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Cited by 386

The DOI matches its Crossref record; 56 of the 56 references it cites were found in a registry or an index.

Carbon dioxide capture and conversion by an acid-base resistant metal-organic framework

Open access
Liang, Linfeng, Liu, Caiping, Jiang, Feilong, Chen, Qihui, Zhang, Linjie, Xue, Hui, Jiang, Hai-Long, Qian, Jinjie, Yuan, Daqiang, Hong, Maochun·2017·Nature Communications
DOI 10.1038/s41467-017-01166-3
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Abstract

Considering the rapid increase of CO 2 emission, especially from power plants, there is a constant need for materials which can effectively eliminate post-combustion CO 2 (the main component: CO 2/N 2 = 15/85). Here, we show the design and synthesis of a Cu(II) metal-organic framework (FJI-H14) with a high density of active sites, which displays unusual acid and base stability and high volumetric uptake (171 cm 3 cm−3) of CO 2 under ambient conditions (298 K, 1 atm), making it a potential adsorbing agent for post-combustion CO 2. Moreover, CO 2 from simulated post-combustion flue gas can be smoothly converted into corresponding cyclic carbonates by the FJI-H14 catalyst. Such high CO 2 adsorption capacity and moderate catalytic activity may result from the synergistic effect of multiple active sites.

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Metadata

Authors
Liang, L., Liu, C., Jiang, F., Chen, Q., Zhang, L., Xue, H., Jiang, H.-L., Qian, J., Yuan, D., & Hong, M.
Venue
Nature Communications
Publisher
Springer Science and Business Media LLC
Published
2017-11-01
Volume
8
Issue
1
Pages
1233-1233
ISSN
2041-1723 (ISSN-L)
DOI
10.1038/s41467-017-01166-3
OpenAlex
W2765856370
Cited by
386
References
56
FWCI
33.33
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Carbon dioxide capture and conversion by an acid-base resistant metal-organic framework. https://app.cochat.ai/papers/10.1038/s41467-017-01166-3
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Liang, L., Liu, C., Jiang, F., Chen, Q., Zhang, L., Xue, H., Jiang, H.-L., Qian, J., Yuan, D., & Hong, M. (2017). Carbon dioxide capture and conversion by an acid-base resistant metal-organic framework. Nature Communications. https://doi.org/10.1038/s41467-017-01166-3

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