journal article·2015-10-15

Exciton Formation and Quenching in a Au/CdS Core/Shell Nanostructure

Dirk Ziemannn, Volkhard May

Publisher page

Abstract

An atomistic description is presented of the excited state dynamics in spherical Au/CdS core/shell nanocrystals up to a diameter of 15 nm. Au-core excited states are considered in a multipole plasmon scheme, whereas a tight-binding description combined with a configuration interaction approach is used to compute single electron-hole pair excitations in the CdS-shell. The electron-hole pair energy-shift and screening due to an Au-core polarization is found of minor importance. For the studied system, the energy transfer coupling can be identified as the essential core-shell interaction. Characterizing the CdS-shell excitons by atomic centered transition charges and the Au-core by its multipole plasmon moments, an energy transfer coupling can be introduced that gives a complete microscopic description beyond any dipole-dipole approximation and with values around 10 meV. Together with a considerable plasmon-exciton energy mismatch, these coupling values explain the measured 300 ps lifetime of shell excitons due to energy transfer to the Au-core.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Gold and Silver Nanoparticles Synthesis and Applications

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

Affiliations

Institute für Physik, Humboldt-Universität zu Berlin, Netwonstraße 15, D-12489 Berlin, Germany

Funding

Deutsche Forschungsgemeinschaft

References (34)

Show source-provided references
1. 10.1021/nl048822810.1021/nl0488228 ↗
2. 10.1021/nl802427810.1021/nl8024278 ↗
3. 10.1016/j.nanoen.2011.09.00210.1016/j.nanoen.2011.09.002 ↗
4. 10.1038/nphoton.2011.28510.1038/nphoton.2011.285 ↗
5. 10.1038/nature0831810.1038/nature08318 ↗
6. 10.1021/nl401582710.1021/nl4015827 ↗
7. 10.1021/ja047107x10.1021/ja047107x ↗
8. 10.1021/nl060083310.1021/nl0600833 ↗
9. 10.1126/science.118476910.1126/science.1184769 ↗
10. 10.1021/nn404264w10.1021/nn404264w ↗
11. 10.1021/jp405430m10.1021/jp405430m ↗
12. 10.1021/jp500009k10.1021/jp500009k ↗
13. 10.1021/jp512105m10.1021/jp512105m ↗
14. 10.1021/nl402730m10.1021/nl402730m ↗
15. 10.1021/jz500302310.1021/jz5003023 ↗
16. 10.1021/jp511169610.1021/jp5111696 ↗
17. 10.1103/PhysRevB.53.957910.1103/PhysRevB.53.9579 ↗
18. 10.1103/PhysRevB.60.181910.1103/PhysRevB.60.1819 ↗
19. 10.1103/PhysRevB.73.24532710.1103/PhysRevB.73.245327 ↗
20. 10.1103/PhysRevB.76.07531010.1103/PhysRevB.76.075310 ↗
21. 10.1063/1.311723110.1063/1.3117231 ↗
22. 10.1103/PhysRevB.82.24530410.1103/PhysRevB.82.245304 ↗
23. 10.1103/PhysRevB.74.20530910.1103/PhysRevB.74.205309 ↗
24. 10.1103/PhysRevB.66.20520210.1103/PhysRevB.66.205202 ↗
25. 10.1103/PhysRevB.69.04531610.1103/PhysRevB.69.045316 ↗
26. 10.1002/crat.20041053410.1002/crat.200410534 ↗
27. 10.1021/jp803708r10.1021/jp803708r ↗
28. 10.1021/nl010080k10.1021/nl010080k ↗
29. 10.1103/PhysRevB.81.23530810.1103/PhysRevB.81.235308 ↗
30. 10.1103/PhysRevB.89.03530710.1103/PhysRevB.89.035307 ↗
31. 10.1021/jp305505c10.1021/jp305505c ↗
32. 10.1021/nl050062t10.1021/nl050062t ↗
33. 10.1103/PhysRevB.65.11542110.1103/PhysRevB.65.115421 ↗
34. 10.1103/PhysRevLett.78.219210.1103/PhysRevLett.78.2192 ↗