Composite magnetoelectrics implemented as thin film heterostructures are discussed in view of their applicability as highly sensitive magnetic field sensors. Here, either PZT or AlN served as piezoelectric component. The magnetostrictive phase consisted of layer systems based on FeCo or (Fe90Co10)78Si12B10. All functional layers were deposited with thicknesses of a few micrometers on Si cantilever structures with typical lateral dimensions of 25 mm by 2.2 mm. Magnetoelectric coefficients as large as 6900 V/cm Oe and a limit of detection as low as 1 pT/(Hz)1/2 were measured. Currently, the best result demonstrates a detection limit of 500 fT/(Hz)1/2 at 958 Hz frequency using a set of two sensors for external noise suppression. A frequency conversion technique is proposed to broaden the applicability of resonant magnetoelectric sensors to a wider frequency range. Finally, the achieved sensor performance is evaluated with regard to typical magnetic field amplitudes in medical applications.

Magneto polymer matrix composites (MPMC) is a new class of magnetic polymer materials which are being developed and under investigation as potential materials for tomorrow’s aircraft structures. It encompasses magnetic, particulate strengthening (dispersion strengthening) as well as fiber reinforcement/strengthening characteristics which are sought out to be utilized toward making efficient future aerospace composite materials. Various types of ferrites including barium, cobalt, iron, and strontium were explored for being used in making new composites. Here a comprehensive review of the synthesis, structure, properties, thermodynamics, surface chemistry, and phase transformations of individual ferrites and clusters of ferrites as fillers is presented. In particular a discussion about the rational control of the mechanical, physical, thermal, electrical, and magnetic properties of magneto polymer matrix composites through surface functionalization, modification, emulsification/compounding/blending, heat treatment (phase transformation and separation), and control of processing conditions (temperature, pressure and geometry of mold) is provided. These smart materials have a wide range of potential applications in medicine, drug delivery, bio imaging, bio marking, tissue engineering, electromagnetic interference (EMI) and electromagnetic force (EMF) shielding, and as competent materials for aerospace structural applications.

Magnesium alloy has great potential for bone implantation. However, its corrosion rate is fast in physiological environment. In this paper, biological Mg–Zn–Ca alloy was processed by high pressure torsion (HPT) and subsequently annealed at 90–270 °C for 30 min. The microstructure and corrosion resistance in simulated body fluid were investigated. The results revealed that with the rise of the annealing temperature, the grain size of the HPT alloy gradually increased and the relative diffraction peak intensity of (0002) grain orientation decreased. The amount of second phases increased first and then decreased, while the surface stress decreased first and then increased. All of these changes affected the corrosion rate simultaneously. The corrosion resistance of the HPT alloy increased first and then decreased with the rise of annealing temperature. After annealing at 210 °C for 30 min, the corrosion resistance was the best. Therefore, it was feasible to control the corrosion rate via annealing treatment.

A CeO2/ZrO2-hydroxyapatite (HA) composite bio-ceramic coating was prepared on ZK60 magnesium (Mg) alloy by using micro-arc oxidation (MAO) and electrophoretic deposition (EPD). MAO coating was done as the basal layer was grown in alkaline electrolyte with the addition of nanoparticles (CeO2 and ZrO2) to improve the mechanical properties of coating. A HA coating as the covering layer was deposited on the surface of MAO coating for improving the biological properties of the coating. The phase compositions and morphology of coatings were monitored with X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. Adhesion and wear resistance of coatings were evaluated using a scratch test and a pin-on-disc sliding wear test. The corrosion resistance of coatings was evaluated in a simulated body fluid (SBF) using electrochemical tests at 36.5 ± 0.5 °C. The experimental results showed that the CeO2/ZrO2-HA composite coating on Mg alloy effectively improved its mechanical properties and corrosion resistance. Combining MAO and EPD is a promising modification technology for degradable Mg alloys as biomaterials.

