Tuning the Crystallinity and Coverage of SiO2–ZnIn2S4 Core–Shell Nanoparticles for Efficient Hydrogen Generation
Source abstract
Abstract
The coverage, thickness, and crystallinity of ZnIn2S4 (ZIS) shells on SiO2 core nanoparticles (SiO2@ZIS) were systematically investigated using microwave-assisted solvothermal methods aided by the addition of acid in ethanolic medium. The surface modification of the SiO2 cores with (3-mercaptopropyl)trimethoxysilane was found to be critical to generate a homogeneous coverage of ZnIn2S4. The SiO2@ZIS core–shell nanoparticles exhibited the best coverage but poor crystallinity when synthesized in pure ethanol, whereas best crystallinity but poor coverage was observed when synthesized in an aqueous solution. The addition of selected amounts of acid (HCl) led to improved crystallinity in the ethanolic medium. The thickness of the ZIS shell could be controlled in an ethanolic solution by judiciously varying the amounts of acid and the concentration of the ZIS precursor. Increasing the concentration of the ZIS precursor to twice the standard concentration in ethanolic solution with the addition of 100 μL of HCl afforded better crystallinity, homogeneous coverage, and optimal photocatalytic hydrogen production.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Copper-based nanomaterials and applications · Quantum Dots Synthesis And Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical and Materials Engineering, National Central University, 300 Jhongda Road, Jhongli City 32001, Taiwan
Sustainability Science and Engineering Program, International College, Tunghai University, Taichung 40704, Taiwan
Department of Chemistry, University of Houston, 4800 Calhoun Road, Houston, Texas 77204-5003, United States
Funding
Welch Foundation · Air Force Office of Scientific Research · Ministry of Science and Technology, Taiwan
References (42)
Show source-provided references
1. 10.1038/3510460710.1038/35104607 ↗
2. 10.1021/jacs.5b0410710.1021/jacs.5b04107 ↗
3. 10.1021/jz100796610.1021/jz1007966 ↗
4. 10.1023/A:102348050771010.1023/A:1023480507710 ↗
5. 10.1039/C6CC03199D10.1039/C6CC03199D ↗
6. 10.1002/anie.20050031410.1002/anie.200500314 ↗
7. 10.1021/acs.jpcc.5b0206810.1021/acs.jpcc.5b02068 ↗
8. 10.1021/cr400366s10.1021/cr400366s ↗
9. 10.1016/j.jpowsour.2011.08.10310.1016/j.jpowsour.2011.08.103 ↗
10. 10.1021/cg060767o10.1021/cg060767o ↗
11. 10.1039/C3NJ00266G10.1039/C3NJ00266G ↗
12. 10.1021/jp804525q10.1021/jp804525q ↗
13. 10.1039/C3CP51857D10.1039/C3CP51857D ↗
14. 10.1002/anie.20131051310.1002/anie.201310513 ↗
15. 10.1016/j.ijhydene.2010.02.01710.1016/j.ijhydene.2010.02.017 ↗
16. 10.1039/C1DT11308A10.1039/C1DT11308A ↗
17. 10.1021/acsami.6b0119710.1021/acsami.6b01197 ↗
18. 10.1021/am503208310.1021/am5032083 ↗
19. 10.1021/ja058084510.1021/ja0580845 ↗
20. 10.1016/j.materresbull.2008.03.02710.1016/j.materresbull.2008.03.027 ↗
21. 10.1016/j.ijhydene.2008.05.04310.1016/j.ijhydene.2008.05.043 ↗
22. 10.1063/1.509966610.1063/1.5099666 ↗
23. 10.1021/acs.chemrev.9b0020110.1021/acs.chemrev.9b00201 ↗
24. 10.1002/admi.20150028010.1002/admi.201500280 ↗
25. 10.1021/AM200832210.1021/AM2008322 ↗
26. 10.1021/ja305603t10.1021/ja305603t ↗
27. 10.1016/j.jpcs.2008.04.03510.1016/j.jpcs.2008.04.035 ↗
28. 10.1021/jp111272910.1021/jp1112729 ↗
29. 10.1039/C3CY00952A10.1039/C3CY00952A ↗
30. 10.1021/ic800752t10.1021/ic800752t ↗
31. 10.1016/0021-9797(68)90272-510.1016/0021-9797(68)90272-5 ↗
32. 10.1021/cm052888210.1021/cm0528882 ↗
33. 10.1021/nl201820r10.1021/nl201820r ↗
34. 10.1039/C1JA10025D10.1039/C1JA10025D ↗
35. 10.1021/am402310u10.1021/am402310u ↗
36. 10.1021/cr300143v10.1021/cr300143v ↗
37. 10.1016/j.cplett.2013.11.04310.1016/j.cplett.2013.11.043 ↗
38. 10.1021/acs.langmuir.5b0101910.1021/acs.langmuir.5b01019 ↗
39. 10.1039/C1EE02533C10.1039/C1EE02533C ↗
40. 10.1021/cg060929g10.1021/cg060929g ↗
41. 10.1021/cr990001d10.1021/cr990001d ↗
42. 10.1016/0022-1902(67)80453-610.1016/0022-1902(67)80453-6 ↗