Facile room temperature synthesis of Ag@AgBr core–shell microspheres with high visible-light-driven photocatalytic performance
Source abstract
Abstract
The uniform Ag@AgBr core–shell microspheres were synthesized by a very facile wet-chemical route in aqueous solution, including a reduction process to prepare sphere-like Ag core and a deposition process to synthesize AgBr shell. X-ray diffraction, x-ray photoelectron spectroscopy, field emission scanning electron microscopy, and high-resolution transmission electron microscopy results confirmed the formation of Ag@AgBr core–shell heterostructures which had been achieved by this simple method. Field emission scanning and high-resolution transmission electron microscopy results of the as-synthesized Ag@AgBr composite revealed that AgBr particles were deposited on the surface of sphere-like Ag core. Under visible-light (λ >420 nm) and real sunlight irradiation, the as-synthesized Ag@AgBr samples exhibit high activity and good stability for the photodegradation of Rhodamine 6G (R6G) in water. The present work suggests that the as-synthesized Ag@AgBr core–shell microsphere can be applied as a visible light-activated photocatalyst in efficient utilization of solar energy for treating water polluted by some chemically stable azo dyes in environment. The enhanced photocatalytic performance of the as-synthesized Ag@AgBr composite might be attributed to accelerated separation efficiency of electron–hole pairs on the interface of the Ag@AgBr hybrids and improved visible-light absorption abilities when AgBr is coupled with Ag.
Source: expertdata · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Quantum Dots Synthesis And Properties · ZnO doping and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (36)
Show source-provided references
1. 10.1126/science.116417010.1126/science.1164170 ↗
2. 10.1016/j.catcom.2013.04.00610.1016/j.catcom.2013.04.006 ↗
3. 10.1038/nature0114110.1038/nature01141 ↗
4. 10.1039/c3dt32813a10.1039/c3dt32813a ↗
5. 10.1021/am403349m10.1021/am403349m ↗
6. 10.1016/j.jphotochem.2013.04.00810.1016/j.jphotochem.2013.04.008 ↗
7. 10.1016/j.apcatb.2009.12.02210.1016/j.apcatb.2009.12.022 ↗
8. 10.1039/c0cp00414f10.1039/c0cp00414f ↗
9. 10.1016/j.physb.2006.11.04610.1016/j.physb.2006.11.046 ↗
10. 10.1016/j.jallcom.2013.02.03610.1016/j.jallcom.2013.02.036 ↗
11. 10.1002/jctb.384110.1002/jctb.3841 ↗
12. 10.1016/j.apcatb.2013.12.00810.1016/j.apcatb.2013.12.008 ↗
13. 10.1016/j.chemosphere.2014.01.02210.1016/j.chemosphere.2014.01.022 ↗
14. 10.1021/am402929d10.1021/am402929d ↗
15. 10.1016/j.jphotochemrev.2013.10.00110.1016/j.jphotochemrev.2013.10.001 ↗
16. 10.1016/j.apcatb.2013.11.03310.1016/j.apcatb.2013.11.033 ↗
17. 10.1016/j.apcatb.2013.06.02310.1016/j.apcatb.2013.06.023 ↗
18. 10.1016/j.matlet.2012.10.02010.1016/j.matlet.2012.10.020 ↗
19. 10.1016/j.solidstatesciences.2012.08.00210.1016/j.solidstatesciences.2012.08.002 ↗
20. 10.1016/j.jallcom.2013.08.02810.1016/j.jallcom.2013.08.028 ↗
21. 10.1021/ie404283d10.1021/ie404283d ↗
22. 10.1016/j.cattod.2010.02.06810.1016/j.cattod.2010.02.068 ↗
23. 10.1007/s11144-011-0291-610.1007/s11144-011-0291-6 ↗
24. 10.1016/j.apsusc.2013.06.12110.1016/j.apsusc.2013.06.121 ↗
25. 10.1039/c2dt12089e10.1039/c2dt12089e ↗
26. 10.1039/c3nr05466g10.1039/c3nr05466g ↗
27. 10.1016/j.matlet.2013.12.11110.1016/j.matlet.2013.12.111 ↗
28. 10.1016/j.matlet.2011.03.07010.1016/j.matlet.2011.03.070 ↗
29. 10.1039/C3RA45341C10.1039/C3RA45341C ↗
30. 10.1016/j.seppur.2011.07.01610.1016/j.seppur.2011.07.016 ↗
31. 10.1002/adma.20130417310.1002/adma.201304173 ↗
32. 10.1016/j.jallcom.2010.04.18910.1016/j.jallcom.2010.04.189 ↗
33. 10.1016/j.apcatb.2013.11.01510.1016/j.apcatb.2013.11.015 ↗
34. 10.1016/j.jhazmat.2012.03.00210.1016/j.jhazmat.2012.03.002 ↗
35. 10.1039/c1cp20488b10.1039/c1cp20488b ↗
36. 10.1016/j.apcatb.2013.12.04210.1016/j.apcatb.2013.12.042 ↗