广角SS-OCT En Face结构投射图揭示未成年人玻璃体早期液化特征

目的:应用广角扫频源光学相干断层扫描成像(swept-source optical coherence tomography,SS-OCT)的en face结构投射图研究玻璃体早期液化特征。方法:使用SS-OCT进行18 mm×18 mm的容积(Cube)扫描,创建并分析健康未成年人(年龄5~18岁)70眼的系列玻璃体en face结构投射图。结果:在未成年人中,视网膜前的玻璃体包含4种液化结构,分别为后皮质前玻璃体囊袋(posterior precortical vitreous pocket,PPVP)、视盘前Martegiani区(the area of Martegiani,AM)、血管前液化裂隙(prevascular vitreous fissures,PVF)和液化池(cistern)。所有研究眼均能检出PPVP、AM和PVF,其中22眼(31.4%)的PPVP和AM连通。41眼(58.6%)可检出液化池,且其年龄大于未检出液化池的个体(P=0.01),液化池的发生与年龄呈正相关(r_(s)=0.315,P=0.008)。液化池的象限空间分布频率依次为颞上(90.2%)、鼻上(58.5%)、颞下(36.6%)、鼻下(24.4%),最常累及颞上象限(P<0.001)。结论:PPVP、AM和PVF是健康人群视网膜前玻璃体早期液化过程中均出现的特征。液化池的发生与年龄呈正相关,最常出现在颞上象限,可能是年龄相关性玻璃体液化变性的结果。

Boosting catalytic activities of carbon felt electrode towards redox reactions of vanadium ions by defect engineering

Vanadium redox flow batteries(VRFBs)are one of the most promising energy storage systems owing to their safety,efficiency,flexibility and scalability.However,the commercial viability of VRFBs is still hindered by the low electrochemical performance of the available carbon-based electrodes.Defect engineering is a powerful strategy to enhance the redox catalytic activity of carbon-based electrodes for VRFBs.In this paper,uniform carbon defects are introduced on the surfaces of carbon felt(CF)electrode by Ar plasma etching.Together with a higher specific surface area,the Ar plasma treated CF offers additional catalytic sites,allowing faster and more reversible oxidation/reduction reactions of vanadium ions.As a result,the VRFB using plasma treated electrode shows a power density of 1018.3 mW/cm^(2),an energy efficiency(EE)of 84.5%,and the EE remains stable over 1000 cycles.

Structure characterization and electrochemical properties of new lithium salt LiODFB for electrolyte of lithium ion batteries

Lithium difluoro(axalato)borate (LiODFB) was synthesized in dimethyl carbonate (DMC) solvent and purified by the method of solventing-out crystallization. The structure characterization of the purified LiODFB was performed by Fourier transform infrared (FTIR) spectrometry and nuclear magnetic resonance (NMR) spectrometry. The electrochemical properties of the cells using 1 mol/L LiPF6 and 1 mol/L LiODFB in ethylene carbonate (EC)/DMC were investigated, respectively. The results indicate that LiODFB can be reduced at about 1.5 V and form a robust protective solid electrolyte interface (SEI) film on the graphite surface in the first cycle. The graphite/LiNi1/3Mn1/3Co1/3O2 cells with LiODFB-based electrolyte have very good capacity retention at 55 ℃, and show very good rate capability at 0.5C and 1C charge/discharge rate. Therefore, as a new salt, LiODFB is a most promising alternative lithium salt to replace LiPF6 for lithium ion battery electrolytes in the future.

Effect of the amount of zinc-doped on the electrochemical performance of nickel hydroxide

The nickel hydroxide prepared by micro-emulsion method was doped by coprecipitated Zn. The effect of the amount of zinc-doped on the properties of Ni(OH)2 such as the reversibility of the electrode reaction, the charge efficiency and active material utilization ratio of nickel electrode, and discharge specific capacity was studied by cyclic voltammetry and constant current charge-discharge tests. The results indicate that the specific discharge capacity of nickel hydroxide obtained by micro-emulsion method is much less than its theoretical value because the transfer of electrons and the diffusion of protons H+ are hindered owing to its crystal grain size in a nanometer range and thus possessing higher crystal interface resistance. The crystal cells are swelled and the crystal defects increased in prepared material due to part of Ni2+ substituted by Zn2+ when zinc and nickel hydroxide are coprecipitated. Hence, the electrons and protons H+ in the electrode reaction are transferred easily, the electrochemical behavior of nickel electrode is improved and discharge specific capacity is promoted. However, the performance of Ni(OH)2 is gradually enhanced with the addition of zinc-doped at first, while slowly decreased after the content of zinc is added to a certain value. The best electrode reaction reversibility, the highest electrode charge efficiency, the highest active material utilization ratio and the largest specific capacity on discharge are available when the mass fraction of Zn doped in nickel hydroxide by coprecipitation reaches 2.5 %.

