充电电极特性的测量与计算

本文主要阐述了了实际掌握和测量各种不同充电电极在各种不同工作条件下的充电特性，并依据已掌握的充电特性推算充电电极对光导体在充电过程中的作用，即光导体最终表面静电电位，这在复印机工程设计中的一定的指导意义，当前，依此理论，反过来推算，亦然。

锯齿状充电电极的充电特性及其改善

本文介绍了什么是锯齿状充电电极，锯齿状充电电极的由来和发展历史，详细阐述了锯齿状充电电极的工作原理和特性，以及该充电电极如何在光导体表面建立静电电位，如何通过调整该电极的各组成部分来改善其输出特性，文章用图片来展示实验的结果。

TiO_(2)提高富碳氮化碳的光生电荷存储性能

氮化碳材料固有的导电性差、电子迁移率低等问题导致高光生电荷复合率,阻碍了其光生电荷存储性能的提高.为此,构建了TiO_(2)富碳氮化碳共轭聚合物(CPCN)界面异质结,以提高光生电荷分离率.采用具有高比表面积(220.03 m^(2)/g)的TiO_(2)纳米晶介孔薄膜作为电子传输物质,通过增大TiO_(2)与CPCN之间的界面面积提高了电极反应活性,促进了光生空穴的高效抽取,获得了197 C/g的光生电荷存储容量.

Effects of dispersant on performance of Ni-Zn batteries

A new additive of sodium hexametaphosphate （SHMP） was introduced to the paste of zinc electrode, with the purpose of preventing the zinc active materials from agglomerating and improving the stability of batteries. The properties of the zinc electrodes were characterized by scanning electron microscopy （SEM）, constant current charge/discharge measurement, self-discharge test and hydrogen collection experiment. The photographs of zinc electrode show that SHMP can significantly break up the agglomeration, uniforrnize the particle distribution and increase the surface area, which are advantageous to improve the electrochemical performance of zinc electrode. The experimental battery shows a 97 times cycling life and a 30.2% remaining capacity after 4 d storage. The hydrogen collection experimental results indicate that the SHMP can decrease the ratio of hydrogen evolution. Therefore, the corrosion of zinc electrode is suppressed and the charge/discharge efficiency is enhanced.

Controllable Spin Polarization of Charge Current by Rashba Spin Orbital Coupling

We report a theoretic study on modulating the spin polarization of charge current in a mesoscopic fourterminal device of cross structure by using the inverse spin hall effect. The scattering region of device is a two-dimensional electron gas （2DEG） with Rashba spin orbital interaction （RSOI）, one of lead is ferromagnetic metal and other three leads are spin-degenerate normal metals. By using Landauer-Biittiker formalism, we found that when a longitudinal charge current flows through 2DEG scattering region from FM lead by external bias, the transverse current can be either a pure spin current or full-polarized charge current due to the combined effect of spin hall effect and its inverse process, and the polarization of this transverse current can be easily controlled by several device parameters such as the Fermi energy, ferromagnetic magnetization, and the RSOI constant. Our method may pave a new way to control the spin polarization of a charge current.

Electrochemical Behavior of Electrodeposited Sn Films： Possible Negative Electrode for Na^＋ Rechargeable Batteries

Tin films on copper substrate, obtained by electrodeposition procedure, were structural and electrochemical characterized. In particular to investigate the possibility to use such metal as possible negative electrode in Na＋ rechargeable batteries, EPS （electrochemical potential spectroscopy） and galvanostatic charge/discharge cycling of the electrodes were investigated, at room temperature in organic electrolyte. Three crystalline and one amorphous phases were identified as well as high discharge capacity （738 mAb/g） was obtained after 4 cycles. Unfortunately material fading, due to the internal stress during sodiation/desodiation process, causes poor cyclability.

