Hollow Functional Materials Derived from Metal–Organic Frameworks: Synthetic Strategies,Conversion Mechanisms,and Electrochemical Applications

Hollow materials derived from metal–organic frameworks (MOFs), by virtue of their controllable configuration, composition, porosity, and specific surface area, have shown fascinating physicochemical properties and widespread applications, especially in electrochemical energy storage and conversion. Here, the recent advances in the controllable synthesis are discussed, mainly focusing on the conversion mechanisms from MOFs to hollow‐structured materials. The synthetic strategies of MOF‐derived hollow‐structured materials are broadly sorted into two categories: the controllable synthesis of hollow MOFs and subsequent pyrolysis into functional materials, and the controllable conversion of solid MOFs with predesigned composition and morphology into hollow structures. Based on the formation processes of hollow MOFs and the conversion processes of solid MOFs, the synthetic strategies are further conceptually grouped into six categories: template‐mediated assembly, stepped dissolution–regrowth, selective chemical etching, interfacial ion exchange, heterogeneous contraction, and self‐catalytic pyrolysis. By analyzing and discussing 14 types of reaction processes in detail, a systematic mechanism of conversion from MOFs to hollow‐structured materials is exhibited. Afterward, the applications of these hollow structures as electrode materials for lithium‐ion batteries, hybrid supercapacitors, and electrocatalysis are presented. Finally, an outlook on the emergent challenges and future developments in terms of their controllable fabrications and electrochemical applications is further discussed.     

Hydrogen Storage in Metal–Organic Frameworks

Metal–organic frameworks (MOFs) are highly attractive materials because of their ultra‐high surface areas, simple preparation approaches, designable structures, and potential applications. In the past several years, MOFs have attracted worldwide attention in the area of hydrogen energy, particularly for hydrogen storage. In this review, the recent progress of hydrogen storage in MOFs is presented. The relationships between hydrogen capacities and structures of MOFs are evaluated, with emphasis on the roles of surface area and pore size. The interaction mechanism between H₂ and MOFs is discussed. The challenges to obtain a high hydrogen capacity at ambient temperature are explored.     

2D Metal–Organic Frameworks as Multifunctional Materials in Heterogeneous Catalysis and Electro/Photocatalysis

Metal–organic frameworks (MOFs) are composed of particles with 3D geometry and are currently among the most widely studied heterogeneous catalysts. To further increase their activity, one of the recent trends is to develop related 2D materials with a high aspect ratio derived from a large lateral size and a small thickness. Here, the use of these 2D MOFs as catalysts, electrocatalysts, and photocatalysts is summarized, illustrating the advantages of these 2D materials compared to analogous 3D MOFs. The state of the art is summarized in tables and, when possible, pertinent turnover number (TON) and frequency (TOF) values. This enhanced activity of 2D MOFs derives from the accessibility of the active sites, the presence of a higher density of defects, and exchangeable coordination positions around the MOFs, as well as from their ability to form thin films on electrodes or surfaces. The importance of providing convincing evidence of the stability of 2D MOFs under reaction conditions and general characterization data of the used 2D material after catalysis is highlighted. In the last part, views regarding challenges in the field and new developments that can be expected are presented.     

Semiconductor Metal–Organic Frameworks: Future Low‐Bandgap Materials

Metal–organic frameworks (MOFs) with low density, high porosity, and easy tunability of functionality and structural properties, represent potential candidates for use as semiconductor materials. The rapid development of the semiconductor industry and the continuous miniaturization of feature sizes of integrated circuits toward the nanometer (nm) scale require novel semiconductor materials instead of traditional materials like silicon, germanium, and gallium arsenide etc. MOFs with advantageous properties of both the inorganic and the organic components promise to serve as the next generation of semiconductor materials for the microelectronics industry with the potential to be extremely stable, cheap, and mechanically flexible. Here, a perspective of recent research is provided, regarding the semiconducting properties of MOFs, bandgap studies, and their potential in microelectronic devices.     

Explosives in the Cage: Metal–Organic Frameworks for High‐Energy Materials Sensing and Desensitization

An overview of the current status of coordination polymers and metal–organic frameworks (MOFs) pertaining to the field of energetic materials is provided. The explosive applications of MOFs are discussed from two aspects: one for detection of explosives, and the other for explosive desensitization. By virtue of their adjustable pore/cage sizes, high surface area, tunable functional sites, and rich host–guest chemistry, MOFs have emerged as promising candidates for both explosive sensing and desensitization. The challenges and perspectives in these two areas are thoroughly discussed, and the processing methods for practical applications are also discussed briefly.     

