MOF‐Confined Sub‐2 nm Atomically Ordered Intermetallic PdZn Nanoparticles as High‐Performance Catalysts for Selective Hydrogenation of Acetylene

Controllable synthesis of ultrasmall atomically ordered intermetallic nanoparticles is a challenging task, owing to the high temperature commonly required for the formation of intermetallic phases. Here, a metal–organic framework (MOF)‐confined co‐reduction strategy is developed for the preparation of sub‐2 nm intermetallic PdZn nanoparticles, by employing the well‐defined porous structures of calcinated ZIF‐8 (ZIF‐8C) and an in situ co‐reduction therein. HAADF‐STEM, HRTEM, and EDS characterizations reveal the homogeneous dispersion of these sub‐2 nm intermetallic PdZn nanoparticles within the ZIF‐8C frameworks. XRD, XPS, and EXAFS measurements further confirm the atomically ordered intermetallic phase nature of these sub‐2 nm PdZn nanoparticles. Selective hydrogenation of acetylene evaluation results show the excellent catalytic properties of the sub‐2 nm intermetallic PdZn, which result from the energetically more favorable path for acetylene hydrogenation and ethylene desorption over the ultrasmall particles than over larger‐sized intermetallic PdZn as revealed by density functional theory (DFT) calculations. Moreover, this protocol is also extendable for the preparation of sub‐2 nm intermetallic PtZn nanoparticles and is expected to provide a novel methodology in synthesizing ultrasmall atomically ordered intermetallic nanomaterials by rationally functionalizing MOFs.     

Kinetic‐Controlled Formation of Bimetallic Metal–Organic Framework Hybrid Structures

Heterometallic metal–organic frameworks (MOFs) are constructed from two or more kinds of metal ions, while still remaining their original topologies. Due to distinct reaction kinetics during MOF formation, partial distribution of different metals within a single MOF crystal can lead to sophisticated heterogeneous nanostructures. Here, this study reports an investigation of reaction kinetics for different metal ions in a bimetallic MOF system, the ZIF‐8/67 (M(2‐mIM)₂, M = Zn for ZIF‐8, and Co for ZIF‐67, 2‐mIM = 2‐methylimidazole), by in situ optical method. Distinct kinetics of the two metals forming single‐component MOFs are revealed, and when both Co and Zn ions are present in the starting solution, homogeneous distributions of the two metals are only achieved at high Co/Zn ratio, while at low Co/Zn ratio concentration gradient from Co‐rich cores to Zn‐rich shells is observed. Further, by adding the two metals in sequence, more sophisticated structures are achieved. Specifically, when Co²⁺ is added first, ZIF‐67@ZIF‐8/67 core–shell nanocrystals are achieved with tunable core/shell thickness ratio depending on the time intervals; while when Zn²⁺ is added first, only agglomerates of irregular shape form due to the weak nucleation ability of Zn²⁺.     

Ternary Alloys Encapsulated within Different MOFs via a Self‐Sacrificing Template Process: A Potential Platform for the Investigation of Size‐Selective Catalytic Performances

Functional nanoparticles encapsulated within metal–organic frameworks (MOFs) as an emerging class of composite materials attract increasing attention owing to their enhanced or even novel properties caused by the synergistic effect between the two functional materials. However, there is still no ideal composite structure as platform to systematically analyze and evaluate the relation between the enhanced catalytic performance of composites and the structure of MOF shells. In this work, taking RhCoNi ternary alloy nanoflowers, for example, first the RhCoNi@MOF composite catalysts sheathed with different structured MOFs via a facile self‐sacrificing template process are successfully fabricated. The structure type of MOF shells is easily adjustable by using different organic molecules as etchant and coordination reagent (e.g., 2,5‐dihydroxyterephthalic acid or 2‐methylimidazole), which can dissolve out the Co or Ni element in the alloy template in a targeted manner, thereby producing ZIF‐67(Co) or MOF‐74(Ni) shells accordingly. With the difference between the two MOF shells in the aperture sizes, the as‐prepared two RhCoNi@MOF composites preform distinct size selectivity during the alkene hydrogenation. This work would help us to get more comprehensive understanding of the intrinsic role of MOFs behind the enhanced catalytic performance of nanoparticle@MOF composites.     

