Metal Oxide Nanoparticles: Review of Synthesis, Characterization and Biological Effects.

In the last few years, the progress made in the field of nanotechnology has allowed researchers to develop and synthesize nanosized materials with unique physicochemical characteristics, suitable for various biomedical applications. Amongst these nanomaterials, metal oxide nanoparticles (MONPs) have gained increasing interest due to their excellent properties, which to a great extent differ from their bulk counterpart. However, despite such positive advantages, a substantial body of literature reports on their cytotoxic effects, which are directly correlated to the nanoparticles' physicochemical properties, therefore, better control over the synthetic parameters will not only lead to favorable surface characteristics but may also increase biocompatibility and consequently lower cytotoxicity. Taking into consideration the enormous biomedical potential of MONPs, the present review will discuss the most recent developments in this field referring mainly to synthesis methods, physical and chemical characterization and biological effects, including the pro-regenerative and antitumor potentials as well as antibacterial activity. Moreover, the last section of the review will tackle the pressing issue of the toxic effects of MONPs on various tissues/organs and cell lines.

Transfer of a Photocatalytically Active TiO2 Nanotube Array onto Cementitious Materials.

Due to a recent change concerning the risk and hazard regulations of titanium dioxide powders, which possibly leads to restrictions in the use of those materials in photocatalytic applications, an alternative utilization of titanium dioxide is shown in this work. This is achieved by covering surfaces of cement-based materials with a regular-shaped monolayer of photocatalytically active titanium dioxide nanotube arrays which are not affected by the regulation changes due to their shape and size. This study delivers a proposal for the synthesis of TiO2 nanotubes via anodization and their post-treatment to generate detached crystalline nanotube arrays which can be easily transferred onto material surfaces. We show that the transfer of such nanostructured materials can be achieved by modifying the cement mold, showing the opportunity for applying the material to precast elements. The composite material is characterized by referencing the morphology and photocatalytic activity.

Fibronectin Functionalized Electrospun Fibers by Using Benign Solvents: Best Way to Achieve Effective Functionalization.

The aim of this study is to demonstrate the feasibility of different functionalization methods for electrospun fibers developed using benign solvents. In particular three different approaches were investigated to achieve the functionalization of poly(epsilon caprolactone) (PCL) electrospun fibers with fibronectin. Protein surface entrapment, chemical functionalization and coaxial electrospinning were performed and compared. Moreover, bilayered scaffolds, with a top patterned and functionalized layer with fibronectin and a randomly oriented not functionalized layer were fabricated, demonstrating the versatility of the use of benign solvents for electrospinning also for the fabrication of complex graded structures. Besides the characterization of the morphology of the obtained scaffolds, ATR-FTIR and ToF-SIMS were used for the surface characterization of the functionalized fibers. Cell adhesion and proliferation were also investigated by using ST-2 cells. Positive results were obtained from all functionalized scaffolds and the most promising results were obtained with bilayered scaffolds, in terms of cells infiltration inside the fibrous structure.

Electronically Tuned Asymmetric meso-Substituted Porphyrins for p-Type Solar Cells.

A series of electronically tuned asymmetric porphyrins have been synthesized for use in p-type solar cells. The porphyrin derivatives were strategically designed with electron-withdrawing capability and an electronic dipole gradient to aid in electron-harvesting capacity from a nickel oxide cathode. Specifically, the porphyrins were substituted at the meso position with different arrangements of the electron-withdrawing pentafluorobenzene moiety, electron-donating/coordinating 4-pyridyl ligand, and an electron withdrawing/synthetically modifiable 4-cyanophenyl unit. Two distinct free-base porphyrins were synthesized, one of which was further metallated with nickel(II). The porphyrins were fully characterized and their electronic properties explored experimentally by electrochemistry, and both steady state and time-resolved spectroscopy. Finally, the porphyrins were incorporated into a p-type solar cell device utilizing NiO as the cathode, and demonstrating a preliminary maximum performance of η(%)=0.082 and IPCEMAX (%)=26.0 without co-sensitization.

