Evolution of Superconducting-Transition Temperature with Superfluid Density and Conductivity in Pressurized Cuprate Superconductors

What factors fundamentally determine the value of superconducting transition temperature Tc in high temperature superconductors has been the subject of intense debate.Following the establishment of an empirical law known as Homes'law,there is a growing consensus in the community that the Tc value of the cuprate superconductors is closely linked to the superfluid density(ρ_(s))of its ground state and the conductivity(σ)of its normal state.However,all the data supporting this empirical law(ρ_(s)=AσT_(c))have been obtained from the ambientpressure superconductors.In this study,we present the first high-pressure results about the connection of the quantities of ρ_(s) and σ with T_(c),through the studies on the Bi_(1.74)Pb_(0.38)Sr_(1.88)CuO_(6+δ)and Bi_(2)Sr_(2)CaCu_(2)O_(8+δ),in which the value of their high-pressure resistivity(ρ=1/σ)is achieved by adopting our newly established method,while the quantity ofρs is extracted using Homes'law.We highlight that the Tc values are strongly linked to the joint response factors of magnetic field and electric field,i.e.,ρ_(s) and σ,respectively,implying that the physics determining T_(c) is governed by the intrinsic electromagnetic fields of the system.

Hierarchical structures on platinum-iridium substrates enhancing conducting polymer adhesion

Conducting polymers(CPs),including poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)(PEDOT:PSS),are promising coating materials for neural electrodes.However,the weak adhesion of CP coatings to substrates such as platinum-iridium is a significant challenge that limits their practical application.To address this issue,we used femtosecond laser-prepared hierarchical structures on platinum-iridium(Pt-Ir)substrates to enhance the adhesion of PEDOT:PSS coatings.Next,we used cyclic voltammetry(CV)stress and accelerated aging tests to evaluate the stability of both drop cast and electrodeposited PEDOT:PSS coatings on Pt-Ir substrates,both with and without hierarchical structures.Our results showed that after 2000 CV cycles or five weeks of aging at 60℃,the morphology and electrochemical properties of the coatings on the Pt-Ir substrates with hierarchical structures remained relatively stable.In contrast,we found that smooth Pt-Ir substrate surfaces caused delamination of the PEDOT:PSS coating and exhibited both decreased charge storage capacity and increased impedance.Overall,enhancing the stability of PEDOT:PSS coatings used on common platinum-iridium neural electrodes offers great potential for improving their electrochemical performance and developing new functionalities.

An ultrathin and robust single-ion conducting interfacial layer for dendrite-free lithium metal batteries

The practical application of rechargeable lithium metal batteries(LMBs) encounters significant challenges due to the notorious dendrite growth triggered by uneven Li deposition behaviors. In this work,a mechanically robust and single-ion-conducting interfacial layer, fulfilled by the strategic integration of flexible cellulose acetate(CA) matrix with rigid graphene oxide(GO) and Li F fillers(termed the CGL layer), is rationally devised to serve as a stabilizer for dendrite-free lithium(Li) metal batteries. The GCL film exhibits favorable mechanical properties with high modulus and flexibility that help to relieve interface fluctuations. More crucially, the electron-donating carbonyl groups(C=O) enriched in GCL foster a strengthened correlation with Li^(+), which availably aids the Li^(+)desolvation process and expedites facile Li^(+)mobility, yielding exceptional Li^(+) transference number of 0.87. Such single-ion conductive properties regulate rapid and uniform interfacial transport kinetics, mitigating the growth of Li dendrites and the decomposition of electrolytes. Consequently, stable Li anode with prolonged cycle stabilities and flat deposition morphologies are realized. The Li||LiFePO_(4) full cells with CGL protective layer render an outstanding cycling capability of 500 cycles at 3 C, and an ultrahigh capacity retention of 99.99% for over 220 cycles even under harsh conditions. This work affords valuable insights into the interfacial regulation for achieving high-performance LMBs.

