Measurement of Electric Charge in a Charged Hydroxyapatite Dielectric Using Pendant Drop.

A simple noninvasive measurement method which allows one to determine the trapped charge in a biocompatible hydroxyapatite dielectric is developed. The hydroxyapatite samples are charged by electron beam with energy 30 keV and total irradiated charge ranging from 2 × 10-9 C to 2 × 10-7 C. The value of the trapped charge is determined by analyzing the shape change of a liquid droplet hanging from a needle in proximity of the charged sample surface. The shape change of the pendant drop in the field of gravity is commonly utilized in the measurements of the surface free tension (SFT) of liquids. The external electric field leads to a further modification of the droplet shape and to an effective change of the SFT. The change of the SFT as a function of distance between the droplet and sample and the critical distance at which the droplet detaches from the needle are measured for various values of the irradiated charge. These two quantities are also derived theoretically by considering the trapped charge as a single fitting parameter. We can thus determine the trapped charge in two independent noninvasive ways. It is noteworthy that our method is easily implementable into the standard pendant drop setups. As a practical application of the method, a long-term charge stability of the charged hydroxyapatite is demonstrated, thus paving the way toward quantitative studies of its bioactivity in dependence on the value of the trapped charge.

Surface charge and carbon contamination on an electron-beam-irradiated hydroxyapatite thin film investigated by photoluminescence and phase imaging in atomic force microscopy.

The surface properties of hydroxyapatite, including electric charge, can influence the biological response, tissue compatibility, and adhesion of biological cells and biomolecules. Results reported here help in understanding this influence by creating charged domains on hydroxyapatite thin films deposited on silicon using electron beam irradiation and investigating their shape, properties, and carbon contamination for different doses of incident injected charge by two methods. Photoluminescence laser scanning microscopy was used to image electrostatic charge trapped at pre-existing and irradiation-induced defects within these domains, while phase imaging in atomic force microscopy was used to image the carbon contamination. Scanning Auger electron spectroscopy and Kelvin probe force microscopy were used as a reference for the atomic force microscopy phase contrast and photoluminescence laser scanning microscopy measurements. Our experiment shows that by combining the two imaging techniques the effects of trapped charge and carbon contamination can be separated. Such separation yields new possibilities for advancing the current understanding of how surface charge influences mediation of cellular and protein interactions in biomaterials.

Reactive HiTUS TiNbVTaZrHf-Nx Coatings: Structure, Composition and Mechanical Properties.

High entropy metal sub-lattice stabilized nitride coatings based on multicomponent refractory transition metals (TM = Ti, Nb, V, Ta, Zr, Hf) are promising candidates for extreme conditions due to their high thermal, mechanical, and corrosion properties. The aims of the current work included the investigations of the possibilities of the novel High Target Utilization Sputtering (HiTUS) technique applied to reactive sputtering of TiNbVTaZrHf-xN coatings from the viewpoints of hysteresis behavior during reactive sputtering as well as the structure, composition, stoichiometry, and mechanical properties of the resulting coatings. With increasing nitrogen content, coating structures varied from amorphous in metallic alloy coatings to textured nano-columnar fcc structures. Despite certain deviations of TM from equiatomic concentrations, homogeneous solid solutions corresponding to single-phase multicomponent nitride analogous to high entropy stabilized compounds were obtained. Mechanical properties were found to be proportional to nitrogen content. The highest hardness HIT ~ 33 GPa and indentation modulus EIT ~ 400 GPa were found in a slightly sub-stoichiometric (~42 at% nitrogen) composition. HIT/EIT and limited pillar split measurements suggested that these coatings exhibit low fracture toughness (around 1 MPa.m1/2). The work confirmed that reactive HiTUS is suitable for the preparation of multicomponent nitrides with the control of their stoichiometry and mechanical properties only via nitrogen additions.

Application of MXene for remediation of low-level radioactive aqueous solutions contaminated with 133Ba and 137Cs.

MXene is an innovative multilayered material that has been prepared by an acid-salt (HCl + NH4F) etching route and tested for the removal of 133Ba and 137Cs in radioactive conditions for the first time. MXene has exhibited high uptake capacity of about 154.9 and 121.5 mg g-1 for 133Ba and 137Cs, respectively, in 0.01 mol L-1 solution and using 5 g L-1 of adsorbent at natural pH.

