Large-scale inverted-V channels of upflowing oxygen ions pumped by Alfvén waves

Large-scale inverted-V channels of upflowing oxygen ions are frequently identified in data collected by Cluster,at all local times,near the open-closed field line boundary over Earth’s high-latitude ionosphere-occur with downward propagating MHD Alfvén waves which have cascaded into kinetic regimes of plasma.The transverse acceleration of the oxygen ions in the center of these structures is interpreted as the integrated energization by these waves along the channels.Also observed within the channels are upward parallel electric fields,a key characteristic of kinetic Alfvén waves,which may contribute not only to lifting the ions but also to precipitating aurora electrons that might initiate ion upflow in the ionosphere below.Statistics on five-year observations of Cluster show that the channels typically form during geomagnetic perturbations,particularly when solar-wind dynamic pressure is high or highly fluctuated.Near the open-closed field line boundary,the stronger the wave power,the higher the upward oxygen flux and the higher the beam energy,indicating that these waves provide a simple but efficient way to drive oxygen upflows.

Surface defects,stress evolution,and laser damage enhancement mechanism of fused silica under oxygen-enriched condition

Oxygen ions(O;)were implanted into fused silica at a fixed fluence of 1×10^(17) ions/cm^(2) with different ion energies ranging from 10 ke V to 60 ke V.The surface roughness,optical properties,mechanical properties and laser damage performance of fused silica were investigated to understand the effect of oxygen ion implantation on laser damage resistance of fused silica.The ion implantation accompanied with sputtering effect can passivate the sub-/surface defects to reduce the surface roughness and improve the surface quality slightly.The implanted oxygen ions can combine with the structural defects(ODCs and E′centers)to reduce the defect densities and compensate the loss of oxygen in fused silica surface under laser irradiation.Furthermore,oxygen ion implantation can reduce the Si-O-Si bond angle and densify the surface structure,thus introducing compressive stress in the surface to strengthen the surface of fused silica.Therefore,the laser induced damage threshold of fused silica increases and the damage growth coefficient decreases when ion energy up to30 ke V.However,at higher ion energy,the sputtering effect is weakened and implantation becomes dominant,which leads to the surface roughness increase slightly.In addition,excessive energy aggravates the breaking of Si-O bonds.At the same time,the density of structural defects increases and the compressive stress decreases.These will degrade the laser laser-damage resistance of fused silica.The results indicate that oxygen ion implantation with appropriate ion energy is helpful to improve the damage resistance capability of fused silica components.

Oxygen ion conductivity of La_(0.8)Sr_(0.2)Ga_(0.83)Mg_(0.17-x)Co_xO_(3-δ) synthesized by laser rapid solidification

Materials Lao.8Sro.2Gao.83Mgo.17_xCox03_6 with x = 0, 0.05, 0.085, 0.10, and 0.15 are synthesized by laser rapid solidification. It is shown that the samples prepared by laser rapid solidification give rise to unique spear-like or leaf-like microstructures which are orderly arranged and densely packed. Their electrical properties each show a general depen dence of the Co content and the total conductivities of Lao.8Sro.2Gao.83Mgo.085Coo.08503_6 prepared by laser rapid solidification are measured to be 0.067, 0.124, and 0.202 S.cm-1 at 600, 700, and 800 ℃, respectively, which are much higher than by conventional solid state reactions. Moreover, the electrical conductivities each as a function of the oxy gen partial pressure are also measured. It is shown that the samples with the Co content values 〈 8.5 mol% each exhibit basically ionic conduction while those for Co content values 〉 10 mol % each show ionic mixed electronic conduction under oxygen partial pressures from 10-16 atm （1 atm = 1.01325 x 105 Pa） to 0.98 atm. The improved ionic conductivity of Lao.sSro.2Gao.83Mgo.085Coo.08503 prepared by laser rapid solidification compared with by solid state reactions is attributed to the unique microstructure of the sample generated during laser rapid solidification.

