Abstract

Streak camera measurements of luminescence from ZnO single crystals as a function of temperature show that the spontaneous radiative lifetime of the “free exciton” band at 380nm is 440ps at room temperature, decreasing to 290ps at 85K. The donor-bound exciton lifetime is 50ps from 85K down to 16K, the lowest temperature we measured. This is significantly faster than is consistent with the dipole matrix element of any single atom transition scaled to the same wavelength. We discuss the oscillator strength of extended exciton states based on the theory of defect-bound excitons, and examine its limit for free excitons. In that regard, we ask what physically limits the coherent dipole size and how a material might be engineered for “giant” exciton oscillator strength. The phenomenon applies to single excitons, not just coherently produced multiple excitations.

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