Laser CVD Growth of Uniquely <010>-oriented ß-Ga2 O3 Films on Quartz Substrate with Ultrafast Photoelectric Response.

The oriented growth of ß-Ga2 O3 films has triggered extensive interest due to the remarkable and complex anisotropy found in the ß-Ga2 O3 bulks. Remarkable properties, including stronger solar-blind ultraviolet (SBUV) absorption, better mobility, and higher thermal conductivity, are usually observed along <010> direction as compared to other low-index axes. So far, <010>-oriented ß-Ga2 O3 film growth has been hindered by the lack of suitable substrates and higher surface energy of the (010) crystal plane. Herein, the first growth of uniquely <010>-oriented ß-Ga2 O3 films on quartz substrates by laser chemical vapor deposition (LCVD) are reported. By investigating the effects of deposition temperature (Tdep ) and O2 flow rate (RO2 ) on the growth of ß-Ga2 O3 films, it is found that the formation of <010> orientation is closely related to the higher stability of oxygen close-packed planes under O-rich condition. As a result, a grain size of up to ≈2 µm and a deposition rate of up to ≈ 40 µm h-1 are obtained. Metal-semiconductor-metal (MSM) type detector based on <010>-oriented ß-Ga2 O3 film exhibits ultra-fast response speed, 1-2 orders of magnitude higher than those of most detectors based on ß-Ga2 O3 films with other orientations.

Atomic Interface Engineering of Single-Atom Pt/TiO2 -Ti3 C2 for Boosting Photocatalytic CO2 Reduction.

Solar-driven CO2 conversion into valuable fuels is a promising strategy to alleviate the energy and environmental issues. However, inefficient charge separation and transfer greatly limits the photocatalytic CO2 reduction efficiency. Herein, single-atom Pt anchored on 3D hierarchical TiO2 -Ti3 C2 with atomic-scale interface engineering is successfully synthesized through an in situ transformation and photoreduction method. The in situ growth of TiO2 on Ti3 C2 nanosheets can not only provide interfacial driving force for the charge transport, but also create an atomic-level charge transfer channel for directional electron migration. Moreover, the single-atom Pt anchored on TiO2 or Ti3 C2 can effectively capture the photogenerated electrons through the atomic interfacial PtO bond with shortened charge migration distance, and simultaneously serve as active sites for CO2 adsorption and activation. Benefiting from the synergistic effect of the atomic interface engineering of single-atom Pt and interfacial TiOTi, the optimized photocatalyst exhibits excellent CO2 -to-CO conversion activity of 20.5 µmol g-1  h-1 with a selectivity of 96%, which is five times that of commercial TiO2 (P25). This work sheds new light on designing ideal atomic-scale interface and single-atom catalysts for efficient solar fuel conversation.

Doped Lead Halide White Phosphors for Very High Efficiency and Ultra-High Color Rendering.

Near-UV-pumped white-light-emitting diodes with ultra-high color rendering and decreased blue-light emission is highly desirable. However, discovering a single-phase white light emitter with such characteristics remains challenging. Herein, we demonstrate that Mn doping as low as 0.027 % in the hybrid post-perovskite type (TDMP)PbBr4 (TDMP=trans-2,5-dimethylpiperaziniium) enables to achieve a bright pure white emission replicating the spectrum of the sun's rays. Thus, a white phosphor exhibiting an emission with CIE coordinates (0.330, 0.365), a high photoluminescence quantum yield of 60 % (new record for white light emission of hybrid lead halides), and an ultra-high color rendering index (CRI=96, R9=91.8), corresponding to the record value for a single phase emitter was obtained. The investigation of the photoluminescence properties revealed how free excitons, self-trapped excitons, and low amount of Mn dopants are coupled to give rise to such pure white emission.

Evidence for an oxygen-depleted liquid outer core of the Earth.

On the basis of geophysical observations, cosmochemical constraints, and high-pressure experimental data, the Earth's liquid outer core consists of mainly liquid iron alloyed with about ten per cent (by weight) of light elements. Although the concentrations of the light elements are small, they nevertheless affect the Earth's core: its rate of cooling, the growth of the inner core, the dynamics of core convection, and the evolution of the geodynamo. Several light elements-including sulphur, oxygen, silicon, carbon and hydrogen-have been suggested, but the precise identity of the light elements in the Earth's core is still unclear. Oxygen has been proposed as a major light element in the core on the basis of cosmochemical arguments and chemical reactions during accretion. Its presence in the core has direct implications for Earth accretion conditions of oxidation state, pressure and temperature. Here we report new shockwave data in the Fe-S-O system that are directly applicable to the outer core. The data include both density and sound velocity measurements, which we compare with the observed density and velocity profiles of the liquid outer core. The results show that we can rule out oxygen as a major light element in the liquid outer core because adding oxygen into liquid iron would not reproduce simultaneously the observed density and sound velocity profiles of the outer core. An oxygen-depleted core would imply a more reduced environment during early Earth accretion.

