Investigating the origin of the nonradiative decay of bound excitons in GaN nanowires
Christian Hauswald, Pierre Corfdir, Johannes K. Zettler, Vladimir M., Kaganer, Karl K. Sabelfeld, Sergio Fern\'andez-Garrido, Timur Flissikowski,, Vincent Consonni, Tobias Gotschke, Holger T. Grahn, Lutz Geelhaar, Oliver, Brandt

TL;DR
This study investigates the rapid nonradiative recombination of excitons in GaN nanowires, revealing that point defects, rather than surface or coalescence defects, dominate the decay process across a range of temperatures.
Contribution
It demonstrates that nonradiative decay in GaN nanowires is primarily caused by point defects, challenging previous assumptions about surface or coalescence-related defects being the main factors.
Findings
Nonradiative decay dominates between 10 and 300 K.
Bound and free excitons are strongly coupled with a common lifetime.
Decay times do not correlate with surface-to-volume ratio or coalescence degree.
Abstract
We investigate the origin of the fast recombination dynamics of bound and free excitons in GaN nanowire ensembles by temperature-dependent photoluminescence spectroscopy using both continuous-wave and pulsed excitation. The exciton recombination in the present GaN nanowires is dominated by a nonradiative channel between 10 and 300 K. Furthermore, bound and free excitons in GaN NWs are strongly coupled even at low temperatures resulting in a common lifetime of these states. By solving the rate equations for a coupled two-level system, we show that one cannot, in practice, distinguish whether the nonradiative decay occurs directly via the bound or indirectly via the free state. The nanowire surface and coalescence-induced dislocations appear to be the most obvious candidates for nonradiative defects, and we thus compare the exciton decay times measured for a variety of GaN nanowire…
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