Structure-evolution-designed amorphous oxides for dielectric energy storage.

Recently, rapidly increased demands of integration and miniaturization continuously challenge energy densities of dielectric capacitors. New materials with high recoverable energy storage densities become highly desirable. Here, by structure evolution between fluorite HfO2 and perovskite hafnate, we create an amorphous hafnium-based oxide that exhibits the energy density of ~155 J/cm3 with an efficiency of 87%, which is state-of-the-art in emergingly capacitive energy-storage materials. The amorphous structure is owing to oxygen instability in between the two energetically-favorable crystalline forms, in which not only the long-range periodicities of fluorite and perovskite are collapsed but also more than one symmetry, i.e., the monoclinic and orthorhombic, coexist in short range, giving rise to a strong structure disordering. As a result, the carrier avalanche is impeded and an ultrahigh breakdown strength up to 12 MV/cm is achieved, which, accompanying with a large permittivity, remarkably enhances the energy storage density. Our study provides a new and widely applicable platform for designing high-performance dielectric energy storage with the strategy exploring the boundary among different categories of materials.

High-Resolution Magnetoelectric Sensor and Low-Frequency Measurement Using Frequency Up-Conversion Technique.

The magnetoelectric (ME) sensor is a new type of magnetic sensor with ultrahigh sensitivity that suitable for the measurement of low-frequency weak magnetic fields. In this study, a metglas/PZT-5B ME sensor with mechanical resonance frequency fres of 60.041 kHz was prepared. It is interesting to note that its magnetic field resolution reached 0.20 nT at fres and 0.34 nT under a DC field, respectively. In order to measure ultralow-frequency AC magnetic fields, a frequency up-conversion technique was employed. Using this technique, a limit of detection (LOD) under an AC magnetic field lower than 1 nT at 8 Hz was obtained, and the minimum LOD of 0.51 nT was achieved at 20 Hz. The high-resolution ME sensor at the sub-nT level is promising in the field of low-frequency weak magnetic field measurement technology.

Perpendicular magnetization anisotropy induced dynamical coherence reduction in stripe domain film.

We investigated the magnetization dynamics of the 350 nm permalloy film with in plane domain (IPD), stripe domain (SD), and labyrinth domain (LD) patterns. Experimental and micromagnetic simulation results showed that the change in magnetic domain structure from IPD to LD was due to the increasing perpendicular magnetic anisotropy (PMA) of the film. The magnetization dynamics indicated that the resonant modes of the film strongly depended on the magnetic domain structure. IPD films presented a uniform precession mode. The film with well-regular SD exhibited clear acoustic and optical resonance modes, and the formation of LD suppressed both resonance modes. Finally, the dynamics of magnetization dependent on the domain structure in these films were discussed by using the phenomenological resonance models.

Reacquainting the Electrochemical Conversion Mechanism of FeS2 Sodium-Ion Batteries by Operando Magnetometry.

In spite of the excellent electrochemical performance in lithium-ion batteries (LIBs), transition-metal compounds usually show inferior capacity and cyclability in sodium-ion batteries (SIBs), implying different reaction schemes between these two types of systems. Herein, coupling operando magnetometry with electrochemical measurement, we peformed a comprehensive investigation on the intrinsic relationship between the ion-embedding mechanisms and the electrochemical properties of the typical FeS2/Na (Li) cells. Operando magnetometry together with ex-situ transmission electron microscopy (TEM) measurement reveal that only part of FeS2 is involved in the conversion reaction process, while the unreactive parts form "inactive cores" that lead to the low capacity. Through quantification with Langevin fitting, we further show that the size of the iron grains produced by the conversion reaction are much smaller in SIBs than that in LIBs, which may lead to more serious pulverization, thereby resulting in worse cycle performance. The underlying reason for the above two above phenomena in SIBs is the sluggish kinetics caused by the larger Na-ion radius. Our work paves a new way for the investigation of novel SIB materials with high capacity and long durability.

Construction of the POMOF@Polypyrrole Composite with Enhanced Ion Diffusion and Capacitive Contribution for High-Performance Lithium-Ion Batteries.

