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In this paper, we developed a sequential chemical etching and selenization processes to synthesize Co-MoSex double-shelled hollow nanocages (CMS DSHNCs) as high performance electrode materials for supercapacitor applications. Co-MoOx yolk-shelled hollow nanocages were firstly synthesized using a solvothermal process through facile ion-exchange reactions between zeolitic imidazolate framework-67 (ZIF-67) and MoO42- ions. By applying a solvothermal temperature of 160 oC in the presence of SeO32- and subsequently annealing strategy, CMS-DSHNCs were successfully synthesized with a yolk-shell hierarchically hollow and porous morphology of mixed metal selenides. The CMS-DSHNCs exhibit superior electrochemical properties as electrode materials for supercapacitor: e.g., a specific capacity of 1029.8 C g-1 at 2 A g-1 (3.089 C cm-2 at 6mA cm-2), a rate capability of ~76.14, a capacity retention at 50 A g-1, and a good cycle stability (95.2 capacity retention over 8000 cycles). A hybrid supercapacitor was constructed using the CMS-DSHNCs as the cathode and activated carbon (AC) as the anode in a solution of 3 M KOH, and achieved a high specific energy of 45 Wh kg−1, and a specific power up to 2222 W kg−1 with a good cycling stability of 94 after 8000 cycles.

Poor ductility of titanium matrix composites with medium/high-strength reinforced with carbonaceous nanomaterials (eg., graphene, carbon nanotubes etc.), has seriously restricted their wide-range engineering and practical industry utility. Herein, we propose a new methodology to significantly and simultaneously enhance both ductility and tensile strength of the titanium matrix composites. We ball milled Ti–6Al–4V (TC4) powders with in-situ chemically synthetized Ni decorated multi-walled carbon nanotubes (i.e MWCNTs@Ni), and then sintered the composites powders using spark plasma sintering (SPS). We achieved both a significant balanced between superior strength and increased ductility of the composite using the MWCNTs@Ni nanopowders. The enhanced strength in composites is mainly attributed to the interfacial structures for effectively enhanced load transfer capability between MWCNTs@Ni and Ti matrix, e.g., the formation of coherent/semi-coherent interfaces among interfacial phases Ti2Ni, TiC and Ti matrix. Furthermore, we applied the dislocation theory to reveal the toughening mechanisms of MWCNTs@Ni in the MWCNTs@Ni/TC4 composites. This study provides a new methodology of fabricating metal matrix composites (reinforced with carbon based nanomaterial) with both high strength and good ductility.

Cation substitution in spinel cobaltites (e.g., ACo2O4, in which A = Mn, Fe, Co, Ni, Cu, or Zn) is a promising strategy to precisely modulate their electronic structure/properties and thus improve the corresponding electrochemical performance for water splitting. However, the fundamental principles and mechanisms are not fully understood. This research aims to systematically investigate the effects of cation substitution in spinel cobaltites derived from mixed-metal-organic frameworks on the oxygen evolution reaction (OER). Among the obtained ACo2O4 catalysts, FeCo2O4 showed excellent OER performance with a current density of 10 mA·cm−2 at an overpotential of 164 mV in alkaline media. Both theoretical calculations and experimental results demonstrate that the Fe substitution in the crystal lattice of ACo2O4 can significantly accelerate charge transfer, thereby achieving enhanced electrochemical properties. The crystal field of spinel ACo2O4, which determines the valence states of cations A, is identified as the key factor to dictate the OER performance of these spinel cobaltites.

For conventional titanium matrix composites (TiMCs), there is always a trade-off issue between enhanced strength and ductility of these materials. In this study, we explore a new design methodology by reinforcing titanium alloy matrix with carbonaceous nanomaterials and investigate the mechanisms for achieving a good balance of their strength and ductility. The TiMCs were synthesized through a low-cost powder metallurgy route using pre-mixed Ti-6Al-4V (TC4) powders and various carbon based nanofillers, including graphite powders (GPs), graphene oxide nanosheets (GONs) and graphene nanoplates (GNPs), and were further rolled at a temperature of 1173 K with a deformation of 66.7%. Among these three types of carbon reinforcing sources, the GNPs are more easily reacted with TC4 matrix and form more contents of TiC phases after sintering owing to their larger amounts of defects than those of the GPs and GONs. TiC products are identified to play a bridging role for not only connecting the TC4 matrix but also forming coherent interfaces with the TC4 matrix, thus facilitating a strong interfacial bonding of the composites. The as-rolled GNPs/TC4 composites exhibit a 0.2% yield strength of 1146.36 MPa (with an elongation of ∼8.1%), which is 24.6%, 9.22% and 5.62% higher than those of pure TC4, GPs/TC4 and GONs/TC4 composites. The GNPs/TC4 nanocomposites show a better balance of strength and ductility than those of the other two types of nanocomposites. The synergetic strengthening mechanisms are identified to be Orowan strengthening effect, effective load transfer capability of GNPs, and in-situ formation of interfacial TiC structures, which provide optimum interfacial microstructures to achieve good mechanical properties of the TiMCs.

In this paper, we for the first time report the catalytic activity and durability of nickel cobaltite telluride (NiCo2Te4) nanocluster bifunctional catalysts can be significantly boosted by surface modification with perylene-tetracarboxylic-dianhydride for overall water-splitting in neutral solution. We reveal that tuning energy distribution of nanoclusters via a simple surface ligand can drastically increase the catalytic activity towards efficient hydrogen and oxygen evolution reaction simultaneously. A two-electrode based water electrolysis cell using this newly developed nanocluster catalyst operates at a low bias voltage of 1.55 V to achieve a current density of 10 mA·cm−2 in near-neutral pH solution for overall water-splitting. This, to the best of our knowledge, represents the most efficient mixed-transition-metal-based electrode that has so far been reported for electrochemical water splitting.

