Covalent Organic Framework Thin Films Research Articles

Photochemical and Patternable Synthesis of 2D Covalent Organic Framework Thin Film Using Dynamic Liquid/Solid Interface.

2D covalent organic frameworks (COFs) are highly porous crystalline materials with promising applications in organic electronics. Current methods involve either on-surface synthesis (solid surface) or interfacial synthesis (liquid/liquid, liquid/gas interface) to create thin films for these applications, each with its drawbacks. On-surface synthesis can lead to contamination from COF powder or unreacted chemicals, while interfacial synthesis risks damaging the film during post-transfer processes. These challenges necessitate the development of alternative synthesis methods for high-quality 2D COF films. This study presents a novel approach for synthesizing homogeneous 2D COF thin films by combining photochemistry and a liquid-flowing system. Leveraging previous work on liquid flow systems to prevent contamination during solvothermal synthesis, this approach to the photochemical method, resulting in the synthesis of high-crystalline 2D COF films with tunable thickness is adopted. The photochemical approach offers spatially controllable energy sources, enabling patternable COF synthesis. Notably, it is successfully fabricated ultrasmooth patterned 2D COF films on hexagonal boron nitride, offering a streamlined process for optoelectronic device fabrication without additional pre, post-processing steps.

Orientation and morphology control in acid-catalyzed covalent organic framework thin films.

As thin films of semiconducting covalent organic frameworks (COFs) are demonstrating utility for ambipolar electronics, channel materials in organic electrochemical transistors (OECTs), and broadband photodetectors, control and modulation of their thin film properties is paramount. In this work, an interfacial growth technique is utilized to synthesize imine TAPB-PDA COF films at both the liquid-liquid interface as well as at the liquid-solid interface on a Si/SiO2 substrate. The concentration of acetic acid catalyst in the aqueous phase is shown to significantly influence the thin film morphology of the liquid-solid growth, with concentrations below 1 M resulting in no film nucleation, concentrations of 1-4 M enabling smooth film formation, and concentrations greater than 4 M resulting in films with a higher density of particulates on the surface. Importantly, while the films grown at the liquid-liquid interface are mixed-orientation, those grown directly at the liquid-solid interface on the Si/SiO2 surface have highly oriented COF layers aligned parallel to the substrate surface. Moreover, this liquid-solid growth process affords TAPB-PDA COF thin films with p-type charge transport having a transconductance of 10 μS at a gate voltage of -0.9 V in an OECT device structure.

3D Covalent Organic Frameworks from Design, Synthesis to Applications in Optoelectronics.

Covalent organic frameworks (COFs), a new class of crystalline materials connected by covalent bonds, have been developed rapidly in the past decades. However, the research on COFs is mainly focused on two-dimensional (2D) COFs, and the research on three-dimensional (3D) COFs is still in the initial stage. In 2D COFs, the covalent bonds exist only in the 2D flakes and can form 1D channels, which hinder the charge transport to some extent. In contrast, 3D COFs have a more complex pore structure and thus exhibit higher specific surface area and richer active sites, which greatly enhance the 3D charge carrier transport. Therefore, compared to 2D COFs, 3D COFs have stronger applicability in energy storage and conversion, sensing, and optoelectronics. In this review, it is first introduced the design principles for 3D COFs, and in particular summarize the development of conjugated building blocks in 3D COFs, with a special focus on their application in optoelectronics. Subsequently, the preparation of 3D COF powders and thin films and methods to improve the stability and functionalization of 3D COFs are summarized. Moreover, the applications of 3D COFs in electronics are outlined. Finally, conclusions and future research directions for 3D COFs are presented.

