Evaluating the Structural Response of Amphiphilic Monolayers to Environmental Stimuli
Source abstract
Abstract
Amphiphilic monolayers composed of end groups with distinct polar and nonpolar functional groups offer rapid and reversible interfacial adaptation in response to environmental stimuli such as a change in interfacial medium polarity. We have synthesized and characterized a suite of monolayers with functional groups of competing polarity designed to reconfigure their interfacial chemical composition in response to solvent polarity. In these films, the end group is designed to be able to reorient and expose the functional groups that minimize the interfacial free energy between the film and the environment. Using a combination of spectroscopic, computational, and wettability studies, we have investigated the responsive interfacial behavior of different end groups upon exposure to environments with varying polarities. Contact angle measurements across a series of polar and dispersive probe liquids reveal trends that reflect the underlying molecular flexibility and composition. Vibrational sum frequency generation (SFG) spectroscopy and atomistic molecular dynamics (MD) simulations confirm solvent-driven reorientation of the end groups, with restructuring observed at the interface. To quantify these effects, we have developed a surface energy calculation model that incorporates solvent-induced surface rearrangements into the estimations. Our findings reveal a strong dependence of surface energy and switching behavior on the length and flexibility of the functionalities in the end group, which affects the exposure of certain interfacial compositions under different solvents. These results offer new insights into the design of adaptive monolayers and provide a framework for evaluating solvent-responsive surfaces.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Spectroscopy and Quantum Chemical Studies · Electrostatics and Colloid Interactions · Material Dynamics and Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical and Biomolecular Engineering
Vanderbilt University
Interdisciplinary Materials Science Program
Chemical Sciences Division
Oak Ridge National Laboratory
School of Engineering and Physical Sciences
Heriot-Watt University
Funding
Oak Ridge National Laboratory · Division of Chemical, Bioengineering, Environmental, and Transport Systems
References (73)
Show source-provided references
1. 10.1039/C8TC02049C10.1039/C8TC02049C ↗
2. 10.1021/acsami.9b0129310.1021/acsami.9b01293 ↗
3. 10.1002/advs.20210012610.1002/advs.202100126 ↗
4. 10.5004/dwt.2021.2681510.5004/dwt.2021.26815 ↗
5. 10.1039/D3TB02164E10.1039/D3TB02164E ↗
6. 10.1016/j.progpolymsci.2004.03.00110.1016/j.progpolymsci.2004.03.001 ↗
7. 10.1126/science.107599710.1126/science.1075997 ↗
8. 10.1021/acs.accounts.6b0013210.1021/acs.accounts.6b00132 ↗
9. 10.1016/j.progpolymsci.2009.11.00110.1016/j.progpolymsci.2009.11.001 ↗
10. 10.1021/ma00070a02010.1021/ma00070a020 ↗
11. 10.1021/ma301513s10.1021/ma301513s ↗
12. 10.1021/ja038051u10.1021/ja038051u ↗
13. 10.1021/la950294f10.1021/la950294f ↗
14. 10.1021/jacs.1c1283210.1021/jacs.1c12832 ↗
15. 10.1016/j.jcis.2022.02.00610.1016/j.jcis.2022.02.006 ↗
16. 10.1073/pnas.160308011310.1073/pnas.1603080113 ↗
17. Craven, N. C.; Cordova-Huaman, A.; Iacovella, C. R.; Jennings, G. K.; McCabe, C.Evaluating the Terminal Group Switching of Responsive Monolayer Films: Examining Structural Rearrangements via Molecular Simulations and Experimental Wetting Measurements J. Mater. Chem. A 2025 10.1039/D5TA00366K.10.1039/D5TA00366K ↗
