journal article·2014-02-25

Aerosolized Droplet Mediated Self-Assembly of Photosynthetic Pigment Analogues and Deposition onto Substrates

Vivek B. Shah, Pratim Biswas

ACS Nano· Volume 8· Issue 2
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Abstract

Self-assembled photosynthetic molecules have a high extinction coefficient and a broad absorption in the infrared region, and these properties can be used to improve the efficiency of solar cells. We have developed a single-step method for the self-assembly of synthetic chlorin molecules (analogues of native bacteriochlorophylls) in aerosolized droplets, containing a single solvent and two solvents, to synthesize biomimetic light-harvesting structures. In the single-solvent approach, assembly is promoted by a concentration-driven process due to evaporation of the solvent. The peak absorbance of Zn(II) 3-(1-hydroxyethyl)-10-phenyl-13(1)-oxophorbine (1) in methanol shifted from 646 nm to 725 nm (∼ 80 nm shift) after assembly, which is comparable to the shift observed in the naturally occurring assembly of bacteriochlorophyll c. Although assembly is thermodynamically favorable, the kinetics of self-assembly play an important role, and this was demonstrated by varying the initial concentration of the pigment monomer. To overcome kinetic limitations, a two-solvent approach using a volatile solvent (tetrahydrofuran) in which the dye is soluble and a less volatile solvent (ethanol) in which the dye is sparingly soluble was demonstrated to be effective. The effect of molecular structure is demonstrated by spraying the sterically hindered Zn(II) 3-(1-hydroxyethyl)-10-mesityl-13(1)-oxophorbine (2), which is an analogue of 1, under similar conditions. The results illustrate a valuable and facile aerosol-based method for the formation of films of supramolecular assemblies.
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Research context

OpenAlex topics: Photosynthetic Processes and Mechanisms · Porphyrin and Phthalocyanine Chemistry · Spectroscopy and Quantum Chemical Studies

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

Affiliations

Aerosol and Air Quality Research Laboratory, Department of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, Missouri 63130, United States

References (51)