Microstructure and Thermal Conductivity of Carbon Nanotube Reinforced Cu Composites.

Microstructure and thermal conductivity (TC) of carbon nanotubes reinforced Cu (CNT-Cu) composites have been studied. When CNTs were coated with nano Cu by electroless plating, the TC of CNT-Cu composites showed a noticeable improvement and increased with CNT contents. When 1.0 vol% CNTs was added, the TC of CNT-Cu composites increased to 420.4 W/(m · K), 30% higher than that of monolithic Cu (323.1 W/(m · K)). According to the measured TC of CNT-Cu composites, the interfacial thermal resistance of CNT-Cu composites was calculated as 3.0 × 10⁻9 m² K/W which was lower than the reported values of CNTs reinforced polymer matrix composites and ceramic matrix composites. Microstructures showed that CNTs modified with nano Cu were homogeneously dispersed and embedded in the Cu matrix, indicating that there was strong bonding between CNTs and Cu. The homogeneously dispersed CNTs and reduction of interfacial thermal resistance resulted in the improvement of thermal conductivity of CNT-Cu composites. Therefore, the prepared CNT-Cu composites are promising materials for thermal management applications.

Optimizing low loss negative index metamaterial for visible spectrum using differential evolution: reply.

We reply to the comment written by Aslam and Güney on our previous paper, Zhao et al. [Opt. Express 19(12), 11605-11614 (2011)]. We maintain that the proposed implementation of the DE algorithm for NIMs optimization in our work is correct, and the mentioned ambiguities in the comment due to the existence of multiple branches for n' in the retrieval procedure have been considered and eliminated by using the proposed robust retrieval method. Furthermore, the FOM of 15.2 for the DE-designed optimal fishnet structure reported in our work is reasonable for ideal fabrication conditions.

Optimal structure of light trapping in thin-film solar cells: dielectric nanoparticles or multilayer antireflection coatings?

Recent research has found an alternative way to enhance light trapping of thin-film solar cells by using dielectric nanoparticles deposited on the cell surface. To improve the performance of light trapping, a systematic study on the influence of dielectric nanoparticles on enhancement efficiency is performed in this paper. We prove that the optimal dielectric nanoparticles are substantially equivalent to the multilayer antireflection coatings (ARCs) with a "low-high-low" dielectric constant profile. Moreover, it is demonstrated that the use of a simple two-layer SiO2/SiC ARC can reach 34.15% enhancement, which has exceeded the ideal limit of 32% of nanoparticles structure including plasmonic Ag nanoparticles, dielectric SiC, and TiO2 nanoparticles. That means the optimal multilayer ARCs structure is obviously superior to the optimal dielectric nanoparticles structure, and the deposition of a simple two-layer SiO2/SiC structure on top of a thin-film silicon solar cell can significantly enhance photoelectron generation and hence, result in superior performance of thin-film solar cells.

Dual-Coordination-Induced Poly(vinylidene fluoride)/Li6.4Ga0.2La3Zr2O12/Succinonitrile Composite Solid Electrolytes Toward Enhanced Rate Performance in All-Solid-State Lithium Batteries.

Pursuing high energy and power density in all-solid-state lithium batteries (ASSLBs) has been the focus of attention. However, due to their inferior ion transport, their rate performance is limited compared to traditional lithium-ion batteries. Herein, a dual-coordination mechanism is first proposed to construct a high-performance poly(vinylidene fluoride)/Li6.4Ga0.2La3Zr2O12/succinonitrile (PVDF/LLZO/SN) composite solid electrolyte. The dual-coordination interactions of SN with both LLZO and Li+ in lithium salts allow SN to act like a branched chain of PVDF, realizing an increase in the free volume of the composite electrolyte. Meanwhile, SN molecules are immobilized within the electrolyte membrane by coordinating with LLZO, ensuring good interfacial stability. Profiting from the dual-coordination mechanism, the PVDF/LLZO/SN composite solid electrolyte combines enhanced electrochemical performance and interfacial compatibility. When applied to ASSLBs, the composite solid electrolyte enables the battery to operate at rates up to 6 C. The LiFePO4/Li batteries operated at 4 C can still deliver a high capacity retention rate of 96.4% after 50 cycles. Notably, these batteries also exhibit good long-cycle stability. After 500 cycles at 0.5 C, the discharge capacity was maintained at 145.9 mAh g-1.

