journal article·2023-06-07

Trinuclear Fe Clusters for Highly Efficient CO2 Photoreduction

Jixin Li, Kaiyue Ma, Chunguang Li, Zhan Shi, Shouhua Feng

ACS Applied Materials & Interfaces· Volume 15· Issue 22
Publisher page

Abstract

Photocatalytic reduction of CO 2 into valuable chemicals or fuels is considered a promising solution to mitigate the energy crisis. In this work, efficient CO 2 to CO conversion was achieved, accompanied by a class of trinuclear Fe clusters as photocatalysts. Under optimal conditions, the highest catalytic rate could be up to 140.9 μmol/h in 6 h with the assistance of photosensitizers (PS). The trinuclear Fe Clusters can be used as secondary building units to construct Fe-based metal–organic frameworks (MOFs). However, the catalytic activity of Fe-based MOFs is weaker than that of clusters in both the cases of extra PS-assisted MOFs and integrated PS into MOFs. The simpler synthesis, lower cost, and higher catalytic activity make the Fe clusters a better catalyst. Additionally, steady-state fluorescence tests confirmed the transfer of photogenerated electrons from PS to the clusters during the photocatalytic reaction.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: CO2 Reduction Techniques and Catalysts · Advanced Photocatalysis Techniques · Nanocluster Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130012, P. R. China

Funding

Jilin University · Department of Science and Technology of Jilin Province · National Natural Science Foundation of China · Higher Education Discipline Innovation Project

References (42)

Show source-provided references
1. 10.1039/C9CS00163H10.1039/C9CS00163H ↗
2. 10.1021/acs.chemrev.8b0040010.1021/acs.chemrev.8b00400 ↗
3. 10.1038/s41563-018-0033-510.1038/s41563-018-0033-5 ↗
4. 10.1002/adma.20170464910.1002/adma.201704649 ↗
5. 10.1039/C4CS00103F10.1039/C4CS00103F ↗
6. 10.1016/j.cej.2020.12551810.1016/j.cej.2020.125518 ↗
7. 10.1021/acs.inorgchem.0c0194110.1021/acs.inorgchem.0c01941 ↗
8. 10.1002/chem.20190515510.1002/chem.201905155 ↗
9. 10.1039/C8SC03471K10.1039/C8SC03471K ↗
10. 10.1021/acscatal.0c0449510.1021/acscatal.0c04495 ↗
11. 10.1039/D0GC01497D10.1039/D0GC01497D ↗
12. 10.1021/jacs.1c1308110.1021/jacs.1c13081 ↗
13. 10.1021/acscatal.1c0441510.1021/acscatal.1c04415 ↗
14. 10.1002/adma.20170551210.1002/adma.201705512 ↗
15. 10.1039/D1QI00742D10.1039/D1QI00742D ↗
16. 10.1002/anie.20191328410.1002/anie.201913284 ↗
17. 10.1021/cs501169t10.1021/cs501169t ↗
18. 10.1016/j.apcatb.2020.11917310.1016/j.apcatb.2020.119173 ↗
19. 10.1002/anie.20130942610.1002/anie.201309426 ↗
20. 10.1002/anie.20181154510.1002/anie.201811545 ↗
21. 10.1021/acsami.9b1978510.1021/acsami.9b19785 ↗
22. 10.1039/C4CS00097H10.1039/C4CS00097H ↗
23. 10.1021/ja201165c10.1021/ja201165c ↗
24. 10.1021/jacs.8b0361310.1021/jacs.8b03613 ↗
25. 10.1016/S1872-2067(19)63329-210.1016/S1872-2067(19)63329-2 ↗
26. 10.1016/j.apcatb.2020.11868610.1016/j.apcatb.2020.118686 ↗
27. 10.1039/C6TA00429F10.1039/C6TA00429F ↗
28. 10.1007/BF0257831610.1007/BF02578316 ↗
29. 10.1021/acsami.7b0604110.1021/acsami.7b06041 ↗
30. 10.1038/ncomms672310.1038/ncomms6723 ↗
31. 10.1039/D1CY01311D10.1039/D1CY01311D ↗
32. 10.1016/j.joule.2021.01.00110.1016/j.joule.2021.01.001 ↗
33. 10.1021/acs.chemmater.6b0290710.1021/acs.chemmater.6b02907 ↗
34. 10.1038/ncomms697910.1038/ncomms6979 ↗
35. 10.1021/ja507269n10.1021/ja507269n ↗
36. 10.1039/C8TA00154E10.1039/C8TA00154E ↗
37. 10.1021/acscatal.0c0337210.1021/acscatal.0c03372 ↗
38. 10.1021/acscatal.2c0484510.1021/acscatal.2c04845 ↗
39. 10.1016/j.cej.2018.10.03610.1016/j.cej.2018.10.036 ↗
40. 10.1039/C3CS60296F10.1039/C3CS60296F ↗
41. 10.1039/D0EE00900H10.1039/D0EE00900H ↗
42. 10.1002/adma.20160514810.1002/adma.201605148 ↗