Revealing the Formation of Well-Dispersed Polystyrene@ZIF-8 Core–Shell Nanoparticles by Analytical Ultracentrifugation
Source abstract
Abstract
Significant progress has been made in the synthesis and application of core-shell nanoparticles in the past decade. But particle agglomerations are hard to avoid as the formation mechanisms of core-shell nanoparticles are still vague and not clear even for the simplest and most straightforward hard-templating method. Here, analytical ultracentrifugation (AUC) is applied to investigate the formation of polystyrene@ZIF-8 core-shell nanoparticles, as a model to understand the hard-templating method. It has been found that the concentration of the ZIF-8 precursor influences both the ZIF-8 shell formation and the agglomeration of the polystyrene (PS) template. An overdiluted ZIF-8 precursor is not suitable for ZIF-8 shell formation, while a highly concentrated ZIF-8 precursor causes strong aggregation of the PS core. By applying the optimal precursor concentration identified by AUC, well-dispersed polystyrene@ZIF-8 core-shell nanoparticles can be obtained.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Innovative Microfluidic and Catalytic Techniques Innovation · Protein purification and stability · Microfluidic and Capillary Electrophoresis Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Precision Spectroscopy, Shanghai Key Laboratory of Magnetic Resonance, School of Physics and Electronic Science, East China Normal University, 3663 North Zhongshan Road, Shanghai 200062, China
Funding
National Natural Science Foundation of China
References (27)
Show source-provided references
1. 10.1039/C5NR07004J10.1039/C5NR07004J ↗
2. 10.1126/science.282.5391.111110.1126/science.282.5391.1111 ↗
3. 10.1021/acs.chemrev.5b0073110.1021/acs.chemrev.5b00731 ↗
4. 10.1016/j.memsci.2015.01.03810.1016/j.memsci.2015.01.038 ↗
5. 10.1002/adma.20180093910.1002/adma.201800939 ↗
6. 10.1002/smll.20170139210.1002/smll.201701392 ↗
7. 10.1039/D0SM00026D10.1039/D0SM00026D ↗
8. 10.1002/anie.20160384410.1002/anie.201603844 ↗
9. 10.1038/ncomms133810.1038/ncomms1338 ↗
10. 10.1021/nn503205k10.1021/nn503205k ↗
11. 10.1021/acsnano.6b0137710.1021/acsnano.6b01377 ↗
12. 10.1039/C6AN02236G10.1039/C6AN02236G ↗
13. 10.1021/jacs.6b0913510.1021/jacs.6b09135 ↗
14. 10.1039/C1CC16213F10.1039/C1CC16213F ↗
15. 10.1126/science.aao340310.1126/science.aao3403 ↗
16. 10.1021/cm900166h10.1021/cm900166h ↗
17. 10.1016/j.colsurfa.2009.07.03610.1016/j.colsurfa.2009.07.036 ↗
18. 10.1002/chem.20170210910.1002/chem.201702109 ↗
19. 10.1007/s00396-014-3276-y10.1007/s00396-014-3276-y ↗
20. Rowe A. J. · 1988
21. 10.1017/S003358350000208010.1017/S0033583500002080 ↗
22. 10.1529/biophysj.106.08137210.1529/biophysj.106.081372 ↗
23. 10.1016/S0006-3495(00)76713-010.1016/S0006-3495(00)76713-0 ↗
24. 10.1016/S0006-3495(01)75838-910.1016/S0006-3495(01)75838-9 ↗
25. 10.1038/385141a010.1038/385141a0 ↗
26. 10.1021/acsnano.5b0111610.1021/acsnano.5b01116 ↗
27. 10.1006/jcis.2000.719010.1006/jcis.2000.7190 ↗