Preparation of Li4TisO12 Microspheres with a Pure Cr2O3 Coating Layer and its Effect for Lithium Storage

The pure Cr2O3 coated Li4Ti5O12 microspheres were prepared by a facile and cheap solution- based method with basic chromium（III） nitrate solution （pH=ll.9）. And their Li-storage properties were investigated as anode materials for lithium rechargeable batteries. The pure Cr2O3 works as an adhesive interface to strengthen the connections between Li4Ti5O12 par- ticles, providing more electric conduction channels, and reduce the inter-particle resistance. Moreover, Li2Cr2O3, formed by the lithiation of Cr2O3, can further stabilize LiTTi5O12 with high electric conductivity on the surface of particles. While in the acid chromium solution （pH=3.2） modification, besides Cr2O3, Li2CrO4 and TiO2 phases were also found in the final product. Li2CrO4 is toxic and the presence of TiO2 is not welcome to im- prove the electrochemical performance of Li4Ti5O12 microspheres. The reversible capacity of 1% Cr2O3-coated sample with the basic chromium solution modification was 180 mAh/g at 0.1 C, and 134 mAh/g at 10 C. Moreover, it was even as high as 127 mAh/g at 5 C after 600 cycles. At -20 ℃, its reversible specific capacity was still as high as 118 mAh/g.

Evaluation of substrates for zinc negative electrode in acid PbO_2–Zn single flow batteries

An investigation was performed on the suitability of carbon materials, metallic lead and its alloys as substrates for zinc negative electrode in acid PbO2-Zn single flow batteries. The zinc deposition process was carried out in the mediumofl mol.L 1H2SO4 at room temperature. No maximum current appears on the potentiostatic current transients for the zinc deposition on lead and its alloys. With increasing overpotential, the progressive nucleation turns to be a 3D-instantaneous nucleation process for the resin-graphite composite. Hydrogen evolution on the graphite composite is effectively suppressed with the doping of a polymer resin. The hydrogen evolution reaction on the lead is relatively weak, while on the lead alloys, it becomes serious to a certain degree. Although the ex- change current density of zinc deposition and dissolution process on the graphite composite is relatively low, the zinc corrosion is weakened to a great extent. With the increase of deposition time, zinc deposits are more compact. The cyclings of zinc galvanostatic charge-discharge on the graphite composite provide more than 90% of coulombic and 80% of energy efficiencies, and exhibit superior cycling stability during the first 10 cycles.

Electrochemical Energy Storage Technologies and Applications

The current need to fasten the implementation of renewable energies greatly depends on the development of competitive storage devices, and while there is not a single technology which is likely capable to competitively cover the wide range of possible demands, electrochemical technologies are one of the most promising for many of them. For the realization of this promise, new materials fulfilling criteria such as high energy density, high power density, competitive cost, reliability, and environmental compatibility need to be developed in the near future. Electrochemical energy storage devices can be classified into two main technologies： supercapacitors and batteries （including redox flow batteries）. Materials and applications for these technologies are discussed and compared, listing current status, technical and strategic challenges.

Recent progress in ether-based electrolytes for high-voltage lithium metal batteries

Ether-based solvents generally show better affinity for lithium metal,and thus ether-based electrolytes(EBEs)are more inclined to form a uniform and thin solid electrolyte interface(SEI),ensuring the long cycle stability of the lithium metal batteries(LMBs).Nonetheless,EBEs still face the challenge of oxidative decomposition under high voltage,which will corrode the structure of cathodes,destroy the stability of the electrode−electrolyte interface,and even cause safety risks.Herein,the types and challenges of EBEs are reviewed,the strategies for improving the high voltage stability of EBEs and constructing stable electrode−electrolyte interfaces are discussed in detail.Finally,the future perspectives and potential directions for composition optimization of EBEs and electrolyte−electrode interface regulation of high-voltage LMBs are explored.