Shape‐Defined Hollow Structural Co‐MOF‐74 and Metal Nanoparticles@Co‐MOF‐74 Composite through a Transformation Strategy for Enhanced Photocatalysis Performance

In recent years, metal–organic frameworks (MOFs) have received extensive interest because of the diversity of their composition, structure, and function. To promote the MOFs' function and performance, the construction of hollow structural metal–organic frameworks and nanoparticle–MOF composites is significantly effective but remains a considerable challenge. In this article, a transformation strategy is developed to synthesize hollow structural Co‐MOF‐74 by solvothermal transformation of ZIF‐67. These Co‐MOF‐74 particles exhibit a double‐layer hollow shell structure without remarkable shape change compared to original ZIF‐67 particles. The formation of hollow structure stemmed from the density difference of Co between ZIF‐67 and Co‐MOF‐74. By this strategy, hollow structural Co‐MOF‐74 with different sizes and shapes are obtained from corresponding ZIF‐67, and metal nanoparticles@Co‐MOF‐74 is synthesized by corresponding nanoparticles@Co‐ZIF‐67. To verify the structural advantages of hollow structural Co‐MOF‐74 and Ag nanoparticles@Co‐MOF‐74, photocatalytic CO₂ reduction is used as a model reaction. Conventionally synthesized Co‐MOF‐74 (MOF‐74‐C), hollow structural Co‐MOF‐74 synthesized by transformation method (MOF‐74‐T) and Ag nanoparticles@Co‐MOF‐74 (AgNPs@MOF‐74) are used as cocatalysts in this reaction. As a result, the cocatalytic activity of MOF‐74‐T and AgNPs@MOF‐74 is 1.8 times and 3.8 times that of MOF‐74‐C, respectively.     

A Hydrangea‐Like Superstructure of Open Carbon Cages with Hierarchical Porosity and Highly Active Metal Sites

Carbon micro‐/nanocages have attracted great attention owing to their wide potential applications. Herein, a self‐templated strategy is presented for the synthesis of a hydrangea‐like superstructure of open carbon cages through morphology‐controlled thermal transformation of core@shell metal–organic frameworks (MOFs). Direct pyrolysis of core@shell zinc (Zn)@cobalt (Co)‐MOFs produces well‐defined open‐wall nitrogen‐doped carbon cages. By introducing guest iron (Fe) ions into the core@shell MOF precursor, the open carbon cages are self‐assembled into a hydrangea‐like 3D superstructure interconnected by carbon nanotubes, which are grown in situ on the Fe–Co alloy nanoparticles formed during the pyrolysis of Fe‐introduced Zn@Co‐MOFs. Taking advantage of such hierarchically porous superstructures with excellent accessibility, synergetic effects between the Fe and the Co, and the presence of catalytically active sites of both metal nanoparticles and metal–N_x species, this superstructure of open carbon cages exhibits efficient bifunctional catalysis for both oxygen evolution reaction and oxygen reduction reaction, achieving a great performance in Zn–air batteries.     

