Covalent organic frameworks with high quantum efficiency in sacrificial photocatalytic hydrogen evolution

Organic semiconductors offer a tunable platform for photocatalysis, yet the more difficult exciton dissociation, compared to that in inorganic semiconductors, lowers their photocatalytic activities. In this work, we report that the charge carrier lifetime is dramatically prolonged by incorporating a...

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Bibliographic Details
Main Authors: Li, C. (Author), Li, H. (Author), Liu, J. (Author), Wang, J. (Author), Wu, K. (Author), Yang, Q. (Author)
Format: Article
Language:English
Published: Nature Research 2022
Online Access:View Fulltext in Publisher
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001 10.1038-s41467-022-30035-x
008 220706s2022 CNT 000 0 und d
020 |a 20411723 (ISSN) 
245 1 0 |a Covalent organic frameworks with high quantum efficiency in sacrificial photocatalytic hydrogen evolution 
260 0 |b Nature Research  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1038/s41467-022-30035-x 
520 3 |a Organic semiconductors offer a tunable platform for photocatalysis, yet the more difficult exciton dissociation, compared to that in inorganic semiconductors, lowers their photocatalytic activities. In this work, we report that the charge carrier lifetime is dramatically prolonged by incorporating a suitable donor-acceptor (β-ketene-cyano) pair into a covalent organic framework nanosheet. These nanosheets show an apparent quantum efficiency up to 82.6% at 450 nm using platinum as co-catalyst for photocatalytic H2 evolution. Charge carrier kinetic analysis and femtosecond transient absorption spectroscopy characterizations verify that these modified covalent organic framework nanosheets have intrinsically lower exciton binding energies and longer-lived charge carriers than the corresponding nanosheets without the donor-acceptor unit. This work provides a model for gaining insight into the nature of short-lived active species in polymeric organic photocatalysts. © 2022, The Author(s). 
700 1 0 |a Li, C.  |e author 
700 1 0 |a Li, H.  |e author 
700 1 0 |a Liu, J.  |e author 
700 1 0 |a Wang, J.  |e author 
700 1 0 |a Wu, K.  |e author 
700 1 0 |a Yang, Q.  |e author 
773 |t Nature Communications