ‾ space group. In addition, the uniform crystal growth of this MOF on a conducting glass (FTO) substrate was successfully achieved using electrochemical deposition techniques. Only a handful of MOFs have been reposed to grown on conductive surfaces, which makes this study an important focal point for future research on the applications of MOF-based devices in microelectronics.

Suppressing Defect Formation in Metal-Organic Framework Membranes via Plasma-Assisted Synthesis for Gas Separations.

Metal-organic frameworks (MOFs) are considered as promising materials for membrane gas separations. Structural defects within a pure MOF membrane can considerably reduce its selectivity and possibly result in a nonselective separation. This work proposes a solution-phase synthesis with dielectric barrier discharge (DBD) plasma to suppress the formation of defects in the pure MOF membrane of CPO-8-BPY. Through comprehensive solid-state characterization with XRD, SEM, XPS, solid-state NMR, and XAFS, DBD plasma is demonstrated to facilitate deprotonation in the H2aip linker, which leads to a smaller and more uniform particle size of CPO-8-BPY. The narrow grain size distribution effectively reduces the pinhole-type defects in the pure CPO-8-BPY membrane and endows it with good ideal selectivity for H2/CH4 (αH2/CH4 = 28.2) and N2/CH4 (αN2/CH4 = 5.4). The selectivity for H2/CH4 of this membrane from a mixed-gas permeation test is found to be 15.4. Molecular simulations are also performed to gain insights into the gas transport properties of this MOF. The results suggest that ligand rotation plays an important role in CPO-8-BPY when being applied to the membrane separation of N2/CH4.

Zinc(II)-Organic Framework Films with Thermochromic and Solvatochromic Applications.

Multiple-stimuli-responsive photoluminescence films based on a ZnII -organic framework, {[Zn2 (Htpim)(3,4-pydc)2 ]⋅4 DMF⋅4 H2 O}n (1, Htpim=2,4,5-tri(4-pyridyl)imidazole, 3,4-H2 pydc=3,4-pyridinedicarboxylic acid), were fabricated. This compound consisted of a 2D corrugated layer, {Zn(3,4-pydc)}n , which was further pillared using a Y-shaped pillar N-donor ligand (Htpim) to form a 3D-pillared-layer framework with 1D open channels. The rectangular channels in the as-synthesized compound are fully occupied by guest DMF and H2 O molecules. The framework exhibits instant and reversible thermochromic properties corresponding to the removal of different H2 O and DMF guest molecules as temperature increases. The pale-yellow crystal undergoes significant redshifting to a greenish emission centered at 530 nm. Compound 1 also showed remarkable solvatochromic effects in the presence of various organic solvents without affecting its structural integrity. In addition, polycrystalline MOF films were grown on an α-Al2 O3 support for switchable and fast-response thermochromic and solvatochromic sensors.

Hexagonal Superalignment of Nano-Objects with Tunable Separation in a Dilute and Spacer-Free Solution.

Manipulating building-block nanomaterials to form an ordered superstructure in a dilute and spacer-free solution phase challenges the existing 5-nm node lithography and nanorobotics. The cooperative nature of nanocrystals, polymers, and cells can lead to superarrays or colloidal crystals. For known highly ordered systems, the characteristic length of materials, defined as the shortest dimension of objects, is generally larger than their separations. A spacer (small-molecule surfactant or polymer) is typically required to diminish short range van der Waals attraction, which results in a glassy or liquid state. Herein we propose a new concept of achieving highly ordered nano-objects in a dilute and spacer-free system via the synergistic effects of excellent solvation and appropriate constraints on rotational motion. As a proof of concept, this study demonstrates that aluminosilicate nanotubes (AlSiNTs) suspended in water under dilute conditions (e.g., 1.0 wt%) can spontaneously form hexagonal arrays with an intertubular distance as large as tens of nanometers. The separation distance of the ordered superstructure is also tunable via controlling the concentration and length of nanotubes. These superaligned structures are probed using small-angle x-ray scattering and cryo-TEM characterizations, with underlying mechanisms investigated at an atomic level using molecular dynamics simulations. The concept and discovery of this work can open up opportunities to a variety of applications including visible-UV photonics and nanolithography, and may be generalizable to other nano-object systems that fulfill similar requirements.

