Ultrasmall La2O3 Nanoparticles Supported on Cu2O/Copper Foam for CO2 Energization
Source abstract
Abstract
Electrochemical CO 2 energization represents a promising strategy to mitigate its emission and promote resourceful utilization. The production of alcohols offers a sustainable pathway for converting CO 2 into value-added chemicals, which is often hindered by low selectivity and high overpotential. In this work, a class of ultrasmall La 2 O 3 nanoparticle-modified Cu 2 O-based catalyst has been synthesized in situ on a copper foam substrate through a simple hydrothermal method. The optimized catalyst demonstrated a high ethanol Faradaic efficiency of 51.7% at −1.0 V versus the reversible hydrogen electrode (RHE); simultaneously, syngas (CO/H 2 ) was generated with Faradaic efficiencies of 28.27% for CO and 4.8% for H 2 . This product distribution characteristic enables efficient separation and utilization of both liquid (ethanol) and gaseous (syngas) products. This study highlights the pivotal role of rare earth elements in enhancing CO 2 RR efficiency by stabilizing reaction intermediates for facilitating C–C coupling. Furthermore, it presents a scalable and cost-effective approach for CO 2 energization, paving the way for sustainable green energy production and carbon resource management.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: CO2 Reduction Techniques and Catalysts · Catalytic Processes in Materials Science · Catalysis and Oxidation Reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Tianjin Key Laboratory of Organic Solar Cells and Photochemical Conversion, School of Chemistry and Chemical Engineering
Tianjin University of Technology
Funding
Natural Science Foundation of Tianjin Municipality · National Natural Science Foundation of China
References (37)
Show source-provided references
1. 10.1126/science.aav350610.1126/science.aav3506 ↗
2. 10.1002/adma.20180425710.1002/adma.201804257 ↗
3. 10.1126/science.aad499810.1126/science.aad4998 ↗
4. 10.1002/anie.20200061710.1002/anie.202000617 ↗
5. 10.1002/anie.20220926810.1002/anie.202209268 ↗
6. 10.1021/acscatal.8b0157310.1021/acscatal.8b01573 ↗
7. 10.1021/ja00250a04410.1021/ja00250a044 ↗
8. 10.1039/ft990860268310.1039/ft9908602683 ↗
9. 10.1038/s41467-022-31427-910.1038/s41467-022-31427-9 ↗
10. 10.1016/j.xcrp.2022.10094910.1016/j.xcrp.2022.100949 ↗
11. 10.1021/acscatal.3c0379710.1021/acscatal.3c03797 ↗
12. 10.1021/jacs.3c0897410.1021/jacs.3c08974 ↗
13. 10.1002/anie.20231562110.1002/anie.202315621 ↗
14. 10.1039/C9TA03611C10.1039/C9TA03611C ↗
15. 10.1021/acsmaterialslett.2c0092210.1021/acsmaterialslett.2c00922 ↗
16. 10.1021/acsenergylett.3c0269310.1021/acsenergylett.3c02693 ↗
17. 10.1002/cey2.58810.1002/cey2.588 ↗
18. 10.1016/j.cej.2025.16015510.1016/j.cej.2025.160155 ↗
19. 10.1021/jacs.3c0046710.1021/jacs.3c00467 ↗
20. 10.1002/adma.20240064010.1002/adma.202400640 ↗
21. 10.1002/adma.20220599410.1002/adma.202205994 ↗
22. 10.1039/D2RA02753D10.1039/D2RA02753D ↗
23. 10.1007/s12274-022-4234-510.1007/s12274-022-4234-5 ↗
24. 10.1016/j.apcatb.2024.12483910.1016/j.apcatb.2024.124839 ↗
25. 10.1126/sciadv.abl491510.1126/sciadv.abl4915 ↗
26. 10.1039/D2EE01710E10.1039/D2EE01710E ↗
27. 10.1002/adfm.20231108710.1002/adfm.202311087 ↗
28. 10.1002/anie.20230209610.1002/anie.202302096 ↗
29. 10.1002/adfm.20231198910.1002/adfm.202311989 ↗
30. 10.1021/jacs.2c0408110.1021/jacs.2c04081 ↗
31. 10.1038/s41929-017-0018-910.1038/s41929-017-0018-9 ↗
32. 10.1007/s12274-023-6301-y10.1007/s12274-023-6301-y ↗
33. 10.1002/anie.20241845910.1002/anie.202418459 ↗
34. 10.1002/smtd.20180044910.1002/smtd.201800449 ↗
35. 10.1021/acscatal.0c0084710.1021/acscatal.0c00847 ↗
36. 10.1002/aenm.20200379910.1002/aenm.202003799 ↗
37. 10.1002/anie.20211167010.1002/anie.202111670 ↗