Amide‐Engineered Metal–Organic Porous Liquids Toward Enhanced CO 2 Photoreduction Performance
Abstract The development of alternative catalytic systems toward high‐performance CO 2 photoreduction is considered to be a promising approach to address the future energy demand and reduce the CO 2 emissions. However, CO 2 molecules are thermodynamically stable in nature, and thus the adsorption an...
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Published in | Advanced functional materials Vol. 34; no. 19 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.05.2024
|
Online Access | Get full text |
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Summary: | Abstract
The development of alternative catalytic systems toward high‐performance CO
2
photoreduction is considered to be a promising approach to address the future energy demand and reduce the CO
2
emissions. However, CO
2
molecules are thermodynamically stable in nature, and thus the adsorption and activation of CO
2
on the surface of catalysts are the key factors to determine the conversion efficiency. Herein, a porous liquid (NH
2
‐UIO‐66 PL) is demonstrated for efficiently facilitating the adsorption and activation of CO
2
by modification of metal–organic framework (NH
2
‐UIO‐66) with ionic liquid via amide bonds. CdS/NH
2
‐UIO‐66 PL exhibits high‐performance CO
2
‐to‐CO photoreduction with CO yield of 71.37 µmol g
−1
h
−1
and selectivity of 100%. Experiments and theoretical calculations show that the introduced amide moieties not only enriched the electron density at Zr
4+
active sites but also stabilize
*
COOH intermediate. The achievements provide an effective strategy for the development of metal–organic frameworks for energy catalysis. |
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ISSN: | 1616-301X 1616-3028 |
DOI: | 10.1002/adfm.202313695 |