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EN
We demonstrate coexistence of slow and fast components of photoluminescence decay of the Mn^{2+} intra-shell emission in nanoparticles of CdMnS. We explain the observed decrease in PL lifetime of the Mn^{2+} intra-shell transition by high efficiency of spin dependent magnetic interactions between localized spins of Mn^{2+} ions and free carriers. This mechanism is enhanced in nanostructures, but it is also present in bulk samples.
EN
Bulk samples, layers, quantum well, and quantum dot structures of II-Mn-VI samples all show coexistence of slow and fast components of Mn^{2+} photoluminescence decay. Thus, fast photoluminescence decay cannot be related to low dimensionality of a host material. This also means that the model of the so-called quantum confined atom is incorrect. Based on the results of time-resolved photoluminescence and optically detected magnetic resonance investigations we relate the observed lifetime decrease in Mn^{2+} intra-shell transition to spin dependent magnetic interactions between localized spins of Mn^{2+} ions and between Mn^{2+} ions and spins/magnetic moments of free carriers. The latter mechanism is enhanced in nanostructures.
EN
Based on the results of optically detected magnetic resonance and time-resolved investigations we relate the observed lifetime shortening of intra-shell Mn^{2+} emission to spin dependent magnetic interactions between localized spins of Mn^{2+} ions and spins/magnetic moments of free carriers. We show that this mechanism is active in both bulk and in low dimensional structures, such as quantum wells, quantum dots, and nanostructures.
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