Spatiotemporal Magnetocaloric Microenvironment for Guiding the Fate of Biodegradable Polymer Implants

The degradation behavior of implants is significantly important for bone repair. However, it is still unprocurable to spatiotemporally regulate the degradation of the implants to match bone ingrowth. In this paper, a magneto-controlled biodegradation model is established to explore the degradation behavior of magnetic scaffolds in a magnetothermal microenvironment generated by an alternating magnetic field (AMF). The results demonstrate that the scaffolds can be heated by magnetic nanoparticles (NPs) under AMF, which dramatically accelerated scaffold degradation. Especially, magnetic NPs modified by oleic acid with a better interface compatibility exhibit a greater heating efficiency to further facilitate the degradation. Furthermore, the molecular dynamics simulations reveal that the enhanced motion correlation between magnetic NPs and polymer matrix can accelerate the energy transfer. As a proof-of-concept, the feasibility of magneto-controlled degradation for implants is demonstrated, and an optimizing strategy for better heating efficiency of nanomaterials is provided, which may have great instructive significance for clinical medicine.     

Porous agarose/Gd-hydroxyapatite composite bone fillers with promoted osteogenesis and antibacterial activity

Artificial bone fillers are essentially required for repairing bone defects, and developing the fillers with synergistic biocompatibility and anti-bacterial activity persists as one of the critical challenges. In this work, a new agarose/gadolinium-doped hydroxyapatite filler with three-dimensional porous structures was fabricated. For the composite filler, agarose provides three-dimensional skeleton and endows porosity, workability, and high specific surface area, hydroxyapatite (HA) offers the biocompatibility, and the rare earth element gadolinium (Gd) acts as the antibacterial agent. X-ray photoelectron spectroscopy detection showed the doping of Gd in HA lattice with the formation of Gd-HA interstitial solid solution. Attenuated total reflection Fourier transform infrared spectroscopy imaging suggested chemical interactions between agarose and Gd-HA, and the physical structure of agarose was tuned by the Gd-doped HA. Cytotoxicity testing and alizarin red staining experiments using mouse pro-osteoblasts (MC3T3-E1) revealed remarkable bioactivity and osteogenic properties of the composite fillers, and proliferation and growth rates of the cells increased in proportion to Gd content in the composites. Antibacterial testing using the gram-positive bacteria S. aureus and the gram-negative bacteria E. coli indicated promising antibacterial properties of the fillers. Meanwhile, the antibacterial properties of composite filles were enhanced with the increase of Gd content. The antibacterial fillers with porous structure and excellent physicomechanical properties show inspiring potential for bone defect repair.     

Remarkable Antibacterial Activity of Reduced Graphene Oxide Functionalized by Copper Ions

Despite long-term efforts for exploring antibacterial agents or drugs, potentiating antibacterial activity and meanwhile minimizing toxicity to the environment remains a challenge. Here, it is experimentally shown that the functionality of reduced graphene oxide (rGO) through copper ions displays selective antibacterial activity that is significantly stronger than that of rGO itself and no toxicity to mammalian cells. Remarkably, this antibacterial activity is two-orders-of-magnitude greater than the activity of its surrounding copper ions. It is demonstrated that rGO is functionalized through the cation–π interaction to massively adsorb copper ions to form a rGO–copper composite and result in an extremely low concentration level of surrounding copper ions (less than ≈0.5 µm ). These copper ions on rGO are positively charged and strongly interact with negatively charged bacterial cells to selectively achieve antibacterial activity, while rGO exhibits the functionality to not only actuate rapid delivery of copper ions and massive assembly onto bacterial cells but also result in the valence shift in the copper ions from Cu²⁺ into Cu⁺, which greatly enhances the antibacterial activity. Notably, this rGO functionality through cation–π interaction with copper ions can similarly achieve algaecidal activity but does not exert cytotoxicity against neutrally charged mammalian cells.     

Iron diffusivity into superconducting YBa2Cu3O7−δ at oxygen-assisted sintering: structural,magnetic, and transport properties

Optimization of materials exhibiting high-temperature superconductivity for producing controllable nano-devices is crucial for industrial applications. Herein we report a comprehensive study of the diffusion process between YBa₂Cu₃O_7−δ (YBCO) and iron particles. Fe diffusion into the YBCO matrix could be fundamental for multilayer systems with YBCO/Fe-alloy interfaces. We have found that the orthorhombic YBCO structure adopts to 3 wt% Fe, while for higher Fe content, a formation of BaFeO_3−δ and iron oxides was observed. Complementary measurements confirmed the strong superconductivity suppression in YBCO-Fe materials containing more than 7 wt% Fe. The YBCO with diffused Fe material retain the unit cell orthorhombicity (max. 3 wt% Fe), and their superconducting properties follow the principle of critical scaling with different exponents (γ). The critical current density (J_c), pinning fields (H_P) exhibit γ = 1, the first critical field (H_c1) shows γ = 1/2, and critical temperature (T_c) demonstrates γ = 7/4.     