The push–pull fatigue characteristics of the peak-aged Mg–0.2Zn–0.5Zr alloys with different addition levels of neodymium (Nd) have been investigated. The fatigue strength (σf) of the Mg–xNd–0.2Zn–0.5Zr (NZx0K) alloy increases proportionally with the increase of the Nd content (C Nd) as follows: σf (T6) ≈ (13.8–14.0) C Nd + 46 (for x between 0 and 3.0 wt%). The cyclic stress amplitude also increases but the plastic strain value decreases with the increase of the Nd content. The studied alloys exhibit the strain hardening followed by cyclic softening during fatigue test. During the low-cycle fatigue (LCF) test, the cracks originate from the cyclic deformation and cumulative damage. In high-cycle fatigue (HCF), the failure is due to the cyclic deformation and damage irreversibly caused by environment-assisted cyclic slip. The LCF lives of the alloys fitted well with the Coffin–Manson relation and Basquin laws, the three-parameter equation, and the energy-based concepts. The developed multi-scale fatigue (MSF) life models can be used to predict the LCF and HCF lives of the alloys. Among these models, the MSF life can well capture the influence of Nd addition on fatigue.

The effects of minor Cu (0–0.29 wt%) and Mg (0–0.1 wt%) additions on the microstructure, electrical conductivity, mechanical, and creep properties of 8xxx aluminum conductor alloys were studied. The microstructure evolution was investigated using an optical microscope and the electron backscattered diffraction technique. The creep property was characterized by the primary creep strain and the minimum creep rate during creep deformation. The results demonstrated that additions of minor Cu and Mg reasonably improved the ultimate tensile strength but slightly reduced electrical conductivity. The addition of Cu remarkably decreased the primary creep strain but had a negligible effect on the minimum creep rate, leading to a beneficial effect on the short-term creep resistance but no advantage to the creep resistance under the long-term creep process. The minor addition of Mg greatly reduces both the primary creep strain and minimum creep rate, resulting in a significant and effective improvement in the creep resistance.

Al–Zn–Mg–Cu–Zr alloys are very important aeronautical materials because of their low density, high strength, and high ductility. Corrosion failure is a significant factor causing aviation accidents, which should be investigated to develop an aeronautical material but has not been done yet. In this work, the effects of aging mechanisms on the exfoliation corrosion behavior of a spray deposited Al–Zn–Mg–Cu–Zr alloy were investigated. Natural aging (NA), single-stage aging (SA), and retrogression and re-aging (RRA) were treated on specimens before exfoliation corrosion testing. Corrosion attacks were evaluated using the optical microscope (OM) and scanning electron microscope (SEM). Corrosion mechanisms were deduced on the basis of polarization curve results and an equivalent circuit. The RRA sample exhibited the smallest corrosion attack among the three samples, while the NA sample showed the largest corrosion attack. Intergranular corrosion on grain boundaries was discussed to understand the exfoliation corrosion process in the RRA sample. The amount and size of precipitates in grain interior and grain boundary of RRA samples are larger than those in SA and NA samples, leading to the low corrosion susceptibility of the RRA sample.

Hot isotherm compression tests were performed in temperature range of 350–500 °C and at strain rates of 0.0005 to 0.5 s−1 for Al6061 alloy reinforced with alumina nanoparticles. Effect of deformation parameters and optimal conditions for hot working this nanocomposite were comprehended thoroughly via hot working data analyses, electron microscopy images, and X-ray diffractograms. The results indicated the severity of hot deformation process and an increase in the activation energy to 320 kJ/mol due to the addition of nanoparticles. Dynamic recovery (DRV) was considered as the individual determinative softening mechanism during hot deformation of this nanocomposite, and no sign of dynamic recrystallization (DRX) phenomenon observed in the same domain. The unstable region occurred at high strain rates and temperature range of 350–500 °C accompanied with happening drastic defects such as shear bands and cracks. Furthermore, the value of both critical strain and critical stress increased with increasing the strain rate and alumina addition. On the other hand, increasing the temperature decreased the value of critical strain and facilitated the initiation of softening mechanisms.

(Ti,Mo)Al/Al2O3 composites were successfully synthesized utilizing in situ reactive hot pressing method with Ti, Al, and MoO3 powders as starting materials. A possible synthesis mechanism was proposed to explain the formation of (Ti,Mo)Al/Al2O3 composites. The investigation results indicate a probable reaction process that molten Al reacted with MoO3 to form Al2O3 and Mo, and the TiAl matrix grains were refined increasingly by Al2O3 with the addition of MoO3 increased, accompanying with a small quantity of Mo containing phase AlMoTi2 formed in the fabricated composites. Meanwhile, the microstructure and mechanical properties of the (Ti,Mo)Al/Al2O3 composites were characterized. The as-synthesized composites exhibited lamellar structure of TiAl intermetallic compound and the in situ formed fine Al2O3 particles dispersed at the stratified TiAl matrix grain boundaries hindering the growth of the grain size of the matrix. And the Rockwell hardness, flexural strength, and fracture toughness of the as-prepared (Ti,Mo)Al/Al2O3 composite were 44.08 HRC, 684 MPa, 7.63 MPa·m1/2, which improved by 57.4%, 107.3%, and 38.7% compared to monolithic TiAl, respectively. The reinforcing mechanism of the material was also discussed.

