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Atomically dispersed metal atoms on supports exhibit distinctive advantages in maximizing atomic utilization, which plays an indispensable role in the fabrication of cost‐effective catalysts. In particular, dual‐atom catalysts (DACs) containing dual active sites not only retain the merits of single‐atom catalysts (SACs), but also introduce diverse interactions between the two adjacent metal atoms, endowing them with superior catalytic performance and a broad range of applications. With the development of DACs, it is important to identify active sites and establish intrinsic catalytic mechanisms relationship. The general characterization methods for DACs are comprehensively summarized here, especially the structural nature of dual active sites is discussed in detail. Subsequently, the representative scientific research efforts in various applications including thermocatalysis, electrocatalysis, and photocatalysis are described, with emphasis on structure‐property relationships. Finally, a summary and some prospects for the future of advanced DACs are presented. [ABSTRACT FROM AUTHOR]

The N‐methylation reaction of amines with methanol via the borrowing‐hydrogen strategy is an important method for the construction of C−N bonds. Compared with other C1 sources, such as toxic formaldehyde or expensive formic acid, methanol is more suitable for N‐methylation reactions due to its eco‐friendliness and low price. Using this strategy, various types N‐methylated products, including biological and pharmaceutical molecules have been prepared. Here, we present a thorough survey of decades of articles showing current developments in N‐methylation reactions with methanol. We discuss homogenous, heterogenous and light‐driven catalytic systems for both N‐methylation and N,N‐dimethylation reactions. This review presents the shortcomings of current developments and provides future development progress in N‐methylation reactions with methanol. [ABSTRACT FROM AUTHOR]

The support is pivotal for stabilizing single metal atoms and contributes to enhance the catalytic activity of single-atom catalysts. With the merits of versatile structures, tailored electronic structure, as well as high stability, manganese oxide octahedral molecular sieve (OMS-2) can be used as an ideal support to immobilize single atoms. Herein, we report a single-atom Pd catalyst (Pd1–OMS-2) that can afford a silane conversion of above 99% with silanol selectivity of over 99% using water as oxidant under mild conditions, outperforming the original OMS-2. The as-synthesized catalyst exhibits great functional group tolerance and good catalyst stability without aggregation after reaction. And the enhanced catalytic activity is attributed to the decoration of atomic Pd and the increase in content of oxygen vacancies. Characterization of Pd1–OMS-2 indicates that the highly dispersed Pd species is trapped into the framework of OMS-2 by substituting Mn ions, which results in the formation of Pd–O bonds with the adjacent O atoms. [ABSTRACT FROM AUTHOR]

Diethyl carbonate (DEC) was synthesized from ethanol and ethyl carbamate (EC) over Mg–Y composite oxides with excellent yield. Mg–Y composite oxide calcined at 450 °C demonstrated excellent catalytic activity and 70.3% yield was obtained. Note that the production capacity of catalysts (PCC) reached 5987 mgDEC gcat−1 h−1 under the optimized conditions, which was far higher than that reported in previous literature reports. Furthermore, other carbamates such as methyl carbamate (MC) and butyl carbamate (BC) could be also successfully converted into the corresponding dialkyl carbonates. The catalyst could be easily recovered four times under identical conditions. The origin of the catalytic performance was studied using various characterization techniques, and the TPD results showed that the MgY-450 catalyst exhibited more accessible moderate and strong basic sites, which was beneficial to expressing excellent catalytic performance. [ABSTRACT FROM AUTHOR]

With the continuous increase in CO2 emissions, primarily from the combustion of coal and oil, the ecosystem faces a significant threat. Therefore, as an effective method to minimize the issue, the Reverse Water Gas Shift (RWGS) reaction which converts CO2 towards CO attracts much attention, is an environmentally‐friendly method to mitigate climate change and lessen dependence on fossil fuels. Nevertheless, the inherent thermodynamic stability and kinetic inertness of CO2 is a big challenge under mild conditions. In addition, it remains another fundamental challenge in RWGS reaction owing to CO selectivity issue caused by CO2 further hydrogenation towards CH4. Up till now, a series of catalysis systems have been developed for CO2 reduction reaction to produce CO. Herein, the research progress of the well‐performed heterogeneous catalysts for the RWGS reaction were summarized, including the catalyst design, catalytic performance and reaction mechanism. This review will provide insights into efficient utilization of CO2 and promote the development of RWGS reaction. [ABSTRACT FROM AUTHOR]

Catalytic conversion of CO2 to valuable products is a promising way to reduce anthropogenic CO2 emission. Herein, a strategy for coupling conversion of CO2 and high‐carbon alkane to CO and gasoline is developed, which is a feasible choice for the combination of CO2 recycling and petroleum refining. The CO2 conversion reaches 2.6% under mild condition (270 °C), and the selectivity of gasoline in the cracking products exceeds 70 wt%. Additionally, the introduction of CO2 improves the selectivity of aromatic hydrocarbons and increases the octane number of gasoline. Mechanism studies indicate that synergistic effect between Brønsted acid centers and Ni sites on the Beta zeolite supported Ni (20 wt%) catalyst (20Ni/β) plays the key role in alkane cracking and CO2 reduction. Notably, 13CO2 isotopic experiments show that the hydrogen produced during the aromatization can be captured by CO2, inhibiting undesired hydrogen transfer pathways and enhanced the yield of aromatics, while CO2 is converted into valuable CO. [ABSTRACT FROM AUTHOR]

With the continuous increase in CO 2 emissions, primarily from the combustion of coal and oil, the ecosystem faces a significant threat. Therefore, as an effective method to minimize the issue, the Reverse Water Gas Shift (RWGS) reaction which converts CO 2 towards CO attracts much attention, is an environmentally-friendly method to mitigate climate change and lessen dependence on fossil fuels. Nevertheless, the inherent thermodynamic stability and kinetic inertness of CO 2 is a big challenge under mild conditions. In addition, it remains another fundamental challenge in RWGS reaction owing to CO selectivity issue caused by CO 2 further hydrogenation towards CH 4 . Up till now, a series of catalysis systems have been developed for CO 2 reduction reaction to produce CO. Herein, the research progress of the well-performed heterogeneous catalysts for the RWGS reaction were summarized, including the catalyst design, catalytic performance and reaction mechanism. This review will provide insights into efficient utilization of CO 2 and promote the development of RWGS reaction., (© 2024 Wiley-VCH GmbH.)