Co9S8 Nanoparticles‐Embedded N/S‐Codoped Carbon Nanofibers Derived from Metal–Organic Framework‐Wrapped CdS Nanowires for Efficient Oxygen Evolution Reaction

Metal–organic frameworks (MOFs) with tunable compositions and morphologies are recognized as efficient self‐sacrificial templates to achieve function‐oriented nanostructured materials. Moreover, it is urgently needed to develop highly efficient noble metal‐free oxygen evolution reaction (OER) electrocatalysts to accelerate the development of overall water splitting green energy conversion systems. Herein, a facile and cost‐efficient strategy to synthesize Co₉S₈ nanoparticles‐embedded N/S‐codoped carbon nanofibers (Co₉S₈/NSCNFs) as highly active OER catalyst is developed. The hybrid precursor of core–shell ZIF‐wrapped CdS nanowires is first prepared and then leads to the formation of uniformly dispersed Co₉S₈/N, S‐codoped carbon nanocomposites through a one‐step calcination reaction. The optimal Co₉S₈/NSCNFs‐850 is demonstrated to possess excellent electrocatalytic performance for OER in 1.0 m KOH solution, affording a low overpotential of 302 mV to reach the current density of 10 mA cm^?2, a small Tafel slope of 54 mV dec^?1, and superior long‐term stability for 1000 cyclic voltammetry cycles. The favorable results raise a concept of exploring more MOF‐based nanohybrids as precursors to induce the synthesis of novel porous nanomaterials as non‐noble‐metal electrocatalysts for sustainable energy conversion.     

Integration of Metal Nanoparticles into Metal–Organic Frameworks for Composite Catalysts: Design and Synthetic Strategy

Metal–organic frameworks (MOFs) are constructed by periodically alternate metal ions with organic ligands, which offer structural diversity and a wide range of interesting properties as an attractive classification of crystalline porous materials. Integration of MOFs with other size‐limited functional centers can supply new multifunctional composites, which exhibit both the properties of the components and new characteristics due to the combination of MOFs with the selected loadings. In recent years, integration of metal/metal oxide nanoparticles (MNPs) into MOFs to form the composite catalysts has attracted considerable attention due to the superior performance. In this review, the latest studies and up‐to‐date developments on the design and synthetic strategy of new MNP@MOF composite catalysts are specifically highlighted. Both the achievements and problems are evaluated and proposed, and the opportunities and challenges of MNP@MOF composite catalysts are discussed.     

Hybridization of MOFs and COFs: A New Strategy for Construction of MOF@COF Core–Shell Hybrid Materials

The exploration of new porous hybrid materials is of great importance because of their unique properties and promising applications in separation of materials, catalysis, etc. Herein, for the first time, by integration of metal–organic frameworks (MOFs) and covalent organic frameworks (COFs), a new type of MOF@COF core–shell hybrid material, i.e., NH₂‐MIL‐68@TPA‐COF, with high crystallinity and hierarchical pore structure, is synthesized. As a proof‐of‐concept application, the obtained NH₂‐MIL‐68@TPA‐COF hybrid material is used as an effective visible‐light‐driven photocatalyst for the degradation of rhodamine B. The synthetic strategy in this study opens up a new avenue for the construction of other MOF–COF hybrid materials, which could have various promising applications.     

Coordination‐Induced Interlinked Covalent‐ and Metal–Organic‐Framework Hybrids for Enhanced Lithium Storage

Covalent organic frameworks (COF) or metal–organic frameworks have attracted significant attention for various applications due to their intriguing tunable micro/mesopores and composition/functionality control. Herein, a coordination‐induced interlinked hybrid of imine‐based covalent organic frameworks and Mn‐based metal–organic frameworks (COF/Mn‐MOF) based on the Mn? N bond is reported. The effective molecular‐level coordination‐induced compositing of COF and MOF endows the hybrid with unique flower‐like microsphere morphology and superior lithium‐storage performances that originate from activated Mn centers and the aromatic benzene ring. In addition, hollow or core–shell MnS trapped in N and S codoped carbon (MnS@NS‐C‐g and MnS@NS‐C‐l) are also derived from the COF/Mn‐MOF hybrid and they exhibit good lithium‐storage properties. The design strategy of COF–MOF hybrid can shed light on the promising hybridization on porous organic framework composites with molecular‐level structural adjustment, nano/microsized morphology design, and property optimization.     

