journal article·2004-11-01

Conjugated Oligothiophene-Dendron-Capped CdSe Nanoparticles: Synthesis and Energy Transfer

Jason Locklin, Derek Patton, Suxiang Deng, Akira Baba, Mitchel Millan, Rigoberto C. Advincula

Chemistry of Materials· Volume 16· Issue 24
Publisher page

Abstract

In this study, we demonstrate the synthesis of branched oligothiophene dendrons that act as electroactive surfactants for the capping of CdSe nanocrystals through a ligand exchange process. The number of dendrons per nanocrystal and the nature of surface coordination interactions were studied in detail using UV−vis, FT-IR, AFM, and photoluminescence spectroscopies. These dendron/nanocrystal complexes are very soluble in nonpolar solvents and exhibit photoinduced charge-transfer interactions between the two species. One-layer photovoltaic cells were fabricated that showed initial power conversion efficiencies of 0.29%.
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Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Perovskite Materials and Applications

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

Affiliations

Department of Chemistry, University of Houston, Houston, Texas 77204

References (29)

Show source-provided references
1. Peng Z. A. · J. Am. Chem. Soc. · 2001 · 123 · 18310.1021/ja003633m ↗
2. Peng X. · Chem.Eur. J. · 2002 · 8 · 33410.1002/1521-3765(20020118)8:2<334::AID-CHEM334>3.0.CO;2-T ↗
3. Murray C. B. · J. Am. Chem. Soc. · 1993 · 115 · 870610.1021/ja00072a025 ↗
4. Peng X. G. · J. Am. Chem. Soc. · 1998 · 120 · 534310.1021/ja9805425 ↗
5. Aldana J. · J. Am. Chem. Soc. · 2001 · 123 · 884410.1021/ja016424q ↗
6. Wang Y. A. · J. Am. Chem. Soc. · 2002 · 124 · 229310.1021/ja016711u ↗
7. Guo W. · J. Am. Chem. Soc. · 2003 · 125 · 390110.1021/ja028469c ↗
8. Xia C. · Org. Lett. · 2002 · 4 · 206710.1021/ol025943a ↗
9. Xia C. · J. Am. Chem. Soc. · 2004 · 126 · 873510.1021/ja0484404 ↗
10. Mattoussi H. · J. Appl. Phys. · 1998 · 83 · 796510.1063/1.367978 ↗
11. Dabbousi B. O. · Appl. Phys. Lett. · 1995 · 66 · 131610.1063/1.113227 ↗
12. Gao M. · J. Phys. Chem. B · 1998 · 102 · 409610.1021/jp980620a ↗
13. Huynh W. U. · Adv. Mater. · 1999 · 11 · 92310.1002/(SICI)1521-4095(199908)11:11<923::AID-ADMA923>3.0.CO;2-T ↗
14. Huynh W. U. · Science · 2002 · 295 · 242510.1126/science.1069156 ↗
15. Sun B. · Nano Lett. · 2003 · 3 · 96110.1021/nl0342895 ↗
16. Milliron D. J. · J. Adv. Mater. · 2003 · 15 · 5810.1002/adma.200390011 ↗
17. Tavs P. · Chem. Ber. · 1970 · 103 · 242810.1002/cber.19701030815 ↗
18. McKenna C. E. · Tetrahedron Lett. · 1977 · 2 · 15510.1016/S0040-4039(01)92575-4 ↗
19. Kern W. · Semicond. Int. · 1984 · 94
20. Katari J. E. B. · J. Phys. Chem. · 1994 · 98 · 410910.1021/j100066a034 ↗
21. Eilon M. J. · J. Phys. Chem. B · 2001 · 105 · 1272610.1021/jp012577o ↗
22. Kuno M. · J. Chem. Phys. · 1997 · 106 · 986910.1063/1.473875 ↗
23. Peng Z. A. · J. Am. Chem. Soc. · 2002 · 124 · 334310.1021/ja0173167 ↗
24. Corbridge D. E. C. · 1969 · 6
25. Artzi R. · Langmuir · 2003 · 19 · 739210.1021/la0344534 ↗
26. Chalmers J. M. · 2002
27. Hotta S. · Macromolecules · 1987 · 20 · 21210.1021/ma00167a038 ↗
28. Socrates G. · 1980
29. Yu W. W. · Chem. Mater. · 2003 · 15 · 285410.1021/cm034081k ↗