Polyoxometalate (POM) as an "electronic sponge" can store a great number of electrons; however, shortcomings of poor conductivity and solubility in electrolytes cause a significant decrease in specific capacity and poor rate capability. To address the aforementioned disadvantages, a dual strategy was proposed, including coating the conductive polypyrrole (PPy) and utilizing nitrogenous ligands (1,10-phenanthroline monohydrate = 1,10-phen) for metal-organic frameworks (MOFs) to fabricate a [Cu(1,10-phen)(H2O)2]2[Mo6O20]@PPy (Cu-POMOF@PPy) composite, effectively confining the POM in MOFs to avoid dissolution of POM in the electrolyte and improve electrochemical stability. Simultaneously, the PPy shell could improve the conductivity, contribute extra capacity, and alleviate volume variation of Cu-POMOF during cycling. Therefore, the final Cu-POMOF@PPy composite provides an excellent specific capacity of around 769 mA h g-1 at 0.1 A g-1 after 160 cycles and good rate performance, associated with great cycling stability (319 mA h g-1 at 2 A g-1 after 500 cycles). Moreover, the electrochemical reaction mechanism of Cu-POMOF@PPy was investigated by ex situ XPS measurements, indicating that storage of electrons results from the reduction/oxidation of Mo atoms (Mo6+ ↔ Mo4+) and Cu atoms (Cu2+ ↔ Cu0). As a consequence, this work not only proposes a novel method for preparing POM-based lithium-ion batteries but also expands the variety of anode materials.

Reversible control of magnetization in Fe3O4 nanoparticles by a supercapacitor.

The manipulation of magnetism by electrical means is one of the most intensely pursued research topics of recent times aiming at the development of efficient and low-energy consumption devices in spintronics, microelectronics and bioelectronics. Herein, we successfully tuned the saturated magnetization of Fe3O4 by a supercapacitor. Through increasing the surface area of magnetic particles and activation of carbon cloth, fully reversible and robust saturation magnetization variation with low power consumption and remarkable switching speed can be realized on Fe3O4/ionic liquid interfaces at room temperature. The associated magnetism modulation can be attributed to ionic transition between Fe2+ and Fe3+ resulting from both electrostatic and electrochemical doping. This work paves the way for the development of high-performance spintronic devices.

Nanosized MoSe2@Carbon Matrix: A Stable Host Material for the Highly Reversible Storage of Potassium and Aluminum Ions.

Owing to their low cost and abundant reserves relative to conventional lithium-ion batteries (LIBs), potassium-ion batteries (PIBs), and aluminum-ion batteries (AIBs) have shown appealing potential for electrochemical energy storage, but progress so far has been limited by the lack of suitable electrode materials. In this work, we demonstrated a facile strategy to achieve highly reversible potassium and aluminum ions storage in strongly coupled nanosized MoSe2@carbon matrix, induced through an ion complexation strategy. We present a broad range of electrochemical characterization of the synthesized product that exhibits high specific capacities, good rate capability, and excellent cycling stability toward PIBs and AIBs. Through a series of systematic ex situ X-ray photoelectron spectroscopy (XPS) characterizations and density functional theory (DFT) calculations, the Al3+ intercalation mechanism of MoSe2-based AIBs are elucidated. Moreover, both the assembled PIBs and AIBs worked well when exposed to low and high temperatures within the range of -10 to 50 °C, showing promise for energy storage devices in harsh environment. The present study provides new insights into the exploration of MoSe2 as high-performance electrode materials for PIBs and AIBs.

Ultrahigh Frequency and Anti-Interference Optical-Mode Resonance with Biquadratic Coupled FeCoB/Ru/FeCoB Trilayers.

Microwave soft magnetic films (SMFs) are the key materials to effectively miniaturize and multifunctionalize the microwave electromagnetic components and devices. However, currently, single-layer SMFs encounter a frequency bottleneck at around 10 GHz. The ferromagnet/nonmagnetic spacer/ferromagnet sandwiched films with strong interlayer exchange coupling are possible solutions to break through that frequency limitation because they exhibit ultrahigh optical-mode (OM) resonance frequency frO up to 50 GHz, while the tiny permeability and the limited thickness are their own obstacles to overcome. In this study, biquadratic coupled FeCoB25nm/Ru0.25nm/FeCoB25nm sandwiched films with uniaxial magnetic anisotropy were deposited by a composition gradient sputtering method. Pure OM resonance with self-bias frO up to 18.21 GHz and a relative permeability µrO as high as 169 at the cut-off frequency was achieved. Moreover, both the frO and µrO remain unchanged in the magnetic field range of 0-80 Oe, indicating a strong anti-interference capability to small interference field. These results demonstrate that the biquadratic coupled OM resonance can solve the current frequency bottleneck of microwave SMFs by providing ultrahigh resonance frequency while maintaining considerable permeability, thus leading to potential applications of OM resonance in Ku-band microwave magnetic components.

Three-Dimensional Hierarchical Flowerlike FeP Wrapped with N-Doped Carbon Possessing Improved Li+ Diffusion Kinetics and Cyclability for Lithium-Ion Batteries.

