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Despite the prevalent of hexagonal, tetragonal, and triangular pore structures in two-dimensional covalent organic frameworks (2D COFs), the pentagonal pores remain conspicuously absent. We herein present the Cairo pentagonal tessellated COFs, achieved through precisely chosen geometry and metrics of the linkers, resulting in unprecedented mcm topology. In each pentagonal structure, porphyrin units create four uniform sides around 15.5 Å with 90° angles, while tetrabiphenyl unit establish a bottom edge about 11.6 Å with 120° angles, aligning precisely with the criteria of Cairo Pentagon. According to the narrow bandgap and strong near-infrared (NIR) absorbance, as-synthesized COFs exhibit the efficient singlet oxygen (1O2) generation and photothermal conversion, resulting in NIR photothermal combined photodynamic therapy to guide cancer cell apoptosis. Mechanistic studies reveal that the good 1O2 production capability upregulates intracellular lipid peroxidation, leading to glutathione depletion, low expression of glutathione peroxidase 4, and induction of ferroptosis. The implementation of pentagonal Cairo tessellations in this work provides a promising strategy for diversifying COFs with new topologies, along with multimodal NIR phototherapy.
Assuntos
Apoptose , Raios Infravermelhos , Fotoquimioterapia , Oxigênio Singlete , Humanos , Oxigênio Singlete/metabolismo , Oxigênio Singlete/química , Fotoquimioterapia/métodos , Estruturas Metalorgânicas/química , Porfirinas/química , Animais , Peroxidação de Lipídeos , Linhagem Celular Tumoral , Ferroptose , Fototerapia/métodos , Camundongos , Glutationa/química , Glutationa/metabolismo , Fármacos Fotossensibilizantes/química , Neoplasias/terapia , Neoplasias/metabolismoRESUMO
The design of three-dimensional covalent organic frameworks (3D COFs) using linear and trigonal linkers remains challenging due to the difficulty in achieving a specific non-planar spatial arrangement with low-connectivity building units. Here, we report the novel 3D COFs with linear and trigonal linkers, termed TMB-COFs, exhibiting srs topology. The steric hindrance provides an additional force to alter the torsion angles of peripheral triangular units, guiding the linear unit to connect with the trigonal unit into 3D srs frameworks, rather than the more commonly observed two-dimensional (2D) hcb structures. Furthermore, we comprehensively examined the hydrogen peroxide photocatalytic production capacity of the TMB-COFs in comparison with analogous 2D COFs. The experimental results and DFT calculations demonstrate a significant enhancement in photocatalytic hydrogen peroxide production efficacy through framework regulation. This work emphasizes the steric configuration using low connectivity building units, offering a fresh perspective on the design and application of 3D COFs.
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Covalent organic frameworks (COFs) are an innovative class of crystalline porous polymers composed of light elements such as C, N, O, etc., linked by covalent bonds. The distinctive properties of COFs, including designable building blocks, large specific surface area, tunable pore size, abundant active sites, and remarkable stability, have led their widespread applications in electrocatalysis. In recent years, COF-based electrocatalysts have made remarkable progress in various electrocatalytic fields, including the hydrogen evolution reaction, oxygen evolution reaction, oxygen reduction reaction, nitrogen reduction reaction, nitrate reduction reaction, and carbon dioxide reduction reaction. This review begins with an introduction to the design and synthesis strategies employed for COF-based electrocatalysts. These strategies include heteroatom doping, metalation of COF and building monomers, encapsulation of active sites within COF pores, and the development of COF-based derived materials. Subsequently, a systematic overview of the recent advancements in the application of COF-based catalysts in electrocatalysis is presented. Finally, the review discusses the main challenges and outlines possible avenues for the future development of COF-based electrocatalysts.
