Preparation of Photoluminescent Porous Silicon Nanoparticles by High‐Pressure Microfluidization
Source abstract
Abstract
The use of high-shear microfluidization as a rapid, reproducible, and high-yield method to prepare nanoparticles of porous silicon (pSi) with a narrow size distribution is described. Porous films prepared by electrochemical etch of a single-crystal silicon wafer are removed from the substrate, fragmented, dispersed in an aqueous solution, and then processed with a microfluidizer, which generates high yields (57%) of pSi nanoparticles of narrow size distribution (PDI = 0.263) without a filtration step. Preparation of pSi nanoparticles via microfluidization improves yields (by 2.4-fold) and particle size uniformity (by 1.8-fold), and it lowers the total processing time (by 36-fold) over standard ultrasonication or ball milling methods. The average diameter of the nanoparticles can be adjusted over the range 150–350 nm by appropriate adjustment of processing steps. If the fluid carrier in the microfluidizer contains an oxidant for Si, the resulting pSi particles are prepared with a core–shell structure, in which an elemental Si core is encased in a silicon oxide shell. When an aqueous sodium tetraborate processing solution is used, microfluidization generates photoluminescent core–shell pSi particles with a quantum yield of 19% in a single step in less than 20 min.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Silicon Nanostructures and Photoluminescence · Nanowire Synthesis and Applications · Semiconductor materials and devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry and Biochemistry University of California, San Diego 9500 Gilman Drive La Jolla CA 92093 USA
Department of Material Science and Engineering University of California, San Diego 9500 Gilman Drive La Jolla CA 92093 USA
Kyoto University Innovation Capital Co., Ltd. 36‐1, Yoshida‐Honmachi Sakyo‐Ku Kyoto 606‐8317 Japan
Funding
National Science Foundation · Defense Advanced Research Projects Agency
References (29)
Show source-provided references
1. 10.1007/978-3-319-05744-610.1007/978-3-319-05744-6 ↗
2. 10.1021/nn901657w10.1021/nn901657w ↗
3. 10.1016/j.jconrel.2005.08.01710.1016/j.jconrel.2005.08.017 ↗
4. 10.1002/jps.2099910.1002/jps.20999 ↗
5. 10.1016/j.powtec.2015.11.01510.1016/j.powtec.2015.11.015 ↗
6. 10.1126/science.255.5040.6610.1126/science.255.5040.66 ↗
7. 10.1021/cm950608k10.1021/cm950608k ↗
8. 10.1149/1.356166110.1149/1.3561661 ↗
9. 10.1016/j.ejps.2014.04.01810.1016/j.ejps.2014.04.018 ↗
10. 10.1016/S0378-5173(99)00422-610.1016/S0378-5173(99)00422-6 ↗
11. 10.1016/S0168-3659(01)00230-910.1016/S0168-3659(01)00230-9 ↗
12. 10.1016/j.jconrel.2008.02.00710.1016/j.jconrel.2008.02.007 ↗
13. Sailor M. J. · 2012 · 249
14. 10.1016/j.biomaterials.2009.02.00810.1016/j.biomaterials.2009.02.008 ↗
15. 10.1063/1.10773610.1063/1.107736 ↗
16. 10.1016/j.tsf.2005.07.35010.1016/j.tsf.2005.07.350 ↗
17. 10.1063/1.310004510.1063/1.3100045 ↗
18. 10.4155/fmc.09.9010.4155/fmc.09.90 ↗
19. 10.1002/adma.20160063410.1002/adma.201600634 ↗
20. 10.1021/acsnano.5b0159410.1021/acsnano.5b01594 ↗
21. 10.1038/nmat239810.1038/nmat2398 ↗
22. 10.1002/adfm.20140058710.1002/adfm.201400587 ↗
23. 10.1016/j.actbio.2014.09.02510.1016/j.actbio.2014.09.025 ↗
24. 10.1016/S0016-7037(99)00218-510.1016/S0016-7037(99)00218-5 ↗
25. Brinker C. J. · 1990
26. 10.1021/ar600032u10.1021/ar600032u ↗
27. 10.1002/ppsc.20130024410.1002/ppsc.201300244 ↗
28. 10.1016/0022-2313(82)90045-X10.1016/0022-2313(82)90045-X ↗
29. 10.1002/adfm.20060107710.1002/adfm.200601077 ↗