Transition-metal phosphides have a potential application in lithium-ion batteries (LIBs) because of their high theoretical capacities and low cost; nevertheless, they possess dramatic volumetric variation during cycling associated with poor conductivity, limiting their practical applications. Here, a three-dimensional (3D) hierarchical flowerlike FeP coated with nitrogen-doped carbon layer (FeP@N,C hybrid) was constructed through a solvothermal method, followed by a phosphating approach under low temperature. N-doped carbon not only suppresses the volume fluctuation of FeP, but also promotes electron transfer, accompanied by catalyzing the decomposition of Li3P to improve the reversibility of the FeP@N,C hybrid during cycling processes. In addition, a 3D flowerlike architecture assembled from porous nanosheets is also beneficial for shortening the migration path of ions as well as improving the contact area of electrode with electrolyte, which enhances the reaction kinetics and is proved by both experimental measurement of Li+ diffusion coefficient and resistivity, along with the calculation of density functional theory. Consequently, the 3D hierarchical flowerlike FeP@N,C hybrid performs excellent cyclic stability (569 mA h g-1 at a current density of 500 mA g-1 for the 300th cycle) and rate performance (331.94 mA h g-1 at a high current density of 5 A g-1) for LIBs. Based on above results, the fabrication strategy in this work could offer a thought to design other high-performance metal phosphide hybrids.

Synaptic memory devices from CoO/Nb:SrTiO3 junction.

Non-volatile memristors are promising for future hardware-based neurocomputation application because they are capable of emulating biological synaptic functions. Various material strategies have been studied to pursue better device performance, such as lower energy cost, better biological plausibility, etc. In this work, we show a novel design for non-volatile memristor based on CoO/Nb:SrTiO3 heterojunction. We found the memristor intrinsically exhibited resistivity switching behaviours, which can be ascribed to the migration of oxygen vacancies and charge trapping and detrapping at the heterojunction interface. The carrier trapping/detrapping level can be finely adjusted by regulating voltage amplitudes. Gradual conductance modulation can therefore be realized by using proper voltage pulse stimulations. And the spike-timing-dependent plasticity, an important Hebbian learning rule, has been implemented in the device. Our results indicate the possibility of achieving artificial synapses with CoO/Nb:SrTiO3 heterojunction. Compared with filamentary type of the synaptic device, our device has the potential to reduce energy consumption, realize large-scale neuromorphic system and work more reliably, since no structural distortion occurs.

Novel superconducting structures of BH2 under high pressure.

The crystal structures of boron hydrides in a pressure range of 50-400 GPa were studied using the genetic algorithm (GA) method combined with first-principles density functional theory calculations. BH4 and BH5 are predicted to be thermodynamically unstable. Two new BH2 structures with Cmcm and C2/c space group symmetries, respectively, were predicted, in which the B atoms tend to form two-dimensional sheets. The calculated band structures showed that in the pressure range of 50-150 GPa, the Cmcm-BH2 phase has very small gaps, while the C2/c-BH2 phase at 200-400 GPa is metallic. The superconductivity of the C2/c-BH2 structure was also investigated, and electron-phonon coupling calculations revealed that the estimated Tc values of C2/c-BH2 are about 28.18-37.31 K at 250 GPa.

Improved Electrochemical Performance Based on Nanostructured SnS2@CoS2-rGO Composite Anode for Sodium-Ion Batteries.

A promising anode material composed of SnS2@CoS2 flower-like spheres assembled from SnS2 nanosheets and CoS2 nanoparticles accompanied by reduced graphene oxide (rGO) was fabricated by a facile hydrothermal pathway. The presence of rGO and the combined merits of SnS2 and CoS2 endow the SnS2@CoS2-rGO composite with high conductivity pathways and channels for electrons and with excellent properties as an anode material for sodium-ion batteries (SIBs). A high capacity of 514.0 mAh g-1 at a current density of 200 mA g-1 after 100 cycles and a good rate capability can be delivered. The defined structure and good sodium-storage performance of the SnS2@CoS2-rGO composite demonstrate its promising application in high-performance SIBs.

Constructing Three-Dimensional Porous Carbon Framework Embedded with FeSe2 Nanoparticles as an Anode Material for Rechargeable Batteries.