Wetting Properties and Thin-Film Quality in the Wet Deposition of Zeolites.

Zeolites are microporous crystalline materials widely used in catalysis and adsorption applications. The fabrication of zeolite thin films and membranes has also opened up the possibility of using zeolites in electronic devices and membrane separations. The existing approach to growing zeolite films involves exposing the substrate to a high-pH environment; however, this process is applicable to only specific types of substrates. Our group has developed the direct wet deposition of zeolites via ultrasonic nozzle spray deposition to address this issue; however, the relationship between wetting properties and thin-film quality has yet to be investigated. In this study, we prepared zeolite CHA (Si:Al:P = 3:10:20) suspensions using different solvents and surfactants in various concentrations. We then examined the relationships among the composition of the cast solution, their wetting behavior on the glass substrate, and the uniformity of the resulting thin films. We found that using ethanol as a solvent with zeolite crystals in low concentrations with added surfactant yielded zeolite films of high quality. We were also able to produce low-haze zeolite coatings on glass. The zeolite coatings with high hydrophilicity and adsorption capacity presented excellent antifogging capability.

Zeolite-Based Antifogging Coating via Direct Wet Deposition.

Zeolites are strongly hydrophilic materials that are widely used as water adsorbents. They are also promising candidates for antifogging coatings; however, researchers have yet to devise a suitable method for coating glass substrates with zeolite-based films. Here, we report on a direct wet deposition technique that is capable of casting zeolite films on glass substrates without exposing the glass to highly basic solutions or the vapors used in zeolite synthesis. We began by preparing cast solutions of pure silica zeolite MFI synthesized in hydrothermal reactions of various durations. The solutions were then applied to glass substrates via spin-on deposition to form zeolite films. The resulting zeolite MFI thin films were characterized in terms of transmittance to visible light, surface topography, thin film morphology, and crystallinity. Wetting and antifogging properties were also probed. We found that hydrophilicity and antifogging capability increased with the degree of thin film crystallinity. We also determined that the presence of the amorphous silica in the thin films is critical to transparency. Fabricating high-performance zeolite-based antifogging coatings requires an appropriate composition of zeolite crystals and amorphous silica.

Scalable Wet Deposition of Zeolite AEI with a High Degree of Preferred Crystal Orientation.

Producing zeolite films with controlled preferred orientation on an industrial scale is a long-standing challenge. Herein we report on a scalable approach to the direct wet deposition of zeolite thin films and membranes while maintaining a high degree of control over the preferred crystal orientation. As a proof of concept, thin films comprising aluminophosphate zeolite AEI were cast on silicon wafer or porous alumina substrates. Electrical properties and separation performance of the zeolite thin films/membranes were engineered through controlling degree of preferred crystal orientation.

Investigation of the Water Adsorption Properties and Structural Stability of MIL-100(Fe) with Different Anions.

Investigating metal-organic frameworks (MOFs) as water adsorbents has drawn increasing attention for their potential in energy-related applications such as water production and heat transformation. A specific MOF, MIL-100(Fe), is of particular interest for its large adsorption capacity with the occurrence of water condensation at a relatively low partial pressure. In the synthesis of MIL-100(Fe), depending on the reactants, structures with varying anion terminals (e.g., F-, Cl-, or OH-) on the metal trimer have been reported. In this study, we employed molecular simulations and density functional theory calculations for investigating the water adsorption behaviors and the relative structural stability of MIL-100(Fe) with different anions. We also proposed a possible defective structure and explored its water adsorption properties. The results of this study are in good agreement with the experimental measurements and are in support of the observations reported in the literature. Understanding the spatial configurations and energetics of water molecules in these materials has also shed light on their adsorption mechanism at the atomic level.

