Structural regulation enabled stable hollow molybdenum diselenide nanosheet anode for ultrahigh energy density sodium ion pouch cell.

For the continued use of sodium-ion batteries (SIBs), which require matching anode materials, it is crucial to create high energy density energy storage devices. Here, hollow nanoboxes shaped carbon supported sulfur-doped MoSe2 nanosheets (S-MoSe2@NC) are fabricated by in situ growth and heterodoping strategy. This ensures that the MoSe2 nanosheets are tightly anchored to the nanoboxes carbon, and the structure can effectively buffer the volume stress caused by sodium ion (de)intercalation, as well as providing abundant ion/electron migration transportations. As anode for SIBs, the S-MoSe2@NC shows a higher rate capability and excellent cycling stability (431.1 mAh/g after 1100 cycles at 10 A/g). This excellent cycle life and high rate ability are due to the structural stability and outstanding electronic conductance with reduced band gap of the S-MoSe2@NC, as evidenced by the diffusion analysis and theoretical calculation. In order to promote the application of SIBs, the S-MoSe2@NC and NaNi1/3Fe1/3Mn1/3O2 were assembled into a pouch cell, and the test found that besides the excellent cycle rate performance, the ultrahigh energy density of 256 Wh kg-1 and flexible characteristics can be achieved. This study has proven that building a structure with a rock-steady foundation and quick ion migration may efficiently control sodium storage and pave the way for novel applications of high-performance transition metal dichalcogenides in sodium storage.

MIMO 5G Smartphone Antenna with Tri-Band and Decoupled Elements.

In this article, a miniaturized antenna is proposed for 4G/5G multiple input, multiple output (MIMO) applications for smartphones. The proposed antenna is composed of an inverted L-shaped antenna with decoupled elements to cover 4G (2000-2600 MHz), and a planar inverted-F antenna (PIFA) with a J-slot to cover 5G (3400-3600 MHz and 4800-5000 MHz). Furthermore, to achieve the purposes of miniaturization and decoupling, the structure adopts a feeding stub, shorting stub, and outstanding floor, additionally adding the slot to the PIFA, to generate additional frequency bands. Due to the advantages such as multiband operation, MIMO configuration for 5G communications, high isolation, and a compact structure, the proposed antenna design is attractive for 4G/5G smartphones. The antenna array is printed on an FR4 dielectric board, measuring 140 × 70 × 0.8 mm3, with the 4G antenna located on a top 15 mm-long headroom.

UWB Frequency-Selective Surface Absorber Based on Graphene Featuring Wide-Angle Stability.

In this paper, an ultra-wideband and polarization-insensitive frequency-selective surface absorber is presented with oblique incident stable behavior. Different from conventional absorbers, the absorption behavior is much less deteriorated with the increase in the incidence angle. Two hybrid resonators, which are realized by symmetrical graphene patterns, are employed to obtain the desired broadband and polarization-insensitive absorption performance. The optimal impedance-matching behavior is designed at the oblique incidence of electromagnetic waves, and an equivalent circuit model is used to analyze and facilitate the mechanism of the proposed absorber. The results indicate that the absorber can maintain a stable absorption performance with a fractional bandwidth (FWB) of 136.4% up to 40°. With these performances, the proposed UWB absorber could be more competitive in aerospace applications.

Unidirectional invisibility induced by parity-time symmetric circuit.

Parity-time (PT) symmetric structures present the unidirectional invisibility at the spontaneous PT-symmetry breaking point. In this paper, we propose a PT-symmetric circuit consisting of a resistor and a microwave tunnel diode (TD) which represent the attenuation and amplification, respectively. Based on the scattering matrix method, the circuit can exhibit an ideal unidirectional performance at the spontaneous PT-symmetry breaking point by tuning the transmission lines between the lumped elements. Additionally, the resistance of the reactance component can alter the bandwidth of the unidirectional invisibility flexibly. Furthermore, the electromagnetic simulation for the proposed circuit validates the unidirectional invisibility and the synchronization with the input energy well. Our work not only provides an unidirectional invisible circuit based on PT-symmetry, but also proposes a potential solution for the extremely selective filter or cloaking applications.

Analysis and modeling of Fano resonances using equivalent circuit elements.

Fano resonance presents an asymmetric line shape formed by an interference of a continuum coupled with a discrete autoionized state. In this paper, we show several simple circuits for Fano resonances from the stable-input impedance mechanism, where the elements consisting of inductors and capacitors are formulated for various resonant modes, and the resistor represents the damping of the oscillators. By tuning the pole-zero of the input impedance, a simple circuit with only three passive components e.g. two inductors and one capacitor, can exhibit asymmetric resonance with arbitrary Q-factors flexiblely. Meanwhile, four passive components can exhibit various resonances including the Lorentz-like and reversely electromagnetically induced transparency (EIT) formations. Our work not only provides an intuitive understanding of Fano resonances, but also pave the way to realize Fano resonaces using simple circuit elements.

Unimolecular beta-hydroxyperoxy radical decomposition with OH recycling in the photochemical oxidation of isoprene.

A novel process in the photochemical oxidation of isoprene that recycles hydroxyl (OH) radicals has been identified using first-principles computational chemistry. Isoprene is the dominant biogenic volatile organic compound (VOC), and its oxidation controls chemistry in the forest boundary layer and is also thought to contribute to cloud formation in marine environments. The mechanism described here involves rapid unimolecular decomposition of the two major peroxy radicals (beta-hydroxyperoxy radicals) produced by OH-initiated isoprene oxidation. Peroxy radicals are well-known as key intermediates in VOC oxidation, but up to now were only thought to be destroyed in bimolecular reactions. The process described here leads to OH recycling with up to around 60% efficiency in environments with low levels of peroxy radicals and NO(x). In forested environments reaction of the beta-hydroxyperoxy radicals with HO2 is expected to dominate, with a small contribution from the mechanism described here. Peroxy radical decomposition will be more important in the unpolluted marine boundary layer, where lower levels of NO and HO2 are encountered.