Low-Temperature Synthesis of Mesoporous Half-Metallic High-Entropy Spinel Oxide Nanofibers for Photocatalytic CO2 Reduction
Source abstract
Abstract
High-entropy oxides (HEOs) exhibit great prospects owing to their varied composition, chemical adaptability, adjustable light-absorption ability, and strong stability. In this study, we report a strategy to synthesize a series of porous high-entropy spinel oxide (HESO) nanofibers (NFs) at a low temperature of 400 °C by a sol–gel electrospinning technique. The key lies in selecting six acetylacetonate salt precursors with similar coordination abilities, maintaining a high-entropy disordered state during the transformation from stable sols to gel NFs. The as-synthesized HESO NFs of (NiCuMnCoZnFe) 3 O 4 show a high specific surface area of 66.48 m 2 /g, a diverse elemental composition, a dual bandgap, half-metallicity property, and abundant defects. The diverse elements provide various synergistic catalytic sites, and oxygen vacancies act as active sites for electron–hole separation, while the half-metallicity and dual-bandgap structure offer excellent light absorption ability, thus expanding its applicability to a wide range of photocatalytic processes. As a result, the HESO NFs can efficiently convert CO 2 into CH 4 and CO with high yields of 8.03 and 15.89 μmol g –1 h –1, respectively, without using photosensitizers or sacrificial agents.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electronic and Structural Properties of Oxides · Advanced Photocatalysis Techniques · Copper-based nanomaterials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Textiles, Donghua University, Shanghai 201620, People’s Republic of China
Innovation Center for Textile Science and Technology, Donghua University, Shanghai 200051, People’s Republic of China
School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074, People’s Republic of China
Funding
Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China
References (53)
Show source-provided references
1. 10.1016/j.matdes.2021.10953410.1016/j.matdes.2021.109534 ↗
2. 10.1002/smll.20210532910.1002/smll.202105329 ↗
3. 10.1002/smll.20210720710.1002/smll.202107207 ↗
4. 10.1016/j.matdes.2021.10953410.1016/j.matdes.2021.109534 ↗
5. 10.1038/s44160-021-00004-110.1038/s44160-021-00004-1 ↗
6. 10.1038/s41563-020-00816-010.1038/s41563-020-00816-0 ↗
7. 10.1002/adma.20220075610.1002/adma.202200756 ↗
8. 10.1126/science.abn310310.1126/science.abn3103 ↗
9. 10.1016/j.apsusc.2021.15171910.1016/j.apsusc.2021.151719 ↗
10. 10.1016/j.chemosphere.2021.12973410.1016/j.chemosphere.2021.129734 ↗
11. 10.1016/j.apcatb.2021.12089610.1016/j.apcatb.2021.120896 ↗
12. 10.1016/j.cej.2022.13792610.1016/j.cej.2022.137926 ↗
13. 10.1002/adma.20220486510.1002/adma.202204865 ↗
14. 10.1002/smll.20210635810.1002/smll.202106358 ↗
15. 10.3390/pr1001004910.3390/pr10010049 ↗
16. 10.1039/C5DT02964C10.1039/C5DT02964C ↗
17. 10.1039/c0jm02913k10.1039/c0jm02913k ↗
18. 10.1021/acsami.8b2238610.1021/acsami.8b22386 ↗
19. 10.1016/j.mtchem.2022.10121410.1016/j.mtchem.2022.101214 ↗
20. 10.1016/j.apsusc.2006.02.03510.1016/j.apsusc.2006.02.035 ↗
21. 10.1021/jacs.8b1370110.1021/jacs.8b13701 ↗
22. 10.1021/acs.nanolett.1c0442510.1021/acs.nanolett.1c04425 ↗
23. 10.1016/0009-2614(87)80291-910.1016/0009-2614(87)80291-9 ↗
24. 10.1002/pssa.221134021110.1002/pssa.2211340211 ↗
25. 10.1016/j.jallcom.2021.16139010.1016/j.jallcom.2021.161390 ↗
26. 10.1021/jp064290310.1021/jp0642903 ↗
27. 10.1103/PhysRev.98.39110.1103/PhysRev.98.391 ↗
28. 10.1016/S0169-4332(00)00378-010.1016/S0169-4332(00)00378-0 ↗
29. 10.1007/s10853-017-1800-410.1007/s10853-017-1800-4 ↗
30. 10.1021/acsami.0c0356210.1021/acsami.0c03562 ↗
31. 10.1021/jp900028t10.1021/jp900028t ↗
32. 10.1039/C9CC01876J10.1039/C9CC01876J ↗
33. 10.1021/acs.jpclett.8b0289210.1021/acs.jpclett.8b02892 ↗
34. 10.1021/acsami.1c1836210.1021/acsami.1c18362 ↗
35. 10.1021/acs.chemrev.0c0132810.1021/acs.chemrev.0c01328 ↗
36. 10.1016/j.mtener.2021.10089910.1016/j.mtener.2021.100899 ↗
37. 10.1016/j.apcatb.2015.09.03110.1016/j.apcatb.2015.09.031 ↗
38. 10.1016/j.apcatb.2018.08.07310.1016/j.apcatb.2018.08.073 ↗
39. 10.1002/anie.20210921210.1002/anie.202109212 ↗
40. 10.1002/smll.20220787510.1002/smll.202207875 ↗
41. 10.1002/adma.20211051110.1002/adma.202110511 ↗
42. 10.1039/D2TA01376B10.1039/D2TA01376B ↗
43. 10.1021/acsaem.1c0319010.1021/acsaem.1c03190 ↗
44. 10.1016/j.cis.2021.10248610.1016/j.cis.2021.102486 ↗
45. 10.1021/acsami.0c1880910.1021/acsami.0c18809 ↗
46. 10.1039/C7CY01869J10.1039/C7CY01869J ↗
47. 10.1016/j.chempr.2020.06.03310.1016/j.chempr.2020.06.033 ↗
48. 10.1016/j.colsurfa.2020.12491210.1016/j.colsurfa.2020.124912 ↗
49. 10.1038/s41467-019-12858-310.1038/s41467-019-12858-3 ↗
50. 10.1038/s41560-019-0431-110.1038/s41560-019-0431-1 ↗
51. 10.1021/acsami.0c1923310.1021/acsami.0c19233 ↗
52. 10.1016/j.jallcom.2023.17015910.1016/j.jallcom.2023.170159 ↗
53. 10.1038/s41598-020-75134-110.1038/s41598-020-75134-1 ↗