Metal–Organic Framework (MOF)‐Based Drug/Cargo Delivery and Cancer Therapy

Metal–organic frameworks (MOFs)—an emerging class of hybrid porous materials built from metal ions or clusters bridged by organic linkers—have attracted increasing attention in recent years. The superior properties of MOFs, such as well‐defined pore aperture, tailorable composition and structure, tunable size, versatile functionality, high agent loading, and improved biocompatibility, make them promising candidates as drug delivery hosts. Furthermore, scientists have made remarkable achievements in the field of nanomedical applications of MOFs, owing to their facile synthesis on the nanoscale and alternative functionalization via inclusion and surface chemistry. A brief introduction to the applications of MOFs in controlled drug/cargo delivery and cancer therapy that have been reported in recent years is provided here.     

Surface‐Mounted Metal–Organic Frameworks: Crystalline and Porous Molecular Assemblies for Fundamental Insights and Advanced Applications

Metal–organic frameworks (MOFs) are crystalline coordination polymers, assembled from inorganic nodes connected by organic linker molecules. An enormous surface area, huge compositional variety, regular structure, and favorable mechanical properties are among their outstanding properties. Monolithic MOF thin films, i.e., surface‐mounted metal–organic frameworks (SURMOFs), with high degree of structural order and adjustable defect density, can be prepared on solid substrates using layer‐by‐layer techniques. Recent studies where SURMOFs served as model systems for quantitative studies of molecular interactions in porous media, including diffusion, are reviewed. Moreover, SURMOFs are ideally suited for the incorporation of photoactive molecules as well as to study electrical transport through crystalline molecular assemblies. Recent work has demonstrated that the realization of crystalline chromophore assemblies via the SURMOF approach allows the study of fundamental aspects of exciton transport, exciton channeling, and photon upconversion at internal interfaces in organic semiconductor materials. Due to their crystalline nature, MOF materials are well suited for quantitative comparisons with theoretical results; especially, since defect densities and types can be characterized and varied in a straightforward fashion. The active role of these nanoporous films in advanced applications, like for remote‐controlled release of molecules, membranes with photoswitchable selectivity, and ion‐conductors with adjustable conductivity, are also emphasized.     

Strategies for Improving the Functionality of Zeolitic Imidazolate Frameworks: Tailoring Nanoarchitectures for Functional Applications

Zeolitic imidazolate frameworks (ZIFs), a subclass of metal–organic frameworks (MOFs) built with tetrahedral metal ions and imidazolates, offer permanent porosity and high thermal and chemical stabilities. While ZIFs possess some attractive physical and chemical properties, it remains important to enhance their functionality for practical application. Here, an overview of the extensive strategies which have been developed to improve the functionality of ZIFs is provided, including linker modifications, functional hybridization of ZIFs via the encapsulation of guest species (such as metal and metal oxide nanoparticles and biomolecules) into ZIFs, and hybridization with polymeric matrices to form mixed matrix membranes for industrial gas and liquid separations. Furthermore, the developed strategies for achieving size and shape control of ZIF nanocrystals are considered, which are important for optimizing the textural characteristics as well as the functional performance of ZIFs and their derived materials/hybrids. Moreover, the recent trends of using ZIFs as templates for the derivation of nanoporous hybrid materials, including carbon/metal, carbon/oxide, carbon/sulfide, and carbon/phosphide hybrids, are discussed. Finally, some perspectives on the potential future research directions and applications for ZIFs and ZIF‐derived materials are offered.     

