Hostname: page-component-8448b6f56d-gtxcr Total loading time: 0 Render date: 2024-04-16T21:46:01.224Z Has data issue: false hasContentIssue false
  • English
  • Français

Chemically Functional Semiconductor Nanocrystals: Electrochemistry and Self-Assembly on Surfaces

Published online by Cambridge University Press:  11 February 2011

Benjamin M. Hutchins ,
Andrew H. Latham  and
Mary Elizabeth Williams
Benjamin M. Hutchins
Affiliation:
Department of Chemistry, The Pennsylvania State University, University Park, PA 16802
Andrew H. Latham
Affiliation:
Department of Chemistry, The Pennsylvania State University, University Park, PA 16802
Mary Elizabeth Williams
Affiliation:
Department of Chemistry, The Pennsylvania State University, University Park, PA 16802
Get access

Abstract

Semiconductor nanocrystals (i.e., Quantum Dots, QDs) exhibit size-dependent emission properties and have synthetically adjustable ligand shells, making them interesting materials for applications ranging from luminescent displays to biomolecular tags. In this paper, the electrochemical properties of two types of nanocrystal are studied with an emphasis on the effect of core/shell vs core structures. The band gap energy of CdSe particles, measured using optical spectroscopy, was shown to increase slightly with the application of a ZnSe shell, as expected based on the increased energy required to transfer an electron through the shell material. The electrochemically determined band gaps are overestimated in the case of CdSe/ZnSe core/shell nanoparticles, reflecting the band gap of the ZnSe shell. Finally, QDs were self-assembled onto gold surfaces by electrostatic and covalent attachment, and their presence confirmed by fluorescence spectroscopy. The high intensity of emitted light shows that the QDs can be self-assembly onto metallic surfaces, without energy transfer quenching of the luminescence.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 737 , 2002 , E13.27
Copyright
Copyright © Materials Research Society 2003

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Trindade, T.; O'Brien, P.; Pickett, N. L. Chem. Mater. 2001, 13, 3843–3858.Google Scholar
2. Eychmuller, A. J. Phys. Chem. B 2000, 104, 6514–6528.Google Scholar
3. Murray, C. B.; Kagan, C. R.; Bawendi, M. G. Annu. Rev. Mater. Sci. 2000, 30, 545.Google Scholar
4. Ding, Z.; Quinn, B. M.; Haram, S. K.; Pell, L. E.; Korgel, B. A.; Bard, A. J. Science 2002, 296, 1293–1297.Google Scholar
5. Wang, Congjun; Shim, Moonsub; Guyot-Sionnest, Philippe Science 2001, 291, 2390–2392.Google Scholar
6. Haram, S. K.; Quinn, B. M.; Bard, A. J. J. Am. Chem. Soc. 2001, 123, 8860–8861.Google Scholar
7. Reiss, P.; Bleuse, J.; Pron, A. Nano Lett. 2002, 2, 781–784.Google Scholar
8. Peng, X.; Schlamp, M. C.; Kadavanich, A. V.; Alivisatos, A. P. J. Am. Chem. Soc. 1997, 119, 7019–1029.Google Scholar
9. Dabbousi, B. O.; Rodriquez-Veijo, J.; Mikulec Frederic, V.; Heine, J. R.; Mattoussi, Hedi; Ober, R.; Bawendi, M. G. J. Phys. Chem. B 1997, 101, 9463–9475.Google Scholar
10. Hines, M. A.; Guyot-Sionnest, P. J. Phys. Chem. 1996, 100, 468–471.Google Scholar