Electrochemical analysis of rationally designed ZnO nanostructures for biodegradable cellular scaffolds

This work shows a preliminary analysis of a wet-chemistry synthesized platform based on ZnO nanostructures (n-ZnO) for application in regenerative medicine. n-ZnO stability is investigated by electrochemical in-situ sensing of zinc ions released by n-ZnO soaked in simulated biofluids. Impedance analysis allows detecting subtle changes in the bulk solutionimpedance in the range 1 Hz-50 kHz, which can be ascribed to the release of ionic species in solution, among which Zn2+ ions. In parallel, a voltammetry analysis by low-cost mercury-free screen-printed sensors shows the release of Zn2+ ions at not harmful concentrations

Printing ZnO Inks: From Principles to Devices

Solution-based printing approaches permit digital designs to be converted into physical objects by depositing materials in a layer-by-layer additive fashion from microscale to nanoscale resolution. The extraordinary adaptability of this technology to different inks and substrates has received substantial interest in the recent literature. In such a context, this review specifically focuses on the realization of inks for the deposition of ZnO, a well-known wide bandgap semiconductor inorganic material showing an impressive number of applications in electronic, optoelectronic, and piezoelectric devices. Herein, we present an updated review of the latest advancements on the ink formulations and printing techniques for ZnO-based nanocrystalline inks, as well as of the major applications which have been demonstrated. The most relevant ink-processing conditions so far explored will be correlated with the resulting film morphologies, showing the possibility to tune the ZnO ink composition to achieve facile, versatile, and scalable fabrication of devices of different natures

Freestanding Cellulose Acetate/ZnO Flowers Composites for Solar Photocatalysis and Controlled Zinc Ions Release

The versatile properties of ZnO micro- and nano- structures have resulted in many applications in piezotronics, biosensors and photocatalysis. However, ZnO can easily dissolve in aqueous fluids, potentially resulting in the release of reactive oxygen species and zinc ions at toxic concentrations. Such an issue can be solved by dispersing ZnO within biocompatible polymeric matrices to reduce the direct exposure to the aqueous fluid and control the release of zinc ions. Herein, this work explores tailored ZnO flowers/cellulose acetate photocatalytic composites at different ZnO weight percentages (1-15 wt%). The photocatalytic degradation of methylene blue dye under simulated solar light is studied, finding an optimal value of ZnO filler loading in the polymer (10 wt %), resulting from a compromise between the photodegradation efficiency and the hydrophobicity induced by ZnO flowers. The reusability of the composites is investigated, finding a surprising improvement in the photodegradation efficiency after the first cycle. Simulated solar light stimulation induces the controllable release of zinc ions in aqueous solution at ppm-levels from the composites at the optimal ZnO filler loading. Finally, the release of ionic species in the absence of light stimulation is found to be directly proportional to the ZnO-loading in the composite, as a result of its degradation in aqueous environments

Chromium inhibition and size-selected Au nanocluster catalysis for the solution growth of low-density ZnO nanowires

he wet chemical synthesis of nanostructures has many crucial advantages over high-temperature methods, including simplicity, low-cost, and deposition on almost arbitrary substrates. Nevertheless, the density-controlled solution growth of nanowires still remains a challenge, especially at the low densities (e.g. 1 to 10 nanowires/100\u2009\u3bcm2) required, as an example, for intracellular analyses. Here, we demonstrate the solution-growth of ZnO nanowires using a thin chromium film as a nucleation inhibitor and Au size-selected nanoclusters (SSNCs) as catalytic particles for which the density and, in contrast with previous reports, size can be accurately controlled. Our results also provide evidence that the enhanced ZnO hetero-nucleation is dominated by Au SSNCs catalysis rather than by layer adaptation. The proposed approach only uses low temperatures ( 6470\u2009\ub0C) and is therefore suitable for any substrate, including printed circuit boards (PCBs) and the plastic substrates which are routinely used for cell cultures. As a proof-of-concept we report the density-controlled synthesis of ZnO nanowires on flexible PCBs, thus opening the way to assembling compact intracellular-analysis systems, including nanowires, electronics, and microfluidics, on a single substrate

Self-Cleaning Bending Sensors Based on Semitransparent ZnO Nanostructured Films

The design of multifunctional nanostructured materials is the key to the development of smart wearable devices. For instance, nanostructures endowed with both piezoelectric and photocatalytic activities could well be the workhorse for solar-light-driven self-cleaning wearable sensors. In this work, a simple strategy for the assembly of a flexible, semitransparent piezophotocatalytic system is demonstrated by leveraging rational wet chemistry synthesis of ZnO-based nanosheets/nanoflowers (NSs/NFs) under basic pH conditions onto flexible ITO/PET supports. A KMnO4 pretreatment before the ZnO synthesis (seeded ZnO) allows for the control of the density, size, and orientation of the NSs/NFs systems compared to the systems produced in the absence of seeding (seedless ZnO). The electrical response of the sensors is extracted at a 1 V bias as a function of bending in the interval between 0 and 90°, being the responsivity toward bending significantly enhanced by the KMnO4 treatment effect. The photocatalytic activity of the sensors is analyzed in aqueous solution (methylene blue, 25 μM) by a solar simulator, resulting in similar values between seedless and seeded ZnO. Upon bending the sensor, the photocatalytic activity of seedless ZnO is almost unaffected, whereas that of seeded ZnO is improved by about 25%. The sensor’s reusability and repeatability are tested in up to three different cycles. These results open up the way toward the seamless integration of bending sensitivity and photocatalysis into a single device