Phase Transition and Oxygen Ion Diffusion in （La1-xLnx）2Mo2O9 （Ln=Nd, Gd, x=0.05-0.25） Using Dielectric Relaxation Method

Dielectric relaxation method was employed to study the properties of oxygen ion diffusion and phase transition in the oxide-ion conductors （Lal-xLnx）2Mo209 （Ln=Nd, Gd, x=0.05-0.25）. Two dielectric loss peaks were observed： peak Pd at about 600 K and peak P5 around 720 K. Peak Pd is a relaxational peak and associated with the short-range diffusion of oxygen ions, while peak P5 hardly changes its position and dramatically decreases in height with increasing frequency, exhibiting non-relaxational nature. With increasing Ln^3＋ concentration, the heights of peak Ph and Pd increase at first and then decrease after passing a maximum at 15% doping. It is suggested that peak P5 is related to the phase transition of a static disordered state to a dynamic disordered state in oxygen ions/vacancies distribution. It is found that the 15%Gd or 15%Nd doped La2Mo209 samples exhibit the highest conductivity in accordance with the highest height of peak Pd at this doping content.

Advanced rare earth tantalate RETaO_(4)(RE=Dy,Gd and Sm) with excellent oxygen/thermal barrier performance

Thermal barrier coatings(TBCs) materials with lowered the rmal and oxygen ion conductivity can provide thermal and oxidative protection for high te mperature hot-end components in aero nautical engines and gas turbines,The rare-earth tantalate RETaO_(4)(RE=Dy,Gd and Sm) ceramics with monoclinic(m) phase were successfully synthesized via spark plasma sintering.Oxygen vacancies responsible for the thermal and oxygen ion conductivities of RETaO_(4) were demonstrated by atomic-resolution energy dispersive Xray and X-ray photoelectron spectroscopy.Among the three samples,DyTaO_(4) has excellent oxygen/thermal barrier performance.Compared to the current service thermal barrier coating material ZrO_(2)-8 wt% Y_(2)O_(3)(8 YSZ),DyTaO_(4) has an ultra-low oxygen ion conductivity benefiting from low oxygen vacancy concentration and strong stretching force constants.The intrinsic thermal conductivity of DyTaO_(4)is 68.2% less than that of 8 YSZ.Additionally,the thermal expansion rate curves indicate that the phase transformation does not happen from room te mperature to 1200℃.The above results demonstrate that high-growth rate the rmally grown oxide can be retarded by creating dense DyTaO_(4) coating with lowered thermal and oxygen ion conductivity.

Study on Conductivity of Ceramics LaFe_(1 - x) Ni_xO_(3-δ)

The LaFe 1-x Ni x O 3-δ serial ceramics were prepared by standard solid phase reaction method. Two arm electric bridge principal and four electrode method were adopted to measure the resistivity. The results indicate that LaFe 1-x Ni x O 3-δ ceramics are of metallic state conductivity when x varies from 0 6 to 0 8. There are oxygen vacancies and conductive electrons in the ceramics, which results in highly mixed conductivity of electrons and oxygen ions. The amount of oxygen vacancies depends on the sintering techniques, so the proper increase of sintering temperature can decrease the room temperature resistivity. A phase transition is found at around 120 K in the low temperature experiment.

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.

Sintering of Ce_(0.8)Sm_(0.2)O_(1.9)

Ce0.8Sm0.2O1.9（SDC）powder was prepared with an oxalate coprecipitation route.SDC solid solutions were sintered at various temperatures ranging from 1100~1450 ℃,and characterized by X-ray diffraction（XRD）,scanning electron microscopy（SEM）,density measurements,and electrical conductivity measurements.The optimized processing parameters for densification were to uniaxially press the sample at 200~400 MPa and sinter it at 1350~1400 ℃ for 4 h.The density of the sintered pellets was 〉90% of the theoretical density;their soakage was 〈0.5%;and the average grain size was 1~2 μm.The conductivities of the typical sintered specimen were 0.0133 and 0.0211 S·cm-1 at 550 and 600 ℃,respectively;Its activation energy for ionic conductivity was 0.62 eV.The dense SDC bulk material could be used as the electrolyte layer of low temperature solid oxide fuel cells.

