Abstract
DNA-stabilized silver nanoclusters (DNA-AgNCs) are promising fluorophores whose photophysical properties and synthesis procedures have received increased attention in the literature. However, depending on the preparation conditions and the DNA sequence, the DNA-AgNC samples can host a range of different emitters, which can influence the reproducibility of the optical response and the evolution over time of the populations of these emitters. We have developed a simple method to characterize the spectral heterogeneity and time evolution of these emissive species at any given point in time after preparation, by plotting the average decay time as a function of emission wavelength. These so-called average decay time spectra were acquired for different excitation wavelengths of AgNCs stabilized by an oligonucleotide containing 24 cytosines (C24-AgNCs). The average decay time spectra allowed the comparison of sample preparation and the judgment of reproducibility. Therefore, we propose the use of the average decay time spectra as a robust and easy tool to characterize and compare different as-synthesized DNA-AgNC samples. The average decay time spectra can in general also be used to characterize the spectral heterogeneity of other fluorophores, such as luminescent colloidal nanoparticles, and to assess the reproducibility of a synthetic procedure containing an unknown distribution of emissive species.
Highlights
Since the pioneering work of Petty and Dickson, the use of DNA for stabilizing small silver nanoclusters (AgNCs) has been growing rapidly in the last ten years.[1]
C24 was selected since it is known that polycytosine oligonucleotides can stabilize a whole range of emitters that span the visible and near infrared (NIR) region.[12,25,26]
We used the average decay time spectra as a readout to characterize the distribution of emissive AgNCs at a given point in time and for different excitation wavelengths, which is an easy and robust tool providing information on the as-synthesized emissive species distribution
Summary
Since the pioneering work of Petty and Dickson, the use of DNA for stabilizing small silver nanoclusters (AgNCs) has been growing rapidly in the last ten years.[1]. It is well established that polycytosine oligonucleotides stabilize a large range of emissive AgNCs with emission spectra covering the visible range, and some of these emitters show spectral evolution over time.[6,12,25,26,31] High performance liquid chromatography (HPLC) is one method to separate and investigate in detail what was produced during the synthesis. Using the average decay times, the reproducibility, distribution and evolution of the emissive species in the samples can be monitored at various emission wavelengths. This analysis method enables investigation of the composition and evolution of heterogeneous fluorescent samples avoiding tedious separation procedures
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