Sviluppo di una tecnologia laser MBE e deposizione di films sottili di ossidi polifunzionali per applicazioni ai microsistemi

Dottorato di ricerca in ingegneria dei microsistemi. 12. ciclo. A.a. 1999-2000. Tutore G. Balestrino. Coordinatore A. TucciaroneConsiglio Nazionale delle Ricerche - Biblioteca Centrale - P.le Aldo Moro, 7, Rome; Biblioteca Nazionale Centrale - P.za Cavalleggeri, 1, Florence / CNR - Consiglio Nazionale delle RichercheSIGLEITItal

Layered Double Hydroxides in Bioinspired Nanotechnology

Layered Double Hydroxides (LDHs) are a relevant class of inorganic lamellar nanomaterials that have attracted significant interest in life science-related applications, due to their highly controllable synthesis and high biocompatibility. Under a general point of view, this class of materials might have played an important role for the origin of life on planet Earth, given their ability to adsorb and concentrate life-relevant molecules in sea environments. It has been speculated that the organic–mineral interactions could have permitted to organize the adsorbed molecules, leading to an increase in their local concentration and finally to the emergence of life. Inspired by nature, material scientists, engineers and chemists have started to leverage the ability of LDHs to absorb and concentrate molecules and biomolecules within life-like compartments, allowing to realize highly-efficient bioinspired platforms, usable for bioanalysis, therapeutics, sensors and bioremediation. This review aims at summarizing the latest evolution of LDHs in this research field under an unprecedented perspective, finally providing possible challenges and directions for future research

Layered Double Hydroxides: A Toolbox for Chemistry and Biology

Layered double hydroxides (LDHs) are an emergent class of biocompatible inorganic lamellar nanomaterials that have attracted significant research interest owing to their high surface-to-volume ratio, the capability to accumulate specific molecules, and the timely release to targets. Their unique properties have been employed for applications in organic catalysis, photocatalysis, sensors, drug delivery, and cell biology. Given the widespread contemporary interest in these topics, time-to-time it urges to review the recent progresses. This review aims to summarize the most recent cutting-edge reports appearing in the last years. It firstly focuses on the application of LDHs as catalysts in relevant chemical reactions and as photocatalysts for organic molecule degradation, water splitting reaction, CO2 conversion, and reduction. Subsequently, the emerging role of these materials in biological applications is discussed, specifically focusing on their use as biosensors, DNA, RNA, and drug delivery, finally elucidating their suitability as contrast agents and for cellular differentiation. Concluding remarks and future prospects deal with future applications of LDHs, encouraging researches in better understanding the fundamental mechanisms involved in catalytic and photocatalytic processes, and the molecular pathways that are activated by the interaction of LDHs with cells in terms of both uptake mechanisms and nanotoxicology effects

Superconductivity in artificial cuprate structures grown by laser molecular beam epitaxy

Pulsed laser deposition in a molecular beam epitaxy environment has been used to deposit high quality thin films of BaCuO2+x, CaCuO2, and superconducting (BaCuO2+x)(2)/(CaCuO2)(2) artificial superlattices. In situ reflection high energy electron diffraction (RHEED) has shown that the situ x-ray diffraction spectra growth mechanism is two dimensional, and ex confirmed the growth rate deduced from RHEED oscillations. The BaCuO2+xCaCuO2 films alone are not superconducting; however, in infinite layer based heterostructures the occurrence of charge transfer amongst layers containing different alkaline earth ions can give rise to superconductivity. Structural features of these heterostructures can be engineered over a wide range and, consequently, their superconducting properties studied

Novel Electrochemical Sensors Based on L-Proline Assisted LDH for H2O2 Determination in Healthy and Diabetic Urine

In this paper, a novel non-enzymatic modified glassy carbon (GC) sensor, of the (GC-Ag-paste)-catalytic proline-assisted LDH type, for H2O2 determination was fabricated, studied, characterized and employed to determine the hydrogen peroxide content in healthy and diabetic human urine. LDH (whose composition can be schematized as [(ZnAlIII)-Al-II (OH)(2)](+) NO3-center dot nH(2)O) is glued to glassy carbon by means of silver paste, while proline, which increases the catalytic properties of LDH, is used free in solution in the phosphate buffer. A voltametric survey was first conducted to ascertain the positive effect induced by the presence of proline, i.e., the increase of sensor sensitivity. Then a deep study of the new three-electrode amperometric proline-assisted LDH sensor, whose working electrode was of the same type as the one used to perform the cyclic voltammetry, was carried out, working at first in static air, then in a nitrogen atmosphere. Possible interferences from various substances, both oxidants and antioxidants, were also investigated. Lastly, the new amperometric sensor was successfully used to determine the H2O2 level in human urine from both healthy and diabetic subjects. The effect of proline in enhancing the properties of the sensor system was also investigated. The limit of detection (LOD) of the new catalytic sensor was of the order of 0.15 mmol L-1, working in air, and of 0.05 mu mol L-1, working in nitrogen atmosphere