State‐of‐the‐Art Advances and Challenges of Iron‐Based Metal Organic Frameworks from Attractive Features,Synthesis to Multifunctional Applications

Metal organic frameworks (MOFs), as an original kind of organic–inorganic porous material, are constructed with metal centers and organic linkers via a coordination complexation reaction. Among uncountable MOF materials, iron‐containing metal organic frameworks (Fe‐MOFs) have excellent potential in practical applications owing to their many fascinating properties, such as diverse structure types, low toxicity, preferable stability, and tailored functionality. Here, recent research progresses of Fe‐MOFs in attractive features, synthesis, and multifunctional applications are described. Fe‐MOFs with porosity and tailored functionality are discussed according to the design of building blocks. Four types of synthetic methods including solvothermal, hydrothermal, microwave, and dry gel conversion synthesis are illustrated. Finally, the applications of Fe‐MOFs in Li‐ion batteries, sensors, gas storage, separation in gas and liquid phases, and catalysis are elucidated, focusing on the mechanism. The aim is to provide prospects for extending Fe‐MOFs in more practical applications.     

Mechanistic insight into gold nanorod transformation in nanoscale confinement of ZIF-8

Core-shell hybrid nanomaterials have shown new properties and functions that are not attainable by their single counterparts.Nanoscale confinement effect by porous inorganic shells in the hybrid nanostructures plays an important role for chemical transformation of the core nanoparticles.However,metal-organic frameworks(MOFs)have been rarely applied for understanding mechanical insight into such nanoscale phenomena in confinement,although MOFs would provide a variety of properties for the confining environment than other inorganic shells such as silica and zeolite.Here,we examine chemical transformation of a gold nanorod core enclosed by a zeolitic imidazolate framework(ZIF)through chemical etching and regrowth,followed by quantitative analysis in the core dimension and curvature.We find the nanorod core shows template-effective behavior in its morphological transformation.In the etching event,the nanorod core is spherically carved from its tips.The regrowth on the spherically etched core inside the ZIF gives rise toformation of a raspberry-like branched nanostructure in contrast to the growth of an octahedral shape in bulk condition.We attribute the shell-directed regrowth to void space generated at the interfaces between the etched core and the ZIF shell,intercrystalline gaps in mult-domain ZIF shells,and local structural deformation from the acidic reaction conditions.     

Well‐Defined Metal Nanoparticles@Covalent Organic Framework Yolk–Shell Nanocages by ZIF‐8 Template as Catalytic Nanoreactors

Yolk–shell nanoreactors have received considerable interest for use in catalysis. However, the controlled synthesis of continuous crystalline shells without imperfections or cracks remains challenging. Here, a strategy for the synthesis of yolk–shell metal nanoparticles@covalent organic framework (MNPs@COF) nanoreactors by using MNPs@ZIF‐8 core–shell nanostructures as a self‐template is designed and developed. The COF shell is formed through an amorphous‐to‐crystalline transformation process of a polyimine shell in a mildly acidic solution, while the ZIF‐8 is etched in situ, generating a void space between the MNPs core and the COF shell. With the protection of the COF shell, multiple ligand‐free MNPs are confined inside of the hollow nanocages. Importantly, the synthetic strategy can be generalized to engineer the functions and properties of the designed yolk–shell nanocages by varying the structure of the COF shell and/or the composition of the core MNPs. Representative Pd@H‐TpPa yolk–shell nanocages with active Pd NP cores and permeable TpPa shells exhibit high catalytic activity and stability in the reduction of 4‐nitrophenol by NaBH₄ at room temperature.     

Multifunctional Nanoparticle@MOF Core–Shell Nanostructures

Controllable integration of inorganic nanoparticles (NPs) and metal–organic frameworks (MOFs) is leading to the creation of many new multifunctional materials. In this Research News, an emerging type of core–shell nanostructure, in which the inorganic NP cores are encapsulated by the MOF shells, is briefly introduced. Unique functions originating from the property synergies of different types of inorganic NP cores and MOF shells are highlighted, and insight into their future development is suggested. It is highly expected that this Research News could arouse research enthusiasm on such NP@MOF core–shell nanostructures, which have great application potential in devices, energy, the environment, and medicine.     