Zinc cobalt sulfide (ZCS) is a promising and high performance electrode material for pseudocapacitors due to its good electrical conductivity, abundant active sites and rich valence states. In this work, zinc cobalt oxide (ZCO) nanoparticles are firstly synthesized via a hydrothermal method assisted by hexadecyltrimethyl ammonium bromide (CTAB), and then transformed into zinc cobalt sulfide nanoparticles (ZCS NPs) using a facile sulfuration process. The average diameter of ZCS NPs is estimated to be about 15 nm, which is beneficial for Faradaic redox reactions in energy storage process due to their numerous active surfaces. The ZCS NPs are then coated onto a nickel foam to form the working electrode of supercapacitors. Because the ZCS electrode has lower series and charge transfer resistance, and also higher ion diffusion rate than that of the ZCO electrode, it achieves a large specific capacitance of 1269.1 F g−1 at 0.5 A g−1 in 2 M KOH electrolyte, which is four times more than that of the ZCO electrode (e.g., 295.8 F g−1 at 0.5 A g−1). In addition, an asymmetric supercapacitor using the ZCS NPs as the positive electrode and activated carbon as the negative electrode is assembled, which delivers a high energy density of 45.4 Wh kg−1 at a power density of 805.0 W kg−1, with an excellent cycling stability (91.6% retention of the initial capacitance over 5000 cycles).

The influence of αs precipitates on electrochemical behavior and mechanical degradation of Ti-1300 alloy in artificial seawater have been studied. The results show that corrosion resistance and mechanical degradation have been significantly affected by the formation of acicular αs precipitates. The precipitated αs phase with an acicular shape around 40–60 nm in width are uniformly distributed inside β grain. Many αs precipitates are intersected each other and keep a well-defined Burgers orientation relationship with β matrix, which restricts the growth of other αs phases due to pinning effect. Within the electrolyte, the αs phases can form “microgalvanic cells” with their adjacent intergranular β phases, which dramatically deteriorate its corrosion resistance. The mechanical properties of the alloy are also degraded with the increase of immersion time due to the pitting reaction. The precipitated microstructure exhibits an inferior mechanical degradation behavior, and this is mainly because a lot of corrosion cavities are nucleate d and propagated at the interface between αs precipitates and prior β grains.

CuCo2S4 is regarded as a promising electrode material for supercapacitor, but has inferior conductivity and poor cyclic stability which restrict its wide-range applications. In this work, hierarchically hybrid composite of CuCo2S4/carbon nanotubes (CNTs) was synthesized using a facile hydrothermal and sulfuration process. The embedded CNTs in the CuCo2S4 matrix provided numerous effective paths for electron transfer and ion diffusion, and thus promoted the faradaic reactions of the CuCo2S4 electrode in the energy storage processes. The CuCo2S4/CNTs-3.2% electrode exhibited a significantly increased specific capacitance of 557.5 F g−1 compared with those of the pristine CuCo2S4 electrode (373.4 F g−1) and CuO/Co3O4/CNTs-3.2% electrode (356.5 F g−1) at a current density of 1 A g−1. An asymmetric supercapacitor (ASC) was assembled using the CuCo2S4/CNTs-3.2% as the positive electrode and the active carbon as the negative electrode, which exhibited an energy density of 23.2 Wh kg−1 at a power density of 402.7 W kg−1. Moreover, the residual specific capacitance of this ASC device retained 85.7% of its original value after tested for 10,000 cycles, indicating its excellent cycle stability.

In order to solve problems of significant interfacial reactions and agglomeration in graphene reinforced W Cu composites, powders of copper coated graphene (Cu@Gr) were pre-mechanically mixed with tungsten and copper powders, and then graphene doped W Cu composites were sintered using two different methods, e.g., spark plasma sintering (SPS) and infiltration sintering. Microstructural analysis showed that the doped Cu@Gr powder can effectively inhibit the interfacial reaction between graphene and tungsten, prevent the segregation of graphene, and evenly distribute the copper in the binder phase. When the mixed concentration of Cu@Gr was 0.45 wt%, uniform distributions of W phase and Cu phase were obtained in the composite, and the mechanical properties and conductivity of this composite achieved their best results. When the doping content was further increased to 0.8%, WC phase was found in all alloys, thus resulting in poor mechanical and physical properties. Comparing the microstructures produced using these two methods, the composites prepared using the infiltration sintering method showed network distribution of copper phase and segregation of copper, whereas the composites prepared using the SPS method showed network skeleton phase of tungsten. Although the SPS process was performed in a much shorter time, the mechanical properties of the composites sintered using the SPS process did not show much differences with those sintered using the infiltration sintering method.

The effects of loading rate on creep behavior and shear transformation zone (STZ) in magnetron sputtered La-Co-Al and Zr-Cu-Ni-Al amorphous alloy thin films were characterized through instrumented nanoindentation with a spherical indenter. It was revealed that with an increase in loading rate, both thin films became harder with a narrower distribution of mechanical response, and exhibited more pronounced creep displacement with higher creep strain rate. Based on cooperative shear model, both STZ volume and activation energy were calculated by measuring the strain rate sensitivity during creep, showing an increasing tendency with loading rate. However, the strain rate sensitivity was found to decrease with loading rate. Furthermore, structural heterogeneity density, estimated by analyzing the stressed volume at yielding, decreased with loading rate. Therefore, with increasing loading rate, the STZ event can only be activated at detectable structural heterogeneities with relatively larger volume, and the number of available fertile sites was decreased, resulting in postponed shear band formation and suppressed deformation mode transition.

Propagation of surface acoustic waves (SAWs) on bulk piezoelectric substrates such as LiNbO3 and quartz, exhibits an in-plane anisotropic effect due to their crystal cut orientations. Thin film SAW devices, such as those based on ZnO or AlN, offer potential advantages, including isotropic wave velocities in all in-plane directions, higher power handling capability, and potentially lower failure rates. This paper reports experimental and simulation results of nebulization behaviour for water droplets using ZnO/Si surface acoustic wave devices with focused interdigital transducers (IDTs). Post-deposition annealing of the films at various temperatures was applied to improve the quality of the sputtering-deposited ZnO films, and 500 °C was found to be the optimal annealing temperature. Thin film ZnO/Si focused SAW devices were fabricated using the IDT designs with arc angles ranging from 30° to 90°. Nebulization was significantly enhanced with increasing the arc angles of the IDTs, e.g., increased nebulization rate, reduced critical powers required to initialise nebulization, and concentration of the nebulised plume into a narrower size of spray. Effects of applied RF power and droplet size have been systematically studied, and increased RF power and reduced droplet size significantly enhanced the nebulization phenomena.

