journal article·2016-09-20

Substrate-Mediated Cooperative Adsorption of Sodium Cholate on (6,5) Single-Wall Carbon Nanotubes

Felix F. Bergler, Sabine Stahl, Annika Goy, Friedrich Schöppler, Tobias Hertel

Langmuir· Volume 32· Issue 37
Publisher page

Abstract

The interaction of sodium cholate (NaC) with (6,5) single-wall carbon nanotubes (SWNTs) is investigated using photoluminescence spectroscopy. Dilution of SWNT-NaC suspensions is accompanied by changes in the exciton PL quantum yield and peak emission energy. An abrupt change of the exciton emission peak energy at NaC concentrations between 10 and 14 mM indicates strongly cooperative formation of a micellar phase on (6,5) SWNT surfaces with a Hill coefficient of nH = 65 ± 6. This is in contrast to the formation of free NaC micelles with aggregation numbers of only about 4 and suggests that the cooperativity of NaC micelle formation on nanotube surfaces is strongly substrate-enhanced. The temperature dependence of this previously unobserved transition is used for a determination of ΔmicG(⊖)/(1 + β) = -(11.4 ± 0.2) kJ·mol(-1) which, for typical Na(+) counterion binding with β ≈ 0.2, yields a free SWNT-NaC micellization enthalpy ΔmicG(⊖) of -13.7 kJ·mol(-1).
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Research context

OpenAlex topics: Carbon Nanotubes in Composites · Nanopore and Nanochannel Transport Studies · Graphene research and applications

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

Affiliations

Institute of Physical and Theoretical Chemistry and ‡Röntgen Research Center for Complex Material Systems, Julius-Maximilian University Würzburg, 97070 Würzburg, Germany

References (43)

Show source-provided references
1. 10.1126/science.107263110.1126/science.1072631 ↗
2. 10.1002/adfm.20040013010.1002/adfm.200400130 ↗
3. 10.1021/nl050133o10.1021/nl050133o ↗
4. 10.1038/nnano.2006.5210.1038/nnano.2006.52 ↗
5. 10.1021/ja071553d10.1021/ja071553d ↗
6. 10.1038/nnano.2008.13510.1038/nnano.2008.135 ↗
7. 10.1038/nnano.2010.6810.1038/nnano.2010.68 ↗
8. 10.1103/PhysRevLett.104.20740110.1103/PhysRevLett.104.207401 ↗
9. 10.1038/ncomms131310.1038/ncomms1313 ↗
10. 10.1039/c2cp23436j10.1039/c2cp23436j ↗
11. 10.1002/adma.20130487310.1002/adma.201304873 ↗
12. 10.1021/acsnano.5b0470710.1021/acsnano.5b04707 ↗
13. 10.1021/acs.jpcc.5b0686510.1021/acs.jpcc.5b06865 ↗
14. 10.1126/science.110124310.1126/science.1101243 ↗
15. 10.1063/1.219946110.1063/1.2199461 ↗
16. 10.1002/smll.20120139810.1002/smll.201201398 ↗
17. 10.1021/jp107640610.1021/jp1076406 ↗
18. 10.1021/jp509347710.1021/jp5093477 ↗
19. 10.1002/adma.20070235310.1002/adma.200702353 ↗
20. 10.1021/nn101612b10.1021/nn101612b ↗
21. 10.1021/acs.analchem.5b0256310.1021/acs.analchem.5b02563 ↗
22. 10.1021/acs.jpcc.6b0219810.1021/acs.jpcc.6b02198 ↗
23. 10.1021/la402293310.1021/la4022933 ↗
24. 10.1021/la200779310.1021/la2007793 ↗
25. 10.1002/cphc.20130002010.1002/cphc.201300020 ↗
26. 10.1021/nl050069a10.1021/nl050069a ↗
27. 10.1002/pssb.20077612410.1002/pssb.200776124 ↗
28. 10.1063/1.274522810.1063/1.2745228 ↗
29. 10.1039/b927053a10.1039/b927053a ↗
30. 10.1021/jp403711e10.1021/jp403711e ↗
31. 10.1007/BF0276791610.1007/BF02767916 ↗
32. 10.1016/S0021-9797(02)00191-110.1016/S0021-9797(02)00191-1 ↗
33. Carey M. C. · J. Lipid Res. · 1971 · 12 · 60410.1016/S0022-2275(20)39480-3 ↗
34. 10.1016/j.jct.2014.10.01410.1016/j.jct.2014.10.014 ↗
35. 10.1002/anie.20090249010.1002/anie.200902490 ↗
36. Evans D. · 1999
37. 10.1016/S0927-7757(00)00697-X10.1016/S0927-7757(00)00697-X ↗
38. 10.1021/ed900019u10.1021/ed900019u ↗
39. 10.1021/j100030a01910.1021/j100030a019 ↗
40. 10.1103/PhysRevB.70.04541910.1103/PhysRevB.70.045419 ↗
41. 10.1063/1.308984310.1063/1.3089843 ↗
42. 10.1016/S0927-7765(97)00011-810.1016/S0927-7765(97)00011-8 ↗
43. 10.1021/j100550a00110.1021/j100550a001 ↗