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Designing artificial photocatalysts for CO2 reduction is challenging, mainly due to the intrinsic difficulty of making multiple functional units cooperate efficiently. Herein, three-dimensional metal covalent organic frameworks (3D MCOFs) were employed as an innovative platform to integrate a strong Ru(ii) light-harvesting unit, an active Re(i) catalytic center, and an efficient charge separation configuration for photocatalysis. The photosensitive moiety was precisely stabilized into the covalent skeleton by using a rational-designed Ru(ii) complex as one of the building units, while the Re(i) center was linked via a shared bridging ligand with an Ru(ii) center, opening an effective pathway for their electronic interaction. Remarkably, the as-synthesized MCOF exhibited impressive CO2 photoreduction activity with a CO generation rate as high as 1840 µmol g-1 h-1 and 97.7% selectivity. The femtosecond transient absorption spectroscopy combined with theoretical calculations uncovered the fast charge-transfer dynamics occurring between the photoactive and catalytic centers, providing a comprehensive understanding of the photocatalytic mechanism. This work offers in-depth insight into the design of MCOF-based photocatalysts for solar energy utilization.
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Constructing artificial photocatalysts with panchromatic solar energy utilization remains an appealing challenge. Herein, two complementary photosensitizers, [Ru(bpy)3]2+ (bpy = 2,2'-bipyridine) and porphyrin dyes, have been cosensitized in metal covalent organic frameworks (MCOFs), resulting in the MCOFs with strong light absorption covering the full visible spectrum. Under panchromatic light irradiation, the cosensitized MCOFs exhibited remarkable photocatalytic H2 evolution with an optimum rate of up to 33.02 mmol g-1 h-1. Even when exposed to deep-red light (λ = 700 ± 10 nm), a commendable H2 production (0.79 mmol g-1 h-1) was still obtained. Theoretical calculation demonstrated that the [Ru(bpy)3]2+ and porphyrin modules in our MCOFs have a synergistic effect to trigger an interesting dual-channel photosensitization pathway for efficient light-harvesting and energy conversion. This work highlights the potential of combining multiple PSs in MCOFs for panchromatic photocatalysis.
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Multi-shelled hollow metal-organic frameworks (MH-MOFs) are highly promising as electrode materials due to their impressive surface area and efficient mass transfer capabilities. However, the fabrication of MH-MOFs has remained a formidable challenge. In this study, two types of double-shelled open hollow Prussian blue analogues, one with divalent iron (DHPBA-Fe(II)) and the other with trivalent iron (DHPBA-Fe(III)), through an innovative inner-outer growth strategy are successfully developed. The growth mechanism is found to involve lattice matching growth and ligand exchange processes. Subsequently, DHPBA-Fe(II) and DHPBA-Fe(III) are employed as cathodes in aqueous Zn-ion batteries. Significantly, DHPBA-Fe(II) demonstrated exceptional performance, exhibiting a capacity of 92.5 mAh g-1 at 1 A g-1, and maintaining remarkable stability over an astounding 10 000 cycles. This research is poised to catalyze further exploration into the fabrication techniques of MH-MOFs and offer fresh insights into the intricate interplay between electronic structure and battery performance.
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The water oxidation reaction plays an important role in clean energy conversion, utilization, and storage, but mimicking the oxygen-evolving complex of photosystem II for designing active and stable water oxidation catalysts (WOCs) is still an appealing challenge. Here, we innovatively engineered a molecular ruthenium WOC as a metal complex building unit to construct a series of three-dimensional metal covalent organic frameworks (3D MCOFs) for realizing efficient oxidation catalysis. The resultant MCOFs possessed rare 3D interlocking structures with inclined interpenetration of two-dimensional covalent rhombic nets, and the Ru sites were periodically arranged in the crystalline porous frameworks. Impressively, these MCOFs showed excellent performance towards water oxidation (the O2 evolution rate is as high as 2830 nmol g-1 s-1) via the water nucleophilic attack pathway. Besides, the MCOFs were also reactive for oxidizing organic substrates. This work highlights the potential of MCOFs as a designable platform in integrating molecular catalysts for various applications.
