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      • KCI등재

        Effect of Zn2+ and F- Co-Modification on the Structure and Electrochemical Performance of Li4Ti5O12 Anode Material

        Aijia Wei,Wen Li,Lihui Zhang,Xiaohui Li,Xue Bai,Zhenfa Liu 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2017 NANO Vol.12 No.5

        Zn2+ and F- ions are successfully used to modify pure Li4Ti5O12 via a co-precipitation method followed by calcination at 400℃ for 5 h in an Ar atmosphere in order to further investigate the reaction mechanism of the fluoride modification process. Zn2+ and F- co-modified Li4Ti5O12 samples are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and electrochemical measurements. After the modification process, no ZnF2 coating layer is formed on the surface of Li4Ti5O12, instead, F- ions react with Li4Ti5O12 to generate a new phase, composed of a small amount of anatase TiO2, rutile TiO2, LiF, and Zn2+ ions are suspected to form a ZnO coating layer on Li4Ti5O12 particles. The electrolyte reduction decomposition is suppressed in Zn2+ and F- co-modified Li4Ti5O12 due to the ZnO coating layer. 1 wt.% Zn2+ and F- co-modified Li4Ti5O12 exhibits the best rate capability, which leads to a charge capacity of 236.7, 227.8, 222.1, 202.7, 188.9 and 150.7 mAh g -1 at 0.2C, 0.5C, 1C, 3C, 5C and 10C, respectively, between 0 V and 3 V. Furthermore, 1 wt.% Zn2+ and F- comodified Li4Ti5O12 exhibits 96.0% charge capacity retention at 3C rate after 200 cycles, which is significantly higher than that of pure Li4Ti5O12 (78.4%).

      • In-situ PECVD-enabled graphene-V<sub>2</sub>O<sub>3</sub> hybrid host for lithium–sulfur batteries

        Song, Yingze,Zhao, Wen,Wei, Nan,Zhang, Li,Ding, Feng,Liu, Zhongfan,Sun, Jingyu Elsevier 2018 Nano energy Vol.53 No.-

        <P><B>Abstract</B></P> <P>Lithium–sulfur (Li–S) batteries have been regarded as promising candidates for current energy-storage technologies due to their remarkable advantages in energy density and theoretical capacity. However, one of the daunting challenges remained for advanced Li–S systems thus far deals with the synchronous suppression of polysulfide (LiPS) shuttle and acceleration of redox kinetics. Herein, a cooperative interface bridging adsorptive V<SUB>2</SUB>O<SUB>3</SUB> and conductive graphene is constructed <I>in-situ</I> by virtue of direct plasma-enhanced chemical vapor deposition (PECVD), resulting in the design of a novel V<SUB>2</SUB>O<SUB>3</SUB>-graphene hybrid host to synergize the LiPS entrapment and conversion. The redox kinetics and electrochemical performances of thus-derived cathodes were accordingly enhanced owing to the smooth adsorption-diffusion-conversion of LiPSs even at a sulfur mass loading of 3.7 mg cm<SUP>–2</SUP>. Such interfacial engineering offers us a valuable opportunity to gain insight into the comprehensive regulation of LiPS anchoring ability, electrical conductivity and ion diffusive capability in hybrid hosts on suppressing the LiPS shuttle and propelling the redox kinetics. Our devised PECVD route might pave a new route toward the facial and economic design of hetero-phased multi-functional hosts for high-performance Li–S systems.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Graphene-V<SUB>2</SUB>O<SUB>3</SUB> hybrid host was designed <I>in-situ</I> based on PECVD route. </LI> <LI> Thus-derived cathode showed a low capacity decay of merely 0.046% per cycle at 2 C after 1000 cycles. </LI> <LI> Cathodes with a relatively high sulfur mass loading (3.7 mg cm<SUP>–2</SUP>) were fabricated. </LI> <LI> The smooth adsorption-diffusion-conversion of polysulfides was thoroughly probed <I>via</I> experimental studies and DFT simulations. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>

      • KCI등재

        Structure and Performances of xLiFePO4/C·(1 − x)Li3V2(PO4)3/C Cathode for Lithium-Ion Batteries by Using Poly(vinyl alcohol) as Carbon Source

        Chang-ling Fan,Wei-hua Zhang,Tao-tao Zeng,Ling-fang Li,Xiang Zhang,Shao-chang Han 대한화학회 2015 Bulletin of the Korean Chemical Society Vol.36 No.11