Properties of Single-Walled Aluminosilicate Nanotube/Poly(vinyl alcohol) Aqueous Dispersions.

The properties of (synthesized) single-walled aluminosilicate nanotube (AlSiNT; light-scattering characterized length ∼2000 ± 230 nm and diameter ∼35 ± 4 nm) dispersed in an aqueous poly(vinyl alcohol) (PVA) solution (10 wt %) are systematically explored using a comprehensive combination of (polarized/depolarized) dynamic light scattering, rheological, rheo-optical, and scanning electron microscopy analysis schemes. The nanotube/polymer dispersions under investigation are promising for their fair nanotube dispersion in pristine aqueous media (e.g., without salt or acid addition), as well as for the optical transparency that greatly facilitates systematic exploration of structural features and dispersion state that are practically inaccessible for many of their (opaque) companions such as carbon nanotube dispersions. We provide the first in-depth analysis revealing excellent dispersion state of (unmodified) AlSiNT in the PVA matrix, giving rise to (critical) gel-like features and substantially promoted elasticity that can be utilized, as a practical assessment, to produce uniform and defect-free electrospun nanofibers. Additionally, there is unambiguous evidence of nematic liquid crystal-like "wagging" (strain-invariant, periodic oscillation) under steady shear flow, a phenomenon previously unreported for nanotube composite materials. Overall, the present findings suggest that AlSiNT/PVA dispersions possess promising rheological, optical, and electrospinning properties that are highly desirable for current nanotechnological applications, and may serve as an ideal model system for establishing structure-performance relationships for like nanotube/polymer composite materials.

Atmospheric Pressure Plasma Jet-Assisted Synthesis of Zeolite-Based Low-k Thin Films.

Zeolites are ideal low-dielectric constant (low-k) materials. This paper reports on a novel plasma-assisted approach to the synthesis of low-k thin films comprising pure-silica zeolite MFI. The proposed method involves treating the aged solution using an atmospheric pressure plasma jet (APPJ). The high reactivity of the resulting nitrogen plasma helps to produce zeolite crystals with high crystallinity and uniform crystal size distribution. The APPJ treatment also remarkably reduces the time for hydrothermal reaction. The zeolite MFI suspensions synthesized with the APPJ treatment are used for the wet deposition to form thin films. The deposited zeolite thin films possessed dense morphology and high crystallinity, which overcome the trade-off between crystallinity and film quality. Zeolite thin films synthesized using the proposed APPJ treatment achieve low leakage current (on the order of 10-8 A/cm2) and high Young's modulus (12 GPa), outperforming the control sample synthesized without plasma treatment. The dielectric constant of our zeolite thin films was as low as 1.41. The overall performance of the low-k thin films synthesized with the APPJ treatment far exceed existing low-k films comprising pure-silica MFI.

Multifunctional nanoparticles with controllable dimensions and tripled orthogonal reactivity.

Multifunctional nanoparticles featuring three distinct and orthogonal functionalities for performing catalyst-free click reactions of azide-alkyne and maleimide-thiol and atom transfer radical polymerization (ATRP) are fabricated using a simple chemical vapor deposition copolymerization approach with the flexibility to control the particle size and geometry.

Investigating the Potential of Single-Walled Aluminosilicate Nanotubes in Water Desalination.

Water shortage has become a critical issue. To facilitate the large-scale deployment of reverse-osmosis water desalination to produce fresh water, discovering novel membranes is essential. Here, we computationally demonstrate the great potential of single-walled aluminosilicate nanotubes (AlSiNTs), materials that can be synthesized through scalable methods, in desalination. State-of-the-art molecular dynamics simulations were employed to investigate the desalination performance and structure-performance relationship of AlSiNTs. Free energy profiles, passage time distribution, and water density map were also analyzed to further understand the dependence of transport properties on diameter and water dynamics in the nanotubes. AlSiNTs with an inner diameter of 0.86 nm were found to fully reject NaCl ions while allowing orders of magnitude higher water fluxes compared to currently available reverse osmosis membranes, providing opportunities in water desalination.

