Fundamentals of quantum dots (QDs) sensing phenomena show the predominance of these fluorophores over standard organic dyes, mainly because of their unique optical properties such as sharp and tunable emission spectra, high emission quantum yield and broad absorption. Moreover, they also indicate no photo bleaching and can be also grown as no blinking emitters. Due to these properties, QDs may be used e.g., for multiplex testing of the analyte by simultaneously detecting multiple or very weak signals. Physico-chemical mechanisms used for analyte detection, like analyte stimulated QDs aggregation, nonradiative Förster resonance energy transfer (FRET) exhibit a number of QDs, which can be applied in sensors. Quantum dots-based sensors find use in the detection of ions, organic compounds (e.g., proteins, sugars, volatile substances) as well as bacteria and viruses.

Although neurotransmitters are present in human serum at the nM level, any dysfunction of the catecholamines concentration may lead to numerous serious health problems. Due to this fact, rapid and sensitive catecholamines detection is extremely important in modern medicine. However, there is no device that would measure the concentration of these compounds in body fluids. The main goal of the present study is to design a simple as possible, cost-effective new biosensor-based system for the detection of neurotransmitters, using nontoxic reagents. The miniature Au-E biosensor was designed and constructed through the immobilization of tyrosinase on an electroactive layer of cysteamine and carbon nanoparticles covering the gold electrode. This sensing arrangement utilized the catalytic oxidation of norepinephrine (NE) to NE quinone, measured with voltammetric techniques: cyclic voltammetry and differential pulse voltammetry. The prepared bio-system exhibited good parameters: a broad linear range (1–200 μM), limit of detection equal to 196 nM, limit of quantification equal to 312 nM, and high selectivity and sensitivity. It is noteworthy that described method was successfully applied for NE determination in real samples.

The results presented in this paper show how the optical properties and colloidal stability of quantum dots (QDs) vary depending on pH conditions. For this investigation, as-synthesized hydrophobic CdSe/CdS QDs were transferred to an aqueous medium by surface modification with 3-mercaptopropionic acid. The ligand exchange procedure was applied under three different pH conditions: acidic, neutral and alkaline, to obtain three kinds of hydrophilic QDs dispersed in phosphate buffer. The efficiency of the functionalization of QDs was estimated based on the changes in ABS and the highest value was obtained under acidic conditions (45%). The efficiency of photoluminescence (PL) was also best preserved under these conditions, although it was 30 times less than the PL of hydrophobic QDs. Then, all three kinds of hydrophilic QDs were dispersed in solutions with a wide range of pH (2–12) and investigated by absorbance and PL measurements. The results show that QDs subjected to a ligand exchange procedure are characterized by intensive PL at the selected pH values, which correspond to pK_a of the ligand. This phenomenon is independent of the pH at which the ligand exchange procedure is conducted. Moreover, it was found that the PL intensity is preserved during the experiment for QDs functionalized under neutral conditions, whereas it decreases for acidic and increases for alkaline conditions.

Semiconducting nanoparticles (NPs) find applications in many fields, with a recent focus on medicine and biology. Functionalization of the surface of NPs is necessary, and one of the most commonly employed techniques is ligand exchange (LE). In this paper, the study of pH influence on LE reaction for different types of cadmium-based NPs (quantum dots, nanorods, and nanoplates) is presented. Hydrophobic NPs were transferred to the non-organic medium by functionalization with d-penicillamine (DPA). The LE procedure was conducted at four different pH levels (4, 7, 9, and 11), and obtained hydrophilic NPs were dispersed in phosphate buffer. Results show that the most effective procedure resulted from a reaction carried at pH = 4; however, NPs with higher photoluminescence intensity were obtained when pH = 11 was used. Comparable emission was achieved from samples at pH = 4 and pH = 9. The least effective transfer, resulting in unstable NPs, occurred when the procedure was conducted at pH = 7.

In this paper, the study of surface modification of two-dimensional (2D), non-luminescent CdS nanoplates (NPLs) by thiol-containing ligands is presented. We show that a process of twophase transfers with appropriate ligand exchange transforms non-luminescent NPLs into spherical CdS nanoparticles (NPs) exhibiting a blue photoluminescence with exceptionally high quantum yield ~90%. In the process, transfer from inorganic solvent to water is performed, with appropriately selected ligand molecules and pH values (forward phase transfer), which produces NPs with modified size and shape. Then, in reverse phase transfer, NPs are transferred back to toluene due to surface modification by combined Cd (OL)₂ and Cd (Ac)₂. As a result, spherical NPs are formed (average diameter between 4 and 6 nm) with PL QY as high as 90%. This is unique for core only CdS NPs without inorganic shell.

Heterostructured cadmium-based core–shell nanoparticles (NPs) are the subject of research because of not only fundamental scientific advances but also a range of technological applications. To increase the range of applications of nanoparticles, it is possible to immobilise them in sol–gel glass that can be easily manufactured and shaped, keeping the properties of the dispersed particles. This allows the creation of new bulk optical materials with tailored properties, opening up opportunities for various technological applications such as lighting or sensing. Herein we report the synthesis of core–shell CdSe/CdS triangular-shaped nanoparticles under an atmosphere of oxygen and at room temperature. A detailed characterisation of the obtained NPs was carried out. The interesting effect of the gelling agent (tetra-n-butylammonium fluoride) on the triangular nanoparticles in solution and the stability of the emission properties over time was investigated. Sol–gel glasses with entrapped triangular NPs were prepared, and their photoluminescence properties were compared with those obtained in colloidal solutions.