Magnetoresistance in Organic Spin Valves Based on Acid‐Exfoliated 2D Covalent Organic Frameworks Thin Films

AbstractCovalent organic frameworks (COFs), as a burgeoning class of crystalline porous materials, have made significant progress in their application to optoelectronic devices such as field‐effect transistors, memristors, and photodetectors. However, the insoluble features of microcrystalline two‐dimensional (2D) COF powders limit development of their thin film devices. Additionally, the exploration of spin transport properties in this category of π‐conjugated skeleton materials remains vacant thus far. Herein, an imine‐linked 2D Py‐Np COF nanocrystalline powder was synthesized by Schiff base condensation of 4,4′,4′′,4′′′‐(pyrene‐1,3,6,8‐tetrayl)tetraaniline and naphthalene‐2,6‐dicarbaldehyde. Then, we prepared a large‐scale free‐standing Py‐Np COF film via a top‐down strategy of chemically assisted acid exfoliation. Moreover, high‐quality COF films acted as active layers were transferred onto ferromagnetic La0.67Sr0.33MnO3 (LSMO) electrodes for the first attempt to fabricate organic spin valves (OSVs) based on 2D COF materials. This COF‐based OSV device with a configuration of LSMO/Py‐Np COF/Co/Au demonstrated a remarkable magnetoresistance (MR) value up to −26.5 % at 30 K. Meanwhile, the MR behavior of the COF‐based OSVs exhibited a highly temperature dependence and operational stability. This work highlights the enormous application prospects of 2D COFs in organic spintronics and provides a promising approach for developing electronic and spintronic devices based on acid‐exfoliated COF thin films.

Magnetoresistance in Organic Spin Valves Based on Acid-Exfoliated 2D Covalent Organic Frameworks Thin Films.

Covalent organic frameworks (COFs), as a burgeoning class of crystalline porous materials, have made significant progress in their application to optoelectronic devices such as field-effect transistors, memristors, and photodetectors. However, the insoluble features of microcrystalline two-dimensional (2D) COF powders limit development of their thin film devices. Additionally, the exploration of spin transport properties in this category of π-conjugated skeleton materials remains vacant thus far. Herein, an imine-linked 2D Py-Np COF nanocrystalline powder was synthesized by Schiff base condensation of 4,4',4'',4'''-(pyrene-1,3,6,8-tetrayl)tetraaniline and naphthalene-2,6-dicarbaldehyde. Then, we prepared a large-scale free-standing Py-Np COF film via a top-down strategy of chemically assisted acid exfoliation. Moreover, high-quality COF films acted as active layers were transferred onto ferromagnetic La0.67 Sr0.33 MnO3 (LSMO) electrodes for the first attempt to fabricate organic spin valves (OSVs) based on 2D COF materials. This COF-based OSV device with a configuration of LSMO/Py-Np COF/Co/Au demonstrated a remarkable magnetoresistance (MR) value up to -26.5 % at 30 K. Meanwhile, the MR behavior of the COF-based OSVs exhibited a highly temperature dependence and operational stability. This work highlights the enormous application prospects of 2D COFs in organic spintronics and provides a promising approach for developing electronic and spintronic devices based on acid-exfoliated COF thin films.

Perpendicular Alignment of Covalent Organic Framework (COF) Pore Channels by Solvent Vapor Annealing

Covalent organic frameworks (COFs) have showcased great potential in diverse applications such as separation and catalysis, where mass transfer confined in their pore channels plays a significant role. However, anisotropic orientation usually occurs in polycrystalline COFs, and perpendicular alignment of COF pore channels is ultimately desired to maximize their performance. Herein, we demonstrate a strategy, solvent vapor annealing, to reorient COF pore channels from anisotropic orientation to perpendicular alignment. COF thin films are first synthesized to have flexible N-H bonds in their skeletons, thus having structural mobility to enable molecular rearrangement. A solvent with low relative permittivity and a conjugated structure is then identified to have a strong affinity toward the COFs, allowing its vapor to easily penetrate into the COF interlayers. The solvent vapor weakens the π-π interaction and consequently allows the COF monolayers to dissociate. The COF monolayers undergo a reorientation process that converts from random stacking into the face-on stacking fashion, in which the through COF pores are perpendicularly aligned. The aligned COF film exhibits high separation precision toward ions featuring a size difference down to 2 Å, which is 8 times higher than that of the anisotropically oriented counterpart. This work opens up an avenue for COF orientation regulation by solvent vapor annealing and reveals the essential role of the perpendicular alignment of COF pore channels to enable precision separations.