Triethanolamine-assisted synthesis of NiFe layered double hydroxide ultrathin nanosheets for efficient oxygen evolution reaction.

Water electrolysis is a promising technique for producing high-quality hydrogen, the application of which is impeded by the sluggish oxygen evolution reaction (OER) process. In this study, ultrathin nickel-iron layered double hydroxide (NiFe LDH) nanosheets were successfully synthesized through a facile hydrothermal reaction with the assistance of triethanolamine (TEA). Morphological and structural characterizations revealed that the presence of TEA modified the morphology of NiFe LDH, facilitated the synthesis of high-purity NiFe LDH, improved the crystallinity of NiFe LDH and resulted in a slight decrease in specific surface area. X-ray photoelectron spectroscopy (XPS) analysis demonstrated the modulation of the electronic structure engendered by the addition of TEA, with nickel and iron appearing in high valence state in the resulting NiFe LDH nanosheets. The as-prepared NiFe LDH nanosheets possessed outstanding OER activity with fast kinetics, exhibiting a low overpotential of 261 mV to achieve a current density of 10 mA cm-2 and a small Tafel slope of 32.5 mV dec-1 in 1 M KOH. The excellent OER performance and rapid OER kinetics are mainly attributed to the high-valence Ni and Fe rather than the modification in the morphology and microstructure.

Shear-Thickening Covalent Adaptive Networks for Bifunctional Impact-Protective and Post-Tunable Tactile Sensors.

Shear-thickening materials have been widely applied in fields related to smart impact protection due to their ability to absorb large amounts of energy during sudden shock. Shear-thickening materials with multifunctional properties are expanding their applications in wearable electronics, where tactile sensors require interconnected networks. However, current bifunctional shear-thickening cross-linked polymer materials depend on supramolecular networks or slightly dynamic covalently cross-linked networks, which usually exhibit lower energy-absorption density than the highly dynamic covalently cross-linked networks. Herein, we employed boric ester-based covalent adaptive networks (CANs) to elucidate the shear-thickening property and the mechanism of energy dissipation during sudden shock. Guided by the enhanced energy-absorption capability of double networks and the requirements of the conductive networks for the wearable tactile sensors, tungsten powders (W) were incorporated into the boric ester polymer matrix to form a second network. The W networks make the materials stiffer, with a 13-fold increase in Young's modulus. Additionally, the energy-absorption capacity increased nearly 7 times. Finally, we applied these excellent energy-absorbing and conductive materials to bifunctional shock-protective and strain rate-dependent tactile sensors. Considering the self-healable and recyclable properties, we believe that these anti-impact and tactile sensing materials will be of great interest in wearable devices, smart impact-protective systems, post-tunable materials, etc.

Hydrodynamic simulation of hypervelocity generation by multidimensional graded impactors: Planarity enhancement study.

Hypervelocity impact in the universe can be generated by a three-stage gas gun. Achieving the desirable planarity of the flyer enlarges the experimentally effective area of the flyer under the hypervelocity condition. The multidimensional graded density impactor (MDGDI) enhances the planarity of the flyer. In this investigation, a one-dimensional Lagrange elastoplastic hydrodynamic method and a Euler grid finite difference method were used to examine the relationship between the structure of graded density impactors (GDIs) and the planarity of flyers. MDGDIs lead to a deviation of the stress wave produced by the one-dimensional graded density impactor (1DGDI), which offsets the stress disturbance effect, changes the velocity at each particle, and enhances the planarity of flyers. The proportion of flat areas of the flyer increases from 52.70% to 95.71% by adopting MDGDIs. The proportion of flat areas is linear with the wave impedance of the high-impedance layer for 1DGDIs and the wave impedance near the barrel of the high-impedance layer for MDGDIs. This investigation guides the design of GDIs and expands the application of gas gun technology in the field of hypervelocity impact.

Optimal design of light trapping in thin-film solar cells enhanced with graded SiNx and SiOxNy structure.