A molecular mechanics model for covalent and ionic double-network polymer composites was developed in this study to investigate mechanisms of mechanochemically induced unzipping and scission of chemical bonds. Morse potential function was firstly applied to investigate mechanical unzipping of the covalent bonds, and then stress-dependent mechanical energy for the interatomic covalent bonds was discussed. A new mechanochemical model was formulated for describing the mechanically induced ionic bond scissions based on the Morse potential model and equations for electrostatic forces. Based on this newly proposed model, mechanochemical behaviors of several common interatomic interaction types (e.g., A+B−, A2+B2−/A2+2B−/2A+B2− and A3+B3−/A3+3B−/3A+B3−) of the ionic bonds have been quantitatively described and analyzed. Finally, mechanochemical unzipping of the covalent bonds and dissociation of the ionic bonds have been characterized and analyzed based on the molecular mechanics model, which has well predicted the chemical and mechanochemical activations in the covalent and ionic double-network polymer composites.

Surface acoustic wave (SAW) sensors have great advantages in real-time and in-situ gas detection due to their wireless and passive characteristics. Using nanostructured sensing materials to enhance the SAW sensor’s responses has become a research focus in recent years. In this paper, solution-processed PbS colloidal quantum dots (CQDs) were integrated into quartz SAW devices for enhancing the performance of NO2 detection operated at room temperature. The PbS CQDs were directly spin-coated onto ST-cut quartz SAW delay lines, followed by a ligand exchange treatment using Pb(NO3)2. Upon exposure to 10 ppm of NO2 gas, the sensor coated with untreated PbS CQDs showed response and recovery times of 487 s and 302 s, and a negative frequency shift of −2.2 kHz, mainly due to the mass loading effect caused by the absorption of NO2 gas on the surface of the dense CQD film. Whereas the Pb(NO3)2-treated sensor showed fast response and recovery times of 45 s and 58 s, and a large positive frequency shift of 9.8 kHz, which might be attributed to the trapping of NO2 molecules in the porous structure and thus making the film stiffer. Moreover, the Pb(NO3)2-treated sensor showed good stability and selectivity at room temperature.

In this work, effects of 10 keV argon ion implantation on laser-induced damage threshold (LIDT) of fused silica were systematically investigated with ion fluences ranged from 1 × 1016 ions/cm2 to 1 × 1018 ions/cm2. Results show that only when the ion fluence increases above 1 × 1017 ions/cm2, the surface roughness apparently increases due to the formation of argon bubbles in the surface of fused silica. The concentration of defects decreases with the increased fluences up to 1 × 1017 ions/cm2 but then increases further, especially for the oxygen deficient center (ODC) defect. Based on the nanoindentation test results, Ar ion implantation generates large compressive stress and strengthens the surface of fused silica by surface densification. With the increase of the Ar ion fluences, the LIDTs of the samples increase due to the increases in both surface compressive stress and defects annihilation. However, at higher ion fluences, the increase of the densities of defects and argon bubbles are identified as the key reasons for the decrease of the LIDTs. Therefore, Ar ion implantation can improve the LIDTs of fused silica at moderate fluences.

Colloidal quantum dots (CQDs) have shown their advantages in gas-sensing applications due to their extremely small particle size and facile solution based processes. In this study, a high sensitivity of surface acoustic wave (SAW) NO2 sensor was demonstrated using SnS CQDs as the sensing layer. The delay line based SAW device with a resonant frequency of 200 MHz were fabricated on ST-cut quartz substrate. The SnS CQDs with average sizes of 5.0 nm were synthesized and deposited onto SAW sensors using a spin-coating method. The fabricated SAW sensor was capable of detecting a low concentration of NO2 gas at room temperature with a good efficiency and selectivity e.g., with a 1.8 kHz decrease of center frequency of the SAW delay line when exposed to 10 ppm NO2 at room temperature.

Zinc oxide (ZnO) is an environmental-friendly semiconducting, piezoelectric and non-ferroelectric material, and plays an essential role for applications in microelectromechanical systems (MEMS). In this work, a fully integrated two-degree-of-freedom (2DOF) MEMS piezoelectric vibration energy harvester (p-VEH) was designed and fabricated using ZnO thin films for converting kinetic energy into electrical energy. The 2DOF energy harvesting system comprises two subsystems: the primary one for energy conversion and the auxiliary one for frequency adjustment. Piezoelectric ZnO thin film was deposited using a radio-frequency magnetron sputtering method onto the primary subsystem for energy conversion from mechanical vibration to electricity. Dynamic performance of the 2DOF resonant system was analyzed and optimized using a lumped parameter model. Two closely located but separated peaks were achieved by precisely adjusting mass ratio and frequency ratio of the resonant systems. The 2DOF MEMS p-VEH chip was fabricated through a combination of laminated surface micromachining process, double-side alignment and bulk micromachining process. When the fabricated prototype was subjected to an excitation acceleration of 0.5 g, two close resonant peaks at 403.8 and 489.9 Hz with comparable voltages of 10 and 15 mV were obtained, respectively. Accepted version