Controlled Ag-driven superior rate-capability of Li4Ti5O12 anodes for lithium rechargeable batteries

The morphology and electronic structure of a Li4Ti5012 anode are known to determine its electrical and electrochemical properties in lithium rechargeable batteries. Ag-Li4Ti5012 nanofibers have been rationally designed and synthesized by an electrospinning technique to meet the requirements of one-dimensional （1D） morphology and superior electrical conductivity. Herein, we have found that the 1D Ag-Li4Ti5012 nanofibers show enhanced specific capacity, rate capability, and cycling stability compared to bare Li4Ti5012 nanofibers, due to the Ag nanoparticles （〈5 nm）, which are mainly distributed at interfaces between Li4Ti5O12 primary particles. This structural morphology gives rise to 20% higher rate capability than bare Li4Ti5O12 nanofibers by facilitating the charge transfer kinetics. Our findings provide an effective way to improve the electrochemical performance of Li4Ti5O12 anodes for lithium rechargeable batteries.

Cu_2O nanowires as anode materials for Li-ion rechargeable batteries

Li-ion batteries are a key technology for multiple clean energy applications.In this study,Cu2O nanowires were obtained by the reduction of cupric acetate with pyrrole.The resulting Cu2O nanowires exhibited excellent reversible capacities of 470mAh g-1 at rate of 1 C after 100 cycles.The results show that the Cu2O nanowires had more capacity than materials previously reported.No fading was observed over 100 cycles of charging and discharging.The compound metal Cu and incorporation of the conducting polymer polypyrrole(PPy)improved the conductivity of Cu2O and enhanced the stability of the electrode during cycling.The results from this study imply that Cu2O nanowires with high capacity and good cycle retention could be excellent candidates as anode materials for Li-ion rechargeable batteries.

Revealing the interface-rectifying functions of a Li-cyanonaphthalene prelithiation system for SiO electrode

Chemical prelithiation is regarded as a crucial method for improving the initial Coulombic efficiency(ICE)of Li-storage anodes.Herein,a substituent-engineered Li-cyanonaphthalene chemical prelithiation system is designed to simultaneously enhance the ICE and construct a multifunctional interfacial film for SiO electrodes.X-ray photoelectron spectroscopy(XPS),electron energy-loss spectroscopy(EELS),nuclear magnetic resonance(NMR)spectroscopy and atomic force microscopy(AFM)prove that the Licyanonaphthalene prelithiation reagent facilitates the formation of a rectified solid electrolyte interface(SEI)film in two ways:(1)generation of a gradient SEI film with an organic outer layer(dense Ncontaining organics,ROCO_(2)Li)and an inorganic LiF-enriched inner layer;(2)homogenization of the horizontal distribution of the composition,mechanical properties and surface potential.As a result,the prelithiated SiO electrode exhibits an ICE above 100%,enhanced CEs during cycling,better cycle stability and inhibition of lithium dendrite formation in the overcharged state.Notably,the prelithiated hard carbon/SiO(9:1)‖LHCoO_(2) cell displays an enhancement in the energy density of 62.3%.

Porous CuO nanowires as the anode of rechargeable Na-ion batteries

We report the preparation of porous CuO nanowires that are composed of nanoparticles （-50 nm） via a simple decomposition of a Cu（OH）2 precursor and their application as the anode materials of rechargeable Na-ion batteries. The as-prepared porous CuO nanowires exhibit a Brunauer-Emmett-Teller （BET） surface area of 13.05 m^2.g^-1, which is six times larger than that of bulk CuO （2.16 m^2.g^-1）. The anode of porous CuO nanowires showed discharge capacities of 640 mA.h.g^-1 in the first cycle and 303 mA.h.g^-1 after 50 cycles at 50 mA.g^-1 The high capacity is attributed to porous nanostructure which facilitates fast Na-intercalation kinetics. The mechanism of electrochemical Na-storage based on conversion reactions has been studied through cyclic voltammetry, X-ray diffraction （XRD）, Raman spectroscopy, and high resolution transmission electron microscopy （HRTEM）. It is demonstrated that in the discharge process, Na＋ions first insert into CuO to form a CuⅡ1-x CuⅠ x O1-x/2solid and a Na2O matrix then CuⅡ1-xCu Ⅰ xO1-x/2 reacts with Na＋ to produce Cu2O, and finally Cu2O decompose into Cu nanoparticles enclosed in a Na2O matrix. During the charge process, Cu nanopartides are first oxidized to generate Cu2O and then converted back to CuO. This result contributes to the design and mechanistic analysis of high-performance anodes for rechargeable Na-ion batteries.