Hydrophobic Metal–Organic Frameworks

Metal–organic frameworks (MOFs) have diverse potential applications in catalysis, gas storage, separation, and drug delivery because of their nanoscale periodicity, permanent porosity, channel functionalization, and structural diversity. Despite these promising properties, the inherent structural features of even some of the best‐performing MOFs make them moisture‐sensitive and unstable in aqueous media, limiting their practical usefulness. This problem could be overcome by developing stable hydrophobic MOFs whose chemical composition is tuned to ensure that their metal–ligand bonds persist even in the presence of moisture and water. However, the design and fabrication of such hydrophobic MOFs pose a significant challenge. Reported syntheses of hydrophobic MOFs are critically summarized, highlighting issues relating to their design, characterization, and practical use. First, wetting of hydrophobic materials is introduced and the four main strategies for synthesizing hydrophobic MOFs are discussed. Afterward, critical challenges in quantifying the wettability of these hydrophobic porous surfaces and solutions to these challenges are discussed. Finally, the reported uses of hydrophobic MOFs in practical applications such as hydrocarbon storage/separation and their use in separating oil spills from water are summarized. Finally, the state of the art is summarized and promising future developments of hydrophobic MOFs are highlighted.     

Multifunctional Metal–Organic Frameworks for Photocatalysis

Metal–organic frameworks (MOFs) have attracted significant research attention in diverse areas due to their unique physical and chemical characteristics that allow their innovative application in various research fields. Recently, the application of MOFs in heterogeneous photocatalysis for water splitting, CO₂ reduction, and organic transformation have emerged, aiming at providing alternative solutions to address the world‐wide energy and environmental problems by taking advantage of the unique porous structure together with ample physicochemical properties of the metal centers and organic ligands in MOFs. In this review, the latest progress in MOF‐involved solar‐to‐chemical energy conversion reactions are summarized according to their different roles in the photoredox chemical systems, e.g., photocatalysts, co‐catalysts, and hosts. The achieved progress and existing problems are evaluated and proposed, and the opportunities and challenges of MOFs and their related materials for their advanced development in photocatalysis are discussed and anticipated.     

Hybrid Crystals Comprising Metal–Organic Frameworks and Functional Particles: Synthesis and Applications

Hybrid crystals containing encapsulated functional species exhibit promising novel physical and chemical properties. The realization of many properties critically depends on the selection of suitable functional species for incorporation, the rational control of the crystallinity of the host materials, and the manipulation of the distribution of the encapsulated species; only a few hybrid crystals achieve this. Here, a novel synthetic method enables the encapsulation of functional species within crystalline metal–organic frameworks (MOFs). Various kinds of single‐crystalline MOFs with incorporated particles are presented. The encapsulated particles can be distributed in a controllable manner, and the hybrid crystals are applied to the heterogeneous catalysis of the reduction of nitroarenes. These findings suggest a general approach for the construction of MOF materials with potential applications; by combining species and MOFs with suitable functionalities, new properties—not possible by other means—may arise.     

Casting Nanoporous Platinum in Metal–Organic Frameworks

Nanocasting based on porous templates is a powerful strategy in accessing materials and structures that are difficult to form by bottom‐up syntheses in a controlled fashion. A facile synthetic strategy for casting ordered, nanoporous platinum (NP‐Pt) networks with a high degree of control by using metal–organic frameworks (MOFs) as templates is reported here. The Pt precursor is first infiltrated into zirconium‐based MOFs and subsequently transformed to 3D metallic networks via a chemical reduction process. It is demonstrated that the dimensions and topologies of the cast NP‐Pt networks can be accurately controlled by using different MOFs as templates. The Brunauer–Emmett–Teller surface areas of the NP‐Pt networks are estimated to be >100 m² g^?1 and they exhibit excellent catalytic activities in the methanol electrooxidation reaction (MEOR). This new methodology presents an attractive route to prepare well‐defined nanoporous materials for diverse applications ranging from energy to sensing and biotechnology.     

Integration of Biomolecules with Metal–Organic Frameworks

Owing to the progressive development of metal–organic‐frameworks (MOFs) synthetic processes and considerable potential applications in last decade, integrating biomolecules into MOFs has recently gain considerable attention. Biomolecules, including lipids, oligopeptides, nucleic acids, and proteins have been readily incorporated into MOF systems via versatile formulation methods. The formed biomolecule‐MOF hybrid structures have shown promising prospects in various fields, such as antitumor treatment, gene delivery, biomolecular sensing, and nanomotor device. By optimizing biomolecule integration methods while overcoming existing challenges, biomolecule‐integrated MOF platforms are very promising to generate more practical applications.     