        Poly(vinyl alcohol), whose pyrolysis carbon possesses high conductivity of 8.88 × 10−1 S/cm, was used to synthesize xLiFePO4/C·(1 − x)Li3V2(PO4)3/C cathode. It was characterized by X-ray diffraction, scanning electron microscopy, conductivity, cyclic voltammetry, and galvanostatic charge and discharge experiments. Results show that LiFePO4/C and Li3V2(PO4)3/C coexists in the cathode. The particles sizes of 0.75LiFePO4/C·0.25Li3V2(PO4)3/C (x = 0.75) are much smaller than 100 nm due to the role of poly(vinyl alcohol). Its conductivity is 8.79 × 10−2 S/cm. The oxidative and reductive peaks in cyclic voltammetry are sharp and symmetrical. Their low potential gaps indicate that the extractions and insertions of lithium ion possess excellent reversibility. Its discharge capacities at 1 and 5 C are 141.1 and 100.1 mAh/g. The more Li3V2(PO4)3/C in cathode results in the deterioration of electrochemical performances due to its low theoretical capacity. It is concluded that poly(vinyl alcohol) is an effective carbon source in the preparation of xLiFePO4/C·(1 − x)Li3V2(PO4)3/C composite cathode with excellent performances.

      • KCI등재

        Review on State of Charge Estimation Methods for Li-Ion Batteries

        Xiaoqiang Zhang,Wei-ping Zhang,Hongyu Li,Mao Zhang 한국전기전자재료학회 2017 Transactions on Electrical and Electronic Material Vol.18 No.3

        The state of charge (SOC) is an important parameter in a battery-management system (BMS), and is very significantfor accurately estimating the SOC of a battery. Li-ion batteries boast of excellent performance, and can only remainat their best working state by means of accurate SOC estimation that gives full play to their performances and raisestheir economic benefits. This paper summarizes some measures taken in SOC estimation, including the dischargeexperiment method, the ampere-hour integral method, the open circuit voltage method, the Kalman filter method,the neural network method, and electrochemical impedance spectroscopy (EIS. The principles of the various SOCestimation methods are introduced, and their advantages and disadvantages, as well as the working conditionsadopted during these methods, are discussed and analyzed.

      • KCI등재

        Influence of host plants on the development, survivorship, and fecundity of the summer fruit tortrix moth, Adoxophyes orana (Lepidoptera: Tortricidae)

        Li Guang‐wei,Wang Hui‐min,Yang Wen‐tao,Chen Xiu‐lin,Li Bo‐liao,Chen Yu‐xin 한국곤충학회 2021 Entomological Research Vol.51 No.10

        The summer fruit tortrix moth Adoxophyes orana is a seriously damaged leaf roller pest for fruit trees. In this study, we evaluated the effect of five host plants (apple, Malus domestica B.; peach, Prunus persica var. nectarina; apricot, Armeniaca vulgaris Lam.; mulberry, Morus alba L.; and jujube, Ziziphus jujuba M.) on the development, survival, and fecundity of A. orana under laboratory conditions. Results showed that the development times of A. orana on jujube were significantly longer than those on the other four plants. The preimaginal survival rate was influenced by the host plants, which were fed during the larval stage, and with the highest on peach, followed by apple, apricot, and mulberry, and with the lowest on jujube. Adult females from larvae reared on apricot laid the greatest numbers of eggs (318.11 eggs per female), while that on apple, jujube, and mulberry was smaller, and no significant difference was observed among them. The highest intrinsic rate of increase (rm) was observed on peach and apricot; these two fruit trees were considered to be the most suitable host plant for A. orana because of the shorter developmental duration, higher survival rate, and the highest fecundity.

      • KCI등재

        Membrane technologies for Li+/Mg2+ separation from salt-lake brines and seawater: A comprehensive review

        Ye Zhang,Li Wang,Wei Sun,Yue-hua Hu,Honghu Tang 한국공업화학회 2020 Journal of Industrial and Engineering Chemistry Vol.81 No.-