Disorder effects in NbTiN superconducting resonators

Disordered superconducting materials like NbTiN possess a high kinetic inductance fraction and an adjustable critical temperature, making them a good choice for low-temperature detectors. Their energy gap(D), critical temperature(T_(c)),and quasiparticle density of states(QDOS) distribution, however, deviate from the classical BCS theory due to the disorder effects. The Usadel equation, which takes account of elastic scattering, non-elastic scattering, and electro–phonon coupling,can be applied to explain and describe these deviations. This paper presents numerical simulations of the disorder effects based on the Usadel equation to investigate their effects on the △, Tc, QDOS distribution, and complex conductivity of the NbTiN film. Furthermore, NbTiN superconducting resonators with coplanar waveguide(CPW) structures are fabricated and characterized at different temperatures to validate our numerical simulations. The pair-breaking parameter α and the critical temperature in the pure state T_(c)^(P) of our NbTiN film are determined from the experimental results and numerical simulations. This study has significant implications for the development of low-temperature detectors made of disordered superconducting materials.

Conducting Polymer-Based e-Refinery for Sustainable Hydrogen Peroxide Production

Electrocatalysis enables the industrial transition to sustainable production of chemicals using abundant precursors and electricity from renewable sources.De-centralized production of hydrogen peroxide(H_(2)O_(2))from water and oxygen of air is highly desirable for daily life and industry.We report an effective electrochemical refinery(e-refinery)for H_(2)O_(2)by means of electrocatalysis-controlled comproportionation reaction(2_(H)O+o→2HO),feeding pure water and oxygen only.Mesoporous nickel(Ⅱ)oxide(NiO)was used as electrocatalyst for oxygen evolution reaction(OER),producing oxygen at the anode.Conducting polymer poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate)(PEDOT:PSS)drove the oxygen reduction reaction(ORR),forming H_(2)O_(2)on the cathode.The reactions were evaluated in both half-cell and device configurations.The performance of the H_(2)O_(2)e-refinery,assembled on anion-exchange solid electrolyte and fed with pure water,was limited by the unbalanced ionic transport.Optimization of the operation conditions allowed a conversion efficiency of 80%.

A Room-Temperature Chloride-Conducting Metal-Organic Crystal[Al(DMSO)_(6)]Cl_(3) for Potential Solid-State Chloride-Shuttle Batteries

The growing demand for substitutes of lithium chemistries in battery leads to a surge in budding novel anion-based electrochemical energy storage,where the chloride ion batteries(CIBs)take over the role.The application of CIBs is limited by the dissolution and side reaction of chloride-based electrode materials in a liquid electrolyte.On the flipside,its solid-state electrolytes are scarcely reported due to the challenge in realizing fast Cl^(-)conductivity.The present study reports[Al(DMSO)_(6)]Cl_(3),a solid-state metal-organic material,allows chloride ion transfer.The strong Al-Cl bonds in AlCl_(3)are broken down after coordinating of Al^(3+)by ligand DMSO,and Cl^(-)in the resulting compound is weakly bound to complexions[Al(DMSO)_(6)]^(3+),which may facilitate Cl^(-)migration.By partial replacement of Cl^(-)with PF_(6)^(-),the room-temperature ionic conductivity of as-prepared electrolyte is increased by one order of magnitude from 2.172×10^(-5)S cm^(-1)to 2.012×10^(-4)S cm^(-1).When they are assembled with Ag(anode)/Ag-AgCl(cathode)electrode system,reversible electrochemical redox reactions occur on both sides,demonstrating its potential for solid-state chloride ion batteries.The strategy by weakening the bonding interaction using organic ligands between Cl^(-)and central metallic ions may provide new ideas for developing solid chloride-ion conductors.

Aligned Ion Conduction Pathway of Polyrotaxane‑Based Electrolyte with Dispersed Hydrophobic Chains for Solid‑State Lithium–Oxygen Batteries

A critical challenge hindering the practical application of lithium–oxygen batteries(LOBs)is the inevitable problems associated with liquid electrolytes,such as evaporation and safety problems.Our study addresses these problems by proposing a modified polyrotaxane(mPR)-based solid polymer electrolyte(SPE)design that simultaneously mitigates solvent-related problems and improves conductivity.mPR-SPE exhibits high ion conductivity(2.8×10^(−3)S cm^(−1)at 25℃)through aligned ion conduction pathways and provides electrode protection ability through hydrophobic chain dispersion.Integrating this mPR-SPE into solid-state LOBs resulted in stable potentials over 300 cycles.In situ Raman spectroscopy reveals the presence of an LiO_(2)intermediate alongside Li_(2)O_(2)during oxygen reactions.Ex situ X-ray diffraction confirm the ability of the SPE to hinder the permeation of oxygen and moisture,as demonstrated by the air permeability tests.The present study suggests that maintaining a low residual solvent while achieving high ionic conductivity is crucial for restricting the sub-reactions of solid-state LOBs.