Solution-processed ultra-low-k thin films comprising single-walled aluminosilicate nanotubes.

Nanotube-based ultra-low-k thin films with high Young's modulus composed of single-walled aluminosilicate nanotubes (AlSiNTs) and a trace amount of poly(vinyl alcohol) (PVA) have been developed. The dehydrated AlSiNT film possesses a relative permittivity of 1.05, and a Young's modulus of 25 GPa, which exceed those of most existing ultra-low-k materials.

Relationships between the solution and solid-state properties of solution-cast low-k silica thin films.

This paper reports on the fabrication of low-k (amorphous) silica thin films cast from solutions without and with two different types of surfactants (TWEEN® 80 and Triton™ X-100) to elucidate the relationships between the structural/morphological features of the casting solutions and the physical properties of the resulting thin films. Cryogenic transmission microscopy (cryo-TEM), static/dynamic light scattering (SLS/DLS), and small-angle X-ray scattering (SAXS) revealed contrasting colloidal dispersion states and phase behavior among the three casting solutions. Casting solution with the Triton™ X-100 surfactant produced stable (>90 days) nanoparticles with good dispersion in solution (mean particle size ∼10 nm) as well as good mesopore volume (characterized by nitrogen physisorption) in powder and thin films of high mechanical strength (characterized by the nanoindentation test). The longer main chain and bulkier side units of the TWEEN® 80 surfactant led to stable micelle-nanoparticle coexisting dispersion, which resulted in the highest mesopore volume in powder and thin films with the lowest dielectric constant (∼3) among the samples in this study. The casting solution without the surfactant failed to produce a stabilized solution or thin films of acceptable uniformity. These findings demonstrate the possibility of fine-tuning low-k silica film properties by controlling the colloidal state of casting solutions.

Synthesis of Zeolitic Imidazolate Framework Core-Shell Nanosheets Using Zinc-Imidazole Pseudopolymorphs.

Zeolitic imidazolate frameworks (ZIFs) are an emerging class of microporous materials that possess an organic flexible scaffold and zeolite-like topology. The catalytic and molecular-separation capabilities of these materials have attracted considerable attention; however, crystal-shape engineering in ZIF materials remains in its infancy. This is the first study to report an effective method for tailoring the near-spherical crystal morphology of ZIF-8 using its leaf-like pseudopolymorph, ZIF-L. A thin, uniform layer of ZIF-8 is formed on ZIF-L through heterogeneous surface growth to produce a ZIF-L@ZIF-8 core-shell nanocomposite. This results in ZIF-8 with a crystal morphology comprising two-dimensional nanoflakes. We characterized the resulting core-shell crystals using a number of solid-state techniques, including powder X-ray diffraction, scanning electron microscopy, thermogravimetric analysis, and nitrogen physisorption. Approximately 16 mass% of ZIF-8 in the core-shell composites heterogeneous surfacely grown on ZIF-L core crystals. We also investigated the effects of zinc salts, which were used as a source of zinc in the formation of the ZIF-L@ZIF-8 core-shell nanocomposites. Finally, we assessed the CO2 adsorption properties of ZIF-8, ZIF-L, and ZIF-L@ZIF-8 core-shell crystals, the results of which were used to deduce the dynamic and equilibrium adsorption characteristics of various microporous ZIF crystals. The core-shell materials present hybridized CO2 uptake and diffusivity of the parent crystals. The proposed method for the synthesis of core-shell nanocomposites using pseudopolymorphic crystals is applicable to other ZIF systems.