CoFe2O4/Ag Nanostructures as Highly Sensitive Surface-Enhanced Raman Scattering Substrates
Source abstract
Abstract
At present, there is an urgent need to design sensitive substrates for the Raman analysis system to detect potential substances that have major ramifications for health care and the ecological environment. In this work, CoFe2O4/Ag nanostructures with two different morphologies were successfully synthesized as surface-enhanced Raman scattering (SERS) substrates. The as-prepared strawberry-like CoFe2O4@SiO2@Ag and snowman-like CoFe2O4-Ag Janus not only displayed high sensitivity due to the surface plasma resonance (SPR) of Ag nanoparticles and special micro-nano structure but also showed good stability, which was determined by Raman measurement and enhancement factor calculation. Moreover, excellent magnetic response ensured that the composites could be separated rapidly and reused effectively. It was demonstrated that the as-synthesized CoFe2O4@SiO2@Ag and CoFe2O4-Ag Janus composites had great potential as separable, reusable, and active SERS substrates.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Nanocluster Synthesis and Applications · Advanced Nanomaterials in Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Nanomaterials, School of Materials Science and Engineering, Xi’an University of Architecture and Technology, Xi’an 710055, China
School of Science, Xijing University, Xi’an 710123, China
Funding
National Natural Science Foundation of China · Key Laboratory of Advanced Functional Materials and Mesoscopic Physics, Xi’an Jiaotong University
References (24)
Show source-provided references
1. 10.1016/0009-2614(74)85388-110.1016/0009-2614(74)85388-1 ↗
2. 10.1002/asia.20200084710.1002/asia.202000847 ↗
3. 10.1016/j.colsurfa.2017.01.07010.1016/j.colsurfa.2017.01.070 ↗
4. 10.3390/coatings1007067910.3390/coatings10070679 ↗
5. 10.1007/s11468-020-01176-w10.1007/s11468-020-01176-w ↗
6. 10.1007/s11468-020-01268-710.1007/s11468-020-01268-7 ↗
7. 10.1021/am300781h10.1021/am300781h ↗
8. 10.1016/j.apsusc.2017.12.15710.1016/j.apsusc.2017.12.157 ↗
9. 10.1016/j.aca.2017.12.00210.1016/j.aca.2017.12.002 ↗
10. 10.1016/j.apsusc.2017.07.22910.1016/j.apsusc.2017.07.229 ↗
11. 10.1016/j.cplett.2017.07.04310.1016/j.cplett.2017.07.043 ↗
12. 10.1146/annurev.physchem.58.032806.10460710.1146/annurev.physchem.58.032806.104607 ↗
13. 10.1063/1.179999210.1063/1.1799992 ↗
14. 10.1021/nl050814j10.1021/nl050814j ↗
15. 10.1039/C4TC01550A10.1039/C4TC01550A ↗
16. 10.1007/s11051-013-1954-110.1007/s11051-013-1954-1 ↗
17. 10.1039/C4AN01084A10.1039/C4AN01084A ↗
18. 10.1016/j.saa.2017.08.02910.1016/j.saa.2017.08.029 ↗
19. 10.1016/j.molstruc.2013.04.04810.1016/j.molstruc.2013.04.048 ↗
20. 10.1021/acsami.0c0559610.1021/acsami.0c05596 ↗
21. 10.1039/C5RA17606A10.1039/C5RA17606A ↗
22. 10.1016/j.aca.2017.12.00310.1016/j.aca.2017.12.003 ↗
23. 10.1038/srep0720410.1038/srep07204 ↗
24. 10.1039/c1jm13045e10.1039/c1jm13045e ↗