Abstract
A new technique for measuring extremely fast excited state relaxation times, on the order of or less than the laser pulse width, in the presence of a longer relaxation time is described. The difficulties involved in using the conventional pump-and-probe technique and the corresponding advantages of the new technique are illustrated with numerical examples for specific three-level systems. Qualitative experimental results on semiconductors and organic dye molecules substantiating the results are shown.
| Original language | English |
|---|---|
| Pages (from-to) | 989-991 |
| Number of pages | 3 |
| Journal | Applied Physics Letters |
| Volume | 43 |
| Issue number | 11 |
| DOIs | |
| State | Published - Dec 1 1983 |
| Externally published | Yes |
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