Acoustofluidic platform has great potentials to integrate capillary tubes for controlling and manipulating microparticles and biological cells in both non-flowing and continuous-flow settings. In order to effectively manipulate microparticles/cells inside capillary tubes, it is essential to fully understand and control the patterns generated inside the capillary tubes with different cross-sections, and to investigate the influences of configuration and position arrangement of electrodes along with the capillary tubes. This paper aims to systematically investigate the patterning and alignment of microparticles inside glass capillary tubes using thin film surface acoustic wave (SAW) devices. Through both experimental studies and numerical modelling, effects of various cross-section geometries of the capillary tubes and their positioning with respect to the direction of interdigital transducers (IDTs) of the SAW device in both a stationary fluid and a continuous flow fluid were studied. Results showed that for the rectangular glass capillary tubes, the patterned lines of particles are parallel to the tube's side walls, irrelevant to the tube positions along with the IDTs, which is mainly caused by the standing wave field generated inside the rectangular glass tube. Whereas for the circular glass capillary tubes, alignment patterns of particles are quite different along the tube's height. At the bottom of the circular tube, particles are patterned into lines parallel to the tube direction, because the acoustic waves propagate into the water and form a standing wave along the direction of the circular tube. Whereas at the middle height of the tube, the particles are patterned into lines perpendicular to the tube direction, because the formed standing waves also propagate around the circular cross-section of the tube and are perpendicular to the tube direction. For the cases with a continuous liquid flow, under the agitation of acoustic waves, particles are patterned in lines parallel to the flow directions for both the rectangular and circular glass tubes, and the fluid flow enhances and smoothens the patterned lines of the particles.

Hydrogen gas sensors were fabricated using mesoporous In2O3 synthesized using hydrothermal reaction and calcination processes. Their best performance for the hydrogen detection was found at a working temperature of 260 °C with a high response of 18.0 toward 500 ppm hydrogen, fast response/recovery times (e.g. 1.7 s/1.5 s for 500 ppm hydrogen), and a low detection limit down to 10 ppb. Using air as the carrier gas, the mesoporous In2O3 sensors exhibited good reversibility and repeatability towards hydrogen gas. They also showed a good selectivity for hydrogen compared to other commonly investigated gases including NH3, CO, ethyl alcohol, ethyl acetate, styrene, CH2Cl2 and formaldehyde. In addition, the sensors showed good long-term stability. The good sensing performance of these hydrogen sensors is attributed to the formation of mesoporous structures, large specific surface areas and numerous chemisorbed oxygen ions on the surfaces of the mesoporous In2O3.

Tungsten-copper (W-Cu) composites are used as high temperature frictional materials under special service conditions for electromagnetic gun rail and precision guide for rolled pieces due to their good ablation resistance and electrical conductivity. However, they have poor wear resistance at elevated temperatures. In this paper, surface carburization method was applied on the W-20 wt%Cu composite to investigate the mechanisms of carburization and its effects on the high temperature friction behavior of composite. Carburization process has been done at a temperature of 1100 °C for 30 h. The obtained results showed that carburizing at 1100 °C with a dwelling time of 30 h resulted into formation of a carburized layer and a dense intermediate sub-layer on the substrate. Also, the surface carburized layer with a thickness of about 70 μm composed of mixed phases of graphite, WC and W2C. The hardness of carburized layer (~HV454) was significantly higher than that of substrate (HV223). Also, bending strength of the carburized W-Cu composites has been significantly improved, although their electrical conductivity and tensile strength was decreased slightly. The carburization mechanism of the W-Cu composites was found to be dominant by carbon atom diffusion through reaction with W atoms and formation of surface liquid copper, which promoted migration and diffusion of tungsten and carbon at high temperatures. Average coefficients of friction and wear rate of carburized W-Cu composites are all lower than these of un-carburized W-Cu composites owing to the presence of surface carburized layer. Also, formation of CuWO4 at high temperatures reduced the friction and wear resistance of the W-Cu composites.

W-based alloys are currently considered promising candidates for high heat flux components in future fusion reactors. In this paper, hot pressed W-20 wt%Cu composites were treated at room temperature using a sliding friction severe deformation (SFD) process, with a moving speed of 0.2 m/s and an applied load of 500 N. Microstructural evolution of composites after the SFD treatment was evaluated and compared with that of the untreated composites. Results showed that there was a gradient structure generated and an obvious refinement in tungsten particles size in the surface layer after the SFD process. The average particle size of tungsten in the SFD treated composites was 2.60 μm, whereas it was 4.5 μm for tungsten in the untreated composites. Fracture surfaces of the composites indicated that the SFD treatment destroyed the W skeleton and changed fracture mode from predominant inter-granular one to trans-granular one due to the decrease in contact area of W-W inter-particles. Yield strength and ultimate tensile strength of composites after the SFD treatment were 308 MPa and 553 MPa, respectively. The treated composites exhibited micro-hardness values with an average reading of about 308 HV. Analysis of the facture microstructures clearly suggested that the tungsten particles in the treated composites are consisted of dislocations and boundaries as well as dislocation tangles. The electrical conductivity of the composites was decreased from 33 IACS% to 28.5 IACS% after the SFD treatment, mainly due to loss or squeezing of copper into the inner surface.

Sensors are the foundation of modern Internet of Things, artificial intelligent, smart manufacturing etc, but most of them require power to operate without spontaneous unique identifiable function. Herein we propose a novel instantaneous force-driven self-powered self-identified wireless sensor based on triboelectric effect to meet the huge demand of true self-powered wireless sensors. The device consists of a microswitch controlled triboelectric nanogenerator (TENG) in parallel with a capacitor-inductor oscillating circuit, and a wireless transmitter. The system is fully powered by the output of the TENG to generate a resonant frequency containing sensing and device identity information, which is then coupled to the transmitter for realizing a long-range wireless communication. The device, with the multiple functions of energy harvesting, sensing, identity generation and wireless signal transmission, is a standalone device, which responds to each trigger without losing sensing information. It eliminates the requirement of electric components for traditional wireless communication, such as rectification circuit, energy storage units, microprocessor, wireless communication chip, etc. Thus, we developed a true self-powered identifiable wireless sensor with great potential for widespread applications.