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Non-platinum noble metals are highly desirable for the development of highly active, stable oxygen reduction reaction (ORR) electrocatalysts for fuel cells and metal-air batteries. However, how to improve the utilization of non-platinum noble metals is an urgent issue. Herein, a highly efficient catalyst for ORR was prepared through homogeneous loading of Pd precursors by a domain-limited method in a three-dimensional covalent organic framework (COF) followed by pyrolysis. The morphology of the Pd nanoparticles (Pd NPs) was well maintained after carbonization, which was attributed to the rigid structure of the 3D COF. Thanks to the uniform distribution of Pd NPs in the carbon, the catalyst exhibited a remarkable half-wave potential of 0.906â V and a Tafel slope of 70â mV dec-1 in 0.1â M KOH, surpassing the commercial Pt/C catalyst (0.863â V and 75â mV dec-1 ). Furthermore, a maximum power density of 144.0â mW cm-2 was achieved at 252â mA cm-2 , which was significantly higher than the control battery (105.1â mW cm-2 ). This work not only provides a simple strategy for in-situ preparation of highly dispersible metal catalysts in COFs, but also offers new insights into the ORR electrocatalysis.
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Humidity is one of the most important indicators affecting human health. Here, a pair of covalent organic frameworks (COFs) of positional isomers (p-COF and o-COF) for indoor humidity regulation is reported. Although p-COF and o-COF have the same sql topology and pore size, they exhibit different water adsorption behaviors due to the subtle differences in water adsorption sites. Particularly, o-COF exhibits a steep adsorption isotherm in the range of 45-65% RH with a hysteresis loop, which is perfectly suitable for indoor humidity regulation. In the laboratory experiment, when the humidity of the external environment is 20-75% RH, o-COF can control the humidity of the room in the range of 45-60% RH. o-COF has shown great potential as a dual humidification/dehumidification adsorbent for indoor humidity regulation.
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Glycerol oxidation reaction can be substituted for oxygen evolution reaction for more efficient hydrogen production due to its lower thermodynamic potential. Herein, a series of NiCo hydroxide nanosheets containing abundant Ni3+ species and surface ligands were synthesized by in-situ structural transformation of bimetallic organic frameworks in alkaline media for efficient glycerol oxidation reaction. It is found that the incorporation of Co ions increases the content of the Ni3+ species, and that the Ni/Co ratio of 1.0 lead to the optimal catalytic performance. The oxalate-modified nickel-cobalt hydroxide with the optimized Ni/Co ratio can deliver a current density of 10 mA cm-2 at 1.26 V vs. RHE (reversible hydrogen electrode), and reaches its maximum selectivity and Faradaic efficiency at 1.30 V vs. RHE. A high selectivity of 82.9% and a Faradaic efficiency of 91.0% are achieved. The high catalytic activity can be mainly attributed to the abundant Ni3+ species and surface carboxyl groups.
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Dual-atom catalysts (DAC) are deemed as promising electrocatalysts due to the abundant active sites and adjustable electronic structure, but the fabrication of well-defined DAC is still full of challenges. Herein, bonded Fe dual-atom catalysts (Fe2 DAC) with Fe2 N6 C8 O2 configuration were developed through one-step carbonization of a preorganized covalent organic framework with bimetallic Fe chelation sites (Fe2 COF). The transition from Fe2 COF to Fe2 DAC involved the dissociation of the nanoparticles and the capture of atoms by carbon defects. Benefitting from the optimized d-band center and enhanced adsorption of OOH* intermediates, Fe2 DAC exhibited outstanding oxygen reduction activity with a half-wave potential of 0.898â V vs. RHE. This work will guide more fabrication of dual-atom and even cluster catalysts from preorganized COF in the future.
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Nickel-iron oxides are competitive electrocatalysts for oxygen evolution reaction, but their practical applications are restricted by the less-than-desirable intrinsic activity and working stability. To tackle the challenge, surface coordination chemistry is applied to the nickel-iron oxides through a complex-assisted in-situ crystal growth strategy. The ethylenediaminetetraacetate (EDTA) coordinated NixFe3-xO4 (NixFe3-xO4-EDTA) is prepared by a simple one-pot hydrothermal process. The coordinated EDTA molecules can deeply alter the surface coordination structure of the NixFe3-xO4. The NixFe3-xO4-EDTA demonstrates outstanding intrinsic activity towards oxygen evolution reaction, requiring only a small overpotential of 180 mV to reach 10 mA cm-2 in 1.0 M KOH. Moreover, the NixFe3-xO4-EDTA exhibits extremely stable long-term working stability. Density functional theory calculations show that the highly enhanced intrinsic activity is attributed to the surface coordinated EDTA-induced favorable electronic structure and coordination environment, which tunes the adsorption strength of the intermediates and optimizes the energetics of the elementary steps, while the high stability is ascribed to the strong coordination ability of EDTA.
