UV-Vis Spectroscopic Characterization of Nanomaterials in Aqueous Media.

The physicochemical characterization of nanomaterials (NMs) is often an analytical challenge, due to their small size (at least one dimension in the nanoscale, i.e. 1-100 nm), dynamic nature, and diverse properties. At the same time, reliable and repeatable characterization is paramount to ensure safety and quality in the manufacturing of NM-bearing products. There are several methods available to monitor and achieve reliable measurement of nanoscale-related properties, one example of which is Ultraviolet-Visible Spectroscopy (UV-Vis). This is a well-established, simple, and inexpensive technique that provides non-invasive and fast real-time screening evaluation of NM size, concentration, and aggregation state. Such features make UV-Vis an ideal methodology to assess the proficiency testing schemes (PTS) of a validated standard operating procedure (SOP) intended to evaluate the performance and reproducibility of a characterization method. In this paper, the PTS of six partner laboratories from the H2020 project ACEnano were assessed through an interlaboratory comparison (ILC). Standard gold (Au) colloid suspensions of different sizes (ranging 5-100 nm) were characterized by UV-Vis at the different institutions to develop an implementable and robust protocol for NM size characterization.

Exploring the potential of laser desorption ionisation time-of-flight mass spectrometry to analyse organic capping agents on inorganic nanoparticle surfaces.

Analytical techniques are in high demand for the determination of organic capping agents on surfaces of metallic nanoparticles (NPs) such as gold (Au) and silver (Ag). In this study, the potential of laser desorption ionisation time-of-flight mass spectrometry (LDI-ToF-MS) as a technique fit for this purpose is demonstrated. First, a collection of reference spectra of most commonly used organic capping agents, including small molecules and polymers was established. Second, the robustness of the method was tested towards parameters like NP core material and NP size. In a third step, the quantitative capabilities of LDI-ToF-MS were determined. Finally, the potential to detect chemical alterations of the organic capping agent was evaluated. LDI-ToF-MS is able to detect capping agents ranging from small molecules (citric acid, tannic acid, lipoic acid) to large polymers (polyvinylpyrrolidone, branched polyethylenimine and methoxy polyethylene glycol sulfhydryl) on Au and Ag NPs based on characteristic signals for each capping agent. Small molecules showed characteristic fragment ions with low intensities, whereas polymers showed intense signals of the monomeric subunit. The NP concentration range comprises about two orders of magnitude with lowest detection limits of 5 mg/L or a capping agent concentration in the lower nM range. Changes in capping agent composition are detectable at NP concentrations in the g/L range. Thus, LDI-ToF-MS is particularly suitable for characterisation of polymer-capped NPs with high NP concentrations. This may be the case for quality control as part of the material synthesis and testing. Graphical abstract.

Surface cleaning and sample carrier for complementary high-resolution imaging techniques.

Nowadays, high-resolution imaging techniques are extensively applied in a complementary way to gain insights into complex phenomena. For a truly complementary analytical approach, a common sample carrier is required that is suitable for the different preparation methods necessary for each analytical technique. This sample carrier should be capable of accommodating diverse analytes and maintaining their pristine composition and arrangement during deposition and preparation. In this work, a new type of sample carrier consisting of a silicon wafer with a hydrophilic polymer coating was developed. The robustness of the polymer coating toward solvents was strengthened by cross-linking and stoving. Furthermore, a new method of UV-ozone cleaning was developed that enhances the adhesion of the polymer coating to the wafer and ensures reproducible surface-properties of the resulting sample carrier. The hydrophilicity of the sample carrier was recovered applying the new method of UV-ozone cleaning, while avoiding UV-induced damages to the polymer. Noncontact 3D optical profilometry and contact angle measurements were used to monitor the hydrophilicity of the coating. The hydrophilicity of the polymer coating ensures its spongelike behavior so that upon the deposition of an analyte suspension, the solvent and solutes are separated from the analyte by absorption into the polymer. This feature is essential to limit the coffee-ring effect and preserve the native identity of an analyte upon deposition. The suitability of the sample carrier for various sample types was tested using nanoparticles from suspension, bacterial cells, and tissue sections. To assess the homogeneity of the analyte distribution and preservation of sample integrity, optical and scanning electron microscopy, helium ion microscopy, laser ablation inductively coupled plasma mass spectrometry, and time-of-flight secondary ion mass spectrometry were used. This demonstrates the broad applicability of the newly developed sample carrier and its value for complementary imaging.