Preparation of YBa_2Cu_3O_(7-δ) superconducting thick film on Ni-W tapes via electrophoretic deposition

The preparation of La0.4Sr0.6TiO3 （LSTO） buffer layer and YBa2Cu3O7-δ（YBCO） superconducting thick film by a low cost technology was studied. The crystal orientation of LSTO and YBCO films was detected by X-ray diffraction, the conductivity of LSTO film and superconductivity of YBCO coating were investigated by standard four-probe method. Excellent in-plane alignment, smooth and dense LSTO buffer layer was successfully prepared on textured Ni-W taps by metal organic deposition （MOD）. YBCO thick film was fabricated by electrophoretic deposition （EPD）. The effects of applied voltage and deposition time on the YBCO coatings properties were studied. The results show that the critical current density of the YBCO coating deposited under 138 V for 35 min was about 600 A/cm2 （0 T, 77 K）.

Conducting Tissue of Leaves in Nageia and Podocarpus

The conducting tissue structure of transverse and longitudinal sections was observed on leaves of Podocarpus and Nageia.Results showed:in Podocarpus leaves,there is only one midrib,the xylem tracheid of midrib vascular bundle is multi-form,transfusion tissue belongs to Cycas-type and transfusion tracheids are isodiametric,the accessory transfusion tracheids between palisade tissue and sponge tissue are developed;in Nageia leaves,there are plenty of parallel leaves,the xylem tracheids of each vein are relatively simple,transfusion tissue belongs to Taxus-type and transfusion tracheids are longer in longitudinal section than that in transverse section,the accessory transfusion tissue between palisade tissue and sponge tissue is absent.Considering other differences that in leaves of Podocarpus there are three resin ducts under vascular bundle of midrib,mesophyll cells are differentiated into palisade tissue and sponge tissue;in leaves of Nageia,there is only one resin duct under vascular bundle in each vein and no obvious differentiation in mesophyll cells,palisade tissue can be found on both sides,and sclereids can also be found in mesophyll tissue.The anatomical differences of leaf veins and mesophylls between Nageia and Podocarpus mentioned above support the viewpoint that Nageia and Podocarpus are two independent genera.

Effect of RF power on the properties of transparent conducting zirconium-doped zinc oxide films prepared by RF magnetron sputtering

Transparent and conducting zirconium-doped zinc oxide films with high transparency and relatively low resistivity have been successfully prepared by radio frequency （RF） msgnetron sputtering at room temperature, The RF power is varied from 75 to 150 W. At first the crystallinity and conductivity of the film are improved and then both of them show deterioration with the increase of the RF power, The lowest resistivity achieved is 2.07 × 10^-3Ωcm at an RF power of 100W with a Hall mobility of 16cm^2V^-1s^-1 and a carrier concentration of 1.95 × 10^20 cm^-3. The films obtained are polycryetalline with a hexagonal structure and a preferred orientation along the c-axis, All the films have a high transmittance of approximately 92% in the visible range. The optical band gap is about 3.33 eV for the films deposited at different RF powers.

Antibacterial Effect of the Conducting Polyaniline

Excellent antibacterial performance of polyaniline （PAni） against Escherichia coli and Gram-positive Staphylococcus aureus microorganisms has been demonstrated under both dark and visible light conditions. The electrostatic adherence between the PAni molecules and the bacteria may play a very important role for the antibacterial reaction of the PAni. As a result of our investigation, conducting PAni and its composites/blends are believed to be useful as a new type of antibacterial agent, self-clean as well as multifunctional material for improving the human health and living environment.

Recent advances and perspectives of fluorite and perovskite-based dual-ion conducting solid oxide fuel cells