A new antisolvent method was developed to prepare CH3NH3PbI3 and electron transport layers for making efficient hybrid perovskite solar cells. By directly using [6,6]-phenyl-C61-butyric acid methyl ester in chlorobenzene solution as antisolvent, CH3NH3PbI3 and electron transport layers were simultaneously formed in the films. This method not only simplifies the fabrication process of devices, but also produces uniform perovskite films and improves the interfacial structures between CH3NH3PbI3 and electron transport layers. Large perovskite grains were observed in these films, with the average grain size of >1 μm. The so-formed CH3NH3PbI3/electron transport layers demonstrated good optical and charge transport properties. And perovskite solar cells fabricated using these simultaneously-formed layers achieved a higher power conversion efficiency of 16.58% compared to conventional antisolvent method (14.92%). This method reduces nearly 80% usage of chlorobenzene during the fabrication, offering a more facile and environment-friendly approach to fabricate efficient perovskite solar cells than the conventional antisolvent method.

Deformation mode transition (DMT) from highly-localized to non-localized in amorphous alloy thin films (AATFs) was expected to depend on the homologous temperature. Here, DMT in Mg-Zn-Ca AATF with high homologous temperature but intrinsic brittleness was monitored during film/substrate co-bending, and its critical size for DMT is much low compared to other compositions. Intrinsically brittle nature of Mg-based AATF that facilitates the shear band to unstable crack transition may be responsible for unexpected low critical size despite of high homologous temperature.

In this paper, a one-step thermal evaporation approach was used for fabrication of indium bismuth sulphide thin films, and the synergetic effects of co-evaporation of two sources (indium granules and Bi2S3 powders) were investigated using different characterization techniques. X-ray diffraction (XRD) analysis confirmed the crystalline orthorhombic structure for the post-annealed samples. Surface roughness and crystal size of the obtained film samples were increased with increasing annealing temperatures. Analysis using X-ray photoelectron spectroscopy showed the formation of the InBiS3 structure for the obtained films, which is also confirmed by the XRD results. The optical absorption coefficient value of the annealed samples was found to be in the order of 105 cm−1 in the visible region of the solar spectrum. The optical band gap energy and electrical resistivity of the fabricated samples were observed to decrease (from 2.2 to 1.3 eV, and from 0.3 to 0.01 Ω–cm, respectively) with increasing annealing temperatures (from 200 to 350 °C), indicating the suitability of the prepared InBiS3 thin films for solar cell applications.

Mg-Zn-Ca thin film metallic glasses were prepared by using direct current magnetron sputtering and their film thickness dependences of density, morphology and local atomic structure were systematically investigated. It is found that all the films prepared are fully amorphous. The film density and the coordination number around Zn atoms decrease while the surface roughness increases with increasing film thickness. When the film thickness is larger than the critical value of 400 nm, the average atomic distance, the granular size on the film surface and the columnar size on the film cross-section remain almost unchanged, demonstrating that the films grow in an equilibrium mode.

Colloidal quantum dots (CQDs) are promising building blocks for low-cost and high-performance gas sensors due to their excellent solution processability and extremely small size. Among chalcogenide CQDs, PbSe has a large exciton Bohr radius and exhibits strong confinement energies, facilitating the fast charge-carrier transport. However, CQDs-based devices are susceptible to degrade due to the poor stability of CQDs. Here, in order to obtain air-stable PbSe CQDs for gas sensing application, we synthesized PbSe CQDs using a cation exchange method with in situ chloride and cadmium passivation. The sharp absorption peak in UV–vis absorption spectra confirmed strong quantum confinement in the PbSe CQDs and their average diameter was estimated to be 2.87 ± 0.23 nm. To construct gas sensors, PbSe CQDs were spin-coated onto ceramic substrates and then Pb(NO 3 ) 2 treatment was carried out to remove the long-chain ligands surrounding PbSe CQDs. At 25 °C, the sensor was highly sensitive and selective to NO 2 with a response of 22.3 at 50 ppm and a fast response time of 7 s. Moreover, the sensor response showed a 85.2% stability as the time increased up to 20 days, suggesting the potential applications of PbSe CQDs for NO 2 monitoring at room temperature.

The silica modified CeO2 gas sensing nanomaterials are synthesized using a sol-hydrothermal route. The 8%silica-CeO2 has larger specific surface areas of 83.75 m2/g and smaller crystalline size of 11.5 nm than pure CeO2, respectively. Compared to pure CeO2, the 8%silica-CeO2 based gas sensor exhibits significant enhancement NH3 gas-sensing performance. At room temperature, it shows much better gas response of 3244% to 80 ppm of NH3 gas and lower detection limit (0.5 ppm) towards NH3 gas. It is also found that the gas response of the NH3 gas sensors increases linearly with the increase of NH3 gas concentration. Moreover, the NH3 gas sensor have good reversibility, stability and selectivity. The reason of enhanced NH3 gas-sensing performance is not only because of the increased specific surface areas, but also due to the electrolytic conductivity of NH4+ and OH− on the surface.

Manganese oxide is considered an ideal pseudo-capacitive electrode material for supercapacitors due to its low cost, environmental friendliness and large theoretical capacity. However, it is difficult to obtain manganese electrodes with a high specific capacitance and a large voltage range. In this study, ultrafine Mn3O4 nanowires with an average diameter of 4.0 nm were synthesized using a colloidal method. They have a large specific surface area of 175.1 m2 g−1, and can provide numerous active sites to enhance their specific capacitances. They also show a large pore volume of 0.7960 cm3 g−1, which can provide essential channels for ion transport during charging and discharging processes. The supercapacitor electrode made of these ultrafine Mn3O4 nanowires exhibits a predominant surface capacitive behavior during charge/discharge processes, and achieves a large specific capacitance of 433.1 F g−1 at a current density of 0.5 A g−1 with a very wide voltage range from -0.5 to 1.1 V in 1 M Na2SO4 electrolyte. An asymmetric supercapacitor (ASC) was assembled using a cathode electrode made of these ultrafine Mn3O4 nanowires and an active carbon (AC) anode electrode, and a high energy density of 26.68 Wh kg−1 at a power density of 442 W kg−1 was achieved. The ASC showed a good cycling stability, and its capacitance value was still maintained at 75.8% after 64,000 charge/discharge cycles.

