In Liquid Observation and Quantification of Nucleation and Growth of Gold Nanostructures Using in Situ Transmission Electron Microscopy

In situ liquid transmission electron microscopy (TEM) is a powerful technique for observing nanoscale processes in their native liquid environment and in real time. However, the imaging electron beam can have major interferences with the processes under study, altering the experimental outcome. Here, we use in situ liquid TEM to understand the differences between beam-induced and electrodeposition processes that result in nucleation and growth of gold crystallites. Through this study, we find that beam-induced and electrodeposition processes result in crystallites that deposit at different locations within the liquid cell and differ significantly in morphology. Furthermore, we develop a strategy based on increasing the liquid layer thickness for reducing the amount of beam-induced crystallites to negligible levels. Through this optimized system, we study the electrodeposition of gold on carbon electrodes by correlating current time transients and their corresponding time-resolved scanning TEM images. This analysis demonstrates that even when the electron-beam plays a negligible role in gold deposition under optimal conditions, there is a large discrepancy between the amount of deposits observed and the amount measured using the current time transients. This finding sheds light on the heterogeneity of the deposition process and provides insights into designing a new class of in situ liquid TEM systems

Relating Redox Properties of Polyvinylamine‑<i>g</i>‑TEMPO/Laccase Hydrogel Complexes to Cellulose Oxidation

The structure and electrochemical properties of adsorbed complexes based on mixtures of polyvinylamine-<i>g</i>-TEMPO (PVAm-T) and laccase were related to the ability of the adsorbed complexes to oxidize cellulose. PVAm-T10 with 10% of the amines bearing TEMPO moieties (i.e., DS = 10%), adsorbed onto gold sulfonate EQCM-D sensor surfaces giving a hydrogel film that was 7 nm thick, 89% water, and encasing laccase (200 mM) and TEMPO moieties (33 mM). For DS values >10%, all of the TEMPOs in the hydrogel film were redox-active in that they could be oxidized by the electrode. With hydrogel layers made with lower-DS PVAm-Ts, only about half of the TEMPOs were redox-active; 10% DS appears to be a percolation threshold for complete TEMPO-to-TEMPO electron transport. In parallel experiments with hydrogel complexes adsorbed onto regenerated cellulose films, the aldehyde concentrations increased monotonically with the density of redox-active TEMPO moieties in the adsorbed hydrogel. The maximum density of aldehydes was 0.24 μmol/m², about 10 times less than the theoretical concentration of primary hydroxyl groups exposed on crystalline cellulose surfaces. Previous work showed that PVAm-T/laccase complexes are effective adhesives between wet cellulose surfaces when the DS is >10%. This work supports the explanation that TEMPO-to-TEMPO electron transport is required for the generation of aldehydes necessary for wet adhesion to PVAm

Redox Properties of Polyvinylamine‑<i>g</i>‑TEMPO in Multilayer Films with Sodium Poly(styrenesulfonate)

Layer-by-layer (LbL) assemblies of polyvinylamine with grafted TEMPO moieties (PVAm-T) with sodium polystyrenesulfonate (PSS) were prepared on gold-sulfonate surfaces, and the redox properties were measured by cyclic voltammetry. LbL compositions were probed by quartz crystal microbalance (wet) and ellipsometric (dry) film measurements. Approximately 30% of the TEMPO moieties in the LbL assemblies were redox-active when the total TEMPO coverage was varied up to 6 μmol/m², by either varying the TEMPO content in PVAm-T or by varying the number of LbL bilayers. Three non-redox-active PVAm/PSS blocking bilayers were required to prevent the electrode from oxidizing PVAm-T in the exterior LbL layer. This suggests significant intermixing between the layers in the LbL film. In addition to contributing to the small but growing body of work on redox polymers based on grafted TEMPO, this work serves as a reference point for understanding the redox properties of colloidal PVAm-T-laccase complexes in future work

In Situ Liquid Cell TEM Study of Morphological Evolution and Degradation of Pt–Fe Nanocatalysts During Potential Cycling

Nanocatalyst degradation is a serious limiting factor for the commercialization of proton exchange membrane fuel cells. Although the degradation has been extensively studied in the past through various ex situ electrochemical methods, employing an in situ technique can greatly improve our understanding of the mechanisms involved during the electrochemical cycling. In this work, we have employed an in situ liquid cell inside a TEM for a simultaneous investigation of the structural evolution and electrochemical response of Pt–Fe nanocatalysts. We demonstrate that the coarsening processes of these nanocatalyst particles, including the nucleation and growth, are not uniform, both in space and in time scale. The growth rate is found to be both site- and potential-dependent. Furthermore, these particles were found to exhibit considerably different behaviors when attached to an electrode as opposed to when isolated in the electrolyte. With Pt–Fe nanoalloy system as a candidate material, this work demonstrates that the in situ structural characterization of nanocatalysts under electrochemical bias and inside the native electrolyte environment provides much deeper insight into the catalyst degradation mechanisms as compared to the routine ex situ electrochemical studies

Three on Three: Universal and High-Affinity Molecular Recognition of the Symmetric Homotrimeric Spike Protein of SARS-CoV‑2 with a Symmetric Homotrimeric Aptamer

Our previously discovered monomeric aptamer for SARS-CoV-2 (MSA52) possesses a universal affinity for COVID-19 spike protein variants but is ultimately limited by its ability to bind only one subunit of the spike protein. The symmetrical shape of the homotrimeric SARS-CoV-2 spike protein presents the opportunity to create a matching homotrimeric molecular recognition element that is perfectly complementary to its structural scaffold, causing enhanced binding affinity. Here, we describe a branched homotrimeric aptamer with three-fold rotational symmetry, named TMSA52, that not only possesses excellent binding affinity but is also capable of binding several SARS-CoV-2 spike protein variants with picomolar affinity, as well as pseudotyped lentiviruses expressing SARS-CoV-2 spike protein variants with femtomolar affinity. Using Pd–Ir nanocubes as nanozymes in an enzyme-linked aptamer binding assay (ELABA), TMSA52 was capable of sensitively detecting diverse pseudotyped lentiviruses in pooled human saliva with a limit of detection as low as 6.3 × 103 copies/mL. The ELABA was also used to test 50 SARS-CoV-2-positive and 60 SARS-CoV-2-negative patient saliva samples, providing sensitivity and specificity values of 84.0 and 98.3%, respectively, thus highlighting the potential of TMSA52 for the development of future rapid tests