Suppressing the Surface Recombination and Tuning the Open-Circuit Voltage of Polymer/Fullerene Solar Cells by Implementing an Aggregative Ternary Compound.

In this work, we present a novel small molecule based on dithienylthienothiadiazole units (named SM1) acting as an efficient component in ternary blend organic solar cells to modify the hole extraction at the interface. Our findings show that the SM1 suppresses the surface recombination and enhances the open-circuit voltage ( Voc). By introducing SM1 in a host system composed of poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl- C61-butyric acid methyl ester (PCBM), we obtained Voc values of up to 0.75 V and fill factors larger than 70% for the ternary blends. As a consequence, the power conversion efficiency is improved by about 30% compared to P3HT:PCBM binary devices. Interestingly, external quantum efficiency and absorption spectra in the near-infrared region do not show any contribution of SM1 in dried films. Instead, the addition of the small molecule improves the Voc by reducing the surface recombination losses. To shed light on the recombination processes, we carried out Fourier-transform photocurrent spectroscopy and impedance spectroscopy measurements. This work shows that the ternary concept can also have functionalities other than photosensitization and can even act as a morphology-directing agent or an interface modifier.

Stabilization of dry protein coatings with compatible solutes.

Exposure of protein modified surfaces to air may be necessary in several applications. For example, air contact may be inevitable during the implantation of biomedical devices, for analysis of protein modified surfaces, or for sensor applications. Protein coatings are very sensitive to dehydration and can undergo significant and irreversible alterations of their conformations upon exposure to air. With the use of two compatible solutes from extremophilic bacteria, ectoine and hydroxyectoine, the authors were able to preserve the activity of dried protein monolayers for up to >24 h. The protective effect can be explained by the preferred exclusion model; i.e., the solutes trap a thin water layer around the protein, retaining an aqueous environment and preventing unfolding of the protein. Horseradish peroxidase (HRP) immobilized on compact TiO2 was used as a model system. Structural differences between the compatible solute stabilized and unstabilized protein films, and between different solutes, were analyzed by static time-of-flight secondary ion mass spectrometry (ToF-SIMS). The biological activity difference observed in a colorimetric activity assay was correlated to changes in protein conformation by application of principal component analysis to the static ToF-SIMS data. Additionally, rehydration of the denatured HRP was observed in ToF-SIMS with an exposure of denatured protein coatings to ectoine and hydroxyectoine solutions.

Incorporation of bioactive glass nanoparticles in electrospun PCL/chitosan fibers by using benign solvents.

The use of bioactive glass (BG) particles as a filler for the development of composite electrospun fibers has already been widely reported and investigated. The novelty of the present research work is represented by the use of benign solvents (like acetic acid and formic acid) for electrospinning of composite fibers containing BG particles, by using a blend of PCL and chitosan. In this work, different BG particle sizes were investigated, namely nanosized and micron-sized. A preliminary investigation about the possible alteration of BG particles in the electrospinning solvents was performed using SEM analysis. The obtained composite fibers were investigated in terms of morphological, chemical and mechanical properties. An in vitro mineralization assay in simulated body fluid (SBF) was performed to investigate the capability of the composite electrospun fibers to induce the formation of hydroxycarbonate apatite (HCA).

Novel Fully Organic Water Oxidation Electrocatalysts: A Quest for Simplicity.

Despite the growing need for readily available and inexpensive catalysts for the half-reactions involved in water splitting, water oxidation and reduction electrocatalysts are still traditionally based on noble metals. One long-standing challenge has been the development of an oxygen evolution reaction catalyzed by easily available, structurally simple, and purely organic compounds. Herein, we first generalize the performance of the known N-ethyl-flavinium ion to a number of derivatives. Furthermore, we demonstrate an unprecedented application of different pyridinium and related salts as very simple, inexpensive water oxidation organocatalysts consisting of earth-abundant elements (C, H, O, and N) exclusively. The results establish the prospects of heterocyclic aromatics for further design of new organic electrocatalysts for this challenging oxidation reaction.