Benzotriazole (BTA) and tolyltriazole (TTA) were used to passivate pure copper and chromium bronze alloys for environmental protection. Using the chemical immersion treatment, a dense film of chromium-free passivation layer was formed on surfaces of both the pure copper and chromium bronze alloys. Microstructure, crystalline phases and chemical bonds of the passivation layers were systematically characterized, and the passivation mechanisms were studied. The passivation layer was mainly consisted of CuO, Cu2O, polymers of Cu-BTA-TTA and Cu(I)BTA-TTA. The formation mechanism of the chromium-free passivation layer was identified as combined oxidation and adsorption, and the main passivation processes included oxidation and dissolution of the matrix, adsorption of BTA and its derivatives, self-stabilization process of the adsorbed film, and filling of passivation film’s voids by oxide particles.

Ti3C2Tx MXene was synthesized and the 2D layers were hybridized with Au nanoparticle (AuNP) through the in-situ method. The study was successfully prepared MXene 2D layer and the same was TEM captured as well. Polyimide/MXene-AuNP (PI/Mxene-AuNP) transducing conducting nanocomposite thin film was synthesized and evaluated the new material’s capability to use as a transducing thin film for biosensing application. The bioreceptor was prepared on the delay line area of the SAW device by covalently immobilizing mouse monoclonal antibody of carcinoembryonic antigen (CEA) through the thioglycolic acid arm linker mechanism. Immunoassay analysis has suggested that the biosensor responds linearly with the increase in the concentration of the CEA sample. The limit of detection was observed at 0.001 ng/mL. The insertion loss of the bioreceptor was recorded at 10 dB, which also mattered in the high sensitivity of the biosensor. The biosensor has shown excellent selectivity within the environment of other common tumour markers and was stable for 75 days under periodical testing conditions. Clinical serum samples were analyzed successfully and the results were compared with values obtained through the ELISA method.

We proposed a surface acoustic wave (SAW) NH3 gas sensor based on nitrogen doped diamond like carbon (N-DLC) film. The N-DLC film, prepared using a microwave electron cyclotron resonance plasma chemical vapor deposition (ECR-PECVD) method, is highly porous and physically and chemically stable, and have active polar groups on its surface, which can selectively absorb polar NH3 gas molecules. These features of the film lead to the high sensitivity, low noise and excellent stability of the sensor. The sensor can achieve capabilities of in-situ monitoring NH3 in a concentration range from 100 ppb to 100 ppm with fast response (∼5 s) and recovery (∼29 s) at room temperature. The NH3 sensing mechanism is attributed to the decreased porosity of the N-DLC film caused by adsorbed NH3 molecules on its polar groups, which leads an increase of the elastic modulus of the film.

Real time monitoring of contamination on antireflection (AR) silica coatings in high peak power laser systems (HPLs) is critically needed in order to avoid reductions of transmission and laser damage to optical surfaces. Herein we proposed to apply a surface acoustic wave (SAW) sensor to real-time monitor trace amounts of airborne molecular contaminants (AMCs) adsorbed on the AR silica coatings. The silica coating is found to be susceptible to AMCs because of its mesoporous structure, huge surface area and polar nature. The adsorbed AMCs caused the increased mass on the silica coating of the SAW sensor, which resulted in a significant increase of its frequency shift. The fabricated sensor showed a high sensitivity of ∼-490 mm2 ng−1Hz and an excellent linearity vs. the areal density of adsorbed AMCs since the frequency shift of the sensor is linearly related to the change of mass of the silica coating.

This paper proposes an encrypted multitone modulation method to achieve low probability of being deciphered for physical layer security (PLS) of communication based on chaotic cryptography. The main objective of the proposed method is to map random, unpredictable, many-to-one relations between a multitone group (MTG) and baseband data. After the baseband data are mapped to several types of MTGs within the available frequency band with the mapping relation, the transmitter first determines the MTG type according to the data to be sent, and then the definite MTG is selected according to the MTG index sequence. Obviously, under this modulation scheme, the mapping relationship and MTG index sequence determine the distribution of frequency points. Inspired by the characteristics of this modulation, the long-term statistical undifferentiated features of different types of MTGs are obtained by encrypting the mapping relationships, and then the index sequence is designed to realize a roughly equal probability of being used for each MTG type. To accurately decipher the baseband data information, the cooperative receiver needs to master the mapping relationship and related secret keys. After establishing the communication system model under this modulation mode, the anti-non-cooperative reception deciphering ability of the system and its performance are analyzed theoretically. The reliability and concealment of the proposed method are experimentally verified and compared with the reliability and security of the orthogonal frequency-division multiplexing- (OFDM) quadrature phase-shift keying (QPSK) and differential frequency hopping (DFH) modulation methods under the same number of subcarriers and channel environments.

W70Cu30(W-30 wt.% Cu) alloys were fabricated using cold pressing and infiltration sintering methods from two types of powders, i.e., mixed copper-tungsten (M-Cu-W) powders and our newly developed copper-coated tungsten composite (Cu@W) powders. Microstructure, mechanical and arc-ablation properties of the W70Cu30 alloys were investigated, and the mechanism of enhanced physical/mechanical properties and arc-erosion resistance of the W70Cu30 alloys was discussed. For the W70Cu30 alloys prepared using the Cu@W powders, their physical properties, including hardness, electrical conductivity and relative density were much better than those prepared from the M-Cu-W powders. The W70Cu30 alloys fabricated from the Cu@W powders were free of cracks, and showed homogenous distributions of W and Cu network structures. Whereas for the alloys prepared from the M-Cu-W powders, segregation of Cu was observed and the segregation size was about 40–100 μm. Characterization of arc-erosion morphologies of the W70Cu30 alloys prepared with the Cu@W powders revealed the occurrence of evaporation of Cu phase; whereas that of W70Cu30 alloys prepared with the M-Cu-W powders revealed the occurrence of the sputtering of Cu. After arc breakdown for 200 times, mass loss of alloys made using the mixed powders was twice as much as those made using the coated composite powders. Based on the experimental results and theoretical analysis, an arc breakdown mechanism of the WCu-C alloys using the composite powders was proposed which is attributed to the formation of a homogeneous Cu-Cu network structure to uniformly disperse arc energy and dissipate the generated heat, thus prolonging the service life of the WCu alloy contacts.

