journal article·2016-08-23

Forming Nanoparticle Monolayers at Liquid–Air Interfaces by Using Miscible Liquids

Datong Zhang, Jiayang Hu, Kathleen M. Kennedy, Irving P. Herman

Langmuir· Volume 32· Issue 33
Publisher page

Abstract

One standard way of forming monolayers (MLs) of nanoparticles (NPs) is to drop-cast a NP dispersion made using one solvent onto a second, immiscible solvent; after this upper solvent evaporates, the NP ML can be transferred to a solid substrate by liftoff. We show that this previously universal use of only immiscible solvent pairs can be relaxed and close-packed, hexagonally ordered NP monolayers can self-assemble at liquid-air interfaces when some miscible solvent pairs are used instead. We demonstrate this by drop-casting an iron oxide NP dispersion in toluene on a dimethyl sulfoxide (DMSO) liquid substrate. The NPs are energetically stable at the DMSO surface and remain there even with solvent mixing. Excess NPs coagulate and precipitate in the DMSO, and this limits NPs at the surface to approximately 1 ML. The ML domains at the surface nucleate independently, which is in contrast to ML growth at the receding edge of the drying drop, as is common in immiscible solvent pair systems and seen here for the toluene/diethylene glycol immiscible solvent pair system. This new use of miscible solvent pairs can enable the formation of MLs for a wider range of NPs.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Gold and Silver Nanoparticles Synthesis and Applications · Nanomaterials and Printing Technologies · Quantum Dots Synthesis And Properties

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Applied Physics and Applied Mathematics, Columbia University, New York, New York 10027, United States

Funding

Division of Materials Research · Honda Motor Co., Ltd.

References (28)

Show source-provided references
1. 10.1039/C4NR04875J10.1039/C4NR04875J ↗
2. 10.1021/acs.chemmater.5b0152210.1021/acs.chemmater.5b01522 ↗
3. 10.1038/nature1238510.1038/nature12385 ↗
4. 10.1103/PhysRevLett.93.13550310.1103/PhysRevLett.93.135503 ↗
5. 10.1021/nl902904810.1021/nl9029048 ↗
6. 10.1038/nmat161110.1038/nmat1611 ↗
7. 10.1002/adfm.20040046810.1002/adfm.200400468 ↗
8. 10.1021/nn504615a10.1021/nn504615a ↗
9. 10.1021/nn204498j10.1021/nn204498j ↗
10. 10.1021/la304573p10.1021/la304573p ↗
11. 10.1021/la303287z10.1021/la303287z ↗
12. 10.1021/nl200468p10.1021/nl200468p ↗
13. 10.1038/nature0918810.1038/nature09188 ↗
14. 10.1021/ja016812s10.1021/ja016812s ↗
15. 10.1039/b207789b10.1039/b207789b ↗
16. Haynes W. M. · 201410.1201/b17118 ↗
17. 10.1021/acs.jpcc.5b0174110.1021/acs.jpcc.5b01741 ↗
18. Lawrence Berkeley National Laboratory Data Base. URL:henke.lbl.gov/optical_constants/atten2.html.
19. 10.1038/nature1034410.1038/nature10344 ↗
20. 10.1038/3982710.1038/39827 ↗
21. 10.1038/361026a010.1038/361026a0 ↗
22. 10.1021/jp104797910.1021/jp1047979 ↗
23. 10.1107/S002188980904012610.1107/S0021889809040126 ↗
24. 10.1103/PhysRevLett.45.56910.1103/PhysRevLett.45.569 ↗
25. 10.1007/s11746-999-0245-610.1007/s11746-999-0245-6 ↗
26. 10.1016/0021-9797(89)90345-710.1016/0021-9797(89)90345-7 ↗
27. Hessel V. · 200510.1002/3527603581 ↗
28. 10.1021/ie50266a00410.1021/ie50266a004 ↗