Metal selenides have caused widespread concern due to their high theoretical capacities and appropriate working potential; however, they suffer from large volume variation during cycling and low electrical conductivity, which limit their practical applications. In this article, a three-dimensional (3D) porous carbon framework embedded with homogeneous FeSe2 nanoparticles (3D porous FeSe2/C composite) was synthesized by a facile calcined approach, following a selenized method without a template. As the uniformity of FeSe2 nanoparticles and 3D porous structure are beneficial to accommodate volume stress upon cycling and shorten electrons/ions transport path, associated with carbon as a buffer matrix for increasing conductivity, the 3D porous FeSe2/C composite displays excellent electrochemical properties with high reversible capacities of 798.4 and 455.0 mA h g-1 for lithium-ion batteries and sodium-ion batteries, respectively, when the current density is 100 mA g-1 after 100 cycles. In addition, the as-prepared composite exhibits good cycling stability as compared to bare FeSe2 nanoparticles. Therefore, the facile synthetic strategy in the current work provides a new perspective in constructing a high-performance anode.

Investigation on the structures and magnetic properties of carbon or nitrogen doped cobalt ferrite nanoparticles.

Carbon or nitrogen doped cobalt ferrite nanoparticles were synthesized in the air by a facile calcination process. X-ray diffraction, mapping, X-ray photoelectron spectroscopy, and mössbauer spectra results indicate that the nonmetal elements as the interstitial one are doped into cobalt ferrite nanoparticles. The morphologies of doped cobalt ferrite nanoparticles change from near-spherical to irregular cubelike shapes gradually with the increased carbon or nitrogen concentration, and their particles sizes also increase more than 200 nm. Furthermore, the saturation magnetization of carbon doped cobalt ferrite is improved. Although the saturation magnetization of N-doped cobalt ferrite is not enhanced obviously due to the involved hematite, they also do not drop drastically. The results reveal an approach to synthesize large scale ferrite nanoparticles, and improve the magnetic properties of ferrite nanoparticles, and also provide the potential candidates to synthesis co-doped functional magnetic materials.

Microstructure and Electrochemical Performance of Co3O4 Nanopillars Calcinated at Various Temperatures.

One-dimensional (1D) Co3O4 nanopillars were prepared by a facile hydrothermal-calcination method, which involved low thermal decomposition of Co(OH)y(CO3)0.5(2-y) · 11H2O at different temperatures. Microstructure, lithium-storage performance and the conductivity of the Co3O4 nanopillars calcined at different temperatures were systematically investigated. It was revealed that the calcined temperature has an effect on the particle size, crystallinity, and morphology of the Co3O4 nanopillars, which further influenced its electrochemical performance. It was found that when the calcined temperature and time were 450 °C and 2 h, respectively, the obtained Co3O4 nanopillars with the length of 60-100 nm and width of 30-40 nm, presented good lithium-storage performance with a high reversible capacity of 805.8 mAh g-1 after 30 cycles at a current density of 100 mA g-1. In addition, the Co3O4 nanopillars electrode possessed the smallest semicircle diameter, which implied that Co3O4 nanopillars presented the lowest contact and charge-transfer impedances, originating from its good crystallinity and 1D nanocolumnar structure.

Stress-Enhanced Interlayer Exchange Coupling and Optical-Mode FMR Frequency in Self-Bias FeCoB/Ru/FeCoB Trilayers.

Nowadays, the most popular method to increase ferromagnetic resonance (FMR) frequency ( fr) in self-bias soft magnetic films is to improve the anisotropy field HK. However, to push fr to higher frequencies only via raising HK becomes increasingly challenging because fr is already higher than 10 GHz by now. In this study, we fabricated a series of magnetically anisotropic FeCoB/Ru/FeCoB sandwich films possessing antiferromagnetic-like coupling and gradually increased uniaxial stress in the FeCoB sublayers from 52 to 110 MPa. It is quite remarkable that the acoustic mode of FMR gradually disappears, whereas the optical mode is enhanced in these structures. We observed simultaneous enhancement of HK and interlayer coupling field ( JIEC) with the uniaxial stress, which leads to a very pronounced optical-mode frequency increase from 8.67 to 11.62 GHz with a very sensitive stress response of 51 Hz/Pa. In contrast, the fr in a FeCoB single layer (acoustic mode) only varies from 3.47 to 5.05 GHz under similar stress. We believe that the strain-induced electron density variation of the Ru spacer's Fermi surface in the out-of-plane direction is responsible for the enhancement of JIEC. This study demonstrates that the antiferromagnetic coupling is a new route to achieve higher fr and provides the possibility of engineering and manipulating optical-mode resonance simply by controlling the interlayer coupling strength via stress.

A Nanocrystalline Fe2O3 Film Anode Prepared by Pulsed Laser Deposition for Lithium-Ion Batteries.

