In Situ Growth of Metal–Organic Framework on BiOBr 2D Material with Excellent Photocatalytic Activity for Dye Degradation
Source abstract
Abstract
The in situ growth of Bi-based metal–organic framework (MOF) (CAU-17) on BiOBr 2D material was prepared for the first time by using a facile solvothermal transformation approach. The BiOBr was applied both as template to support the growth of MOF and as Bi 3+ source of MOF. The BiOBr/CAU-17-2h composite exhibited enhanced photocatalytic activity for degradation of Rhodamine B (RhB), methylene blue (MB), and methyl orange (MO) under visible light irradiation, suggesting a good synergy between BiOBr and CAU-17 MOF.
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
Key Laboratory for Molecular Design and Nutrition Engineering of Ningbo, Ningbo Institute of Technology, Zhejiang University, Ningbo, Zhejiang 315100, China
Funding
National Natural Science Foundation of China · K. C. Wong Magna Fund, Ningbo Universit · Social Development Foundation of Ningbo
References (45)
Show source-provided references
1. 10.1021/cr200304e10.1021/cr200304e ↗
2. 10.1039/c3cc49440c10.1039/c3cc49440c ↗
3. 10.1002/chem.20150080810.1002/chem.201500808 ↗
4. 10.1016/j.jhazmat.2014.11.03910.1016/j.jhazmat.2014.11.039 ↗
5. 10.1039/C5CC09127F10.1039/C5CC09127F ↗
6. 10.1038/nmat343910.1038/nmat3439 ↗
7. 10.1021/ja404523s10.1021/ja404523s ↗
8. 10.1021/am301310410.1021/am3013104 ↗
9. 10.1002/admi.20150003710.1002/admi.201500037 ↗
10. 10.1039/C4TA04230A10.1039/C4TA04230A ↗
11. 10.1021/nn503834u10.1021/nn503834u ↗
12. 10.1039/C6DT02083F10.1039/C6DT02083F ↗
13. 10.1039/C4NR02553A10.1039/C4NR02553A ↗
14. 10.1021/ja402956f10.1021/ja402956f ↗
15. 10.1021/jacs.5b0310510.1021/jacs.5b03105 ↗
16. 10.1002/anie.20090717310.1002/anie.200907173 ↗
17. 10.1038/ncomms240110.1038/ncomms2401 ↗
18. 10.1002/adfm.20090221810.1002/adfm.200902218 ↗
19. 10.1016/j.apsusc.2015.12.24910.1016/j.apsusc.2015.12.249 ↗
20. 10.1016/j.apcatb.2016.02.01810.1016/j.apcatb.2016.02.018 ↗
21. 10.1016/j.cej.2015.10.11210.1016/j.cej.2015.10.112 ↗
22. 10.1039/C5RA04869A10.1039/C5RA04869A ↗
23. 10.1016/S1003-6326(15)64047-X10.1016/S1003-6326(15)64047-X ↗
24. 10.1039/C6DT02912D10.1039/C6DT02912D ↗
25. 10.1021/jacs.5b1248410.1021/jacs.5b12484 ↗
26. 10.1016/j.jphotochem.2010.03.00410.1016/j.jphotochem.2010.03.004 ↗
27. 10.1016/j.apcatb.2015.10.03610.1016/j.apcatb.2015.10.036 ↗
28. 10.1039/c3ta14617k10.1039/c3ta14617k ↗
29. 10.1016/j.apsusc.2015.12.24910.1016/j.apsusc.2015.12.249 ↗
30. 10.1039/C5NR05154A10.1039/C5NR05154A ↗
31. 10.1021/es902011h10.1021/es902011h ↗
32. 10.1016/j.apcatb.2013.04.05810.1016/j.apcatb.2013.04.058 ↗
33. 10.1021/jp503507910.1021/jp5035079 ↗
34. 10.1039/c3ta14349j10.1039/c3ta14349j ↗
35. 10.1016/j.apcata.2011.02.03310.1016/j.apcata.2011.02.033 ↗
36. 10.1021/ja211433h10.1021/ja211433h ↗
37. 10.1039/C5TA05440K10.1039/C5TA05440K ↗
38. 10.1039/C4RA16948D10.1039/C4RA16948D ↗
39. 10.1016/j.apcatb.2015.03.03710.1016/j.apcatb.2015.03.037 ↗
40. 10.1016/j.cej.2013.02.03410.1016/j.cej.2013.02.034 ↗
41. 10.1016/j.apcatb.2011.10.01610.1016/j.apcatb.2011.10.016 ↗
42. 10.1016/j.apcatb.2015.07.03510.1016/j.apcatb.2015.07.035 ↗
43. 10.1021/acscatal.6b0129310.1021/acscatal.6b01293 ↗
44. 10.1002/anie.20160399010.1002/anie.201603990 ↗
45. 10.1016/j.apsusc.2013.11.05510.1016/j.apsusc.2013.11.055 ↗