Metallic phase-change materials (PCMs) attract much attention due to their high thermal conductivity in thermal energy storage. Our previous work reported a kind of Cu@Cr@Ni bilayer capsules, which could endure at least 1000 thermal cycles between 1323 and 1423 K without leakage, and might be a potential high-temperature metallic PCM. This study numerically investigates the thermal energy charging performance of Cu@Cr@Ni capsules for recovering high-temperature waste heat at both constant and periodically fluctuant heat transfer fluid temperatures. It was revealed that only a short and slight sloped melting platform existed in the curve of outlet temperature due to the ultrahigh thermal conductivity of copper; with higher inlet velocities, the outlet and mean temperatures of such PCM increased and meanwhile the energy transfer efficiency decreased; the outlet and mean temperatures of the PCM and the liquid fraction in it were rather insensitive to the period of the inlet temperature fluctuation; and the amplitude of inlet temperature fluctuation, ±50 K, was sharply reduced to 5 K due to the thermal damping of the PCM.

There is a need to discover new thermoelectric materials that can convert waste heat into electrical energy. In this paper, study has been done to observe the effect of shape and dimension of nanopores embedded in graphene nanoribbons (GNRs) as to tune their thermoelectric performance that can lead to enhancement of thermoelectric figure of merit (ZT). It is observed that incorporation of pores in GNRs greatly reduces the thermal conductivity. Although the Seebeck coefficient decreases with the introduction of the pore while the conductance depends upon the pore shape, the decreasing trend in thermal conductivity leads to enhancement of thermoelectric performance. The aim of this work is to study the effect of various circular and the triangular shaped dimensions so as to tune the pore to its optimal dimension that would enhance the overall thermoelectric efficiency. Ballistic transport regime and semiempirical method using Huckel basis set is used to obtain the electrical properties while the Tersoff potential is used for the phononic system.

Thermoelectric properties of oxygen-deficient filled strontium barium niobates (SBN, Sr x Ba6−x Nb10O30−δ) in the composition range from the barium end member to a Sr:Ba ratio of 80:20 were investigated. The electrical conductivity, Seebeck coefficients, and power factors for ceramic samples annealed at 1300–1310 °C for 30 h under forming gas (∼10−16 pO2 atm) were evaluated from ∼350 to 970 K. The conduction mechanism in the filled SBNs was found to be similar to that of the heavily-reduced unfilled SBNs reported in literature. However, relative to the unfilled counterparts heat-treated at 10−16 atm pO2, larger power factors were observed in the filled SBNs. The thermoelectric performance of these filled SBNs was composition-sensitive; lower Sr contents showed higher electrical conductivities, and power factors. Electron diffraction and Hall experiments suggest that both mobility and carrier concentration are enhanced with decreasing Sr. For ceramic samples, the highest power factors achievable were found for low Sr, heavily-reduced filled compositions.

Two series of lithium iron phosphate (LiFePO4) nanocomposites are prepared by a solvothermal method coupled with high temperature calcination using mononuclear and binuclear metal hexaaminophthalocyanines as modulatory additives, respectively. Physical and electrochemical performances of the composites as cathode materials of lithium-ion batteries are characterized by inductively coupled plasma (ICP), X-ray diffraction (XRD), infrared (IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and electrochemical techniques. The results indicate that the as-synthesized samples modified with binuclear metal phthalocyanines can improve electrochemical properties of LiFePO4 (LFP) for lithium-ion batteries. The composite using binuclear manganese hexaaminophthalocyanine as additive can achieve the highest initial specific discharge capacity of 152.3 mAh/g at 0.1 C, higher than that of ones modified with the corresponding mononuclear phthalocyanine 143.0 mAh/g. Furthermore, the most excellent product exhibits a pretty good capacity retention of 93.0% after 50 cycles at 0.1 C, cycling stability, and low charge transfer resistance of 58.7 Ω.