Self-assembled α-MnO2 urchin-like microspheres as a high-performance cathode for aqueous Zn-ion batteries

Aqueous Zn-ion batteries(AZIBs)are one of the promising battery technologies for the green energy storage and electric vehicles.As one attractive cathode material for AZIBs,α-MnO2 materials exhibit superior electrochemical properties.However,their long-term reversibility is still in great suspense.Considering the decisive effect of the structure and morphology on theα-MnO2 materials,hierarchicalα-MnO2 materials would be promising to improve the cycle performance of AZIB.Here,we synthesized theα-MnO2 urchin-like microspheres(AUM)via a self-assembled method.The porous microspheres composed of one-dimensionalα-MnO2 nanofibers with high crystallinity,which improved the surface area and active sites for Zn2+intercalation.The AUM-based AZIB realized a high initial capacity of 308.0 mA hg-1,and the highest energy density was 396.7 W hkg-1.The kinetics investigation confirmed the high capacitive contribution and fast ion diffusion of the AUM.Ex-situ XRD measurement further verified the synergistic insertion/extraction of H+and Zn2+ions during the charge/discharge process.The superiority of the AUM guaranteed good electrochemical performance and reversible phase evolution,and this application would promote the follow-up research on the advanced AZIB.

Rational synthesis of SnS_2@C hollow microspheres with superior stability for lithium-ion batteries

Tin-based nanomaterials have been extensively explored as high-capacity anode materials for lithium ion batteries（LIBs）. However,the large volume changes upon repeated cycling always cause the pulverization of the electrode materials. Herein,we report the fabrication of uniform SnS_2@C hollow microspheres from hydrothermally prepared SnO_2@C hollow microspheres by a solid-state sulfurization process. The as-prepared hollow SnS_2@C microspheres with unique carbon shell,as electrodes in LIBs,exhibit high reversible capacity of 814 mA h g^（-1） at a current density of 100 mA g^（-1）,good cycling performance（783 mA h g^（-1） for 200 cycles maintained with an average degradation rate of 0.02% per cycle） and remarkable rate capability（reversible capabilities of 433 mA h g^（-1）at 2C）. The hollow space could serve as extra space for volume expansion during the charge-discharge cycling,while the carbon shell can ensure the structural integrity of the microspheres. The preeminent electrochemical performances of the SnS_2@C electrodes demonstrate their promising application as anode materials in the next-generation LIBs.

Cubic imidazolate frameworks-derived CoFe alloy nanoparticles-embedded N-doped graphitic carbon for discharging reaction of Zn-air battery

The construction of transition metal-based catalysts with high activity and stability has been widely regarded as a promising method to replace the precious metal Pt for oxygen reduction reaction(ORR).Herein,we synthesized CoFe alloy nanoparticle-embedded N-doped graphitic carbon(CoFe/NC)nanostructures as ORR electrocatalysts.The ZIF-67(zeolitic imidazolate framework,ZIF)nanocubes were first synthesized,followed by an introduction of Fe2+ions to form CoFe-ZIF precursors via a simple ion-exchange route.Subsequently,the CoFe/NC composites were synthesized through a facile pyrolysis strategy.The ORR activity and the contents of cobalt and iron could be effectively adjusted by controlling the solution concentration of Fe2+ions used for the ion exchange and the pyrolysis temperature.The CoFe/NC-0.2-900 composite(synthesized with 0.2 mmol of FeSO4·7H2O at a pyrolysis temperature of 900℃)exhibited ORR activity that was superior to the other samples owing to a synergistic effect of the bimetal,especially considering the extremely high limiting current density of 6.4 mA cm^-2 compared with that of Pt/C(5.1 mA cm^-2).Rechargeable Zn-air batteries were assembled employing CoFe/NC-0.2-900 and NiFeP/NF(NiFeP supported on nickel foam(NF))as the catalysts for the discharging and charging processes,respectively,The above materials achieved reduced discharging and charging platforms,high power density,and prolonged cycling stability compared with conventional Pt/C+RuO2/C catalysts.