A high potential biphenol derivative cathode: toward a highly stable air-insensitive aqueous organic flow battery

Aqueous organic flow batteries have attracted dramatic attention for stationary energy storage due to their resource sustainability and low cost. However, the current reported systems can normally be operated stably under a nitrogen or argon atmosphere due to their poor stability. Herein a stable airinsensitive biphenol derivative cathode, 3,30,5,50-tetramethylaminemethylene-4,40-biphenol(TABP), with high solubility(>1.5 mol L^(-1)) and redox potential(0.91 V vs. SHE) is designed and synthesized by a scalable one-step method. Paring with silicotungstic acid(SWO), an SWO/TABP flow battery shows a stable performance of zero capacity decay over 900 cycles under the air atmosphere. Further, an SWO/TABP flow battery manifests a high rate performance with an energy efficiency of 85% at a current density of60 m A cm^(-2) and a very high volumetric capacity of more than 47 Ah L^(-1). This work provides a new and practical option for next-generation practical large-scale energy storage.

Lamella-like electrode with high Br_(2)-entrapping capability and activity enabled by adsorption and spatial confinement effects for brominebased flow battery

Bromine-based flow batteries(Br-FBs)are well suitable for stationary energy storage owing to their high energy density and low cost.However,their power density and lifespan are limited by relatively low reaction kinetics of Br_(2)/Br-couple and serious self-discharge caused by bromine migration.Herein,lamella-like porous carbon nitride nanosheets(PCNS)with adsorption and spatial confinement effects are used to modify cathodes for Br-FBs.The large specific surface area and plentiful N-containing groups enable PCNS with excellent adsorption capacity,which captures bromine species into the pores on PCNS layers.The captured bromine species is subsequently confined in PCNS interlayers due to the strong interaction between bromine species and N-containing groups,thus effectively depressing bromine diffusion/migration.Moreover,the strong bromine adsorption capacity significantly improves the electrochemical activity of PCNS.Consequently,a zinc-bromine flow battery(ZBFB)employing PCNS-modified cathode achieves a high current density of 180 m A cm^(-2),with an ultra-high coulombic efficiency of 99.22%.It also exhibits better self-discharge performance and a long cycle life of 500 cycles.Furthermore,a complexing agent-free ZBFB is successfully realized based on the superior bromineentrapping/retaining capacity of the PCNS-modified cathode.Consequently,this work provides a promising strategy toward electrode modifications for high-performance and long-lifespan Br-FBs.

Anion exchange membranes based on long side-chain quaternary ammonium-functionalized poly(arylene piperidinium)s for vanadium redox flow batteries

A new series of poly(arylene piperidinium)-based anion exchange membranes(AEMs)are proposed for vanadium redox flow batteries(VRFBs).The AEMs are fabricated via the Menshutkin reaction between poly(arylene piperidine)without ether bonds in the backbone and various quaternizing agents,including iodomethane,1-bromopentane,and(5-bromopentyl)-trimethylammonium bromide.The properties of the AEMs are investigated in terms of sulfuric acid doping content,swelling,vanadium permeability,ion selectivity,area-specific resistance,mechanical properties,VRFB performance,and cyclic testing.Particularly,a method of measuring the H^(+) permeability of the AEM is developed.It demonstrates that the poly(p-terphenyl-N-methylpiperidine)-quaternary ammonium(PTP-QA)membrane with a QA cation-tethered alkyl chain exhibits high H^(+) permeability,resulting in low area resistance.Combined with its low vanadium permeance,the PTP-QA membrane achieves nearly 370 times higher ion selectivity than Nafion 115.The VRFB based on PTP-QA-based AEM displays high Coulombic efficiencies above 99% at current densities of 80-160 mA cm^(-2).The higher energy efficiency of 89.8% is achieved at 100 mA cm^(-2)(vs.73.6% for Nafion 115).Meanwhile,the PTPQA-based AEM shows good cycling stability and capacity retention,proving great potential as the ion exchange membrane for VRFB applications.

The dual role of hydrogen peroxide in fuel cells

Clean and highly efficient energy production has long been sought after, as a way to solve global energy and environmental problems. Fuel cells, which convert the chemical energy stored in fuel directly into electricity, are expected to be a key enabling technology for the pressing energy issues that plague our planet. Fuel cells require oxygen as an oxidant and require oxygen tank containers when used in air-free environments such as outer space and underwater. Hydrogen peroxide has been extensively uti- lized as an alternative liquid oxidant in place of gaseous oxygen. In addition to being an oxidant, hydrogen peroxide can donate electrons in the oxidation reaction to act as a fuel. This article provides an overview of the dual role of hydrogen peroxide in fuel-cell applications, including working principle, system design, and cell performance. Recent innovations and future perspectives of fuel cells that use hydrogen peroxide are particularly emphasized.

