Issue 24, 2021

Observation of microsecond luminescence while studying two DNA-stabilized silver nanoclusters emitting in the 800–900 nm range

Abstract

We investigated two DNA-stabilized silver nanoclusters (DNA-AgNCs) that show multiple absorption features in the visible region, and emit around 811 nm (DNA811-AgNC) and 841 nm (DNA841-AgNC). Both DNA-AgNCs have large Stokes shifts and can be efficiently excited with red light. A comparison with the commercially available Atto740 yielded fluorescence quantum yields in the same order of magnitude, but a higher photon output above 800 nm since both DNA-AgNCs are more red-shifted. The study of both DNA-AgNCs also revealed previously unobserved photophysical behavior for this class of emitters. The fluorescence quantum yield and decay time of DNA841-AgNC can be increased upon consecutive heating/cooling cycles. DNA811-AgNC has an additional absorption band around 470 nm, which is parallel in orientation to the lowest energy transition at 640 nm. Furthermore, we observed for the first time a DNA-AgNC population (as part of the DNA811-AgNC sample) with green and near-infrared emissive states with nanosecond and microsecond decay times, respectively. A similar dual emissive DNA-AgNC stabilized by a different 10-base DNA strand is also reported in the manuscript. These two examples highlight the need to investigate the presence of red-shifted microsecond emission for this class of emitters.

Graphical abstract: Observation of microsecond luminescence while studying two DNA-stabilized silver nanoclusters emitting in the 800–900 nm range

Supplementary files

Article information

Article type
Paper
Submitted
21 Apr 2021
Accepted
03 Jun 2021
First published
03 Jun 2021
This article is Open Access
Creative Commons BY license

Phys. Chem. Chem. Phys., 2021,23, 13483-13489

Observation of microsecond luminescence while studying two DNA-stabilized silver nanoclusters emitting in the 800–900 nm range

V. Rück, C. Cerretani, V. A. Neacşu, M. B. Liisberg and T. Vosch, Phys. Chem. Chem. Phys., 2021, 23, 13483 DOI: 10.1039/D1CP01731D

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