A DNA‐Stabilized Ag1812+ Cluster with Excitation‐Intensity‐Dependent Dual Emission

Author:

Rück Vanessa1ORCID,Liisberg Mikkel B.1ORCID,Mollerup Christian Brinch2ORCID,He Yanmei3,Chen Junsheng1ORCID,Cerretani Cecilia1ORCID,Vosch Tom1ORCID

Affiliation:

1. Department of Chemistry University of Copenhagen Universitetsparken 5 2100 Copenhagen Denmark

2. Department of Forensic Medicine University of Copenhagen Frederik V's Vej 11 2100 Copenhagen Denmark

3. Division of Chemical Physics and NanoLund Lund University P.O. Box 124 22100 Lund Sweden

Abstract

AbstractDNA‐stabilized silver nanoclusters (DNA‐AgNCs) are easily tunable emitters with intriguing photophysical properties. Here, a DNA‐AgNC with dual emission in the red and near‐infrared (NIR) regions is presented. Mass spectrometry data showed that two DNA strands stabilize 18 silver atoms with a nanocluster charge of 12+. Besides determining the composition and charge of DNA2[Ag18]12+, steady‐state and time‐resolved methods were applied to characterize the picosecond red fluorescence and the relatively intense microsecond‐lived NIR luminescence. During this process, the luminescence‐to‐fluorescence ratio was found to be excitation‐intensity‐dependent. This peculiar feature is very rare for molecular emitters and allows the use of DNA2[Ag18]12+ as a nanoscale excitation intensity probe. For this purpose, calibration curves were constructed using three different approaches based either on steady‐state or time‐resolved emission measurements. The results showed that processes like thermally activated delayed fluorescence (TADF) or photon upconversion through triplet‐triplet annihilation (TTA) could be excluded for DNA2[Ag18]12+. We, therefore, speculate that the ratiometric excitation intensity response could be the result of optically activated delayed fluorescence.

Funder

Villum Fonden

Teknologi og Produktion, Det Frie Forskningsråd

Novo Nordisk Fonden

China Scholarship Council

Publisher

Wiley

Subject

General Chemistry,Catalysis

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