Solvating power regulation enabled low concentration electrolyte for lithium batteries

Li^(+) solvation structures have a decisive influence on the electrode/electrolyte interfacial properties and battery performances.Reduced salt concentration may result in an organic rich solid electrolyte interface(SEI)and catastrophic cycle stability,which makes low concentration electrolytes(LCEs)rather challenging.Solvents with low solvating power bring in new chances to LCEs due to the weak salt-solvent interactions.Herein,an LCE with only 0.25 mol L^(-1) salt is prepared with fluoroethylene carbonate(FEC)and 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropylether(D_(2)).Molecular dynamics simulations and experiments prove that the low solvating power solvent FEC not only renders reduced desolvation energy to Li^(+) and improves the battery kinetics,but also promotes the formation of a LiF-rich SEI that hinders the electrolyte consumption.Li||Cu cell using the LCE shows a high coulombic efficiency of 99.20%,and LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)||Li cell also exhibits satisfying capacity retention of 89.93%in 200 cycles,which demonstrates the great potential of solvating power regulation in LCEs development.

Gelation of a liquid electrolyte with aniline for use in a quasi-solid-state dye-sensitized solar cell

A new kind of gel electrolyte containing only organic solvents and an iodide salt-namely 3-methoxypropionitrile(MPN),aniline and AlI 3 -has been prepared.Gel formation results from the Lewis acid-base interaction between the Lewis acid ionic conductor AlI 3 and the Lewis base organic solvent aniline and no additional gelling agent is required.The AlI 3-aniline complex acts both as an ionic conductor and as a gelling agent.The differences between the peaks characteristic of the-NH 2 group and aromatic ring in the FTIR spectra of free aniline and the AlI 3-aniline hybrid confirm the formation of the AlI 3-aniline complex.The photovoltaic performance and long-term stability of dye-sensitized solar cells can be greatly enhanced by the addition of aniline to the AlI 3-MPN liquid electrolyte.

Effect of cations in ionic liquids on the electrochemical performance of lithium-sulfur batteries

Lithium-sulfur(Li-S) battery is a promising choice for the next generation of high-energy rechargeable batteries, but its application is impeded by the high dissolution of the polysulfides in commonly used organic electrolyte. Room temperature ionic liquids(RTILs) have been considered as appealing candidates for the electrolytes in Li-S batteries. We investigated the effect of cations in RTILs on the electrochemical performance for Li-S batteries. Ex situ investigation of lithium anode for Li-S batteries indicates that during the discharge/charge process the RTIL with N-methyl-N-propylpyrrolidine cations(P13) can effectively suppress the dissolution of the polysulfides, whereas the RTIL with 1-methyl-3-propyl imidazolium cation(PMIM) barely alleviates the shuttling problem. With 0.5 mol L-1 LiTFSI/P13 TFSI as the electrolyte of Li-S battery, the ketjen black/ sulfur cathode material exhibits high capacity and remarkable cycling stability, which promise the application of the P13-based RTILs in Li-S batteries.

A low-temperature solution-processed copper antimony iodide rudorffite for solar cells

A copper antimony iodide rudorffite,Cu3SbI6, was first prepared by using a low-temperature solution-pro- cessing approach.Its film absorbs 320-520nm fight and has an indirect bandgap of 2.43eV.Solar cells with a structure of ITO/PEDOT:PSS/CusSbIJPC6~BM/AI were made,giving a power conversion efficiency of 0.50%and a fill factor of 67.09%.

Application of facile solution-processed ternary sulfide Ag_8SnS_6 as light absorber in thin film solar cells

Light absorber is critical to the further applications of thin film solar cells. Here, we report a facile solution-processed method with an annealing temperature below250°C to fabricate Ag8 SnS6(ATS) light absorber for thin film solar cells. After optimization, the ATS-based thin film solar cells exhibited a reproducible power conversion efficiency(PCE) of about 0.25% and an outstanding long-term stability with 90% of the initial PCE retained after a more than 1,000 h degradation test. This research revealed the potential application of ATS as an earth-abundant, low toxic and chemically stable light absorber in thin film solar cells.