In this paper, a graded SiNx and SiOxNy structure is proposed as antireflection coatings deposited on top of amorphous silicon (α-Si) thin-film solar cell. The structural parameters are optimized by differential evolution in order to enhance the optical absorption of solar cells to the greatest degree. The optimal design result demonstrates that the nonlinear profile of dielectric constant is superior to the linear profile, and discrete multilayer graded antireflection coatings can outperform near continuously graded antireflection coatings. What's more, the electric field intensity distributions clearly demonstrate the proposed graded SiNx and SiOxNy structure can remarkably increase the magnitude of electric field of a-Si:H layer and hence, enhance the light trapping of a-Si:H thin-film solar cells in the whole visible and near-infrared spectrum. Finally, we have compared the optical absorption enhancements of proposed graded SiNx and SiOxNy structure with nanoparticles structure, and demonstrated that it can result in higher enhancements compared to the dielectric SiC and TiO2 nanoparticles. We have shown that the optimal graded SiNx and SiOxNy structure optimized by differential evolution can reach 33.31% enhancement which has exceeded the ideal limit of 32% of nanoparticles structure including plasmonic Ag nanoparticles, dielectric SiC and TiO2 nanoparticles.

Light-trapping design of graphene transparent electrodes for efficient thin-film silicon solar cells.

In this paper, the performance of solar cells with graphene transparent electrodes is compared with cells using conventional indium tin oxide (ITO) electrodes, and it is demonstrated the optical absorption of solar cells with bare graphene structure is worse than that of bare ITO structure because of the higher refractive index of graphene. To enhance the light trapping of graphene-based thin-film solar cells, a simple two-layer SiO(2)/SiC structure is proposed as antireflection coatings deposited on top of graphene transparent electrodes, and the thickness of each layer is optimized by differential evolution in order to enhance the optical absorption of a-Si:H thin-film solar cells to the greatest degree. The optimization results demonstrate the optimal SiO(2)/SiC/graphene structure can obtain 37.30% enhancement with respect to bare ITO structure, which has obviously exceeded the light-trapping enhancement of 34.15% for the optimal SiO(2)/SiC/ITO structure. Therefore, with the aid of the light-trapping structure, the graphene films are a very promising indium-free transparent electrode substitute for the conventional ITO electrode for use in cost-efficient thin-film silicon solar cells.

Structure Characterization and Impact Effect of Al-Cu Graded Materials Prepared by Tape Casting.

With the need of developing new materials, exploring new phenomenon, and discovering new mechanisms under extreme conditions, the response of materials to high-pressure compression attract more attention. However, the high-pressure state deviating from the Hugoniot line is difficult to realize by conventional experiments. Gas gun launching graded materials could reach the state. In our work, the corresponding Al-Cu composites and graded materials are prepared by tape casting and hot-pressing sintering. The microstructure and the acoustic impedance of the corresponding Al-Cu composites are analyzed to explain the impact behavior of Al-Cu graded materials. Computed tomographic testing and three-dimension surface profilometry machine results demonstrated well-graded structure and parallelism of the graded material. Al-Cu GMs with good parallelism are used to impact the Al-LiF target at 2.3 km/s using a two-stage light-gas gun, with an initial shock impact of 20.6 GPa and ramping until 27.2 GPa, deviating from the Hugoniot line.

Optimizing low loss negative index metamaterial for visible spectrum using differential evolution.

A novel negative index metamaterial design methodology for the visible spectrum with low losses was presented in this paper. A robust differential evolution (DE) was employed to optimize the metamaterial design to achieve a desired set of values for the index of refraction. By using numerical simulation of a wedge-shaped model and S-parameter retrieval method, we found that the DE-designed optimal solution can exhibit a low loss LH frequency band with simultaneously negative values of effective permittivity and permeability at the violet-light wavelength of 408 nm, and the figure of merit is 15.2, that means it may have practical applications because of its low loss and high transmission. Therefore, the design methodology presented in this paper is a very convenient and efficient way to pursue a novel metamaterial with desired electromagnetic characteristics in the visible spectrum.

A Review on Mechanical Models for Cellular Media: Investigation on Material Characterization and Numerical Simulation.

Cellular media materials are used for automobiles, aircrafts, energy-efficient buildings, transportation, and other fields due to their light weight, designability, and good impact resistance. To devise a buffer structure reasonably and avoid resource and economic loss, it is necessary to completely comprehend the constitutive relationship of the buffer structure. This paper introduces the progress on research of the mechanical properties characterization, constitutive equations, and numerical simulation of porous structures. Currently, various methods can be used to construct cellular media mechanical models including simplified phenomenological constitutive models, homogenization algorithm models, single cell models, and multi-cell models. This paper reviews current key mechanical models for cellular media, attempting to track their evolution from their inception to their latest development. These models are categorized in terms of their mechanical modeling methods. This paper focuses on the importance of constitutive relationships and microstructure models in studying mechanical properties and optimizing structural design. The key issues concerning this topic and future directions for research are also discussed.