High-temperature solid-state electrolyte is a key component of several important electrochemical devices,such as oxygen sensors for automobile exhaust control,solid oxide fuel cells(SOFCs) for power generation,and solid oxide electrolysis cells for H_(2) production from water electrolysis or CO_(2) electrochemical reduction to value-added chemicals.In particular,internal diffusion of protons or oxygen ions is a fundamental and crucial issue in the research of SOFCs,hypothetically based on either oxygen-ionconducting electrolytes or proton-conducting electrolytes.Up to now,some electrolyte materials based on fluorite or perovskite structure were found to show certain degree of dual-ion transportation capability,while in available electrolyte database,particularly in the field of SOFCs,such dual-ion conductivity was seriously overlooked.Actually,few concerns arising to the simultaneous proton and oxygen-ion conductivities in electrolyte of SOFCs inevitably induce various inadequate and confusing results in literature.Understanding dual-ion transportation behavior in electrolyte is indisputably of great importance to explain some unusual fuel cell performance as reported in literature and enrich the knowledge of solid state ionics.On the other hand,exploration of novel dual-ion conducting electrolytes will benefit the development of SOFCs.In this review,we provide a comprehensive summary of the understanding of dual-ion transportation in solid electrolyte and recent advances of dual-ion conducting SOFCs.The oxygen ion and proton conduction mechanisms at elevated temperature inside oxide-based electrolyte materials are first introduced,and then(mixed) oxygen ion and proton conduction behaviors of fluorite and perovskite-type oxides are discussed.Following on,recent advances in the development of dual-ion conducting SOFCs based on fluorite and perovskite-type single-phase or composite electrolytes,are reviewed.Finally,the challenges in the development of dual-ion conducting SOFCs are discussed and future prospects are proposed.

A Study on Damage Rules on Insulators by Conducting Sols

Insulating parts are easily subjected to pollution which may cause damage to the electric system. A typical disc insulator is chosen as the target to test its flashover voltage by using an artificial pollution system. This test system aims at obtaining characteristic parameters of damage for chosen conducting sola to the selected insulator. Experimental results show that thickness and electric conductivity of pollutant layer over insulators are the main parameters in damage evaluation. The flashover voltage decreases with increase of thickness and/or conductivity. These results provide a better basis on further revealing the damaging nature of conducting sol materials.

ANALYSIS OF DAMAGE NEAR A CONDUCTING CRACK IN A PIEZOELECTRIC CERAMIC

The finite element formulation for analyzing static damage near a conducting crack in a thin piezoelectric plate is established from the virtual work principle of piezoelectricity.The damage fields under various mechanical and electrical loads are calculated carefully by using an effective iterative procedure.The numerical results show that all the damage fields around a crack tip are fan-shaped and the electric field applied has great influence on the mechanical damage, which is related to the piezoelectric properties.

Preparation and Conducting Behavior of Amphibious Organic/Inorganic Hybrid Proton Exchange Membranes Based on Benzyltetrazole

A series of novel amphibious organic/inorganic hybrid proton exchange membranes with H3PO4 doped which could be used under both wet and dry conditions was prepared through a sol-gel process based on acrylated triethoxysilane（A-TES） and benzyltetrazole-modified triethoxysilane（BT-TES）.The dual-curing approach including UV-curing and thermal curing was used to obtain the crosslinked membranes.Polyethylene glycol（400） diacrylate（PEGDA） was used as an oligomer to form the polymeric matrix.The molecular structures of precursors were characterized by 1 H,13 C and 29 Si NMR spectra.The thermogravimetric analysis（TGA） results show that the membranes exhibit acceptable thermal stability for their application at above 200 oC.The differential scanning calorimeter（DSC） determination indicates that the crosslinked membranes with the mass ratios of below 1.6 of BT-TES to A-TES and the same mass of H3PO4 doped as that of A-TES possess the-T g s,and the lowest T g（-28.9 ℃） exists for the membrane with double mass of H3PO4 doped as well.The high proton conductivity in a range of 9.4―17.3 mS/cm with the corresponding water uptake of 19.1%―32.8% of the membranes was detected at 90 oC under wet conditions.Meanwhile,the proton conductivity in a dry environment for the membrane with a mass ratio of 2.4 of BT-TES to A-TES and double H3PO4 loading increases from 4.89×10-2 mS/cm at 30 ℃ to 25.7 mS/cm at 140 ℃.The excellent proton transport ability under both hydrous and anhydrous conditions demonstrates a potential application in the polymer electrolyte membrane fuel cells.

