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Perovskite solar cells (PSCs) are usually modified and passivated to improve their performance and stability. The interface modification and bulk doping are the two basic strategies. Fluorine (F)‐containing materials are highly favored because of their unique hydrophobicity and coordination ability. This review discusses the basic characteristics of F, and the basic principles of improving the photovoltaic performance and stability of PSC devices using F‐containing materials. We systematically summarized the latest progress in the application of F‐containing materials to achieve efficient and stable PSCs on several key interface layers. It is believed that this work will afford significant understanding and inspirations toward the future application directions of F‐containing materials in PSCs, and provide profound insights for the development of efficient and stable PSCs. [ABSTRACT FROM AUTHOR]

Organic transformation by light-driven catalysis, especially, photocatalysis and photothermal catalysis, denoted as photo(thermal) catalysis, is an efficient, green, and economical route to produce value-added compounds. In recent years, owing to their diverse structure types, tunable pore sizes, and abundant active sites, metal–organic framework (MOF)-based photo(thermal) catalysis has attracted broad interest in organic transformations. In this review, we provide a comprehensive and systematic overview of MOF-based photo(thermal) catalysis for organic transformations. First, the general mechanisms, unique advantages, and strategies to improve the performance of MOFs in photo(thermal) catalysis are discussed. Then, outstanding examples of organic transformations over MOF-based photo(thermal) catalysis are introduced according to the reaction type. In addition, several representative advanced characterization techniques used for revealing the charge reaction kinetics and reaction intermediates of MOF-based organic transformations by photo(thermal) catalysis are presented. Finally, the prospects and challenges in this field are proposed. This review aims to inspire the rational design and development of MOF-based materials with improved performance in organic transformations by photocatalysis and photothermal catalysis. [ABSTRACT FROM AUTHOR]

Achieving industrial-level current density and pH-universal CO2 reduction using single atom catalysts is a significant but challenging task. In this work, we demonstrate that isolated cobalt–nitrogen sites supported on high-curvature carbon could achieve industrial-level current density and pH-universal CO2 electroreduction to CO. In an H-type cell, the catalyst achieves a remarkable maximum CO faradaic efficiency of 98.2%, while maintaining CO faradaic efficiency above 90% over a wide potential window from −0.4 to −1.4 V vs. RHE. In a gas-diffusion flow cell, the CO faradaic efficiency could reach 98.9%, 96.5% and 98.6% in alkaline, acidic and neutral electrolytes, respectively. Impressively, the CO current density could reach 437, 337 and 367 mA cm−2, exceeding industrial-level current density requirements. In situ characterization studies coupled with theoretical calculations reveal that compared with the planar cobalt–nitrogen structure, the curved cobalt–nitrogen structure could effectively activate CO2, facilitate *COOH formation and inhibit the hydrogen evolution reaction, thus affording high activity, selectivity and pH-universal feasibility. [ABSTRACT FROM AUTHOR]

Hydrogen production from photocatalysis via the usage of multicomponent photocatalysts represents a promising pathway for carbon peaking and carbon neutrality, owing to their structural advantages in dealing with the three crucial processes in photocatalysis, namely, light harvesting, charge transfer, and surface redox reactions. We demonstrate the fabrication of a MOF‐based multicomponent photocatalyst, denoted as semiconductor/MOF/cocatalyst, by a one‐pot electrochemical synthetic route. The as‐fabricated multicomponent photocatalyst has a clean interface among the components, leading to close connections that contribute to high‐quality heterojunction and facilitate photogenerated charge transfer and separation, thereby the efficient hydrogen evolution. The hydrogen production rate of the resultant ZrO2/Zr‐MOF/Pt is 1327 μmol ⋅ g−1 ⋅ h−1, which is much higher than that of ZrO2/Zr‐MOF (15 μmol ⋅ g−1 ⋅ h−1) and pure Zr‐MOF (10.1 μmol ⋅ g−1 ⋅ h−1), as well as the photodeposited‐Pt products ZrO2/Zr‐MOF/PtPD (287 μmol ⋅ g−1 ⋅ h−1) and Zr‐MOF/PtPD (192 μmol ⋅ g−1 ⋅ h−1) obtained by the step‐wise synthetic approach. The work gives a good inspiration for the rational design and construction of MOF‐based multicomponent photocatalysts through the one‐pot electrosynthesis. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) represent a novel class of crystalline inorganic–organic hybrid materials with tunable semiconducting behavior. MOFs have potential for application in photocatalysis to produce sustainable solar fuels, owing to their unique structural advantages (such as clarity and modifiability) that can facilitate a deeper understanding of the structure–activity relationship in photocatalysis. This review takes the photocatalytic active sites as a particular perspective, summarizing the progress of MOF‐based photocatalysis for solar fuel production; mainly including three categories of solar‐chemical conversions, photocatalytic water splitting to hydrogen fuel, photocatalytic carbon dioxide reduction to hydrocarbon fuels, and photocatalytic nitrogen fixation to high‐energy fuel carriers such as ammonia. This review focuses on the types of active sites in MOF‐based photocatalysts and discusses their enhanced activity based on the well‐defined structure of MOFs, offering deep insights into MOF‐based photocatalysis. [ABSTRACT FROM AUTHOR]