Preparation of Li_4Ti_5O_(12) submicrospheres and their application as anode materials of rechargeable lithium-ion batteries

We report on the preparation of spinel Li4Ti5O12 submicrospheres and their application as anode materials of rechargeable lithium-ion batteries. The spinel Li4Ti5O12 submicrospheres are synthesized with three steps of the hydrolysis of TiCl4 to form rutile TiO2, the hydrothermal treatment of rutile TiO2 with LiOH to prepare an intermediate phase of LiTi2O4+δ, and the calcinations of LiTi2O4+δ to obtain spinel Li4Ti5O12. The as-prepared products are investigated by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The diameters of Li4Ti5O12 submicrospheres with novel hierarchical microstructures are about 200–300 nm with the assembly of 20–30 nm nanoparticles. The electrochemical properties of Li4Ti5O12 submicrospheres are measured by galvanostatical discharge/charge test and cyclic voltammetry (CV). The as-prepared Li4Ti5O12 display excellent discharge/charge rate and cycling capability. A high discharge capacity of 174.3 mAh/g is obtained in the first discharge at 1 C rate. Meanwhile, there is only tiny capacity fading with nearly 100% columbic efficiency in the sequential 5–50 cycles. Moreover, lithium-ion diffusion coefficient in Li4Ti5O12 is calculated to be 1.03 × 10-7 cm2/s. The present results indicate that the as-prepared Li4Ti5O12 submicrospheres are promising anode candidates of rechargeable Li-ion batteries for high-power applications.

Achieving superior high-temperature sodium storage performance in a layered potassium vanadate

The high-temperature sodium-ion batteries(SIBs)used for large-scale energy storage have attracted extensive attention in recent years.However,the development of SIBs is still hampered mainly by their poor charge/discharge efficiency and stability,necessitating the search for appropriate electrodes.A simple potassium ion intercalation process is used herein to obtain the potassium vanadate(KV_(3)O_(8))nanobelts.When serving as the anode for SIBs at a high temperature(60℃),the KV_(3)O_(8) nanobelts display superior sodium storage performance with a high capacity of 414mA h g^(-1) at 0.1Ag^(-1),remarkable rate capability(220mAh g^(-1) at 20Ag^(-1)),and super-long cycle life(almost no capacity fading at 10Ag^(-1) over 1000 cycles).Moreover,the ex-situ X-ray powder diffraction reveals no structural changes throughout the whole charge/discharge process,which further confirms their outstanding stability,indicating KV_(3)O_(8) nanobelts are a promising candidate for high-temperature SIBs.

High-performance aluminum-polyaniline battery based on the interaction between aluminum ion and-NH groups

Aluminum-ion batteries(AIBs)are a type of promising energy storage device due to their high capacity,high charge transfer efficiency,low cost,and high safety.However,the most investigated graphitic and metal dichalcogenide cathodes normally possess only a moderate capacity and a relatively low cycling stability,respectively,which limit the further development of high-performance AIBs.Here,based on the results of first principles calculations,we developed a polyaniline/graphene oxide composite that exhibited outstanding performances as a cathode material in AIBs(delivering 180 mA h g^−1 after 4000 cycles),considering both the discharge capacity and the cycling performance.Ex-situ characterizations verified that the charge storage mechanism of polyaniline depended on the moderate interactions between−NH in the polyaniline chain and the electrolyte anions,such as AlCl4^−.These findings lay the foundation of the development of high-performance AIBs based on conducting polymers.