New Reverse Conversion for Four-Moduli Set and Five-Moduli Set

Most reverse conversions in Residue Number Systems (RNS) are based on the Chinese Remainder Theorem (CRT) and the Mixed Radix Conversion (MRC). The complexity of the circuitry of the CRT is high due to the large modulo-M operation. The MRC has a simple circuitry but it’s a sequential process in nature. The purpose of this research is to obtain an efficient reverse conversion method to reduce the computational overhead found in the conventional reverse conversion algorithms. In this paper, new algorithms for reverse conversion in RNS for four-moduli set and five-moduli set have been proposed and their correctness evaluated. Numerical evaluations to ascertain the correctness and simplicity of the algorithm have been presented. These algorithms have fewer multiplicative index operations than those in the conventional CRT and MRC. The large modulo-M operation has been eliminated which reduces the computational overhead.

Dynamic phase assembled terahertz metalens for reversible conversion between linear polarization and arbitrary circular polarization

If a metalens integrates the circular polarization(CP)conversion function,the focusing lens together with circular-polariz-ing lens(CPL)in traditional cameras may be replaced by a metalens.However,in terahertz(THz)band,the reported metalenses still do not obtain the perfect and strict single-handed CP,because they were constructed via Pancharatnam-Berry phase so that CP conversion contained both left-handed CP(LCP)and right-handed CP(RCP)components.In this paper,a silicon based THz metalens is constructed using dynamic phase to obtain single-handed CP conversion.Also,we can rotate the whole metalens at a certain angle to control the conversion of multi-polarization states,which can simply manipulate the focusing for incident linear polarization(LP)THz wave in three polarization conversion states,in-cluding LP without conversion,LCP and RCP.Moreover,the polarization conversion behavior is reversible,that is,the THz metalens can convert not only the LP into arbitrary single-handed CP,but also the LCP and RCP into two perpen-dicular LP,respectively.The metalens is expected to be used in advanced THz camera,as a great candidate for tradi-tional CPL and focusing lens group,and also shows potential application in polarization imaging with discriminating LCP and RCP.

Understanding the Reversible Reactions of Li-N_(2) Battery Catalyzed With SnO_(2)

Metal–N_(2) battery can be applied in both energy storage and electrochemical nitrogen reduction reaction(NRR);however,there has been only extraordinarily little study on metal–N_(2) battery since its electrochemical reversibility still needs further proofs.And its electrochemical performances also need to be enhanced.Herein,we investigated the discharge–charge reactions between Li anode and N_(2) cathode via designing an efficient catalyst of nanosized SnO_(2) particles dispersed on N-doped carbon nanosheets(SnO 2@NC)for the Li-N_(2) battery,with good cyclic stability and a high specific capacity of 0.25 mA h(~500 mA h g^(−1))at a large current density of 1000 mA g^(−1).The electrochemical reversibility of both NRR in the discharge process and nitrogen extraction reaction in the charge process for Li-N 2 battery is discussed.Time-of-flight secondary ion mass spectrometry results imply that the SnO_(2)@NC can effectively promote the adsorption of N_(2) and the activation of NRR in the discharge process.Furthermore,ex situ X-ray photoelectron spectroscopy and Fourier transform infrared tests are performed to study the electrochemical reversibility of Li-N_(2) battery.It can be proved that the formation and decomposition of discharging product Li_(3)N are electrochemical reversible during cycling in our deigned Li-N_(2) battery system with SnO_(2)@NC catalyst.

High Initial Reversible Capacity and Long Life of Ternary SnO_(2)-Co-carbon Nanocomposite Anodes for Lithium-Ion Batteries

The two major limitations in the application of SnO_2 for lithium?ion battery(LIB) anodes are the large volume variations of SnO_2 during repeated lithiation/delithiation processes and a large irreversible capacity loss during the first cycle, which can lead to a rapid capacity fade and unsatisfactory initial Coulombic e ciency(ICE). To overcome these limitations, we developed composites of ultrafine SnO_2 nanoparticles and in situ formed Co(CoSn) nanocrystals embedded in an N?doped carbon matrix using a Co?based metal–organic framework(ZIF?67). The formed Co additives and structural advantages of the carbon?confined SnO_2/Co nanocomposite e ectively inhibited Sn coarsening in the lithiated SnO_2 and mitigated its structural degradation while facilitating fast electronic transport and facile ionic di usion. As a result, the electrodes demonstrated high ICE (82.2%), outstanding rate capability(～ 800 mAh g^(-1) at a high current density of 5 A g^(-1)), and long?term cycling stability(～ 760 mAh g^(-1) after 400 cycles at a current density of 0.5 A g^(-1)). This study will be helpful in developing high?performance Si(Sn)?based oxide, Sn/Sb?based sulfide, or selenide electrodes for LIBs. In addition, some metal organic frameworks similar to ZIF?67 can also be used as composite templates.