Metal-Phosphate Bilayers for Anatase Surface Modification.

Compared to many other metal oxides, anatase TiO2 shows relatively lower reactivity toward carboxylic acid anchor groups. The latter is crucial for applications, for example, in dye-sensitized solar cells (DSSCs), where the most used dyes bind to the metal oxide surface through carboxylic acid terminations. To improve the surface reactivity, metal-phosphate bilayers of Ni or Co were synthesized on anatase TiO2 compact oxide and nanotubes. In both cases, time-of-flight secondary ion mass spectrometry (ToF-SIMS) and X-ray photoelectron spectroscopy (XPS) results showed that the bilayers were successfully formed and that the phosphate layer works as an intermediate between TiO2 and the other species. ToF-SIMS depth profiles of modified nanotubes showed that Ni and Co are present through the whole tube length and reduce in content after heat treatment, in agreement with XPS results. Phosphate groups, on the other hand, are more present in the tubes' depth, and their content on the surface is reduced upon exposure to temperature. The reactivity of the modified surfaces toward carboxylic acid-terminated molecules, as stearic acid and Ru-based N719 dye, was evaluated. Contact angle measurements together with dye desorption experiments demonstrated that the Co-phosphate bilayers heat-treated at 300 °C resulted in the largest enhancement compared to the reference. Bilayer-modified compact anatase TiO2 and anatase TiO2 nanotubes were utilized as photoanodes in DSSCs. An increase in efficiency was observed for all modified electrodes with phosphate-Co treatment, leading to the highest JSC values and an efficiency improvement of 48%.

Tuning Anatase Surface Reactivity toward Carboxylic Acid Anchor Groups.

The effect of different post-treatments on TiO2 anatase surface reactivity was investigated in order to obtain the best techniques for enhancing anatase performance in diverse applications, e.g., in photocatalysis and especially as photoelectrodes for dye-sensitized solar cells (DSSCs). Different post-treatments of compact anodic anatase TiO2 were compared, including O2 plasma, UV irradiation, immersion in H2O2, vapor thermal treatment, and post-anodization, evaluating the increase of the amount of OH reactive groups on the surface and removal of surface contamination. In XPS spectra, the increase of OH groups is evident by the O 1s peak at higher binding energy. ToF-SIMS principal component analysis demonstrated that treatments performed in aqueous media led to a cleaner surface, with substantial removal of electrolyte residues. Stearic acid and the organic dye N719 were adsorbed to the differently post-treated anatase, and adsorption was evaluated by contact angle and dye desorption measurements. A higher loading with molecules containing carboxylic acid functionalities was confirmed by both techniques on the treated samples. The post-treatments that presented the highest amounts of dye were used to prepare photoelectrodes, and these were tested in DSSCs where the efficiency values doubled in comparison with the non-post-treated electrode.

A generic interface to reduce the efficiency-stability-cost gap of perovskite solar cells.

A major bottleneck delaying the further commercialization of thin-film solar cells based on hybrid organohalide lead perovskites is interface loss in state-of-the-art devices. We present a generic interface architecture that combines solution-processed, reliable, and cost-efficient hole-transporting materials without compromising efficiency, stability, or scalability of perovskite solar cells. Tantalum-doped tungsten oxide (Ta-WO x )/conjugated polymer multilayers offer a surprisingly small interface barrier and form quasi-ohmic contacts universally with various scalable conjugated polymers. In a simple device with regular planar architecture and a self-assembled monolayer, Ta-WO x -doped interface-based perovskite solar cells achieve maximum efficiencies of 21.2% and offer more than 1000 hours of light stability. By eliminating additional ionic dopants, these findings open up the entire class of organics as scalable hole-transporting materials for perovskite solar cells.

Alternating Current Electrophoretic Deposition for the Immobilization of Antimicrobial Agents on Titanium Implant Surfaces.