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NiOOH has been considered as the active center for urea oxidation reaction (UOR), but it remains challenging to synthesize high-performance NiOOH-based catalysts. Herein, we realize the synthesis of a high-performance NiOOH-based catalyst through in-situ transformation from the NiMn-based metal-organic framework to NiMnOOH. X-ray photoelectron spectroscopy characterization shows that the Ni3+/Ni2+ ratio in the NiMnOOH is 3.9 times as big as that in the Ni(OH)2, and in-situ Raman characterization further consolidates the presence of the NiOOH species in the NiMnOOH and as well unveils the faciliated Ni2+/Ni3+ redox reaction. The abundant NiOOH species, the markedly facilitated Ni2+/Ni3+ redox reaction and the Ni-Mn synergy contribute to the high intrinsic activity of the NiMnOOH towards UOR. The NiMnOOH exhibits an impressively low onset potential of 1.305 V vs reversible hydrogen electrode (RHE) and requires only a small potential of 1.34 V vs RHE to deliver a current density of 100 mA cm-2 in 1.0 M KOH + 0.33 M urea. In addition, the NiMnOOH catalyst possesses good long-term working stability.
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Applications of urea oxidation reaction (UOR) in various sustainable energy-conversion systems are greatly hindered by its slow kinetics. Herein, we demonstrate an in-situ confined synthesis method that produces amorphous chromium oxide confined Ni/NiO nanoparticles-assembled nanosheets (Ni/NiO@CrOx) with fast reaction kinetics towards UOR. The confinement effect of the in-situ generated CrOx overlay contributes to ultrafine Ni/NiO nanoparticles, bringing about rich Ni/NiO and NiO/CrOx interfaces. In-situ Raman and electrochemical characterization show that both CrOx and metallic Ni can promote the formation of the NiOOH species and the electron transfer, leading to high intrinsic activity and fast reaction kinetics. At 1.40 V vs. reversible hydrogen electrode, the Ni/NiO@CrOx delivers a current density of 275 mA cm-2, which is about 2.6 and 6.1 times as large as those of the NiO@CrOx and NiO, respectively. In addition, the protective effect of the CrOx overlay leads to robust working stability towards UOR. Further, the Ni/NiO@CrOx nanosheets are used as bifunctional catalysts for overall urea splitting, and a small electrolysis cell voltage of 1.44 V is needed to reach the benchmark current density of 10 mA cm-2.
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Atmospheric moisture is a sustainable clean water source that can solve the shortage of fresh water in arid areas. Herein a 2D covalent organic framework (COF-ok) was reported as a promising porous sorbent for solar-driven atmospheric water harvesting. COF-ok with ortho-ketoenamine linkage was extremely stable in harsh environment, including in boiling water, strong acids and bases. Because of the balanced hydrophilic and hydrophobic sites in channels, COF-ok showed a high water uptake of 0.33â g g-1 at a low relative humidity of 34 % featuring a characteristic S-shaped water sorption isotherm with low regeneration temperature (â¼45 °C) and excellent cyclic stability. A laboratory-scale water harvesting system could collect water of 161â g kg-1 under sunlight.
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Estruturas Metalorgânicas , Água , Temperatura Baixa , Laboratórios , PorosidadeRESUMO
Three metal covalent organic frameworks (MCOFs), namely RuCOF-ETTA, RuCOF-TPB and RuCOF-ETTBA, were synthesized by incorporating the photosensitive RuII tris(2,2'-bipyridine) unit into the skeleton. Interestingly, each RuCOF contains three isostructural covalent organic frameworks that interlock together with the RuII centers serving as point of registry. The covalently linked network coupling with uniformly distributed RuII units allowed the RuCOFs to exhibit superior chemical stability, strong light-harvesting ability, and high photocatalytic activity toward hydrogen evolution (20 308â µmol g-1 h-1 ). This work illustrates the potential of developing versatile MCOFs-based photocatalysts from functionalized metal complex building unit and further enriches the MCOFs family.