Synthesis and Conductivity of Oxyapatite Ionic Conductor La10-xVx（SiO4）6O3＋x

Apatite-lanthanum silicate has attracted considerable interest in recent years due to its high oxide ion conductivity.In this paper,V-doped samples La10-xVx(SiO4) 6O3+x(0≤x≤1.5) were prepared by sol-gel method and the influences of V-dopant content on calcining temperature and conductivity were reported.The samples were characterized by thermal analysis(TG-DSC) ,X-ray diffraction(XRD) and scanning electron micrograph(SEM) . The apatite was obtained at 800°C,a relatively low temperature in comparison to 1500°C with the conventional solid-state method.The ceramic pellets sintered at 1200°C for 5 h showed a higher relative density than La9.33Si6O26 pellets sintered at 1400°C for 20 h.The conductivities of samples were measured by electrochemical impedance spectroscopy.The conductivity was improved with the increase of V-dopant content on La site.

Synthesis and Conducting Properties of La10-x（SiO4）6O3-1.5x

The synthesis of silicate oxyapatitesLa10-x（SiO4）6O3-1.5x（x=0. 0.17, 0.33, 0.50 and 0.67） via a sol-gel method at 800 ℃ was reported. The apatite phases were characterized by X-ray diffraction （XRD） and conducting properties were studied by electrochemical impedance spectroscopy （EIS）. It is found that the conductivities are influenced by the amount of cation vacancies and interstitial oxygen. The conductivity of La9.33 （SiO4）6O2 with more cation vacancies is higher than that of La9.5 （SiO4）6O2.25. The conductivity of La10 （SiO4）6O3 with more interstitial oxygen is 7.98 ×10^-3 S·cm^-1, which is about 5 times higher than that of La9.33（SiO4）6O2 at 700℃. The electrical conductivity is almost independent of the oxygen partial pressure from 105 to 1 Pa, which suggests that the oxyapatites exhibit almost pure O^2- ion conduction over a wide range of oxygen partial pressure.

An Atomic Oxygen Device Based on PIG Oxygen Negative Ion Source

It is an important research subject for the spaceflight countries to conduct equivalent simulation of 5eV atomic oxygen effects for the spaceflight material in low earth orbit.This paper introduces an apparatus used for producing atomic oxygen,which consists of a PIG ion source with permanent magnet,two electrodes extraction system, an electron deflector,an einzel lens,an ion decelerating electrode and a sample bracket.At present it has been used on the small debris accelerator in the Center for Space Science and Applied Research,Chinese Academy of Sciences, and the producing experiments of O^- are carried out.200—300μA of O^- ions are extracted at the extraction voltage of 2—3kV.The experiments for decelerating of O^- ions and erosion of kapton foil are carried out also.Because of the target room used for both the atomic oxygen device and the small debris accelerator,the facility can be used for small debris impinging and atomic erosion for spaceflight materials simultaneouslly.

High-performance oxygen permeation membranes:Cobalt-free Ba_(0.975)La_(0.025)Fe_(1-x)Cu_(x)O_(3)-δceramics

A new group of cobalt-free perovskite oxides,Ba_(0.975)La_(0.025)Fe_(1-x)Cu_(x)O_(3-δ)(BLFC,x=0.05-0.15),was designed,characterized and applied as oxygen permeation membranes.It was found that BLFC oxides with Cu doping range of 0.075-0.15 maintain cubic perovskite phase in a wide range of temperatures.More Cu introduced at the B-site results in a gradual increase of the electrical conductivity,which is attributed to the denser overlapping of electron clouds of CueO bonds.With increasing Cu content,the oxygen vacancy concentration increases and the oxygen ion migration energy decreases,leading to the highest oxygen permeation flux of 1.59 mL cm^(-2)min^(-1)recorded for Ba_(0.975)La_(0.025)Fe_(0.9)Cu_(0.1)O_(3-δ)1mm thick membrane at 950℃.However,the oxygen permeability decreases with further Cu doping,which may be correspond to a presence of defect association.Ba_(0.975)La_(0.025)Fe_(0.9)Cu_(0.10)O_(3-δ)membrane with 0.7mm thickness delivers stable oxygen permeation flux of 1.57 mL cm^(-2)min^(-1)for 200 h at 900℃.All of the obtained results indicate that the developed BLFC with optimized Cu content(i.e.x=0.1)is a very promising material for usage in oxygen separation applications.