Monolayer-Assisted Surface-Initiated Schiff-Base-Mediated Aldol Polycondensation for the Synthesis of Crystalline sp2 Carbon-Conjugated Covalent Organic Framework Thin Films.

sp2 carbon-conjugated covalent organic frameworks (sp2c-COFs) with superb in-plane π-conjugations, high chemical stability, and robust framework structure are expected to be ideal films/membranes for a wide range of applications including energy-related devices and optoelectronics. However, so far, sp2c-COFs have been mainly limited to microcrystalline powders, and this consequently hampered their performances in devices. Herein, we report a simple and robust methodology to fabricate large-area, free-standing, and crystalline sp2c-COF films (TFPT-TMT and TB-TMT) on various solid substrates (e.g., fluorine-doped tin oxide, aluminum sheet, polyacrylonitrile membrane) by self-assembly monolayer-assisted surface-initiated Schiff-base-mediated aldol polycondensation (namely, SI-SBMAP). The resultant sp2c-COF films show lateral sizes up to 120 cm2 and tunable thickness from tens of nanometers to a few micrometers. Owing to the robust framework and highly ordered quasi-1D channels, the sp2c-COF membrane-based osmotic power generator presents an output power density of 14.1 W m-2 under harsh conditions, outperforming most reported COF membranes as well as commercialized benchmark devices (5 W m-2). This work demonstrates a simple and robust interfacial methodology for the fabrication of sp2c-COF films/membranes for green energy applications and potential optoelectronics.

Covalent Organic Framework Thin-Film Photodetectors from Solution-Processable Porous Nanospheres

The synthesis of homogeneous covalent organic framework (COF) thin films on a desired substrate with decent crystallinity, porosity, and uniform thickness has great potential for optoelectronic applications. We have used a solution-processable sphere transmutation process to synthesize 300 ± 20 nm uniform COF thin films on a 2 × 2 cm2 TiO2-coated fluorine-doped tin oxide (FTO) surface. This process controls the nucleation of COF crystallites and molecular morphology that helps the nanospheres to arrange periodically to form homogeneous COF thin films. We have synthesized four COF thin films (TpDPP, TpEtBt, TpTab, and TpTta) with different functional backbones. In a close agreement between the experiment and density functional theory, the TpEtBr COF film showed the lowest optical band gap (2.26 eV) and highest excited-state lifetime (8.52 ns) among all four COF films. Hence, the TpEtBr COF film can participate in efficient charge generation and separation. We constructed optoelectronic devices having a glass/FTO/TiO2/COF-film/Au architecture, which serves as a model system to study the optoelectronic charge transport properties of COF thin films under dark and illuminated conditions. Visible light with a calibrated intensity of 100 mW cm-2 was used for the excitation of COF thin films. All of the COF thin films exhibit significant photocurrent after illumination with visible light in comparison to the dark. Hence, all of the COF films behave as good photoactive substrates with minimal pinhole defects. The fabricated out-of-plane photodetector device based on the TpEtBr COF thin film exhibits high photocurrent density (2.65 ± 0.24 mA cm-2 at 0.5 V) and hole mobility (8.15 ± 0.64 ×10-3 cm2 V-1 S-1) compared to other as-synthesized films, indicating the best photoactive characteristics.

Solvent-free and in situ synthesis of three-dimensional covalent organic frameworks thin films on Zn anodes for Zn–air batteries

Direct synthesis of three-dimensional covalent organic frameworks (3D COFs) thin film on substrates is paramount important to their practical application in devices. Here, solvent-free and in situ synthesis of 3D COFs thin films on Zn substrates by thermal evaporation technique are proposed. Two 3D COFs thin films (i.e., TAM-Tp and TAM-BPDA) are constructed by tetrakis(4-aminophenyl)methane (TAM), 1,3,5-triformylphloroglucinol (Tp), and 4,4′-biphenyldicarboxaldehyde (BPDA). The crystallinity of 3D COFs thin films can rival their powders synthesized by the grinding coupled with hydrothermal methods. In particular, TAM-Tp thin film shows superior transporting ability of hydroxide ions and remarkable suppression for Zn dendrites as compared to TAM-BPDA thin film. Therefore, the assembled quasi-solid state and aqueous Zn–air batteries (ZABs) with TAM-Tp thin films exhibit high power densities (63.8 mW cm−2 and 111.6 mW cm−2) and long cyclic lifespans (58 h and 600 h).