Fluoride-free synthesis of anodic TiO2 nanotube layers: a promising environmentally friendly method for efficient photocatalysts.

TiO2 nanotube (TNT) layers are generally prepared in fluoride-based electrolytes via electrochemical anodization that relies on the field-assisted dissolution of Ti metal forming nanoporous/nanotubular structures. However, the usage of fluoride ions is considered hazardous to the environment. Therefore, we present an environmentally friendly synthesis and application of TNT layers prepared in fluoride-free nitrate-based electrolytes. A well-defined nanotubular structure with thickness up to 1.5 µm and an inner tube diameter of ∼55 nm was obtained within 5 min using aqueous X(NO3)Y electrolytes (X = Na+, K+, Sr2+, Ag+). For the first time, we show the photocatalytic performance (using a model organic pollutant), HO˙ radical production, and thorough characterization of TNT layers prepared in such electrolytes. The highest degradation efficiency (k = 0.0113 min-1) and HO˙ radical production rate were obtained using TNT layers prepared in AgNO3 (Ag-NT). The intrinsic properties of Ag-NT such as the valence band maximum of ∼2.9 eV, surface roughness of ∼6 nm, and suitable morphological features and crystal structure were obtained. These results have the potential to pave the way for a more environmentally friendly synthesis of anodic TNT layers in the future using the next generation of fluoride-free nitrate-based electrolytes.

Remarkable Improvement in Hydrogen Sensing Characteristics with Pt/TiO2 Interface Control.

Owing to their excellent hydrogen surface susceptibility, TiO2 thin films have been proven worthy of sensing hydrogen. However, these sensors work best at temperatures of 150-400 °C, with poor selectivity and a low response at room temperature. In this context, the novelty of this paper includes an investigation of the critical role of electrode fabrication that is found to significantly define the surface as well as the performance of a sensor. Sensors prepared with optimized conditions showed the best sensor response (SR) of ∼1.58 × 107 toward 10 000 ppm H2 with excellent linearity (R-square ∼ 0.98 for 300-10 000 ppm) at room temperature (∼20 °C). In addition, the said sensor showed a response time of ∼125 s with full baseline recovery and a selectivity factors (SF) of ∼1754, 2456, and 4723 to 1000 ppm of interfering reducing gases CH4, CO, and NH3, respectively, at 100 °C. At room temperature, the selectivity factor (for 300 ppm H2) of the sensor is ∼3.41 to 90% RH and ∼37.35 to 250 ppm oxygen, 200 ppm CO, and 1600 ppm CO2. Last but not least, our X-ray diffraction, X-ray photoelectron spectroscopy, and electrical transport characteristics enabled us to explain the high sensing mechanism on the basis of the estimated grain size, the quantitative atomic composition, the barrier at the Pt/TiO2 interface, and the thermal activation energy (also known as the intergranular barrier height) of the thin films.

Reversible switching of quantum cascade laser-modes using a pH-responsive polymeric cladding as transducer.

We present a novel approach for the reversible switching of the emission wavelength of a quantum cascade laser (QCL) using a halochromic cladding. An air-waveguide laser ridge is coated with a thin layer of polyacrylic acid. This cladding introduces losses corresponding to the absorption spectrum of the polymer. By changing the state of the polymer, the absorption spectrum and losses change, inducing a shift of 7 cm(-1) in the emission wavelength. This change is induced by exposure to acidic or alkaline vapors under ambient conditions and is fully reversible. Such lasers can be used as multi-color light source and as sensor for atmospheric pH.

Resonant impurity bands in semiconductor superlattices.

It is shown that the confined impurity state of a semiconductor quantum well develops into an excited impurity band in the case of a superlattice. This is studied by following theoretically the transition from a single to a multiple quantum well or superlattice by exactly diagonalizing the three-dimensional Hamiltonian for a quantum well system with random impurities. Intersubband absorption experiments, which can be nearly perfectly reproduced by the theory, corroborate this interpretation, which also requires reinterpretation of previous data.