The mechanism for the enhanced piezoelectricity in multi-elements doped (K,Na)NbO3 ceramics.

(K,Na)NbO3 based ceramics are considered to be one of the most promising lead-free ferroelectrics replacing Pb(Zr,Ti)O3. Despite extensive studies over the last two decades, the mechanism for the enhanced piezoelectricity in multi-elements doped (K,Na)NbO3 ceramics has not been fully understood. Here, we combine temperature-dependent synchrotron x-ray diffraction and property measurements, atomic-scale scanning transmission electron microscopy, and first-principle and phase-field calculations to establish the dopant-structure-property relationship for multi-elements doped (K,Na)NbO3 ceramics. Our results indicate that the dopants induced tetragonal phase and the accompanying high-density nanoscale heterostructures with low-angle polar vectors are responsible for the high dielectric and piezoelectric properties. This work explains the mechanism of the high piezoelectricity recently achieved in (K,Na)NbO3 ceramics and provides guidance for the design of high-performance ferroelectric ceramics, which is expected to benefit numerous functional materials.

Peridynamics Model with Surface Correction Near Insulated Cracks for Transient Heat Conduction in Functionally Graded Materials.

A peridynamic (PD) model of functionally graded materials (FGMs) is presented to simulate transient heat conduction in the FGM plate with insulated cracks. The surface correction is considered in the model to reduce the surface effect near the domain boundary and insulated cracks. In order to verify the proposed model, a numerical example for the FGM plate is carried out. The results show good agreement with the analytical solution. The convergence of the model with the surface correction for FGMs without cracks is then investigated. The results reveal that our model converges to the classical solutions in the limit of the horizon going to zero. The effects of two material points discretization schemes on the accuracy of numerical results are investigated. For transient heat conduction of FGMs with a static crack, the results obtained from the proposed PD model agree well with that from the finite element method. Finally, transient heat conduction of the FGM plate with a dynamic horizontal crack and intersecting cracks is simulated and discussed.

Understanding solute effect on grain boundary strength based on atomic size and electronic interaction.

Solute segregating to grain boundary can stabilize the microstructure of nanocrystalline materials, but a lot of solutes also cause embrittlement effect on interfacial strength. Therefore, uncovering the solute effect on grain boundary strength is very important for nanocrystalline alloys design. In this work, we have systematically studied the effects of various solutes on the strength of a Σ5 (310) grain boundary in Cu by first-principle calculations. The solute effects are closely related to the atomic radius of solutes and electronic interactions between solutes and Cu. The solute with a larger atomic radius is easier to segregate the grain boundary but causes more significant grain boundary embrittlement. The weak electronic interactions between the s- and p-block solutes and Cu play a very limited role in enhancing grain boundary strength. While the strong d-states electronic interactions between transition metallic solutes and Cu can counteract embrittlement caused by size mismatch and significantly improve the grain boundary strength. This work deepens our understanding of solute effects on grain boundary strength based on atomic size and electronic interactions.

Study on rheological behavior of Micro/Nano-silicon Carbide Particles in Ethanol by Selecting Efficient Dispersants.

A colloidal stability study of a nonaqueous silicon carbide suspension is of great significance for preparing special silicon carbide ceramics by colloidal processing. In this paper, three different chemical dispersants, which are amphiphilic, acidophilic, and alkaliphilic, are selected to compare their ability to stabilize nonaqueous slurries of silicon carbide. The analysis of the flow index factor is first used to estimate the colloidal stability of the suspensions. The results show that the addition of only 5 wt.% polyvinylpyrrolidone (PVP) forms a silicon carbide slurry with a low viscosity value of 17 mPas at 25 s-1. In addition, Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS)measurements indicate that the PVP molecule is successfully adsorbed on the surface of silicon carbide. The different adsorption models are fitted, and the adsorption of PVP molecules on the surface of silicon carbide belongs to the Langmuir single-layer adsorption model. At the optimal PVP amount, the volume content of the suspension is as high as 22.27 vol.%, a Newtonian-like fluid still appears, and no agglomerate structure is formed in the system. After the volume content exceeds 22.27 vol.%, the flow index factor of the slurry begins to plummet, indicating that the slurry begins to transform from a Newtonian-like fluid to a shear-thinning fluid. The particles undergo inevitable agglomeration accompanied by the emergence of yield stress. Finally, a maximum solid loading of the system is predicted to be 46 vol.%, using the Krieger-Dougherty model.