Construction of Hierarchical Metal–Organic Frameworks by Competitive Coordination Strategy for Highly Efficient CO2 Conversion

Hierarchical porosity and functionalization help to fully make use of metal–organic frameworks (MOFs) for their diverse applications. Herein, a simple strategy is reported to construct hierarchically porous MOFs through a competitive coordination method using tetrafluoroborate (M(BF₄)_x, where M is metal site) as both functional sites and etching agents. The resulting MOFs have in situ formed defect‐mesopores and functional sites without sacrificing their structure stability. The formation mechanism of the defect‐mesopores is elucidated by a combination of experimental and first‐principles calculation method, indicating the general feasibility of this new approach. Compared with the original microporous counterparts, the new hierarchical MOFs exhibit superior adsorption for the bulky dye molecules and catalytic performance for the CO₂ conversion attributed to their specific hierarchical pore structures.     

Thermal Instability Induced Oriented 2D Pores for Enhanced Sodium Storage

Hierarchical porous structures are highly desired for various applications. However, it is still challenging to obtain such materials with tunable architectures. Here, this paper reports hierarchical nanomaterials with oriented 2D pores by taking advantages of thermally instable bonds in vanadium‐based metal–organic frameworks (MOFs). High‐temperature calcination of these MOFs accompanied by the loss of coordinated water molecules and other components enables the formation of orderly slit‐like 2D pores in vanadium oxide/porous carbon nanorods (VO_x/PCs). This unique combination leads to an increase of the reactive surface area. In addition, optimized VO_x/PCs demonstrate high‐rate capability and ultralong cycling life for sodium storage. The assembled full cells also show high capacity and cycling stability. This report provides an effective strategy for producing MOFs‐derived composites with hierarchical porous architectures for energy storage.     

Thermally Stable Metal‐Organic Framework‐Templated Synthesis of Hierarchically Porous Metal Sulfides: Enhanced Photocatalytic Hydrogen Production

Porous nanostructured materials are demonstrated to be very promising in catalysis due to their well accessible active sites. Thermally stable metal‐organic frameworks (MOFs) as hard templates are successfully utilized to afford porous metal oxides and subsequently metal sulfides by a nanocasting method. The resultant metal oxides/sulfides show considerable Brunauer–Emmett–Teller (BET) surface areas, by partially inheriting the pore character of MOF templates. Preliminary investigation on the obtained hierarchically porous CdS for water splitting, as a proof of concept, demonstrates its much higher activity than both corresponding bulk and nanosized counterparts, under visible light irradiation. Given the structural diversity and tailorability of MOFs, such synthetic approach may open an avenue to the synthesis of advanced porous materials for functional applications.     

Improved Capacitive Energy Storage Nanocomposites at High Temperature Utilizing Ultralow Loading of Bimetallic MOF

It is urgent to develop high-temperature dielectrics with high energy density and high energy efficiency for next-generation capacitor demands. Metal-organic frameworks (MOFs) have been widely used due to their structural diversity and functionally adaptable properties. Doping of metal nodes in MOFs is an effective strategy to change the band gap and band edge positions of the original MOFs, which helps to improve their ability to bind charges as traps. In this work, the incorporation of ultralow loading (<1.5 wt%) of novel bimetallic MOFs (ZIF 8–67) into the polyetherimide (PEI) polymer matrix is exhibited. With the addition of ZIF 8–67, the breakdown strength and energy storage capacity of ZIF 8–67/PEI nanocomposites are significantly improved, especially at high temperatures (200 °C). For example, the energy densitiy of the 0.5 wt% ZIF 8–67/PEI nanocomposite is up to 2.96 J cm⁻³, with an efficiency (η) > 90% at 150 °C. At 200 °C, the discharge energy density of 0.25 wt% ZIF 8–67/PEI nanocomposites can still reach 1.84 J cm⁻³ with a η > 90%, which is nine times higher than that of pure PEI (0.21 J cm⁻³) under the same conditions, and it is the largest improvement compared with the previous reports.