Hostname: page-component-8448b6f56d-qsmjn Total loading time: 0 Render date: 2024-04-23T07:53:21.892Z Has data issue: false hasContentIssue false
  • English
  • Français

Nanocrystal Quantum Dots: Building Blocks for Tunable Optical Amplifiers and Lasers

Published online by Cambridge University Press:  21 March 2011

Jennifer A. Hollingsworth ,
Alexander A. Mikhailovsky ,
Anton Malko ,
Victor I. Klimov ,
Catherine A. Leatherdale ,
Hans –J. Eisler  and
Moungi G. Bawendi
Jennifer A. Hollingsworth
Affiliation:
Physical Chemistry and Applied Spectroscopy, Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM 87545, USA
Alexander A. Mikhailovsky
Affiliation:
Physical Chemistry and Applied Spectroscopy, Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM 87545, USA
Anton Malko
Affiliation:
Physical Chemistry and Applied Spectroscopy, Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM 87545, USA
Victor I. Klimov
Affiliation:
Physical Chemistry and Applied Spectroscopy, Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM 87545, USA
Catherine A. Leatherdale
Affiliation:
Department of Chemistry and Center for Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
Hans –J. Eisler
Affiliation:
Department of Chemistry and Center for Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
Moungi G. Bawendi
Affiliation:
Department of Chemistry and Center for Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
Get access

Abstract

We study optical processes relevant to optical amplification and lasing in CdSe nanocrystal quantum dots (NQD). NQDs are freestanding nanoparticles prepared using solution-based organometallic reactions originally developed for the Cd chalcogenides, CdS, CdSe and CdTe [J. Am. Chem. Soc. 115, 8706 (1993)]. We investigate NQDs with diameters ranging from 2 to 8 nm. Due to strong quantum confinement, they exhibit size-dependent spectral tunability over an energy range as wide as several hundred meV. We observe a strong effect of the matrix/solvent on optical gain properties of CdSe NQDs. In most of the commonly used solvents (such as hexane and toluene), gain is suppressed due to strong photoinduced absorption associated with carriers trapped at solvent-related interface states. In contrast, matrix-free close packed NQD films (NQD solids) exhibit large optical gain with a magnitude that is sufficiently high for the optical gain to successfully compete with multiparticle Auger recombination [Science 287, 10117 (2000)]. These films exhibit narrowband stimulated emission at both cryogenic and room temperature, and the emission color is tunable with dot size [Science 290, 314 (2000)]. Moreover, the NQD films can be incorporated into microcavities of different geometries (micro-spheres, wires, tubes) that produce lasing in whispering gallery modes. The facile preparation, chemical flexibility and wide-range spectral tunability due to strong quantum confinement are the key advantages that should motivate research into NQD applications in optical amplifiers and lasers.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 667: Symposium G – Luminescence and Luminescent Materials , 2001 , G6.1
Copyright
Copyright © Materials Research Society 2001

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

1. Asada, M., Miyamoto, Y., and Suematsu, Y., IEEE J. Quantum Electron. QE–22, 1915 (1986).Google Scholar
2. Ledentsov, N. N., et al., Semiconductors 28, 832 (1994).Google Scholar
3. Kistaedter, N. et al., Electron. Lett. 30, 1416 (1994).Google Scholar
4. Grundman, M., Physica E 5, 167 (2000).Google Scholar
5. Murray, C. B., Norris, D. J., and Bawendi, M. G., J. Am. Chem. Soc. 115, 8706 (1993).Google Scholar
6. Klimov, V. and McBranch, D., Opt. Lett. 23, 277 (1998).Google Scholar
7. Klimov, V. I., Schwarz, Ch. J., McBranch, D. W., Leatherdale, C. A., and Bawendi, M. G., Phys. Rev. B 60, R2177 (1999).Google Scholar
8. Klimov, V. I., Mikhailovsky, A. A., Xu, Su, Malko, A., Hollingsworth, J. A., Leatherdale, C. A., Eisler, H.-J., and Bawendi, M. G., Science 290, 314 (2000).Google Scholar
9. Nirmal, M. et al., Phys. Rev. Lett. 75, 3728 (1995).Google Scholar
10. Klimov, V. I., Mikhailovsky, A. A., McBranch, D. W., Leatherdale, C. A., and Bawendi, M. G., Science 287, 10117 (2000).Google Scholar
11. Chepic, D., Efros, A. L., Ekimov, A., Ivanov, M., Kharchenko, V. A., and Kudriavtsev, I., J. Luminescence 47, 113 (1990).Google Scholar
12.In progress.Google Scholar