One prominent cause of implant failure is infection; therefore, research is focusing on developing surface coatings that render the surface resistant to colonization by micro-organisms. Permanently attached coatings of antimicrobial molecules are of particular interest because of the reduced cytoxicity and lower risk of developing resistance compared to controlled release coatings. In this study, we focus on the chemical grafting of bioactive molecules on titanium. To concentrate the molecules at the metallic implant surface, we propose electrophoretic deposition (EPD) applying alternating current (AC) signals with an asymmetrical wave shape. We show that for the model molecule bovine serum albumin (BSA), as well as for the clinically relevant antifungal lipopeptide caspofungin (CASP), the deposition yield is drastically improved by superimposing a DC offset in the direction of the high-amplitude peak of the AC signal. Additionally, in order to produce immobilized CASP coatings, this experimental AC/DC-EPD method is combined with an established surface activation protocol. Principle component analysis (PCA) of time-of-flight secondary ion mass spectrometry (ToF-SIMS) data confirm the immobilization of CASP with higher yield as compared to a diffusion-controlled process, and higher purity than the clinical CASP starting suspensions. Scratch testing data indicate good coating adhesion. Importantly, the coatings remain active against the fungal pathogen C. albicans as shown by in vitro biofilm experiments. In summary, this paper delivers a proof-of-concept for the application of AC-EPD as a fast grafting tool for antimicrobial molecules without compromising their activities.

TiO2 Nanotubes: Nitrogen-Ion Implantation at Low Dose Provides Noble-Metal-Free Photocatalytic H2 -Evolution Activity.

Low-dose nitrogen implantation induces an ion and damage profile in TiO2 nanotubes that leads to "co-catalytic" activity for photocatalytic H2 -evolution (without the use of any noble metal). Ion implantation with adequate parameters creates this active zone limited to the top part of the tubes. The coupling of this top layer and the underlying non-implanted part of the nanotubes additionally contributes to an efficient carrier separation and thus to a significantly enhanced H2 generation.

Enhanced Charge Transport in Tantalum Nitride Nanotube Photoanodes for Solar Water Splitting.

In the present work we grow anodic self-organized Ta2O5 nanotube layers, which are converted by ammonolysis to Ta3 N5 nanotubes, and then are used as photoanodes for photoanalytic water splitting. We introduce a two-step anodization process that not only improves order (reduced growth defects) and overall light absorption in the nanotube layers, but also provides a significantly reduced interface charge resistance at the nitride/metal interface due to subnitride (TaNx ) formation. As a result, such nanotube anodes afford a 15-fold increase of the photocurrent compared with conventional nanotubular Ta3 N5 electrodes under AM 1.5 G simulated sunlight (100 mW cm(-2)) conditions.

Protein interactions with corroding metal surfaces: comparison of Mg and Fe.

The influence of bovine serum albumin (BSA) on the electrochemical behaviour of pure Mg and Fe was studied in simulated body fluid (SBF), in view of the possible application of these materials as biodegradable metals. Results indicate a different trend for the BSA-effect on corrosion for the two metals: for Mg, a strong corrosion-inhibiting effect is observed in the presence of BSA in solution, especially for short-term exposure, whereas for Fe only a slight acceleration of corrosion is caused by the addition of BSA to the solution. For both metals, the protein-effect on the electrochemical behaviour shows a complex time-dependence. Surface analysis indicates that stronger BSA adsorption takes place on Mg than on Fe. Moreover, adsorption experiments with BSA and a second protein (lysozyme) were conducted. The results are discussed in view of electrostatic interactions between differently charged metal oxide/hydroxide surfaces and proteins.

Interface chemistry and molecular bonding of functional ethoxysilane-based self-assembled monolayers on magnesium surfaces.

