Excited-State Dynamics in a DNA-Stabilized Ag16 Cluster with Near-Infrared Emission
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Excited-State Dynamics in a DNA-Stabilized Ag16 Cluster with Near-Infrared Emission. / Chen, Junsheng; Kumar, Ajeet; Cerretani, Cecilia; Vosch, Tom; Zigmantas, Donatas; Thyrhaug, Erling.
I: Journal of Physical Chemistry Letters, Bind 14, Nr. 17, 2023, s. 4078-4083.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Excited-State Dynamics in a DNA-Stabilized Ag16 Cluster with Near-Infrared Emission
AU - Chen, Junsheng
AU - Kumar, Ajeet
AU - Cerretani, Cecilia
AU - Vosch, Tom
AU - Zigmantas, Donatas
AU - Thyrhaug, Erling
N1 - Funding Information: T.V. and C.C. acknowledge funding from the Villum Foundation (VKR023115) and the Independent Research Fund Denmark (0136-00024B). D.Z. and E.T. acknowledge support from the Swedish Research Council. J.C. acknowledges support from the Lundbeck Foundation (Grant No. R303-2018-3237). Publisher Copyright: © 2023 The Authors. Published by American Chemical Society.
PY - 2023
Y1 - 2023
N2 - Due to desirable optical properties, such as efficient luminescence and large Stokes shift, DNA-templated silver nanoclusters (DNA-AgNCs) have received significant attention over the past decade. Nevertheless, the excited-state dynamics of these systems are poorly understood, as studies of the processes ultimately leading to a fluorescent state are scarce. Here we investigate the early time relaxation dynamics of a 16-atom silver cluster (DNA-Ag16NC) featuring NIR emission in combination with an unusually large Stokes shift of over 5000 cm-1. We follow the photoinduced dynamics of DNA-Ag16NC on time ranges from tens of femtoseconds to nanoseconds using a combination of ultrafast optical spectroscopies, and extract a kinetic model to clarify the physical picture of the photoinduced dynamics. We expect the obtained model to contribute to guiding research efforts toward elucidating the electronic structure and dynamics of these novel objects and their potential applications in fluorescence-based labeling, imaging, and sensing.
AB - Due to desirable optical properties, such as efficient luminescence and large Stokes shift, DNA-templated silver nanoclusters (DNA-AgNCs) have received significant attention over the past decade. Nevertheless, the excited-state dynamics of these systems are poorly understood, as studies of the processes ultimately leading to a fluorescent state are scarce. Here we investigate the early time relaxation dynamics of a 16-atom silver cluster (DNA-Ag16NC) featuring NIR emission in combination with an unusually large Stokes shift of over 5000 cm-1. We follow the photoinduced dynamics of DNA-Ag16NC on time ranges from tens of femtoseconds to nanoseconds using a combination of ultrafast optical spectroscopies, and extract a kinetic model to clarify the physical picture of the photoinduced dynamics. We expect the obtained model to contribute to guiding research efforts toward elucidating the electronic structure and dynamics of these novel objects and their potential applications in fluorescence-based labeling, imaging, and sensing.
U2 - 10.1021/acs.jpclett.3c00764
DO - 10.1021/acs.jpclett.3c00764
M3 - Journal article
C2 - 37120843
AN - SCOPUS:85156203020
VL - 14
SP - 4078
EP - 4083
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
SN - 1948-7185
IS - 17
ER -
ID: 346453535