CoxPb1−x nanowire arrays within an anodic aluminum oxide (AAO) template were electrodeposited from an appropriate acetate bath by applying alternating current (ac). The effect of the Pb content on magnetic properties of nanowire arrays was investigated. By adding Pb2+ to an electrolyte containing Co2+, the coercivity field of nanowires decreased from 1508 Oe in Co100 to 921 Oe in Co92.5Pb7.5 while squareness increased from 0.74 for Co nanowires to about 0.82 for Co92.5Pb7.5 nanowire alloy sample. The effect of annealing on the magnetic properties of nanowires in the temperature range between 300 °C and 600 °C was also investigated. It was observed that the coercivity field of Co97.5Pb2.5 nanowire increases from 1290 Oe at room temperature to 1785 Oe at 600 °C. Furthermore, the effect of electrodeposition frequency on the magnetic properties of Co97.5Pb2.5 nanowires was studied. The coercivity was enhanced with increasing frequency; however, after annealing all samples exhibited enhanced coercivity regardless of the electrodeposition frequency.

SnSb nanoparticles are dispersed in carbon nanofibers by electrospinning technology and different SnSb precursors, including Sn0.92Sb0.08O2.04 nanoparticles, Sn(CH3COO)2/Sb(CH3COO)3, and SnCl4·5H2O/SbCl3, are used to tune the morphology of the resultant SnSb/C nanofibers. Porous SnSb/C nanofibers are formed during carbonization Sn0.92Sb0.08O2.04 nanoparticles and Sn(CH3COO)2/Sb(CH3COO)3 are used as precursors of SnSb, while solid nanofibers are observed with SnCl4·5H2O/SbCl3 as the precursor indicating the formation mechanism is closely related to the properties of SnSb precursors. Excellent cycling preference (99% capacity retention after 200 cycles) and high coulombic efficiency (above 99% after 10 cycles) are obtained for the SnSb/C nanofibers using Sn0.92Sb0.08O2.04 as precursor, due to its high surface area and stable SnSb/C structure. It is demonstrated that the uniquely designed composite nanofiber structure with excellent lithium storage performance can be realized simply by selecting precursors with appropriate dissolution and decomposition properties.

Using in situ transmission electron microscopy, we report the observation of the melting behavior of one-dimensional nanostructures of Sn with different length/width aspect ratios. The melting of small aspect-ratio nanowires (nanorods) results in the expansion of liquid Sn along both axial and radial directions with the tendency to form an isometric or spherical particle, thereby minimizing the total surface area. For nanowires with the length/width aspect ratio of ∼10.5, perturbation along the liquid stream causes an unstable necking phenomenon and the whole wire tends to shrink into a spherical particle. In contrast, Rayleigh instability sets in for the melting of the nanowires with the length/width aspect ratio as large as ∼21, which gives rise to necking and fragmentation of the wire into particles. The amorphous native surface oxide (SnO x ) layer serves as a confinement tube and plays an important role in the melting induced morphological evolution of Sn nanowires. A thin SnO x layer is flexible with the ability to shrink or expand upon the flow of molten Sn. The increased rigidity for a thick SnO x surface layer kinetically suppresses bulging and necking formation in molten Sn nanowires.

The on-site hydrogen supply is a key issue for the commercialization of the fuel cells, which is one of the important ways for realizing a hydrogen-economy society. Composite NaNH2–NaBH4 is regarded as a promising high-capacity hydrogen storage material. In this paper, the composite NaNH2–NaBH4 (2/1) was synthesized via a solid-state ball milling method. To improve the hydrogen generation kinetics, a multiplex metal boride Mg–Co–B was selected as the catalyst. It was found that Na3BN2 and metal Na were byproducts in the thermal decomposed sample by X-ray diffraction analysis. Thermogravimetry and differential thermal analysis indicated that the main decomposition stages of the catalyst promoted NaNH2–NaBH4 material were split into three stages. The activation energy of the Mg–Co–B promoted NaNH2–NaBH4 (2/1) material below 300 °C was 76.4 KJ/mol, which is only 47.9% of that of the pristine NaNH2–NaBH4 (2/1), and implying much better hydrogen generation kinetics.