The modification of magnesium implants with functional organic molecules is important for increasing the biological acceptance and for reducing the corrosion rate of the implant. In this work, we evaluated by a combined experimental and theoretical approach the adsorption strength and geometry of a functional self-assembled monolayer (SAM) of hydrolyzed (3-aminopropyl)triethoxysilane (APTES) molecules on a model magnesium implant surface. In time-of-flight secondary ion mass spectrometry (ToF-SIMS) and X-ray photoelectron spectroscopy (XPS), only a minor amount of reverse attachment was observed. Substrate-O-Si signals could be detected, as well as other characteristic APTES fragments. The stability of the SAM upon heating in UHV was investigated additionally. Density-functional theory (DFT) calculations were used to explore the preferred binding mode and the most favorable binding configuration of the hydrolyzed APTES molecules on the hydroxylated magnesium substrate. Attachment of the molecules via hydrogen bonding or covalent bond formation via single or multiple condensation reactions were considered. The impact of the experimental conditions and the water concentration in the solvent on the thermodynamic stability of possible APTES binding modes is analyzed as a function of the water chemical potential of the environment. Finally, the influence of van der Waals contributions to the adsorption energy will be discussed.

Anodic nanotubular/porous hematite photoanode for solar water splitting: substantial effect of iron substrate purity.

Anodization of iron substrates is one of the most simple and effective ways to fabricate nanotubular (and porous) structures that could be directly used as a photoanode for solar water splitting. Up to now, all studies in this field focused on achieving a better geometry of the hematite nanostructures for a higher efficiency. The present study, however, highlights that the purity of the iron substrate used for any anodic-hematite-formation approach is extremely important in view of the water-splitting performance. Herein, anodic self-organized oxide morphologies (nanotubular and nanoporous) are grown on different iron substrates under a range of anodization conditions, including elevated temperatures and anodization supported by ultrasonication. Substrate purity has not only a significant effect on oxide-layer growth rate and tube morphology, but also gives rise to a ninefold increase in the photoelectrochemical water-splitting performance (0.250 vs. 0.028 mA cm−2 at 1.40 V vs. reversible hydrogen electrode under AM 1.5 100 mW cm−2 illumination) for 99.99 % versus 99.5 % purity iron substrates of similar oxide geometry. Elemental analysis and model alloys show that particularly manganese impurities have a strong detrimental effect on the water-splitting performance.

Ta-doped TiO2 nanotubes for enhanced solar-light photoelectrochemical water splitting.

A little dopey: Ta-doped titania (TiO2) nanotube (NT) arrays can be grown by electrochemical anodization onto low-Ta-concentration (0.03-0.4 at % Ta) Ti-Ta alloys. Under optimized conditions (0.1 at % Ta, annealing at 650 °C and 7 µm thickness), Ta-doped TiO2 NT arrays show a significantly enhanced activity in photoelectrochemical water splitting under simulated sunlight conditions (see figure).

Albumin coating on magnesium via linker molecules--comparing different coating mechanisms.

As magnesium is a non-toxic and biodegradable metal, it is gaining more and more interest in the biomedical sector. The biodegradability is due to the corrosion of Mg in aqueous, chloride containing environment, as it is present in the body. However, corrosion of pure magnesium occurs too fast and takes place inhomogeneously on the metal surface. Moreover, Mg dissolution is connected with strong hydrogen evolution. Therefore alloying and/or coating of magnesium seem to be promising approaches to slow down corrosion and in return hydrogen evolution. This study explores coating of Mg with albumin via three different linker molecules, aminopropyl-triethoxysilane (APTES) plus ascorbic acid (VitC), carbonyldiimidazole (CDI) and stearic acid (SA). The metal samples were first passivated and after the pre-coating with the linker molecules the protein coating took place by soaking the pre-treated samples in an aqueous albumin solution. The immersion time was varied from 0.25 h up to 24 h. The success and the quality of the different coatings were documented by X-ray Photoelectron Spectroscopy (XPS) and Time of Flight Secondary Ion Mass Spectrometry (ToF-SIMS). Pre-coatings were additionally characterized by contact angle and surface roughness measurements. Electrochemical measurements were carried out in simulated body fluid (SBF) to characterize the coatings in view of their corrosion behavior. Albumin coatings could be produced with every linker molecule investigated. Certain protective effects were observed already for linker SAM coated Mg, overall the systems CDI-BSA and SA-BSA showed the best corrosion resistances.