Sn and Y co-doped BaCo_(0.6)Fe_(0.4)O_(3)-δcathodes with enhanced oxygen reduction activity and CO_(2) tolerance for solid oxide fuel cells

Applying mixed oxygen ionic and electronic conducting(MIEC)oxides as the cathode offers a promis-ing solution to enhance the performance of solid oxide fuel cells(SOFCs).However,the phase instability in CO_(2)-containing air and sluggish oxygen reduction activity of MIEC cathodes remain a long-term chal-lenge for optimizing the electrochemical performance of SOFCs.Herein,a heterovalent co-doping strategy is proposed to enhance the oxygen reduction activity and CO_(2)tolerance of SOFCs cathodes,which can be demonstrated by developing a novel BaCo_(0.6)Fe_(0.4)O_(3)-δ(BCF)-based MIEC oxide,BaCo_(0.6)Fe_(0.2)Sn_(0.1) Y_(0.1)O_(3-δ)(BCFSY).In addition to improving the stability of BCF-based perovskites,this strategy achieves an opti-mized balance of ionic mobility and oxygen vacancies due to the synergies between the effects of the co-dopants.Compared with single-doped materials,BCFSY exhibits improved CO_(2)tolerance and consider-ably higher ORR activity,which is reflected in a significantly lower polarization resistance of 0.15Ωcm^(2) at 600℃.The results of this work provide an efficient tactic for designing electrode materials for SOFCs.

Ultralow oxygen ion diffusivity in pyrochlore-type La_(2)(Zr_(0.7)Ce_(0.3))_(2)O_(7)

Thermally grown oxides(TGOs)at the ceramic top-coat/metallic bond-coat interface are a pressing chal-lenge in advanced thermal barrier coating(TBC)systems as they can affect the performance and ser-vice lifetime of TBCs.Thus,developing novel TBC materials with ultralow oxygen ion diffusivity is very urgent.In this study,we reported the diffusive properties of oxygen ions in a novel pyrochlore-type La_(2)(Zr_(0.7)Ce_(0.3))_(2)O_(7)(LZ7C3)material.The measured ionic conductivity and atomistic simulation revealed that the oxygen ion diffusivity in LZ7C3 grains is two orders of magnitude lower than that in conventional 8 wt.%yttria-stabilized zirconia(8YSZ)grains.This is due to the relatively high energy barrier for oxygen hopping in LZ7C3.In addition,it was found that enhancing the order distribution of cations is a strategy to reduce the intrinsic oxygen diffusion of pyrochlore-type oxides.On the other hand,we observed that La^(3+) cations segregate at the grain boundaries(GBs)of LZ7C3,which results in the electrostatic poten-tial at GBs being comparable to that in the bulk.Furthermore,we found that the oxygen ion diffusion is facilitated at the GBs of LZ7C3 due to the stretched O-Zr/Ce bond and the low coordination at GBs.How-ever,the segregations of Y^(3+)cations and the increase in the number of oxygen vacancies resulted in the formation of an electrostatic layer at the GBs of 8YSZ,which shielded the oxygen ion diffusion.Despite this,the oxygen ion diffusivity in LZ7C3 was still considerably less than that in conventional 8YSZ.This study offers a stepping stone toward utilizing pyrochlore-type LZ7C3 materials as advanced TBCs at high temperatures.

High-temperature ferromagnetic metallic phase in LaMnO_(3)/Sr_(3)Al_(2)O_(6)heterostructure

To achieve a flexible single-crystal multifunctional membrane,the freestanding process of a rigid epitaxial transition metal oxide thin film via a buffered water-dissolution sacrificial layer has attracted reasonable attentions.Owing to the difference in chemical potential,specific element affinity,and lattice constant between the target membrane and the sacrificial layer,the freestanding process may cause an indelible change of physics property once the target thin film is sensitive to the above factors.Here,the heterostructures composed of the generally adopted sacrificial layer Sr_(3)Al_(2)O_(6)(SAO)and LaMnO_(3)(LMO)have been systematically investigated.The electrical and magnetic properties of LMO show extreme sensitivity to the thickness of SAO(tSAO).Then we have also found that LMO/SAO heterostructures can exhibit the coexistence of two ferromagnetic phases,the significantly enhanced Curie temperature~342 K,and the large magnetoresistance-23.3%at 300 K,which is similar to the optimal-doped manganite such as La_(2/3)Sr_(1/3)MnO_(3).X-ray diffraction results show that continuously tunable strain from out-of-plane tension to relaxation and then to compression can be generated by adjusting tSAO.This strain can stabilize the migrated oxygen from LMO to SAO,which is induced by the large oxygen affinity difference between Bsite Mn and Al.It is believed that these unexpected electrical/magnetic phenomena are originated from the combined effects of interfacial element diffusion and strain.Our study provides a strategy for designing new magnetic phases,and a reference for the fundamental understanding of strongly correlated transition metal oxide systems in the freestanding process.