Show source-provided references
1. Peet J. · Acc. Chem. Res. · 2009 · 42 · 170010.1021/ar900065j ↗
2. Tange R. · J. Mater. Res. · 2011 · 26 · 306
3. Fiorini C. · Opto-Electron. Rev. · 2010 · 18 · 37610.2478/s11772-010-0046-3 ↗
4. Tam J. M. · ACS Nano · 2010 · 4 · 217810.1021/nn9015746 ↗
5. Kim D. H. · Adv. Mater. · 2007 · 19 · 67810.1002/adma.200601259 ↗
6. Palmer R. E. · ACS Nano · 2013 · 7 · 641610.1021/nn403955e ↗
7. Lee C. · J. Electron. Mater. · 2005 · 34 · 110.1007/s11664-005-0172-8 ↗
8. Zhang S. · Nat. Biotechnol. · 2003 · 21 · 117110.1038/nbt874 ↗
9. Hirose T. · J. Mol. Catal. A: Chem. · 2003 · 193 · 2710.1016/S1381-1169(02)00478-8 ↗
10. Schmidt-Mende L. · Science · 2001 · 293 · 111910.1126/science.293.5532.1119 ↗
11. De Rosa C. · Nature · 2000 · 405 · 43310.1038/35013018 ↗
12. Lindsey J. S. · New J. Chem. · 1991 · 15 · 153
13. Whitesides G. M. · Science · 1991 · 254 · 131210.1126/science.1962191 ↗
14. Whitesides G. M. · Science · 2002 · 295 · 241810.1126/science.1070821 ↗
15. Miras H. N. · Chem. Commun. · 2009 · 129710.1039/b819534j ↗
16. Frigaard N.-U. · 2006 · 2 · 7910.1007/7171_021 ↗
17. Overmann J. · Limnol. Oceanogr. · 1992 · 37 · 15010.4319/lo.1992.37.1.0150 ↗
18. Blankenship R. E. · 200210.1002/9780470758472 ↗
19. Huijser A. · J. Phys. Chem. C · 2007 · 111 · 1172610.1021/jp072927s ↗
20. Modesto-Lopez L. B. · Energy Env. Sci. · 2010 · 3 · 21610.1039/B914758F ↗
21. Jelley E. E. · Nature · 1936 · 138 · 100910.1038/1381009a0 ↗
22. Mass O. · New J. Chem. · 2011 · 35 · 267110.1039/c1nj20611g ↗
23. Huber V. · Angew. Chem., Int. Ed. · 2005 · 44 · 314710.1002/anie.200462762 ↗
24. Roger C. · J. Am. Chem. Soc. · 2006 · 128 · 654210.1021/ja0584469 ↗
25. Balaban T. S. · Acc. Chem. Res. · 2005 · 38 · 61210.1021/ar040211z ↗
26. Miyatake T. · Helv. Chim. Acta · 1999 · 82 · 79710.1002/(SICI)1522-2675(19990609)82:6<797::AID-HLCA797>3.0.CO;2-9 ↗
27. Shahar C. · ACS Nano · 2013 · 7 · 354710.1021/nn400484y ↗
28. Miyatake T. · Photochem. Photobiol. · 1999 · 69 · 44810.1111/j.1751-1097.1999.tb03311.x ↗
29. Misawa K. · Appl. Phys. Lett. · 1993 · 63 · 57710.1063/1.109954 ↗
30. Mayerhoffer U. · Angew. Chem., Int. Ed. · 2012 · 51 · 561510.1002/anie.201200897 ↗
31. Miyatake T. · Coord. Chem. Rev. · 2010 · 254 · 259310.1016/j.ccr.2009.12.027 ↗
32. Horn D. · Angew. Chem., Int. Ed. · 2001 · 40 · 433010.1002/1521-3773(20011203)40:23<4330::AID-ANIE4330>3.0.CO;2-W ↗
33. Numata M. · Angew. Chem., Int. Ed. · 2012 · 51 · 184410.1002/anie.201106632 ↗
34. Mobius D. · J. Appl. Phys. · 1988 · 64 · 513810.1063/1.342421 ↗
35. Jiao J. · J. Am. Chem. Soc. · 2006 · 128 · 696510.1021/ja060906q ↗
36. Liu Z. · Chem. Mater. · 2005 · 17 · 372810.1021/cm047858y ↗
37. Lu Y. F. · Nature · 1999 · 398 · 22310.1038/18410 ↗
38. Moon J. H. · Adv. Mater. · 2004 · 16 · 60510.1002/adma.200305446 ↗
39. Lee S. Y. · ACS Nano · 2010 · 4 · 471710.1021/nn101297c ↗
40. Wang W. N. · Catal. Sci. Technol. · 2011 · 1 · 59310.1039/c0cy00091d ↗
41. Wu C. · Langmuir · 2010 · 26 · 432710.1021/la903421y ↗
42. Langley G. J. · Rapid Commun. Mass Spectrom. · 1997 · 11 · 16510.1002/(SICI)1097-0231(19970131)11:2<165::AID-RCM732>3.0.CO;2-T ↗
43. Alcalde E. · Rapid Commun. Mass Spectrom. · 2000 · 14 · 101410.1002/(SICI)1097-0231(20000615)14:11<1014::AID-RCM982>3.0.CO;2-N ↗
44. Novoderezhkin V. · Chem. Phys. Lett. · 2001 · 335 · 23410.1016/S0009-2614(01)00045-8 ↗
45. Muenter A. A. · J. Phys. Chem. · 1992 · 96 · 278310.1021/j100186a002 ↗
46. Roden J. · Int. J. Mod. Phys. B · 2010 · 24 · 506010.1142/S0217979210057201 ↗
47. Basak S. · Chem. Eng. Sci. · 2007 · 62 · 126310.1016/j.ces.2006.11.029 ↗
48. Chen D.-R. · Aerosol Sci. Technol. · 1997 · 27 · 36710.1080/02786829708965479 ↗
49. Kashchiev D. · 2000
50. Chen D. R. · J. Aerosol Sci. · 1995 · 26 · 96310.1016/0021-8502(95)00027-A ↗
51. Hinds W. C. · 1999