Python tooth-inspired fixation device for enhanced rotator cuff repair.

Rotator cuff repair surgeries fail frequently, with 20 to 94% of the 600,000 repairs performed annually in the United States resulting in retearing of the rotator cuff. The most common cause of failure is sutures tearing through tendons at grasping points. To address this issue, we drew inspiration from the specialized teeth of snakes of the Pythonoidea superfamily, which grasp soft tissues without tearing. To apply this nondamaging gripping approach to the surgical repair of tendon, we developed and optimized a python tooth-inspired device as an adjunct to current rotator cuff suture repair and found that it nearly doubled repair strength. Integrated simulations, 3D printing, and ex vivo experiments revealed a relationship between tooth shape and grasping mechanics, enabling optimization of the clinically relevant device that substantially enhances rotator cuff repair by distributing stresses over the attachment footprint. This approach suggests an alternative to traditional suturing paradigms and may reduce the risk of tendon retearing after rotator cuff repair.

Astrometrically registered maps of H2O and SiO masers toward VX Sagittarii.

The supergiant VX Sagittarii is a strong emitter of both H2O and SiO masers. However, previous VLBI observations have been performed separately, which makes it difficult to spatially trace the outward transfer of the material consecutively. Here we present the astrometrically registered, simultaneous maps of 22.2 GHz H2O and 43.1/42.8/86.2/129.3 GHz SiO masers toward VX Sagittarii. The H2O masers detected above the dust-forming layers have an asymmetric distribution. The multi-transition SiO masers are nearly circular ring, suggesting spherically symmetric wind within a few stellar radii. These results provide the clear evidence that the asymmetry in the outflow is enhanced after the smaller molecular gas clump transform into the inhomogeneous dust layers. The 129.3 GHz maser arises from the outermost region compared to that of 43.1/42.8/86.2 GHz SiO masers. The ring size of the 129.3 GHz maser is maximized around the optical maximum, suggesting that radiative pumping is dominant.

Cactus-Like Hollow Cu2-x S@Ru Nanoplates as Excellent and Robust Electrocatalysts for the Alkaline Hydrogen Evolution Reaction.

The development of Pt-free electrocatalysts for the hydrogen evolution reaction (HER) recently is a focus of great interest. While several strategies are developed to control the structural properties of non-Pt catalysts and boost their electrocatalytic activities for the HER, the generation of highly reactive defects or interfaces by combining a metal with other metals, or with metal oxides/sulfides, can lead to notably enhanced catalytic performance. Herein, the preparation of cactus-like hollow Cu2-x S@Ru nanoplates (NPs) that contain metal/metal sulfide heterojunctions and show excellent catalytic activity and durability for the HER in alkaline media is reported. The initial formation of Ru islands on presynthesized Cu1.94 S NPs, via cation exchange between three Cu+ ions and one Ru3+ , induces the growth of the Ru phase, which is concomitant with the dissolution of the Cu1.94 S nanotemplate, culminating in the formation of a hollow nanostructure with numerous thin Ru pillars. Hollow Cu2-x S@Ru NPs exhibit a small overpotential of 82 mV at a current density of -10 mA cm-2 and a low Tafel slope of 48 mV dec-1 under alkaline conditions; this catalyst is among state-of-the-art HER electrocatalysts in alkaline media. The excellent performance of hollow Cu2-x S@Ru NPs originates from the facile dissociation of water in the Volmer step.

RhCu 3D Nanoframe as a Highly Active Electrocatalyst for Oxygen Evolution Reaction under Alkaline Condition.

One pot synthesis of RhCu alloy truncated octahedral nanoframes, Cu@Rh core-shell nanoparticles, and a bundle of five RhCu nanowires is demonstrated. The RhCu alloy 3D nanoframe, in particular, exhibits excellent catalytic activity toward the oxygen evolution reaction under alkaline conditions.

Plasmon Enhanced Direct Bandgap Emissions in Cu7 S4 @Au2 S@Au Nanorings.

Nanostructured copper sulfides, promising earth-abundant p-type semiconductors, have found applications in a wide range of fields due to their versatility, tunable low bandgap, and environmental sustainability. The synthesis of hexagonal Cu7 S4 @Au2 S@Au nanorings exhibiting plasmon enhanced emissions at the direct bandgap is reported. The synthesized Cu7 S4 @Au2 S@Au nanorings show greatly enhanced absorption and emission by local plasmons compared to pure copper sulfide nanoparticles.

Position Accuracy Improvement by Implementing the DGNSS-CP Algorithm in Smartphones.