On the Existence of Excitonic Signatures in the Optical Response of Metal–Organic Frameworks: Comment on “van der Waals Metal–Organic Framework as an Excitonic Material for Advanced Photonics”

In a recent experimental paper, it was claimed that pronounced excitonic signatures are observed in optical response of Zn‐based metal–organic frameworks (MOFs) at room temperature. Performing ab initio modelling, it is demonstrated that an alternative interpretation based on single‐electron optical transitions between narrow π‐bands in the system of aromatic rings of the ligand is far more plausible. Although these results do not rule the possibility of exciton formation in MOFs out completely, they show that extreme caution should be taken in attributing the features in photoabsorption spectra alone to excitons, and additional proof, such as data on long‐distance energy transfer, is necessary.     

Hollow Metal–Organic‐Framework Micro/Nanostructures and their Derivatives: Emerging Multifunctional Materials

Hollow metal–organic framework (MOF) micro/nanostructures and their derivatives are attracting a great amount of research interest in recent years because their hierarchical porous structures not only provide abundant, easily accessed metal sites but also endow 3D channels for rapid mass transport. As a result, they demonstrate significant advantages in many applications including catalysis, gas sensors, batteries, supercapacitors, and so on. Nevertheless, studies on hollow MOFs and their derivatives are still at the beginning of this field, and the relationship between their structures and application performances is not yet reviewed comprehensively. Herein, the synthetic strategies and practical applications of hollow micro/nanostructured MOFs and their derivatives are summarized, and their corresponding prospects are also discussed.     

Enhancing Oxygen Evolution Reaction through Modulating Electronic Structure of Trimetallic Electrocatalysts Derived from Metal–Organic Frameworks

The construction of efficient, durable, and non‐noble metal electrocatalysts for oxygen evolution reaction (OER) is of great value but challenging. Herein, a facile method is developed to synthesize a series of trimetallic (W/Co/Fe) metal–organic frameworks (MOFs)‐derived carbon nanoflakes (CNF) with various Fe content, and an Fe‐dependent volcano‐type plot can be drawn out for WCoFe_x ‐CNF. The optimized WCoFe_0.3‐CNF (when the feed ratio of Fe/Co is 0.3) demonstrates superior electrocatalytic performance with a low overpotential of only 254 mV@10 mA cm^?2 and excellent durability of 100 h. Further researches show that appropriate amount of iron doping can regulate the electronic structure, resulting in a favorable synergistic environment. This method may stimulate the exploration of electrocatalysts by utilizing MOFs as precursors while realizing electronic modulation by multimetal doping.     

Heterogeneous Catalysis in Zeolites,Mesoporous Silica,and Metal–Organic Frameworks

Crystalline porous materials are important in the development of catalytic systems with high scientific and industrial impact. Zeolites, ordered mesoporous silica, and metal–organic frameworks (MOFs) are three types of porous materials that can be used as heterogeneous catalysts. This review focuses on a comparison of the catalytic activities of zeolites, mesoporous silica, and MOFs. In the first part of the review, the distinctive properties of these porous materials relevant to catalysis are discussed, and the corresponding catalytic reactions are highlighted. In the second part, the catalytic behaviors of zeolites, mesoporous silica, and MOFs in four types of general organic reactions (acid, base, oxidation, and hydrogenation) are compared. The advantages and disadvantages of each porous material for catalytic reactions are summarized. Conclusions and prospects for future development of these porous materials in this field are provided in the last section. This review aims to highlight recent research advancements in zeolites, ordered mesoporous silica, and MOFs for heterogeneous catalysis, and inspire further studies in this rapidly developing field.     

Separation of Chemical Reaction Intermediates by Metal–Organic Frameworks

HPLC columns custom‐packed with metal–organic framework (MOF) materials are used for the separation of four small intermediates and byproducts found in the commercial synthesis of an important active pharmaceutical ingredient in methanol. In particular, two closely related amines can be separated in the methanol reaction medium using MOFs, but not with traditional C18 columns using an optimized aqueous mobile phase. Infrared spectroscopy, UV–vis spectroscopy, X‐ray diffraction, and thermogravimetric analysis are used in combination with molecular dynamic simulations to study the separation mechanism for the best‐performing MOF materials. It is found that separation with ZIF‐8 is the result of an interplay between the thermodynamic driving force for solute adsorption within the framework pores and the kinetics of solute diffusion into the material pores, while the separation with Basolite F300 is achieved because of the specific interactions between the solutes and Fe³⁺ sites. This work, and the exceptional ability to tailor the porous properties of MOF materials, points to prospects for using MOF materials for the continuous separation and synthesis of pharmaceutical compounds.