Effect of surface morphology on wettability conversion

A hierarchical structural surface of TiO2 film with reversibly light-switchable wettability between superhydrophobicity and superhydrophilicity on metal substrate was fabricated through simply dip-coating method from TiO2 precursor solution containing TiO2 nanoparticles with the average diameter 25 nm (P25),followed by heat-treatment and modification with fluoroalkylsilane (FAS) molecules.The morphology,phase and crystallographic structure,and chemical composite of the as-prepared TiO2 film were characterized by scanning electron microscopy (SEM),X-ray diffraction (XRD),and X-ray photoelectron spectroscopy (XPS).The wettability of TiO2 film was characterized by a drop shape analyzer.The water contact angle of superhydrophobic TiO2 film was up to 165.6°.Under UV irradiation,the water contact angle decreased and the superhydrophobic TiO2 film became superhydrophilic because of hydroxyl groups absorption on the TiO2 surface.Meanwhile,the surface morphology of TiO2 film,which resulted from the TiO2 nanoparticles added in TiO2 precursor solution,had a significant effect on the wettability conversion of TiO2 film and enhanced the switch from hydrophobicity to hydrophilicity.The wettability could be reversibly switched between superhydrophobicity and superhydrophilicity via alternation of UV exposure and dark storage.

CO_(2) and photo-controlled reversible conversion of supramolecular assemblies based on water soluble pillar[5]arene and coumarin-containing guest

In this communication,a new supramolecualr amphiphile was successfully constructed based on water soluble pillar[5]arene and a unique guest which contain a CO_(2) responsive tertiary amine unit and a UV responsive coumarin group.When guest molecule 1 dispersed in water,it self-assembled into sheet-like structures.Upon bubbling CO_(2),1 transformed into 1 H due to the tertiary amine unit was protonated,accompany the nano-sheets transformed into vesicles.Further irradiation of 1 H with 365 nm light for 3 h,the coumarin group reacted with each other to form bola-type amphiphie 2 H.In this case,vesicles collapsed and re-assembled into nano-tubes.However,when addition of WPS into the solution of 1 H,the vesicles transformed into micelles,this is due to the formation of supramolecular amphiphile WP5&1 H.Upon irradiation of WP5&1 H with 365 nm light for 3 h,nano-ribbons observed instead of micelles in the solution.Notably,nanotubes from 2 H could also transform into nano-ribbons after adding WPS.The selfassembly process and the resultant assemblies were characterized by TEM,SEM,DLS,SAXS and NMR technologies.Due to both CO_(2) and light are "green" for living organisms,we anticipated our system can offer the possibilities in "on demand" drug absorption and release.

Catalytic effect of carbon-based electrode materials in energy storage devices

The catalytic effect of electrode materials is one of the most crucial factors for achieving efficient electrochemical energy conversion and storage.Carbon-based metal composites were widely synthesized and employed as electrode materials because of their inherited outstanding properties.Usually,electrode materials can provide a higher capacity than the anticipated values,even beyond the theoretical limit.The origin of the extra capacity has not yet been explained accurately,and its formation mechanism is still ambiguous.Herein,we first summarized the current research progress and drawbacks in energy storage devices(ESDs),and elaborated the role of catalytic effect in enhancing the performance of ESDs as follows:promoting the evolution of the solid electrolyte interphase(SEI),accelerating the reversible conversion of discharge/charge products,and improving the conversion speed of the intermediate and the utilization rate of the active materials,thereby avoiding the shuttling effect.Additionally,a particular focus was placed on the interaction between the catalytic effect and energy storage performance in order to highlight the efficacy and role of the catalytic effect.We hope that this review could provide innovative ideas for designing the electrode materials with an efficient catalytic effect for ESDs to promote the development of this research field.

Recent development of pillar[n]arene-based amphiphiles

Pillar[n]arene-based amphiphiles,mainly including amphiphilic pillar[n]arenes and supra-amphiphilic pillar[n]arenes,have obtained considerable interests in recent years due to their fascinating chemical structures,various self-assembly behaviors,and widely applications.Thanks to the pillar-like frameworks and the rich host-guest recognitions of the cavities,these amphiphiles can be easily controlled to form dimensional and morphologic assemblies for multiple applications.Compared with traditional linear covalent amphiphiles,the introduction of host-guest recognitions facilitated the preparation and controllability of these supramolecular amphiphilic systems.Moreover,the host-guest recognitions endow the assemblies from pillar[n]arene-based amphiphiles with stimuli-responsive functions.In this mini-review,we summarized the chemical structures,self-assembly features,and the applications of pillar[n]arene-based amphiphiles.However,several research topics of pillar[n]arenebased amphiphiles can be further developed in the future,such as larger cavity amphiphilic pillar[n]arenes,co-assembly with 2 D materials and utilization of the host-guest interactions.