Nanocrystalline Fe2O3 thin films are deposited directly on the conduct substrates by pulsed laser deposition as anode materials for lithium-ion batteries. We demonstrate the well-designed Fe2O3 film electrodes are capable of excellent high-rate performance (510 mAh g- 1 at high current density of 15,000 mA g- 1) and superior cycling stability (905 mAh g- 1 at 100 mA g- 1 after 200 cycles), which are among the best reported state-of-the-art Fe2O3 anode materials. The outstanding lithium storage performances of the as-synthesized nanocrystalline Fe2O3 film are attributed to the advanced nanostructured architecture, which not only provides fast kinetics by the shortened lithium-ion diffusion lengths but also prolongs cycling life by preventing nanosized Fe2O3 particle agglomeration. The electrochemical performance results suggest that this novel Fe2O3 thin film is a promising anode material for all-solid-state thin film batteries.

Engineering optical mode ferromagnetic resonance in FeCoB films with ultrathin Ru insertion.

Ferromagnetic resonance (FMR) in soft magnetic films (SMFs) to a large extent determines the maximum working frequency of magnetic devices. The FMR frequency (fr) in an optical mode is usually much higher than that in the corresponding acoustic mode for exchange coupled ferromagnet/nonmagnet/ferromagnet (FM/NM/FM) trilayers. In this study, we prepared a 50 nm FeCoB film with uniaxial magnetic anisotropy (UMA), showing a high acoustic mode fr of 4.17 GHz. When an ultrathin Ru spacer was inserted in the very middle of the UMA-FeCoB film, the zero-field FMR was abruptly switched from an acoustic mode to an optical one with fr dramatically enhanced from 4.17 GHz to 11.32 GHz. Furthermore, the FMR mode can be readily tuned to optical mode only, acoustic mode only, or double mode by simply varying the applied filed, which provides a flexible way to design multi-band microwave devices.

Driving ferromagnetic resonance frequency of FeCoB/PZN-PT multiferroic heterostructures to Ku-band via two-step climbing: composition gradient sputtering and magnetoelectric coupling.

RF/microwave soft magnetic films (SMFs) are key materials for miniaturization and multifunctionalization of monolithic microwave integrated circuits (MMICs) and their components, which demand that the SMFs should have higher self-bias ferromagnetic resonance frequency fFMR, and can be fabricated in an IC compatible process. However, self-biased metallic SMFs working at X-band or higher frequency were rarely reported, even though there are urgent demands. In this paper, we report an IC compatible process with two-step superposition to prepare SMFs, where the FeCoB SMFs were deposited on (011) lead zinc niobate-lead titanate substrates using a composition gradient sputtering method. As a result, a giant magnetic anisotropy field of 1498 Oe, 1-2 orders of magnitude larger than that by conventional magnetic annealing method, and an ultrahigh fFMR of up to 12.96 GHz reaching Ku-band, were obtained at zero magnetic bias field in the as-deposited films. These ultrahigh microwave performances can be attributed to the superposition of two effects: uniaxial stress induced by composition gradient and magnetoelectric coupling. This two-step superposition method paves a way for SMFs to surpass X-band by two-step or multi-step, where a variety of magnetic anisotropy field enhancing methods can be cumulated together to get higher ferromagnetic resonance frequency.

Integrated biological and chemical control of rice sheath blight by Bacillus subtilis NJ-18 and jinggangmycin.

BACKGROUND: Sheath blight caused by Rhizoctonia solani Kühn is a major disease of rice that greatly reduces yield and grain quality and jinggangmycin is the most widely used fungicide to control this disease in China. Bacillus subtilis NJ-18 has broad antimicrobial activity to many phytopathogenic bacteria and fungi; it is especially effective against Rhizoctonia solani. Laboratory, greenhouse and field tests were conducted to determine the effect of combining the biological control agent Bacillus subtilis NJ-18 with the fungicide jinggangmycin for control of rice sheath blight. RESULTS: Growth of NJ-18 in vitro was not affected by jinggangmycin. In a greenhouse experiment, disease control was greater with a mixture of NJ-18 and jinggangmycin than with either alone; a mixture of NJ-18 at 10(8) cfu mL(-1) and jinggangmycin at 50 or 100 mg L(-1) reduced lesion length by 35% and 20%, respectively, and the combinations showed a synergistic action. In three field trials, disease control was significantly greater with a mixture of NJ-18 at 10(8) cfu mL(-1) and jinggangmycin at 75 or 150 g a.i. ha(-1) than with either component alone. CONCLUSION: The results of the study indicate that, when Bacillus subtilis NJ-18 strain was combined with jinggangmycin, there was an increased suppression of rice sheath blight, and thus could provide an alternative disease control option.