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Metal–Organic Framework‐Based Photocatalysis for Solar Fuel Production

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 m...

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Bibliographic Details
Published in:Small methods 2023-01, Vol.7 (1), p.e2201258-n/a
Main Authors: Xiao, Juan‐Ding, Li, Rui, Jiang, Hai‐Long
Format: Article
Language:English
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Summary: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. Metal–organic frameworks (MOFs) have captured widespread attention for application in photocatalysis owing to their semiconductor‐like behavior and unique structural advantages. MOF‐based photocatalysts with readily tailorable structures feature abundant active sites located at metal nodes, organic linkers, and pore space, which have potential for solar fuel production by photocatalytic water splitting, carbon dioxide reduction, and nitrogen fixation reactions.
ISSN:2366-9608
2366-9608
DOI:10.1002/smtd.202201258