Picosecond time-resolved photoluminescence measurements were performed on CdSe core and CdSe/ZnS core/shell colloidal quantum dots (QDs). Photoluminescence (PL) emission is observed to originate from intrinsic ±1U and ±1L bright states with lifetimes of 60 and 450 ps, respectively, and from a long living component with nanosecond lifetimes. The latter is attribuited to the emission from surface states (ss) approximately 16 and 13 meV below the ±1L state for core and core/shell QDs, respectively. We show that in the temperature range between 15 and 70 K the three recombination processes compete and they are thermally populated through different pathways (±1L → ±1U and ss → ±1L) © 2007 American Chemical Society.

Picosecond photoluminescence decay time in colloidal nanocrystals: The role of intrinsic and surface states

Morello G.
Primo
;
Cozzoli P. D.;Manna L.;De Giorgi M.
2007

Abstract

Picosecond time-resolved photoluminescence measurements were performed on CdSe core and CdSe/ZnS core/shell colloidal quantum dots (QDs). Photoluminescence (PL) emission is observed to originate from intrinsic ±1U and ±1L bright states with lifetimes of 60 and 450 ps, respectively, and from a long living component with nanosecond lifetimes. The latter is attribuited to the emission from surface states (ss) approximately 16 and 13 meV below the ±1L state for core and core/shell QDs, respectively. We show that in the temperature range between 15 and 70 K the three recombination processes compete and they are thermally populated through different pathways (±1L → ±1U and ss → ±1L) © 2007 American Chemical Society.
2007
INFM (attivo dal 18/11/1923 al 31/12/2021)
colloidal nanocrystals
time resolved
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/517838
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