Metal-organic frameworks (MOFs) are a class of distinctive porous crystalline materials constructed by metal ions/clusters and organic linkers. Owing to their structural diversity, functional adjustability, and high surface area, different types of MOF-based single metal sites are well exploited, including coordinately unsaturated metal sites from metal nodes and metallolinkers, as well as active metal species immobilized to MOFs. Furthermore, controllable thermal transformation of MOFs can upgrade them to nanomaterials functionalized with active single-atom catalysts (SACs). These unique features of MOFs and their derivatives enable them to serve as a highly versatile platform for catalysis, which has actually been becoming a rapidly developing interdisciplinary research area. In this review, we overview the recent developments of catalysis at single metal sites in MOF-based materials with emphasis on their structures and applications for thermocatalysis, electrocatalysis, and photocatalysis. We also compare the results and summarize the major insights gained from the works in this review, providing the challenges and prospects in this emerging field.

Metal-Organic Framework-Based Catalysts with Single Metal Sites.

Single-atom photocatalysts have shown their compelling potential and arguably become the most active research direction in photocatalysis due to their fascinating strengths in enhancing light-harvesting, charge transfer dynamics, and surface reactions of a photocatalytic system. While numerous comprehensions about the single-atom photocatalysts have recently been amassed, advanced characterization techniques and vital theoretical studies are strengthening our understanding on these fascinating materials, allowing us to forecast their working mechanisms and applications in photocatalysis. In this review, we begin by describing the general background and definition of the single-atom photocatalysts. A brief discussion of the metal-support interactions on the single-atom photocatalysts is then provided. Thereafter, the current available characterization techniques for single-atom photocatalysts are summarized. After having some fundamental understanding on the single-atom photocatalysts, their advantages and applications in photocatalysis are discussed. Finally, we end this review with a look into the remaining challenges and future perspectives of single-atom photocatalysts. We anticipate that this review will provide some inspiration for the future discovery of the single-atom photocatalysts, manifestly stimulating the development in this emerging research area.

Heterogeneous Single-Atom Photocatalysts: Fundamentals and Applications.

Isolated atoms featuring unique reactivity are at the heart of enzymatic and homogeneous catalysts. In contrast, although the concept has long existed, single-atom heterogeneous catalysts (SACs) have only recently gained prominence. Host materials have similar functions to ligands in homogeneous catalysts, determining the stability, local environment, and electronic properties of isolated atoms and thus providing a platform for tailoring heterogeneous catalysts for targeted applications. Within just a decade, we have witnessed many examples of SACs both disrupting diverse fields of heterogeneous catalysis with their distinctive reactivity and substantially enriching our understanding of molecular processes on surfaces. To date, the term SAC mostly refers to late transition metal-based systems, but numerous examples exist in which isolated atoms of other elements play key catalytic roles. This review provides a compositional encyclopedia of SACs, celebrating the 10th anniversary of the introduction of this term. By defining single-atom catalysis in the broadest sense, we explore the full elemental diversity, joining different areas across the whole periodic table, and discussing historical milestones and recent developments. In particular, we examine the coordination structures and associated properties accessed through distinct single-atom-host combinations and relate them to their main applications in thermo-, electro-, and photocatalysis, revealing trends in element-specific evolution, host design, and uses. Finally, we highlight frontiers in the field, including multimetallic SACs, atom proximity control, and possible applications for multistep and cascade reactions, identifying challenges, and propose directions for future development in this flourishing field.

Single-Atom Catalysts across the Periodic Table.

The general synthesis and control of the coordination environment of single-atom catalysts (SACs) remains a great challenge. Herein, a general host-guest cooperative protection strategy has been developed to construct SACs by introducing polypyrrole (PPy) into a bimetallic metal-organic framework. As an example, the introduction of Mg2+ in MgNi-MOF-74 extends the distance between adjacent Ni atoms; the PPy guests serve as N source to stabilize the isolated Ni atoms during pyrolysis. As a result, a series of single-atom Ni catalysts (named NiSA -Nx -C) with different N coordination numbers have been fabricated by controlling the pyrolysis temperature. Significantly, the NiSA -N2 -C catalyst, with the lowest N coordination number, achieves high CO Faradaic efficiency (98 %) and turnover frequency (1622 h-1 ), far superior to those of NiSA -N3 -C and NiSA -N4 -C, in electrocatalytic CO2 reduction. Theoretical calculations reveal that the low N coordination number of single-atom Ni sites in NiSA -N2 -C is favorable to the formation of COOH* intermediate and thus accounts for its superior activity.

Regulating the Coordination Environment of MOF‑Templated Single‑Atom Nickel Electrocatalysts for Boosting CO 2 Reduction

Atomically dispersed metal catalysts (ADCs), as an emerging class of heterogeneous catalysts, have been widely investigated during the past two decades. The atomic dispersion nature of the catalyti...

Surface Coordination Chemistry of Atomically Dispersed Metal Catalysts.

A surfactant-stabilized coordination strategy is used to make two-dimensional (2D) single-atom catalysts (SACs) with an ultrahigh Pt loading of 12.0 wt %, by assembly of pre-formed single Pt atom coordinated porphyrin precursors into free-standing metal-organic framework (MOF) nanosheets with an ultrathin thickness of 2.4±0.9 nm. This is the first example of 2D MOF-based SACs. Remarkably, the 2D SACs exhibit a record-high photocatalytic H2 evolution rate of 11 320 μmol g-1  h-1 via water splitting under visible light irradiation (λ>420 nm) compared with those of reported MOF-based photocatalysts. Moreover, the MOF nanosheets can be readily drop-casted onto solid substrates, forming thin films while still retaining their photocatalytic activity, which is highly desirable for practical solar H2 production.

Ultrathin Metal-Organic Framework Nanosheets with Ultrahigh Loading of Single Pt Atoms for Efficient Visible-Light-Driven Photocatalytic H 2 Evolution

Developing “green” catalytic systems with desirable performance such as good water solubility, recyclability, and switchability is a great challenge. Here, to address this challenge, we extend the ...

https://www.chinesechemsoc.org/doi/pdf/10.31635/ccschem.020.202000486

Single-Metal-Atom Polymeric Unimolecular Micelles for Switchable Photocatalytic H2 Evolution

Poly(ionic liquid)-based polymer composites as high-performance solid-state electrolytes: benefiting from nanophase separation and alternating polymer architecture.

Quan Zuo

Papers

Ultrathin Metal-Organic Framework Nanosheets with Ultrahigh Loading of Single Pt Atoms for Efficient Visible-Light-Driven Photocatalytic H 2 Evolution

Single-Metal-Atom Polymeric Unimolecular Micelles for Switchable Photocatalytic H2 Evolution

Poly(ionic liquid)-based polymer composites as high-performance solid-state electrolytes: benefiting from nanophase separation and alternating polymer architecture.

A supramolecular single-site photocatalyst based on multi-to-one Förster resonance energy transfer.

High-loading single cobalt atoms on ultrathin MOF nanosheets for efficient photocatalytic CO_2 reduction