Polycyclic Aromatic Hydrocarbon for the Detection of Nonpolar Analytes under Counteracting Humidity Conditions
Source abstract
Abstract
Real-world samples contain reducing and oxidizing chemical agents as well as large and small (bio)molecules, which are polar or nonpolar in nature. Sensing nonpolar analytes, which is of paramount importance for a wide variety of applications, is generally more difficult to achieve than sensing polar analytes. Here, we report on empirical observations of a unique polycyclic aromatic hydrocarbon derivative, referred as PAH-A, whose structure has a triangular-shaped aromatic core (with a carbon number of 60) and contains hydrophobic mesogens terminated with hydrophobic alkyl chains. We show that films made of PAH-A enable excellent sensitivity to nonpolar analytes, compared to polar analytes, in a setting of 5-40% counteracting relative humidity. This finding is based on monitoring the changes in the physical/optical properties of thin PAH-A films upon exposure to nonpolar and polar analytes, by means of quartz crystal microbalance and spectroscopic ellipsometry measurements. A comparison with other polycyclic aromatic hydrocarbon derivatives with different cores or organic functionalities is provided and discussed.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Chemical Sensor Technologies · Analytical Chemistry and Chromatography · Metabolomics and Mass Spectrometry Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
The Department of Chemical Engineering and the Russell Berrie Nanotechnology Institute, Technion − Israel Institute of Technology, Haifa 32000, Israel
The Department of Electronics, Electrical and Automatic Engineering, Rovira i Virgili University, 43007 Tarragona, Spain
Max-Planck-Institute for Polymer Research, Postfach 3148, D-55021 Mainz, Germany
References (45)
Show source-provided references
1. Tisch U. · MRS Bull. · 2010 · 35 · 79710.1557/mrs2010.509 ↗
2. Tisch U. · CML–Lung Cancer · 2012 · 5 · 107
3. Tisch U. · Rev. Chem. Eng. · 2010 · 26 · 17110.1515/revce.2010.009 ↗
4. Peng G. · Nat. Nanotechnol. · 2009 · 4 · 66910.1038/nnano.2009.235 ↗
5. Peng G. · Nano Lett. · 2009 · 9 · 136210.1021/nl8030218 ↗
6. Ionescu R. · ACS Chem. Neurosci. · 2011 · 2 · 68710.1021/cn2000603 ↗
7. Barash O. · Nanomedicine · 2012 · 8 · 58010.1016/j.nano.2011.10.001 ↗
8. Barash O. · Small · 2009 · 5 · 261810.1002/smll.200900937 ↗
9. Rock F. · Chem. Rev. · 2008 · 108 · 70510.1021/cr068121q ↗
10. Dickert F. L. · Sens. Actuat. B · 2000 · 70 · 26310.1016/S0925-4005(00)00578-5 ↗
11. Paska Y. · ACS Nano · 2012 · 6 · 33510.1021/nn203653h ↗
12. Paska Y. · ACS Appl. Mater. Interface · 2012 · 4 · 260410.1021/am300288z ↗
13. Paska Y. · ACS Nano · 2011 · 5 · 562010.1021/nn201184c ↗
14. Haick H. · J. Phys. D · 2007 · 40 · 717310.1088/0022-3727/40/23/S01 ↗
15. Angione M. D. · Mater. Today · 2011 · 14 · 42410.1016/S1369-7021(11)70187-0 ↗
16. Crowe L. L. · Langmuir · 2007 · 23 · 622710.1021/la700455b ↗
17. Konvalina G. · ACS Appl. Mater. Interface · 2012 · 4 · 31710.1021/am2013695 ↗
18. Zilberman Y. · ACS Nano · 2011 · 5 · 674310.1021/nn202314k ↗
19. Zilberman Y. · Adv. Mater. · 2010 · 22 · 431710.1002/adma.201001275 ↗
20. Zilberman Y. · Langmuir · 2009 · 25 · 541110.1021/la8042928 ↗
21. Feng X. L. · Adv. Mater. · 2008 · 14 · 268410.1002/adma.200800642 ↗
22. Kastler M. · J. Am. Chem. Soc. · 2005 · 127 · 428610.1021/ja0430696 ↗
23. Stabel A. · Angew. Chem., Int. Ed. · 1995 · 34 · 160910.1002/anie.199516091 ↗
24. Feng X. L. · Angew. Chem., Int. Ed. · 2008 · 47 · 170310.1002/anie.200703967 ↗
25. Feng X. L. · J. Am. Chem. Soc. · 2009 · 131 · 443910.1021/ja808979t ↗
26. Feng X. L. · Nat. Mater. · 2009 · 8 · 42110.1038/nmat2427 ↗
27. Yan H.-Q. · Sens. Actuators, B · 1993 · 10 · 13310.1016/0925-4005(93)80036-B ↗
28. Zarnik M. S. · Metrol. Meas. Syst. · 2012 · 13310.2478/v10178-012-0012-0 ↗
29. Bouhadid M. · Macromol. Symp. · 2008 · 268 · 910.1002/masy.200850802 ↗
30. Bai Z. · Mater. Sci. Eng. · 2008 · 149 · 1210.1016/j.mseb.2007.11.020 ↗
31. Belghachi A. · J. Phys. D · 1990 · 23 · 22310.1088/0022-3727/23/2/014 ↗
32. Eaton K. · Sens. Actuators, B · 2002 · 82 · 9410.1016/S0925-4005(01)00996-0 ↗
33. Vlachos D. S. · Sens. Actuators, B · 1995 · 24 · 49110.1016/0925-4005(95)85105-4 ↗
34. Aspnes D. E. · J. Electrochem. Soc. · 1980 · 127 · 135910.1149/1.2129899 ↗
35. Philipp H. R. · 1985
36. Leinfellner N. · Microelectron. Rel. · 2000 · 40 · 87310.1016/S0026-2714(99)00333-9 ↗
37. Bennett M. E. · J. Phys. Chem. C · 2008 · 112 · 1727210.1021/jp801476f ↗
38. Li B. · Nano Lett. · 2008 · 8 · 356310.1021/nl072314r ↗
39. Ekinci K. L. · Appl. Phys. Lett. · 2004 · 84 · 446910.1063/1.1755417 ↗
40. Ekinci K. L. · J. Appl. Phys. · 2004 · 95 · 268210.1063/1.1642738 ↗
41. Gardner J. W. · 199910.1093/oso/9780198559559.001.0001 ↗
42. Faglia G. · Sens. Actuat. B · 1997 · 44 · 51710.1016/S0925-4005(97)00174-3 ↗
43. Patel S. V. · Sens. Actuators, B · 2003 · 96 · 54110.1016/S0925-4005(03)00637-3 ↗
44. Yu H. · Proc. IEEE Sens. · 2003 · 2 · 1333
45. Di Natale C. · Biosens. Bioelectron. · 2003 · 18 · 120910.1016/S0956-5663(03)00086-1 ↗