Miniaturized Layer-by-Layer Deposition of Metal–Organic Framework Coatings through Digital Microfluidics
Source abstract
Abstract
Digital microfluidics (DMF) was demonstrated as a unique tool to scale down and automate the layer-by-layer deposition (LBL) process for depositing patterned metal-organic frameworks (MOF) coatings by making use of the coordinated movement of individual droplets containing the MOF building blocks. HKUST-1, a MOF material consisting of Cu(II) ions and trimesate (1,3,5-benzenetricarboxylate; BTC) linkers, was chosen. In each step, reactant droplets were kept in contact with the substrate to be coated for a few minutes before several washing droplets were used to remove leftover reactants. As could be expected from previous LBL studies, highly uniform dense HKUST-1 coatings are formed that cover the whole surface of the functionalized gold patches. After removing parts of the coating, it can easily be seen that the coating has a uniform thickness of approximately 550 nm after 40 cycles. A similar enhanced increase in layer thickness has been observed in the preparation of HKUST-1 LBL films by spraying the different solutions onto the substrate.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced biosensing and bioanalysis techniques · Biosensors and Analytical Detection · Metal-Organic Frameworks: Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
BIOSYST-MeBioS, KU Leuven − University of Leuven, Willem de Croylaan 42, B-3001 Leuven, Belgium
MICAS-ESAT, KU Leuven − University of Leuven, Kasteelpark Arenberg 10, B-3001 Leuven, Belgium
Center for Surface Chemistry and Catalysis, KU Leuven − University of Leuven, Kasteelpark Arenberg 23, B-3001 Leuven, Belgium
References (27)
Show source-provided references
1. Sumida K. · Chem. Rev. · 2012 · 112 · 72410.1021/cr2003272 ↗
2. Li J. R. · Chem. Rev. · 2012 · 112 · 86910.1021/cr200190s ↗
3. Farrusseng D. · Angew. Chem., Int. Ed. · 2009 · 48 · 750210.1002/anie.200806063 ↗
4. Lee J. · Chem. Soc. Rev. · 2009 · 38 · 145010.1039/b807080f ↗
5. Bradshaw D. · Chem. Soc. Rev. · 2012 · 41 · 234410.1039/C1CS15276A ↗
6. Falcaro P. · Adv. Mater. · 2012 · 24 · 315310.1002/adma.201200485 ↗
7. Allendorf M. D. · Chem.—Eur. J. · 2011 · 17 · 1137210.1002/chem.201101595 ↗
8. Robinson A. L. · Anal. Chem. · 2012 · 84 · 704310.1021/ac301183w ↗
9. Shekhah O. · Chem. Soc. Rev. · 2011 · 40 · 108110.1039/c0cs00147c ↗
10. Zacher D. · Chem. Soc. Rev. · 2009 · 38 · 141810.1039/b805038b ↗
11. Betard A. · Chem. Rev. · 2012 · 112 · 105510.1021/cr200167v ↗
12. Dimitrakakis C. · Chem. Commun. · 2012 · 48 · 748310.1039/c2cc33292b ↗
13. Ameloot R. · Adv. Mater. · 2010 · 22 · 268510.1002/adma.200903867 ↗
14. Witters D. · Adv. Mater. · 2012 · 24 · 131610.1002/adma.201104922 ↗
15. Carbonell C. · J. Am. Chem. Soc. · 2011 · 133 · 214410.1021/ja2002428 ↗
16. Shekhah O. · J. Am. Chem. Soc. · 2007 · 129 · 1511810.1021/ja076210u ↗
17. Zacher D. · Chem.—Eur. J. · 2011 · 17 · 144810.1002/chem.201002381 ↗
18. Shekhah O. · Nat. Mater. · 2009 · 8 · 48110.1038/nmat2445 ↗
19. Shekhah O. · Dalton Trans. · 2011 · 40 · 495410.1039/c0dt01818j ↗
20. Wheeler A. R. · Science · 2008 · 322 · 53910.1126/science.1165719 ↗
21. Falcaro P. · J. Mater. Chem. C · 2013 · 1 · 4210.1039/C2TC00241H ↗
22. Arslan H. K. · Adv. Funct. Mater. · 2011 · 21 · 422810.1002/adfm.201101592 ↗
23. Vergauwe N. · J. Micromech. Microeng. · 2011 · 21 · 05402610.1088/0960-1317/21/5/054026 ↗
24. Chui S. S. Y. · Science · 1999 · 283 · 114810.1126/science.283.5405.1148 ↗
25. Zybaylo O. · Phys. Chem. Chem. Phys. · 2010 · 12 · 809210.1039/b927601g ↗
26. Pollack M. G. · Appl. Phys. Lett. · 2000 · 77 · 172510.1063/1.1308534 ↗
27. Zacher D. · Angew. Chem., Int. Ed. · 2011 · 50 · 17610.1002/anie.201002451 ↗