Echinacoside Protects Against MPP+-Induced Neuronal Apoptosis via ROS/ATF3/CHOP Pathway Regulation

Echinacoside （ECH） is protective in a mouse model of Parkinson＇ s disease （PD） induced by 1-methyl-4- phenylpyridinium ion （MPP＋）. To investigate the mechanisms involved, SH-SYSY neuroblastoma ceils were treated with MPP＋ or a combination of MPP＋ and ECH, and the expression of ATF3 （activating transcription factor 3）, CHOP （C/EBP-homologous protein）, SCNA （synuclein alpha）, and GDNF （glial cell line-derived neurotrophic factor） was assessed. The results showed that ECH significantly improved cell survival by inhibiting the generation of MPP＋-induced reactive oxygen species （ROS）. In addition, ECH suppressed the ROS and MPP＋- induced expression of apoptotic genes （ATF3, CHOP, and SCNA）. ECH markedly decreased the MPP＋-induced cas- pase-3 activity in a dose-dependent manner. ATF3- knockdown also decreased the CHOP and cleaved caspase- 3 levels and inhibited the apoptosis induced by MPP＋. Interestingly, ECH partially restored the GDNF expression that was down-regulated by MPP＋. ECH also improved dopaminergic neuron survival during MPP＋ treatment and protected these neurons against the apoptosis induced by MPTP. Taken together, these data suggest that the ROS/ ATF3/CHOP pathway plays a critical role in mechanisms by which ECH protects against MPP＋-induced apoptosis in PD.

Effects of synthesis methods on catalytic activities of CoOx–TiO2 for low-temperature NH3-SCR of NO

A series of cobalt doped TiO2（Co-TiO2） and Co Oxloaded TiO2（Co/TiO2） catalysts prepared by sol–gel and impregnation methods respectively were investigated on selective catalytic reduction with NH3（NH3-SCR） of NO. It was found that Co-TiO2 catalyst showed more preferable catalytic activity at low temperature range. From characterization results of XRD,TEM, Raman and FT-IR, Co species were proved to be doped into TiO2 lattice by replaced Ti atoms. After being characterized and analyzed by NH3-TPD, PL, XPS, EPR and DRIFTS, it was found that the better NH3-SCR activities of Co-TiO2 catalysts, compared with Co/TiO2 catalyst, were ascribed to the formation of more oxygen vacancies which further promoted the production of more superoxide ions（O-2）. The superoxide ions were crucial for the formation of low temperature SCR reaction intermediates（NO-3） by reacting with adsorbed NO molecule. Therefore, these aspects were responsible for the higher low temperature NH3-SCR activity of Co-TiO2 catalysts.

A review of transition metal chalcogenide/graphene nanocomposites for energy storage and conversion

To meet the ever-increasing energy demands, advanced electrode materials are strongly requested for the exploration of advanced energy storage and conversion technologies, such as Li-ion batteries, Li-S batteries, Li-]Zn-air batteries, supercapacitors, dye-sensitized solar cells, and other electrocatalysis process （e.g., oxygen reductionlevolution reaction, hydrogen evolution reaction）. Transition metal chalcogenides （TMCs, Le., sulfides and selenides） are forcefully considered as an emerging candidate, owing to their unique physical and chemical properties. Moreover, the integration of TMCs with conductive graphene host has enabled the significant improvement of electrochemical performance of devices. In this review, the recent research progress on TMC]graphene composites for applications in energy storage and conversion devices is summarized. The preparation process of TMC]graphene nanocomposites is also included. In order to promote an in-depth understanding of performance improvement for TMC/graphene materials, the operating principle of various devices and technologies are briefly presented. Finally, the perspectives are given on the design and construction of advanced electrode materials.