Thickness dependency and interfacial structure effects on thermal properties of AlN thin films were systematically investigated by characterizing cross-plane and in-plane thermal conductivities, crystal structures, chemical compositions, surface morphologies and interfacial structures using an extended differential 3ω method, X-ray diffraction (XRD) analysis, X-ray photoelectron spectroscopy, atomic force microscopy (AFM) and transmission electron microscopy. AlN thin films with various thicknesses from 100 to 1000 nm were deposited on p-type doped silicon substrates using a radio frequency reactive magnetron sputtering process. Results revealed that both the cross- and in-plane thermal conductivities of the AlN thin films were significantly smaller than those of the AlN in a bulk form. The thermal conductivities of the AlN thin films were strongly dependent on the film thickness, in both the cross- and in-plane directions. Both the XRD and AFM results indicated that the grain size significantly affected the thermal conductivity of the films due to the scattering effects from the grain boundary.

Copper antimony sulphide (Cu3SbS3) with a p-type conductivity and optical band gaps in the range of 1.38 to 1.84 eV is considered to be a promising solar harvesting material with non-toxic and economical elements. In this study, we reported the fabrication of Cu3SbS3 thin films using successive thermal evaporation of Cu2S and Sb2S3 layers followed by annealing in an argon atmosphere at a temperature range of 300-375°C. The structural and optical properties of the as-deposited and annealed films were investigated. The annealed films notably show the crystalline phase of the Cu3SbS3, identified from the X-ray diffraction analysis and endorsed by the Raman analysis as well. Whereas their chemical state of the constituent elements was characterized with X-ray photoelectron spectroscopy. The measured highest resistivity of the annealed film was found to be ~0.2 Ω-cm. Hence, our obtained results for the fabricated Cu3SbS3 thin films bring to light that Cu3SbS3would be a good absorber layer in solar cells due to their low resistivity, a higher value of the optical absorption coefficient (~105 cm-1), the low transmittance (

Unlike metal electrodes such as Al and Au, aluminum doped zinc oxide (AZO) with high conductivity and transparency can be used as transparent electrodes for surface acoustic wave (SAW) resonators, and thus realize fully transparent and invisible ZnO SAW devices on glass. This paper reports the fabrication of transparent SAW resonators using AZO as the transparent electrode and investigation of effects of deposition parameters on the crystal structures of the AZO thin films deposited by magnetron sputtering. Results show that a low sputtering pressure and an optimal sputtering power are beneficial for the deposition of (0002) orientation of AZO. The optimal deposition parameters are found to be: deposition pressure of 0.3 Pa, sputtering power of 300 W, substrate temperature of 200 °C. The fabricated transparent SAW devices have different wavelengths (from 16 to 32 μm) and all the devices exhibit two types of wave modes: Rayleigh and Sezawa waves. Compared with Sezawa wave, the Rayleigh wave has a large signal amplitude up to 25 dB. In addition, as the wavelength increases, the resonant frequencies of both the Rayleigh and Sezawa waves increase whereas their phase velocities decrease. The transparent SAW devices have also demonstrated their ability to induce a strong acoustic streaming in a water droplet with a streaming velocity up to 2.27 cm/s. This research opens a door for further exploration of the SAW devices in transparent electronics.

A multilayer structure of TeO2/interdigital transducers (IDTs)/ZnO(112¯0)/Si(100) was proposed and investigated to achieve both high sensitivity and temperature-stability for bio-sensing applications. Dispersions of phase velocities, electromechanical coupling coefficients K2, temperature coefficient of delay (TCD) and sensitivity in the multilayer structures were simulated as functions of normalized thicknesses of ZnO (hZnO/λ) and TeO2 (hTeO2/λ) films. The fundamental mode of Love mode (LM) - surface acoustic wave (SAW) shows a larger value of K2 and higher sensitivity compared with those of the first mode. TeO2 film with a positive TCD not only compensates the temperature effect induced due to the negative TCD of ZnO(112¯0)/Si(100), but also enhances the sensitivity of the love mode device. The optimal normalized thickness ratios were identified to be hTeO2/λ=0.021 and hZnO/λ=0.304, and the devices with such structures can which generate a normalized sensitivity of -1.04×10-3m3/kg, a TCD of 0.009ppm/°C, and a K2 value of 2.76%.

Titanium alloys have been applied for many lightweight structural components in the fields of aerospace, automobiles and biomedical implants owing to their light-weight, good mechanical properties and biocompatibility. However, poor tribological performance often restricts their wide-range applications. In this study, we synthesized Cu modified Ti-6Al-4 V (TC4) powders with various Cu contents (0, 1, 3, 5, 10 wt%), which was further strengthened with 0.3 wt% graphene oxide nanosheets (GONs) using a powder metallurgy technology. These composite powders were then synthesized into titanium matrix composites using spark plasma sintering. Effects of Cu contents on microstructure evolution, phase composition and tribological properties of Ti matrix composites were systematically investigated. The synthesized composites were consisted of α-Ti, β-Ti, Ti2Cu, in-situ-formed TiC and remained GONs, and showed better tribological properties than those of TC4 alloy. The average coefficient of friction was reduced from 0.168 to a minimum value of 0.120 as the copper content increased from 0 to 3 wt%, meanwhile the wear volume loss was reduced by 49.3%. Whereas further increasing Cu contents resulted in the increases of both coefficients of friction and wear volume loss. These improvements are mainly attributed to the hardness strengthening effects by Ti-Cu intermetallics and TiC@GONs structure, as well as the self-lubricating effect of GONs. Compared with traditional surface modification processes, the new method proposed in this work is cost-effective and promising for improving the tribological performance of titanium alloys in industry applications.