The position accuracy of Global Navigation Satellite System (GNSS) modules is one of the most significant factors in determining the feasibility of new location-based services for smartphones. Considering the structure of current smartphones, it is impossible to apply the ordinary range-domain Differential GNSS (DGNSS) method. Therefore, this paper describes and applies a DGNSS-correction projection method to a commercial smartphone. First, the local line-of-sight unit vector is calculated using the elevation and azimuth angle provided in the position-related output of Android's LocationManager, and this is transformed to Earth-centered, Earth-fixed coordinates for use. To achieve position-domain correction for satellite systems other than GPS, such as GLONASS and BeiDou, the relevant line-of-sight unit vectors are used to construct an observation matrix suitable for multiple constellations. The results of static and dynamic tests show that the standalone GNSS accuracy is improved by about 30%-60%, thereby reducing the existing error of 3-4 m to just 1 m. The proposed algorithm enables the position error to be directly corrected via software, without the need to alter the hardware and infrastructure of the smartphone. This method of implementation and the subsequent improvement in performance are expected to be highly effective to portability and cost saving.

Formation of a Cu@RhRu core-shell concave nanooctahedron via Ru-assisted extraction of Rh from the Cu matrix and its excellent electrocatalytic activity toward the oxygen evolution reaction.

A facile one step route has been developed for the synthesis of trimetallic Cu@RhRu core-shell concave nanooctahedra by co-decomposition of Ru, Rh and Cu precursors. A mechanistic study reveals that nanoparticles with a CuRh alloy core and a Ru shell are initially formed and a subsequent migration of Rh to the shell results in the Cu@RhRu core-shell concave nanooctahedron. The shell exhibits atomically mixed Ru and Rh phases with an fcc atomic structure, although the hcp atomic structure is commonly found for the bulk Ru. We also report an unusually high catalytic activity of the Cu@RhRu octahedral nanocrystals toward the oxygen evolution reaction in alkaline solution.

Morphological evolution of 2D Rh nanoplates to 3D Rh concave nanotents, hierarchically stacked nanoframes, and hierarchical dendrites.

Impurity doping has yielded a number of useful optical and catalytic alloy nanoparticles, by providing synthetic routes to unprecedented nanostructures. However, Zn is difficult to use as a dopant in alloy nanoparticles due to the difficulty in reduction, and therefore little has been reported on Zn-doped alloy nanoparticles and their potential applications. Herein we report an unusual role of the dopant Zn as a crystal growth modifying agent to cause the formation of novel concave Rh nanostructures, namely nanotents. We could further prepare unprecedented hierarchically stacked Rh nanoframes and dendritic nanostructures derived from them by understanding the role of various surface-stabilizing moieties. We also report the usage of new Rh nanostructures in selective hydrogenation of phthalimides.

One pot synthesis of hollow Cu-doped Ru octahedral nanocages via an in situ generated metastable Cu nanoparticle template.

A facile synthetic strategy was developed for a hollow Ru octahedral nanocage via an in situ generated metastable facet-controlled Cu nanooctahedron. Co-decomposition of Cu and Ru precursors forms a metastable core-shell Cu@Ru nanoparticle, and a subsequent in situ dissolution of the core Cu phase results in a hollow octahedral Cu-doped Ru nanocage. CTAB (cetyltrimethylammonium bromide) was found to effect both the formation and destabilization of the Cu template under the employed reaction conditions, which is the key requirement for one-step synthesis of hollow Cu-doped Ru nanocages. The regioselective, preferential deposition of Ru atoms on the edge and corner of the core template nanoparticle led to a structurally well-defined Cu doped-Ru octahedral nanocage.

Dynamics and mechanism of flame retardants in polymer matrixes: experiment and simulation.

We investigate the dynamics and the mechanism of flame retardants in polycarbonate matrixes to explore for a way of designing efficient and environment-friendly flame retardants. The high phosphorus content of organic phosphates has been considered as a requirement for efficient flame retardants. We show, however, that one can enhance the efficiency of flame retardants even with a relatively low phosphorus content by tuning the dynamics and the intermolecular interactions of flame retardants. This would enable one to design bulkier flame retardants that should be less volatile and less harmful in indoor environments. UL94 flammability tests indicate that even though the phosphorus content of 2,4-di-tert-butylphenyl diphenyl phosphate (DDP) is much smaller with two bulky tertiary butyl groups than that of triphenyl phosphate (TPP), DDP should be as efficient of a flame retardant as TPP, which is a widely used flame retardant. On the other hand, the 2-tert-butylphenyl diphenyl phosphate (2-tBuDP), with a lower phosphorus content than TPP but with a greater phosphorus content than DDP, is less efficient as a flame retardant than both DDP and TPP. Dynamic secondary ion mass spectrometry and molecular dynamics simulations reveal that the diffusion of DDP is slower by an order of magnitude at low temperature than that of TPP but becomes comparable to that of TPP at the ignition temperature. This implies that DDP should be much less volatile than TPP at low temperature, which is confirmed by thermogravimetric analysis. We also find from Fourier transform infrared spectroscopy that Fries rearrangement and char formation are suppressed more by DDP than by TPP. The low volatility and the suppressed char formation of DDP suggest that the enhanced flame retardancy of DDP should be attributed to its slow diffusivity at room temperature and yet sufficiently high diffusivity at high temperature.