Substantial Enhancement toward the Photocatalytic Activity of CdS Quantum Dots by Photonic Crystal-Supporting Films
Source abstract
Abstract
The introduction of photonic crystals (PC) to semiconductors, which usually appear in the form of inverse opal materials, has been proved to be an effective way to enhance the photocatalytic activity, but their enhancement factor is merely two- to fourfold in most previous reports. In this work, a supported thin-film photocatalyst (CdS/SiO2-ETPTA), as a new PC-based catalyst system, is prepared for hydrogen evolution under visible light, which presents an 6.4- to 8.8-fold activity compared to the same CdS quantum dots deposited on a non-PC film. This substantial enhancement originates from the high reflectivity of PCs and absorption of reflected light by CdS, whose absorption edge exactly matches the stopband of PCs. Compared to the traditional inverse opal photocatalysts, the PC-supported photocatalyst possesses many advantages including simplified procedures in synthesis, a substantial enhancement of activity, flexible modification with mature thin-film techniques, good stability, and easy regeneration in reaction.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Photonic Crystals and Applications · Quantum Dots Synthesis And Properties · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, China
Funding
Shanghai Municipal Education Commission · National Natural Science Foundation of China · Shanghai Education Development Foundation
References (42)
Show source-provided references
1. 10.1002/anie.20150620510.1002/anie.201506205 ↗
2. 10.1002/anie.20171045610.1002/anie.201710456 ↗
3. 10.1002/adma.20130465410.1002/adma.201304654 ↗
4. 10.1038/ncomms565910.1038/ncomms5659 ↗
5. 10.1038/nphoton.2007.14010.1038/nphoton.2007.140 ↗
6. 10.1002/smll.20140300510.1002/smll.201403005 ↗
7. 10.1002/adfm.20170282510.1002/adfm.201702825 ↗
8. 10.1002/smll.20160114010.1002/smll.201601140 ↗
9. 10.1038/srep0148410.1038/srep01484 ↗
10. 10.1038/ncomms841610.1038/ncomms8416 ↗
11. 10.1039/c6nr08767a10.1039/c6nr08767a ↗
12. 10.1021/nn200100v10.1021/nn200100v ↗
13. 10.1021/cm502883310.1021/cm5028833 ↗
14. 10.1002/adma.20060058810.1002/adma.200600588 ↗
15. 10.1039/c5nr04663g10.1039/c5nr04663g ↗
16. 10.1039/c4ta01922a10.1039/c4ta01922a ↗
17. 10.1039/c0ee00116c10.1039/c0ee00116c ↗
18. 10.1021/nl302920210.1021/nl3029202 ↗
19. 10.1016/j.apcatb.2015.11.01810.1016/j.apcatb.2015.11.018 ↗
20. 10.1039/c3ta13985a10.1039/c3ta13985a ↗
21. 10.1002/smll.20140097010.1002/smll.201400970 ↗
22. 10.1039/c3ta15044e10.1039/c3ta15044e ↗
23. 10.1039/c3ra42618a10.1039/c3ra42618a ↗
24. 10.1021/jp102525y10.1021/jp102525y ↗
25. 10.1039/c4ta03333g10.1039/c4ta03333g ↗
26. 10.1002/anie.20130268010.1002/anie.201302680 ↗
27. 10.1002/adfm.20160089410.1002/adfm.201600894 ↗
28. 10.1039/c7ta01703k10.1039/c7ta01703k ↗
29. 10.1021/es903833f10.1021/es903833f ↗
30. 10.1039/c1cc11243k10.1039/c1cc11243k ↗
31. 10.1038/srep0284910.1038/srep02849 ↗
32. 10.1039/c5ra18964k10.1039/c5ra18964k ↗
33. 10.1002/aenm.20150124110.1002/aenm.201501241 ↗
34. 10.1002/adma.20170080310.1002/adma.201700803 ↗
35. 10.1016/j.scib.2017.03.00510.1016/j.scib.2017.03.005 ↗
36. 10.1016/j.apcatb.2015.05.04110.1016/j.apcatb.2015.05.041 ↗
37. 10.1002/anie.20140096610.1002/anie.201400966 ↗
38. 10.1021/acs.jpclett.5b0135310.1021/acs.jpclett.5b01353 ↗
39. 10.1039/c5ta05224f10.1039/c5ta05224f ↗
40. 10.1002/1521-3773(20020703)41:13<2368::aid-anie2368>3.0.co;2-g10.1002/1521-3773(20020703)41:13<2368::aid-anie2368>3.0.co;2-g ↗
41. 10.1002/adfm.20130159010.1002/adfm.201301590 ↗
42. 10.1016/j.jechem.2018.05.00610.1016/j.jechem.2018.05.006 ↗