Self-powered wireless sensor systems are highly sought for the forthcoming Internet of Things era. However, most of the technologies take the route of energy harvesting, storage, and power regulation to power wireless sensor systems, which has a limited operation duration due to the low energy utilization efficiency of the multiple energy conversions involved. Here, we propose a triboelectric nanogenerator (TENG) based fully self-powered, instantaneous wireless sensor system which yet does not contain electronic devices and chips, but the passive components only. By integrating a capacitive sensor and an inductor coil with TENG, the pulse voltage output of the TENG is converted into a sinusoidal signal containing the sensing information with a resonant frequency and is transmitted to the receiver in distance wirelessly and continuously. A precise analytical model is developed for the capacitive sensor system with general implication; the oscillating signal generated by the model shows excellent agreement with experimental results. A capacitive humidity sensor is then utilized for sensing demonstration, showing that the maximum transmission distance of the sensor system is 50 and 90 cm for a 1 cm diameter magnetic-core coil pair and 20 cm diameter air-core coil pair, respectively. The wireless humidity sensor exhibits a sensitivity of 1.26 kHz/%RH, fast response speed, and excellent linearity, demonstrating its great application potential of the self-powered technology.

Nanoparticles have been widely used to enhance mechanical properties of polymer matrix, however, the complex mechanisms of interfacial entanglements, coupled confinements and coordinative motions among the polymer macromolecules and nanoparticles have not been well understood. In this study, we develop a coupling model to describe the thermodynamic entanglements and confinement effects within nanoparticle reinforced shape memory polymer (SMP) nanocomposites. We found that thermodynamic relaxation of the SMP nanocomposite is determined by cooperative effects of sub-entanglement and topological entanglement of macromolecule chains, which selectively enhance the relaxation behaviors and enable a high recovery stress of SMP nanocomposites. Finally, the effectiveness of this model is demonstrated by applying it to predict the constitutive relationships and shape memory behaviors, and this fundamental approach can reveal toughening mechanisms of shape recovery strength in the SMP nanocomposites by nanoparticles.

Graphene quantum dots decorated zinc oxide nanowires (GQDs@ZnO-NWs) were applied to enhance sensing performance of highly flexible and transparent surface acoustic wave (SAW) ultraviolet (UV) photodetectors made on ultra-thin flexible glass. The developed flexible SAW sensors possess better performance than that of the previously developed polymer based flexible SAW devices, due to insignificant acoustic loss of flexible glass substrate. UV sensitivity of the flexible glass based SAW sensors was enhanced by three times, and the response time was shorten by four times after the sensor was coated with the GQDs@ZnO-NWs hybrid nanomaterials. These improvements are mainly attributed to: (1) large specific surface areas of ZnO NWs which can generate a large number of photon-generated carriers; (2) introduction of GQDs which can reduce the carrier recombination rate. The resonant frequency of flexible glass SAW UV photodetectors exhibited a good repeatability and stability in responses to cyclic changes of the UV lights at different wavelengths. They also maintained a good performance under a bending angle of ∼30° for 200 times without apparent degradation, showing the excellent flexibility and stability of the UV photodetector.

Two-dimensional transition metal carbides/nitrides, known as MXenes, have recently received significant attention for gas sensing applications. However, MXenes have strong adsorption to many types of volatile organic compounds (VOCs), and therefore gas sensors based on MXenes generally have low selectivity and poor performance in mixtures of VOCs due to cross-sensitivity issues. Herein, we developed a Ti3C2Tx-based virtual sensor array (VSA) which allows both highly accurate detection and identification of different VOCs, as well as concentration prediction of the target VOC in variable backgrounds. The VSA’s responses from the broadband impedance spectra create a unique fingerprint of each VOC without a need for changing temperatures. Based on the methodologies of principal component analysis and linear discrimination analysis, we demonstrate highly accurate identifications for different types of VOCs and mixtures using this MXene based VSA. Furthermore, we demonstrate an accuracy of 93.2% for the prediction of ethanol concentrations in the presence of different concentrations of water and methanol. The high level of identification and concentration prediction shows a great potential of MXene based VSA for detection of VOCs of interest in the presence of known and unknown interferences.

This paper reports significant enhancement of corrosion resistance and electrical properties of waterborne epoxy coatings through additions of ceria modified graphene. Results showed that ceria particles were uniformly distributed and covalently bonded onto the surface of graphene. A dense interface layer was formed between the ceria modified graphene and epoxy matrix by aliphatic ether bonds. The composite coating with a modified graphene content of 0.5 wt% exhibited the best corrosion resistance with the highest impedance modulus (e.g., 103 Ω cm2 for the damaged coating) and the lowest corrosion rate (e.g., 0.002 mm/year). The excellent corrosion resistance of the composite coating is related to the barrier effect of graphene and the inhibition effect of ceria on metal corrosion. Moreover, the coating showed a low percolation threshold of 0.231 vol% and its electrical conductivity reached 10−5 S/m when the content of modified graphene was 0.5 wt%.

Poor wettability and weak interfacial bonding between Cu and Al2O3 have been critical issues for sintering of high-quality Ni@Al2O3/Cu composites. In this paper, we explore an interfacial engineering design methodology to achieve good mechanical properties of Ni@Al2O3/Cu composites using spark plasma sintering method. The Ni coated powders were prepared using a heterogeneous precipitation method, which can significantly improve wettability between Cu and Al2O3 and enhance their interfacial bonding. The sintered Ni@Al2O3/Cu composites with a copper content of 15 vol% showed a compact network structure of alumina well-infiltrated with metallic Cu, and achieved good mechanical (e.g., fracture toughness of 6.72 MPam1/2) and physical properties (e.g., relative density of 99.3% and electrical resistivity of 1.2810−3 Ω m). The key mechanisms for the enhanced properties of the composites synthesized using the Ni coated composite powders have been identified as: (1) well-formed ceramic/metal interfacial structures which improve wettability of Al2O3 with Cu, and promote the formation of a homogeneous network structure; (2) enhanced elemental diffusion and interfacial reactions, which result in formation of Cu2O and CuAlO2 and thus improve interfacial wetting and bonding properties.