Oriented Thiophene‐Extended Benzotrithiophene Covalent Organic Framework Thin Films: Directional Electrical Conductivity (Adv. Funct. Mater. 47/2022)

Covalent Organic Frameworks In article number 2205949, Dana Dina Medina, Ralf Thomas Weitz, Timothy Clark and co-workers describe the synthesis of covalent organic frameworks (COFs) based on a thiophene-extended benzotrithiophene (BTT) building block. Oriented thin films of the BTT COFs show room-temperature in-plane electrical conductivity of up to 10−4 S m−1 and a trap-dominated charge transport via a hopping mechanism. Moreover, electrical conductivity of the COF films is directional with a strong preference for the in-plane over the out-of-plane direction.

Oriented Thiophene‐Extended Benzotrithiophene Covalent Organic Framework Thin Films: Directional Electrical Conductivity

AbstractThe synthesis of covalent organic frameworks (COFs) based on a novel thiophene‐extended benzotrithiophene (BTT) building block is described, which in combination with triazine‐based amines (1,3,5‐triazine‐2,4,6‐triyl)trianiline (TTA) or (1,3,5‐triazine‐2,4,6‐triyl)tris(([1,1´‐biphenyl]‐4‐amine)) (TTTBA)) affords crystalline, and porous imine‐linked COFs, BTT TTA and BTT TTTBA, with surface areas as high as 932 and 1200 m2 g−1, respectively. Oriented thin films are grown successfully on different substrates, as indicated by grazing incidence diffraction (GID). Room‐temperature in‐plane electrical conductivity of up to 10−4 S m−1 is measured for both COFs. Temperature‐dependent electrical conductivity measurements indicate activation energies of ≈123.3 meV for BTT TTA and ≈137.5 meV for BTT TTTBA and trap‐dominated charge transport via a hopping mechanism for both COFs. Moreover, conductive atomic force microscopy reveals directional and defect‐dominated charge transport in the oriented BTT COF films with a strong preference for the in‐plane direction within the molecular 2D‐planes. Quantum mechanical calculations predict BTT TTTBA to conduct holes and electrons effectively in both in‐plane and out‐of‐plane directions. In‐plane, charge carrier transport is of hopping character where the triazine cores represent the barrier. Out‐of‐plane, a continuous charge‐carrier pathway is calculated that is hampered by an imposed structural defect simulated by a rotated molecular COF layer.

Azo-Branched Covalent Organic Framework Thin Films as Active Separators for Superior Sodium-Sulfur Batteries.

Sodium-Sulfur (Na-S) batteries are outstanding for their ultrahigh capacity, energy density, and low cost, but they suffer from rapid cell capacity decay and short lifespan because of serious polysulfide shuttle and sluggish redox kinetics. Herein, we synthesize thin films of covalent organic frameworks (COFs) with azobenzene side groups branched to the pore walls. The azobenzene branches deliver dual functions: (1) narrow the pore size to the sub-nanometer scale thus inhibiting the polysulfide shuttle effect and (2) act as ion-hopping sites thus promoting the Na+ migration. Consequently, the Na-S battery using the COF thin film as the separator exhibits a high capacity of 1295 mA h g-1 at 0.2 C and an extremely low attenuation rate of 0.036% per cycle over 1000 cycles at 1 C. This work highlights the importance of separator design in upgrading Na-S batteries and demonstrates the possibility of functionalizable framework materials in developing high-performance energy storage systems.

Modulated Synthesis of Self-Standing Covalent Organic Framework Films.