Abstract: A wide range of light absorption and rapid electron–hole separation are desired for efficient photocatalysis. Herein, on the basis of a semiconductor‐like metal–organic framework (MOF), a Pt@MOF/Au catalyst with two types of metal–MOF interfaces integrates the surface plasmon resonance excitation of Au nanorods with a Pt‐MOF Schottky junction, which not only extends the light absorption of the MOF from the UV to the visible region but also greatly accelerates charge transfer. The spatial separation of Pt and Au particles by the MOF further steers the formation of charge flow and expedites the charge migration. As a result, the Pt@MOF/Au presents an exceptionally high photocatalytic H2 production rate by water splitting under visible light irradiation, far superior to Pt/MOF/Au, MOF/Au and other counterparts with similar Pt or Au contents, highlighting the important role of each component and the Pt location in the catalyst. [ABSTRACT FROM AUTHOR]

Hydrogen production from photocatalysis via the usage of multicomponent photocatalysts represents a promising pathway for carbon peaking and carbon neutrality, owing to their structural advantages in dealing with the three crucial processes in photocatalysis, namely, light harvesting, charge transfer, and surface redox reactions. We demonstrate the fabrication of a MOF-based multicomponent photocatalyst, denoted as semiconductor/MOF/cocatalyst, by a one-pot electrochemical synthetic route. The as-fabricated multicomponent photocatalyst has a clean interface among the components, leading to close connections that contribute to high-quality heterojunction and facilitate photogenerated charge transfer and separation, thereby the efficient hydrogen evolution. The hydrogen production rate of the resultant ZrO 2 /Zr-MOF/Pt is 1327 μmol ⋅ g -1  ⋅ h -1 , which is much higher than that of ZrO 2 /Zr-MOF (15 μmol ⋅ g -1  ⋅ h -1 ) and pure Zr-MOF (10.1 μmol ⋅ g -1  ⋅ h -1 ), as well as the photodeposited-Pt products ZrO 2 /Zr-MOF/Pt PD (287 μmol ⋅ g -1  ⋅ h -1 ) and Zr-MOF/Pt PD (192 μmol ⋅ g -1  ⋅ h -1 ) obtained by the step-wise synthetic approach. The work gives a good inspiration for the rational design and construction of MOF-based multicomponent photocatalysts through the one-pot electrosynthesis., (© 2024 Wiley-VCH GmbH.)

Electroreduction of carbon dioxide into readily collectable and high-value carbon-based fuels is greatly significant to overcome the energy and environmental crises yet challenging in the development of robust and highly efficient electrocatalysts. Herein, a bismuth (Bi) heterophase electrode with enriched amorphous/crystalline interfaces was fabricated via cathodically in situ transformation of Bi-based metal-phenolic complexes (Bi-tannic acid, Bi-TA). Compared with amorphous or crystalline Bi catalyst, the amorphous/crystalline structure Bi leads to significantly enhanced performance for CO 2 electroreduction. In a liquid-phase H-type cell, the Faraday efficiency (FE) of formate formation is over 90% in a wide potential range from -0.8 to -1.3 V, demonstrating a high selectivity toward formate. Moreover, in a flow cell, a large current density reaching 600 mA cm -2 can further be rendered for formate production. Theoretical calculations indicate that the amorphous/crystalline Bi heterophase interface exhibits a favorable adsorption of CO 2 and lower energy barriers for the rate-determining step compared with the crystalline Bi counterparts, thus accelerating the reaction process. This work paves the way for the rational design of advanced heterointerface catalysts for CO 2 reduction.