Cerium Metal–Organic Framework Incorporating Quinoline Sulfonic Acid for Photocatalytic Carbon Dioxide Reduction
Source abstract
Abstract
Cerium metal–organic frameworks (Ce-MOFs) have attracted extensive attention due to their potential in photocatalytic applications. However, Ce-MOFs constructed with organic carboxylic acids as ligands typically exhibit wide band gaps, which limit their utilization in the visible-light region. This work proposes a strategy to design visible-light-active Ce-MOFs by employing quinoline sulfonic acid as a ligand. The synthesized compound ( 1-Ce ) features a high surface area, open Ce metal sites, and large-sized 1D channels. Benefiting from ligand-to-metal charge transfer, 1-Ce demonstrates good visible light absorption. Additionally, the chelating coordination of nitrogen and oxygen atoms endows 1-Ce with excellent chemical stability. Owing to its abundant metal sites, high porosity, and visible light responsiveness, 1-Ce exhibits outstanding photocatalytic activity for CO 2 reduction under visible light, achieving a CO production rate of 138 μmol·g –1 ·h –1 ─surpassing previously reported Ce-MOF photocatalysts.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Advanced Photocatalysis Techniques · Covalent Organic Framework Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry
Fuzhou University
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter
Chinese Academy of Sciences
Fujian College
University of Chinese Academy of Sciences
Funding
National Natural Science Foundation of China
References (39)
Show source-provided references
1. 10.1002/adma.20200441410.1002/adma.202004414 ↗
2. 10.1002/adma.20170430310.1002/adma.201704303 ↗
3. 10.1016/j.ccr.2020.21354310.1016/j.ccr.2020.213543 ↗
4. 10.1016/j.ccr.2023.21512110.1016/j.ccr.2023.215121 ↗
5. 10.1002/smll.20230273810.1002/smll.202302738 ↗
6. 10.1021/jacs.0c1154610.1021/jacs.0c11546 ↗
7. 10.1016/j.ccr.2020.21362010.1016/j.ccr.2020.213620 ↗
8. 10.1016/j.progpolymsci.2015.04.00810.1016/j.progpolymsci.2015.04.008 ↗
9. 10.14102/j.cnki.0254-5861.2022-013810.14102/j.cnki.0254-5861.2022-0138 ↗
10. 10.1016/j.cattod.2020.12.03810.1016/j.cattod.2020.12.038 ↗
11. 10.1039/D0CS00920B10.1039/D0CS00920B ↗
12. 10.1002/smll.20220768710.1002/smll.202207687 ↗
13. 10.1039/D0DT02813D10.1039/D0DT02813D ↗
14. 10.1016/j.cej.2024.15824010.1016/j.cej.2024.158240 ↗
15. 10.1016/j.ccr.2024.21640510.1016/j.ccr.2024.216405 ↗
16. 10.1021/acsmaterialslett.1c0079710.1021/acsmaterialslett.1c00797 ↗
17. 10.1021/acsmaterialslett.3c0123610.1021/acsmaterialslett.3c01236 ↗
18. 10.1039/D2QI01443B10.1039/D2QI01443B ↗
19. 10.1039/D3QI02645K10.1039/D3QI02645K ↗
20. 10.1007/s12034-020-02225-010.1007/s12034-020-02225-0 ↗
21. 10.1016/j.inoche.2023.11079910.1016/j.inoche.2023.110799 ↗
22. 10.1002/smll.20230965610.1002/smll.202309656 ↗
23. 10.1016/j.jssc.2025.12521010.1016/j.jssc.2025.125210 ↗
24. 10.1002/aoc.761610.1002/aoc.7616 ↗
25. 10.1021/acsami.2c1838910.1021/acsami.2c18389 ↗
26. 10.1021/jacs.8b0361310.1021/jacs.8b03613 ↗
27. 10.1016/j.jallcom.2022.16364910.1016/j.jallcom.2022.163649 ↗
28. 10.1021/acsami.1c0749610.1021/acsami.1c07496 ↗
29. 10.1039/D0CC04116E10.1039/D0CC04116E ↗
30. 10.1016/j.ccr.2020.21361510.1016/j.ccr.2020.213615 ↗
31. 10.1039/D4QI00436A10.1039/D4QI00436A ↗
32. 10.1039/D2TA08921A10.1039/D2TA08921A ↗
33. 10.1021/acs.cgd.3c0015110.1021/acs.cgd.3c00151 ↗
34. 10.1021/acsmaterialslett.3c0086110.1021/acsmaterialslett.3c00861 ↗
35. 10.1002/adma.20170511210.1002/adma.201705112 ↗
36. 10.1016/j.cej.2021.12996810.1016/j.cej.2021.129968 ↗
37. 10.1002/adma.20170366310.1002/adma.201703663 ↗
38. 10.1016/j.seppur.2023.12599410.1016/j.seppur.2023.125994 ↗
39. 10.1002/adma.20170737710.1002/adma.201707377 ↗