The weak interaction of covalent organic framework (COF) nanoparticles makes the preparation of self-standing COF films difficult. Herein, a modulated strategy for the facile synthesis of self-standing COF films with good crystallinity and tunable thickness is reported. As compared with the non-modulated approach, the modulated strategy changes the COF morphology from nanoparticles to nanofibers, enabling the facile preparation of self-standing COF films with improved mechanical properties. The Young's modulus of the self-standing COF film obtained via the modulated strategy could increase by 26 times. Moreover, self-standing LZU-8 film can be used as a membrane for efficient removal of 99 % mercury ions from aqueous solution. Our results open up a new approach to prepare self-standing COF thin films for practical applications.

Detachable all-carbon-linked 3D covalent organic framework films for semiconductor/COF heterojunctions by continuous flow synthesis

Detachable all-carbon-linked 3D covalent organic framework films for semiconductor/COF heterojunctions by continuous flow synthesis

Electrosynthesis of Ionic Covalent Organic Frameworks for Charge‐Selective Separation of Molecules

Covalent organic frameworks (COFs) have emerged as potent material platforms for engineering advanced membranes to tackle challenging separation demands. However, the synthesis of COF membranes is currently hampered by suboptimal productivity and harsh synthesis conditions, especially for ionic COFs with perdurable charges. Herein, ionic COFs with charged nanochannels are electrically synthesized on conductive supports to rapidly construct composite membranes for charge-selective separations of small molecules. The intrinsic charging nature and strong charge intensity of ionic COFs are demonstrated to collectively dominate the membrane growth. Spontaneous repairing to diminish defects under the applied electric field is observed, in favor of generating well-grown COF membranes. Altering electrosynthetic conditions realizes the precise control over the membrane thickness and thus the separation ability. Electrically synthesized ionic COF membranes exhibit remarkable molecular separation performances due to their relatively ordered and charged nanochannels. With these charge-selective pathways, the membranes enable the efficient sieving of charged and neutral molecules with analogous structures. This study reveals an electrical route to synthesizing COF thin films, and showcases the great potential of ionic nanochannels in precise separation based on charge selectivity.

Solvent-Free and in Situ Synthesis of Three-Dimensional Covalent Organic Frameworks Thin Films on Zn Anodes for Zn–Air Batteries

Solvent-Free and in Situ Synthesis of Three-Dimensional Covalent Organic Frameworks Thin Films on Zn Anodes for Zn–Air Batteries

Crystallizing Sub 10 nm Covalent Organic Framework Thin Films via Interfacial-Residual Concomitance.

Synthesis of covalent organic framework (COF) thin films on different supports with high crystallinity and porosity is crucial for their potential applications. We have designed a new synchronized methodology, residual crystallization (RC), to synthesize sub 10 nm COF thin films. These residual crystallized COF thin films showcase high surface area, crystallinity, and conductivity at room temperature. We have used interfacial crystallization (IC) as a rate-controlling tool for simultaneous residual crystallization. We have also diversified the methodology of residual crystallization by utilizing two different crystallization pathways: fiber-to-film (F-F) and sphere-to-film (S-F). In both cases, we could obtain continuous COF thin films with high crystallinity and porosity grown on various substrates (the highest surface area of a TpAzo COF thin film being 2093 m2 g-1). Precise control over the crystallization allows the synthesis of macroscopic defect-free sub 10 nm COF thin films with a minimum thickness of ∼1.8 nm. We have synthesized two COF thin films (TpAzo and TpDPP) using F-F and S-F pathways on different supports such as borosilicate glass, FTO, silicon, Cu, metal, and ITO. Also, we have investigated the mechanism of the growth of these thin films on various substrates with different wettability. Further, a hydrophilic support (glass) was used to grow the thin films in situ for four-probe system device fabrication. All residual crystallized COF thin films exhibit outstanding conductivity values. We could obtain a conductivity of 3.7 × 10-2 mS cm-1 for the TpAzo film synthesized by S-F residual crystallization.