Modeling of conducting bridge evolution in bipolar vanadium oxide-based resistive switching memory

We investigate the resistive switching characteristics of a Cu/VOx/W structure. The VOx film is deposited by radio- frequency magnetron sputtering on the Cu electrode as a dielectric layer. The prepared VOx sample structure shows reproducible bipolar resistive switching characteristics with ultra-low switching voltage and good cycling endurance. A modified physical model is proposed to elucidate the typical switching behavior of the vanadium oxide-based resistive switching memory with a sudden resistance transition, and the self-saturation of reset current as a function of compliance current is observed in the test, which is attributed to the conducting mechanism is discussed in detail. growth pattern of the conducting filaments. Additionally, the related

STUDIES ON ENHANCED CONDUCTIVITY OF STRETCHED CONDUCTING POLYMERS

A physical model of series of the conductivity on chain and the interchain conductivitybetween chains is proposed to explain enhanced conductivity of stretched conducting polymers.This model suggests that the enhanced conductivity for stretched conducting polymers might bedue to increasing of the interchain conductivity between chains along the elongation direction afterdrawing processes if the conductivity on chain is assumed much larger than that of the interchainconductivity between chains. According to this model, it is expected that the temperaturedependence of conductivity measured by four-probe method for stretched conducting polymers iscontrolled by a variation of the interchain conductivity between chains with temperature, whichcan be used to explain that a metallic temperature dependence of conductivity for stretchedconducting polymers is not observed although the conductivity along the elongation direction isenhanced by two or three orders of magnitude.

The properties of transparent conducting molybdenum-doped ZnO films grown by radio frequency magnetron sputtering

Transparent conducting molybdenum-doped zinc oxide films are prepared by radio frequency（RF） magnetron sputtering at ambient temperature.The MoO3 content in the target varies from 0 to 5 wt%,and each film is polycrystalline with a hexagonal structure and a preferred orientation along the c axis.The resistivity first decreases and then increases with the increase in MoO3 content.The lowest resistivity achieved is 9.2 × 10^-4.cm,with a high Hall mobility of 30 cm^2.V-1.s-1 and a carrier concentration of 2.3×10^20 cm^-3 at an MoO3 content of 2 wt%.The average transmittance in the visible range is reduced from 91% to 80% with the increase in the MoO3 content in the target.

Conducting Polyaniline-Electrical Charge Transportation

Conductive polyanilines are synthesized by doping with inorganic and organic acids, namely Hydrochloric acid (HCl) and ±10-camphor sulfonic acid (CSA). The direct current (DC) conductivities (σDC) are found to be about 9.5 ′ 10-8, 1.8, and 95.8 S/cm for PANI base, PANI(HCl) and PANI(CSA), respectively. σDC is measured down to a temperature of ~100 K and the apparent change in the activation energies are found to be 98.16, 74.40, and 57.24 meV for PANI base, HCl, and CSA dopings respectively. σDC is less temperature dependent near room temperature, further decrease in temperature the σDC is strongly dependent. Upon the inspection of AC conductivities (σAC) versus frequency curves, it can be inferred that the conduction process is noticeably influenced upon doping and within the dopants. σAC has shown classical plateau (DC-AC crossover) region, nonetheless shifted crossover frequency (critical frequency) upon doping is rather interesting. Critical frequencies (wc) are obtained from universal power-law for all samples. The variation in the dielectric properties can be attributed to the dopant incorporation. In material characterization, successful doping is corroborated by FTIR, UV-vis spectroscopy and slight influence upon doping can also be seen in thermal properties. Intense photoluminescence (PL) peaks at 322.5, 581.4 and 644.2 nm are observed. PANI(CSA) exhibited highest peak intensity followed by PANI(HCl) and PANI base.

Hemoglobin-biocatalyzed Synthesis of Conducting Molecular Complex of Polyaniline and Lignosulfonate

A new biocatalyst route for the synthesis of a conducting polyaniline （PANI）/ lignosulfonate （LGS） complex was presented.Four different catalysts such as hemoglobin （Hb）,5,10,15,20-tetrakis （meso-hydroxyphenyl） porphyrin,iron （II） tetrasulfophthalocyanine and ferric chloride were used to polymerize aniline in the presence of a natural polyelectrolytes template LGS.The experimental results show that Hb is an effective catalyst in this case and the synthesis is simple,and the conditions are mild in that the polymerization may be carried out in lower pH （1.0-4.0） buffered solution and optimal pH of 2.0.Varying concentrations of aniline,LGS and H2O2 in feed the favorable conditions for the production of PANI were determined.UV-vis absorption,FTIR,elemental analysis,conductivity,cyclic voltammetry and thermogravimetric analyses confirm the formation of thermally stable and electroactive PANI.