Sample fabrication and metrological characterization of single-photon emitters based on nitrogen vacancy centers in nanodiamonds

Author(s):  
Franziska Hirt ◽  
Justus Christinck ◽  
Helmuth Hofer ◽  
Beatrice Rodiek ◽  
Stefan Kueck

Abstract Quantum metrology requires a stable single-photon emission and a high single-photon purity. Since nitrogen-vacancy (NV-) centers provide both features at room temperature, they are promising candidates for the application in this field [1, 2]. The knowledge about a suitable sample preparation technique is crucial, because the quality of the single-photon emission strongly depends on the sample purity and on the spatial resolvability of the emitters. This work presents the comparison and optimization of various sample fabrication techniques of nitrogen vacancy center doped nanodiamonds on standard cover glasses. The preparation is followed by a comparative characterization of the centers of the various samples. The sample fabrication includes the removal of contaminants on the cover glass surface. This was carried out by using peroxymonosulfuric acid (piranha solution, H2SO5) in comparison to the commercially available lye Hellmanex III (by Hellma Analytics). After cleaning the cover glasses, volumes of various nanodiamond dilutions were applied via spin coating. In subsequent steps, the nanodiamonds themselves were cleaned with peroxymonosulfuric acid, too, to remove contaminants resulting from the manufacturing process, e.g. graphite. The samples were analyzed by using a confocal laser scanning microscope with an oil immersion objective. Single-photon purity was determined by measuring the second order correlation function with a Hanbury Brown and Twiss setup. Spectral analysis revealed the presence of NV-- and NV0-centers. It was shown that a suitable cleansing method has an immense impact on single-photon emission, as was proven by a comparative characterization of differently manufactured nanodiamonds.

Pharmaceutics ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 770
Author(s):  
Patrick M. Perrigue ◽  
Richard A. Murray ◽  
Angelika Mielcarek ◽  
Agata Henschke ◽  
Sergio E. Moya

Nanoformulations offer multiple advantages over conventional drug delivery, enhancing solubility, biocompatibility, and bioavailability of drugs. Nanocarriers can be engineered with targeting ligands for reaching specific tissue or cells, thus reducing the side effects of payloads. Following systemic delivery, nanocarriers must deliver encapsulated drugs, usually through nanocarrier degradation. A premature degradation, or the loss of the nanocarrier coating, may prevent the drug’s delivery to the targeted tissue. Despite their importance, stability and degradation of nanocarriers in biological environments are largely not studied in the literature. Here we review techniques for tracing the fate of nanocarriers, focusing on nanocarrier degradation and drug release both intracellularly and in vivo. Intracellularly, we will discuss different fluorescence techniques: confocal laser scanning microscopy, fluorescence correlation spectroscopy, lifetime imaging, flow cytometry, etc. We also consider confocal Raman microscopy as a label-free technique to trace colocalization of nanocarriers and drugs. In vivo we will consider fluorescence and nuclear imaging for tracing nanocarriers. Positron emission tomography and single-photon emission computed tomography are used for a quantitative assessment of nanocarrier and payload biodistribution. Strategies for dual radiolabelling of the nanocarriers and the payload for tracing carrier degradation, as well as the efficacy of the payload delivery in vivo, are also discussed.


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