Facile fabrication of covalent organic framework composite membranes via interfacial polymerization for enhanced separation and anti-fouling performance

Covalent organic frameworks (COFs) have the advantages of high porosity, uniform and adjustable pore size, as well as superior compatibility with polymer, which are favorable for the production of defect-free films with high flux and excellent separation performance. In this work, TAPB-PDA COF thin films were synthesized by interfacial polymerization of benzaldehyde (PDA) and 1,3,5-tris (4-aminophenyl) benzene (TAPB) on polyethersulfone (PES) substrates with the aid of a catalyst. Different thicknesses of the COF films could be achieved by varying the concentration of the monomers. The TAPB-PDA COF/PES composite membranes exhibited enhanced removal capacities for organic matters compared to the pristine PES membrane, e.g., with the rejections of calcon (molecular weight of 416 g mol-1) and humic acid at 92.3% and 98.0%, respectively. Moreover, after the fouling of model organic pollutants or the filtration of natural surface water, the recovery coefficient of water permeability by hydraulic cleaning was 22–35% higher for the TAPB-PDA COF/PES composite membrane than that of the PES membrane. The improved anti-fouling performance was mainly attributed to the increased membrane surface hydrophilicity benefiting from the hydrophilic nature of the TAPB-PDA COF materials.

Chemically Stable Polyarylether-Based Metallophthalocyanine Frameworks with High Carrier Mobilities for Capacitive Energy Storage.

Covalent organic frameworks (COFs) with efficient charge transport and exceptional chemical stability are emerging as an import class of semiconducting materials for opto-/electronic devices and energy-related applications. However, the limited synthetic chemistry to access such materials and the lack of mechanistic understanding of carrier mobility greatly hinder their practical applications. Herein, we report the synthesis of three chemically stable polyarylether-based metallophthalocyanine COFs (PAE-PcM, M = Cu, Ni, and Co) and facile in situ growth of their thin films on various substrates (i.e., SiO2/Si, ITO, quartz) under solvothermal conditions. We show that PAE-PcM COFs thin films with van der Waals layered structures exhibit p-type semiconducting properties with the intrinsic mobility up to ∼19.4 cm2 V-1 s-1 and 4 orders of magnitude of increase in conductivity for PAE-PcCu film (0.2 S m-1) after iodine doping. Density functional theory calculations reveal that the carrier transport in the framework is anisotropic, with the out-of-plane hole transport along columnar stacked phthalocyanine more favorable. Furthermore, PAE-PcCo shows the redox behavior maximumly contributes ∼88.5% of its capacitance performance, giving rise to a high surface area normalized capacitance of ∼19 μF cm-2. Overall, this work not only offers fundamental understandings of electronic properties of polyarylether-based 2D COFs but also paves the way for their energy-related applications.

Patterning, Transfer, and Tensile Testing of Covalent Organic Framework Films with Nanoscale Thickness

Covalent organic frameworks (COFs) are promising materials for a variety of applications, including membrane-based separations, thin-film electronics, and as separators for electrochemical devices. Robust mechanical properties are critical to these applications, but there are no reliable methods for patterning COFs or producing free-standing thin films for direct mechanical testing. Mechanical testing of COFs has only been performed on films supported by a rigid substrate. Here, we present a method for patterning, transferring, and measuring the tensile properties of free-floating nanoscale COF films. We synthesized COF powders by condensation of 1,3,5-tris(4-aminophenyl)benzene (TAPB) and terephthalaldehyde (PDA) and prepared uniform thin films by spin casting from a mixture of trifluoroacetic acid and water. The COF films were then reactivated to recover crystallinity and patterned by plasma etching through a poly(dimethylsiloxane) (PDMS) mask. The films were transferred to the surface of water, and we performed direct tensile tests. We measured a modulus of approximately 1.4 GPa for TAPB-PDA COF and a fracture strain of 2.5%, which is promising for many applications. This work advances the development of COFs for thin-film applications by demonstrating a simple and generally applicable approach to cast, pattern, and transfer COF thin films and to perform direct mechanical analysis.