18. 10.1163/156856192X0062910.1163/156856192X00629 ↗
19. Mazzola L. · 2013 · 17310.1002/9781118795620.ch10 ↗
20. 10.1016/j.matdes.2021.10990210.1016/j.matdes.2021.109902 ↗
21. 10.1021/acs.langmuir.0c0179910.1021/acs.langmuir.0c01799 ↗
22. 10.1126/science.255.5049.123010.1126/science.255.5049.1230 ↗
23. 10.1073/pnas.150264211210.1073/pnas.1502642112 ↗
24. 10.1021/la026515g10.1021/la026515g ↗
25. 10.1016/j.apsusc.2010.03.06410.1016/j.apsusc.2010.03.064 ↗
26. 10.1166/jamr.2010.103510.1166/jamr.2010.1035 ↗
27. 10.1098/rspl.1800.009510.1098/rspl.1800.0095 ↗
28. 10.1021/j100808a52410.1021/j100808a524 ↗
29. 10.1002/app.1969.07013081510.1002/app.1969.070130815 ↗
30. 10.1080/0021846730807843710.1080/00218467308078437 ↗
31. 10.1016/0927-7757(93)80308-210.1016/0927-7757(93)80308-2 ↗
32. Żenkiewicz M. · J. Achiev. Mater. Manuf. Eng. · 2007 · 24 · 137
33. 10.1016/j.tsf.2006.04.00610.1016/j.tsf.2006.04.006 ↗
34. 10.1021/la301033h10.1021/la301033h ↗
35. 10.1038/pj.2014.9110.1038/pj.2014.91 ↗
36. 10.1021/acs.langmuir.9b0125210.1021/acs.langmuir.9b01252 ↗
37. 10.1006/jcis.2002.826210.1006/jcis.2002.8262 ↗
38. 10.1021/acsami.2c0182410.1021/acsami.2c01824 ↗
39. 10.1021/acs.langmuir.8b0178310.1021/acs.langmuir.8b01783 ↗
40. 10.1039/C7RA00708F10.1039/C7RA00708F ↗
41. 10.1021/acs.langmuir.2c0019810.1021/acs.langmuir.2c00198 ↗
42. 10.1016/0032-3861(85)90206-X10.1016/0032-3861(85)90206-X ↗
43. 10.1039/D3NA00977G10.1039/D3NA00977G ↗
44. 10.1021/la00056a01710.1021/la00056a017 ↗
45. 10.1021/acs.jpcc.5b0632110.1021/acs.jpcc.5b06321 ↗
46. 10.1021/la00088a03510.1021/la00088a035 ↗
47. 10.1021/la501832810.1021/la5018328 ↗
48. 10.1002/app.2744610.1002/app.27446 ↗
49. 10.1002/(SICI)1099-0488(19990815)37:16<2039::AID-POLB8>3.0.CO;2-O10.1002/(SICI)1099-0488(19990815)37:16<2039::AID-POLB8>3.0.CO;2-O ↗
50. 10.1364/OE.41246910.1364/OE.412469 ↗
51. 10.1021/acssensors.6b0063410.1021/acssensors.6b00634 ↗
52. 10.1021/acsami.3c0071910.1021/acsami.3c00719 ↗
53. 10.1364/OL.43.00203810.1364/OL.43.002038 ↗
54. 10.1063/1.508497110.1063/1.5084971 ↗
55. 10.1021/jp306838a10.1021/jp306838a ↗
56. 10.1038/s41467-017-01088-010.1038/s41467-017-01088-0 ↗
57. 10.1021/acs.jpcb.3c0038610.1021/acs.jpcb.3c00386 ↗
58. 10.1002/aic.1720610.1002/aic.17206 ↗
59. 10.1021/ja962176010.1021/ja9621760 ↗
60. 10.1016/j.commatsci.2019.05.02610.1016/j.commatsci.2019.05.026 ↗
61. 10.1021/acs.langmuir.7b0247910.1021/acs.langmuir.7b02479 ↗
62. 10.1021/la504985810.1021/la5049858 ↗
63. 10.1016/j.softx.2015.06.00110.1016/j.softx.2015.06.001 ↗
64. Gowers, R.; Linke, M.; Barnoud, J.; Reddy, T.; Melo, M.; Seyler, S.; Domański, J.; Dotson, D.; Buchoux, S.; Kenney, I.; Beckstein, O. MDAnalysis: A Python Package for the Rapid Analysis of Molecular Dynamics Simulations; Proceedings of the Python in Science Conference; SciPy Proceedings: Austin, TX, 2016; pp 98–105 10.25080/majora-629e541a-00e.10.25080/majora-629e541a-00e ↗
65. 10.1002/jcc.2178710.1002/jcc.21787 ↗
66. Morrison R. T. · 1992
67. 10.1021/acs.langmuir.5b0380710.1021/acs.langmuir.5b03807 ↗
68. 10.1021/jp904809h10.1021/jp904809h ↗
69. 10.1021/la053522710.1021/la0535227 ↗
70. 10.1021/jp036674o10.1021/jp036674o ↗
71. 10.1080/0144235050022589410.1080/01442350500225894 ↗
72. 10.1016/j.ijadhadh.2017.12.00210.1016/j.ijadhadh.2017.12.002 ↗
73. 10.1021/ja00005a00410.1021/ja00005a004 ↗