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Hollow structured metal-organic frameworks (MOFs) and their derivatives are desired in catalysis, energy storage, etc. However, fabrication of novel hollow MOFs and revelation of their formation mechanisms remain challenging. Herein, open hollow 2D MOFs in the form of hexagonal nut are prepared through self-template method, which can be readily scaled up at gram scale in a one-pot preparation. The evolution from the initial superstructure to the final stable MOFs is tracked by wide-angle X-ray scattering, transforming from solid hexagon to open hollow hexagon. More importantly, this protocol can be extended to synthesizing a series of open hollow structured MOFs with sizes ranging from ≈120 to ≈1200 nm. Further, open hollow structured cobalt/N-doped porous carbon composites are realized through conformal transformation of the as-prepared MOFs, which demonstrates promising applications in sustainable energy conversion technologies. This study sheds light on the kinetically controlled synthesis of novel 2D MOFs for their extended utilizations.
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Estruturas Metalorgânicas , Catálise , Cobalto/química , Estruturas Metalorgânicas/química , Conformação Molecular , NozesRESUMO
NiFe alloys are among the most promising electrocatalysts for oxygen evolution reaction (OER). However, a comprehensive study is yet to be done to reveal the surface structure-performance relationship of NiFe alloys. In particular, the role of the ultrathin surface oxide layer, which is unavoidable for pure NiFe alloys, is always neglected. Herein, a series of NiFe alloys with different Ni/Fe ratios are fabricated. It is found that different Ni/Fe ratios lead to significant differences in surface composition and structure of the NiFe alloys, and thus affect their catalytic performance. Then, the oxide/metal interface of the Ni4Fe1 alloy is tailored by adjusting the hydrogenation temperature to further understand the surface structure-activity relationship, and the optimal OER performance is achieved at the oxide/metal interfaces that have suitable surface Fe/Ni ratio and an appropriate amount of oxygen vacancies. In-situ Raman characterization shows that the Ni4Fe1 alloy with well-tailored oxide/metal interface facilitates the formation of active species. Density functional theory calculations demonstrate that the ultrathin surface oxide layers are responsible for the high catalytic activity of the NiFe alloys, and that the quantity of oxygen vacancies in the surface oxides affects the adsorption energy of O* and thus to a great extent determines the catalytic activity.
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Edge sites and interlayer space of NiFe layered double hydroxides (LDHs) play an important role in water oxidation. However, the combined effect of interlayer expansion and partial exfoliation on the catalytic activity is yet to be investigated. Herein, scalable synthesis of partially exfoliated citrate-intercalated NiFe LDHs with tunable interlayer space have been achieved. The effect of citrate concentration on the phase, morphology, surface elemental composition, electronic states of surface metals, and electrochemical properties are comprehensively studied. The unique structure results in improved intrinsic catalytic activity and abundant active edge sites for oxygen evolution reaction. The optimal NiFe LDHs show an overpotential of 225 mV at 10 mA cm-2, which is much smaller than that (â¼305 mV) of the single-layer NiFe LDH nanosheets reported in the literature. The high catalytic activity can be mainly attributed to the combined effect between the enlarged interlayer space and the partial exfoliation/nanosheet thickness. That is, the interlayer space is related to the reaction kinetics/mechanism, while the degree of exfoliation affects the magnitude of the current density at a certain potential.
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The construction of heteroporous covalent organic frameworks (COFs) is still a challenge. Herein, a series of 2D COFs with hexagonal and quadrilateral pores were constructed via in situ salphen or metal salphen formation. Metallized salphen-based COFs can be used as electrocatalysts towards water oxidation with an overpotential of 266 mV at 10 mA cm-2.