Preparation,characterization and investigation of molecular films coated on diamond-like carbon substrate

For the successful application of boundary lubrication, detailed investigations about the influence of preparation process on molecular films are needed. In this paper, a specially designed device was used for the film preparation. The scanning electron microscope (SEM) combined with atomic force microscope (AFM) was employed to characterize the surface morphology and nanotribological behavior of molecular films. After the liquid phase deposition, molecular films are randomly and densely distributed over Ti-doped diamond-like carbon (Ti-DLC) substrates. Through rigorous surface treatments, island-like molecular films were finally achieved on substrate surfaces. The surface friction of molecular films is obviously lower than that of Ti-DLC surfaces. Then, pin-on-disk tribotests were performed to study the macrofriction behavior of molecular films under different preparation parameters. Based on the orthogonal experiment, the effect of five preparation parameters (solution weight percent, smearing force and processing time of three smearing steps) on initial friction coefficient of molecular films was investigated. The results indicated that the order of significance levels is as follows: processing time of the second smearing step > solution weight percent > processing time of step 1 > processing time of step 3 > smearing force. For the purpose of friction reduction, the appropriate level ranges are 0.75% (Solution), 2.5 N–15 N (Force), 1 min–10 min (Step 1), 1 min–2 min (Step 2) and 1 min, 2 min, 5 min and 15 min (Step 3). The initial friction coefficient under the optimized conditions is around 0.112, and the equilibrium friction coefficient is around 0.162, which is lower than that of unlubricated Ti-DLC substrates.     

Enhanced transduction coefficient in piezoelectric PZT ceramics by mixing powders calcined at different temperatures

Large transduction coefficient ($d_{33}\times g_{33}$) is difficult to obtain in piezoelectric ceramics because these two parameters show opposite trends with compositional modifications. Herein, the Pb(Zr_0.53Ti_0.47)O₃ ceramic powders were calcinated under different temperatures (A:830 °C, B:860 °C, and C:890 °C), and then mixed together according to different weight ratios (1A:1B:1C, 1A:2B:1C, 1A:2B:3C and 3A:2B:1C) for ceramics preparation. Both d₃₃ and g₃₃ are improved successfully, and the transduction coefficient with the weight ratio of 1A:2B:3C reaches up to 17,500 × 10⁻¹⁵ m²/N, which is 60 % higher than that with the powders calcinated under 830 °C, and at least twice those of commercial PZT-4, PZT-5A and PZT-8 ceramics. The improved transduction coefficient is owing to the enhanced piezoelectric constant and spontaneous polarization resulted from the increased grain size, relative density and the fraction of tetragonal phase. These results indicate that this is a simple but effective way to tailor the transduction coefficient in piezoelectric ceramics.     

Improved optical and structural properties of cadmium sulfide nanostructures for optoelectronic applications

In this study, the effect of ZnO seed layer on the growth of uniform CdS nanostructures was investigated using chemical bath deposition technique. Besides, the influence of molar concentration of reagents on the surface morphology, structural and optoelectrical properties of the deposited CdS thin films were examined. The CdS nanostructures were grown on bare glass and ZnO/glass substrates with different reagent molar concentrations. The results indicated an improvement in the homogeneity and uniformity of the grown CdS nanostructures on ZnO seed layer which can be due to the low lattice mismatch between ZnO and CdS structures. The CdS/ZnO samples were optimized by changing the molar concentration of reagents. A three–dimensional intersecting vertical nanosheet morphology with hexagonal structure was obtained when modified chemical concentration of 0.5 M was applied. The XRD pattern of CdS nanosheets indicated the hexagonal phase of CdS which were strongly orientated along (002) plane. The elevated intensity of dominant peak related to this sample confirmed the improved crystal quality of this CdS nanostructure comparing to the other samples. The UV–Vis spectrum demonstrated a high absorption coefficient for CdS intersecting nanosheets which might be due to the high specific surface area and light trapping behavior of this sample. The photoluminescence study also showed an improvement in optical properties of optimized CdS nanostructures. In order to study the optoelectrical properties of CdS nanostructures, metal–semiconductor–metal photodetectors were fabricated with different CdS samples and their current–voltage characteristics were analyzed. The results indicated an enhancement in photosensitivity, responsivity, and speed of photodetectors based on optimized CdS nanostructures.     

High quality sapphire crystal by advanced chemical transport process

Single crystal sapphire was synthesized by chemical transport of Al-O generated by the reaction of polycrystalline Al₂O₃ ceramic and carbon. Using C-axis oriented polycrystalline Al₂O₃ ceramics as a seed crystal in the deposition temperature range, a C-axis sapphire crystal (Φ5xL35 mm) was grown at a temperature range of 700–1000 °C, and the growth rate in the C-axis direction was about 3.5 mm/h. The transmittance in the visible to infrared region of the synthesized sapphire is a theoretical value (transmission loss is lower than 0.1 %/cm), and the absorption edge was less than 200 nm (the band gap is 6.2 eV), which is shorter than the absorption edge (240 nm) of the commercially available single crystal (band gap 5.2 eV) synthesized by the Czochralski method. The dislocation density in this material was extremely low, and it was confirmed by lattice image observation that it was a high-quality single crystal with very few defects.