        Recent years have seen rapid improvement of technology and large-scale applications of lithium-ionbatteries, which leads to an increasing market demand for lithium. Since the land lithium resources arediminishing drastically, the sources of lithium extraction have shifted to the large amount of waterresources containing salt-lake brines and seawater. Among the varieties of aqueous recovery approaches,membrane technology seems to have huge development potential and good application prospect. This isbecause the membrane technologies exhibit excellent Li/Mg separation selectivity, with low energyconsumption and green process owing to no addition of chemicals. The present work reviews the latestadvances in various membrane technologies, including nanofiltration membrane, electrodialysis,membrane capacitive deionization approaches, solid electrolyte electrolysis-based technology, etc. Therecent developments in positively charged nanofiltration membrane are discussed in terms of thepreparation methods, membrane properties, and Li/Mg separation coefficient. In addition, the effects ofseveral factors on electrodialysis for lithium extraction and relevant mechanisms in both simple andactual saline systems are discussed, including applied voltage, VC/VD, and coexisting ions. Theapplications of electrodialysis with novel selective membrane involving nanofiltration membrane as wellas solid electrolyte membrane and perspectives for further investigation are proposed.

      • KCI등재

        A Mild Strategy to Strengthen Three Dimensional Graphene Aerogel for Supporting Sulfur as a Free‐standing Cathode in Lithium–Sulfur Batteries

        Yinglin Yan,Haichao Qin,Yiqi Wei,Rong Yang,Yunhua Xu,Liping Chen,Qiaole Li,Mangmang Shi 대한화학회 2018 Bulletin of the Korean Chemical Society Vol.39 No.5

        Recently, three dimensional graphene aerogel (3DGA) supported sulfur microparticles was used as a cathode material for lithium?sulfur batteries, which was considered as one of the most promising next generation rechargeable batteries due to its ultra?high theoretical specific capacity (1675 mAh/g). However, the mechanical strength of 3DGA remains an issue for further application. Herein, a strengthened 3DGA (S3DGA) was achieved by soaking in a low concentration ammonia solution at a relative low temperature. Then the S3DGA loaded sulfur (S3DGA?S) was cut into a round piece and directly used as a cathode without additional binders or conductive additives in Li?S batteries. The mechanical strength, microstructure, and electrochemical properties were investigated by compare with a 3DGA prepared without strengthen. The S3DGA?S presented good mechanical strength, excellent capacity retention, and lower electrochemical impedance.

      • Development of ligustrazine-loaded lipid emulsion: Formulation optimizatiom, characterization and biodistribution

        ( Lijun Wei ),( Nirmal Marasini ),( Gao Li ),( Chul Soon Yong ),( Jong Oh Kim ),( Qizhe Quan ) 영남대학교 약품개발연구소 2013 영남대학교 약품개발연구소 연구업적집 Vol.23 No.0

        Ligustrazine is a traditional Chinese medicine used to treat various cardiovascular and neurovascular complications. However, this compound exhibits rapid first-pass metabolism, a short biological half-life, low stability and potential vascular irritation that restrict its use for long-term therapy. The use of a lipid emulsion as a carrier for intravenous administration of ligustrazine might provide sustained and prolonged release, thereby reducing the frequency of administration and improving patient compliance. The main purpose of our study was to develop a highly stable and sterile optimal formulation of a ligustrazine lipid emulsion (LLE) and to evaluate its pharmacokinetic behavior and tissue distribution in rats. The final optimal formulation consisted of soybean oil (12.0%), oleic acid (0.6%), lecithin (1.0%), poloxamer 188 (0.6%) and glycerol (2.25%). The average particle size, polydispersity index (PDI), zeta-potential and pH of the final product were 215.0±2.5 nm, 0.076±0.033, -40.4±5.3 mV and 7.25±0.05, respectively. The LLE was stable for at least three months at room temperature. In vitro drug release studies of the LLE suggested a sustained release profile, which was further confirmed by in vivo pharmacokinetic studies in rats. The area under the drug concentration-time curve from 0 h to 10 h (AUC(0-10h)) for LLE was increased by 1.6-fold compared with that of the commercially available ligustrazine injection (LI), suggesting enhanced bioavailability from the lipid-based emulsion. Furthermore, a tissue distribution study showed significant improvement in the distribution pattern of ligustrazine with a higher AUC(0-180 min) observed in all tissues for LLE than for LI. In conclusion, LLE, with excellent stability, improved pharmacokinetics and tissue distribution, demonstrates great potential for the delivery of ligustrazine for clinical applications.ⓒ2012 Elsevier B.V.All rights reserved.

      • KCI등재

        Effect of Cooling Rate on Solidification and Segregation Characteristics of 904L Super Austenitic Stainless Steel

        Yunong Li,Dening Zou,Wanwan Chen,Yingbo Zhang,Wei Zhang,Fanghong Xu 대한금속·재료학회 2022 METALS AND MATERIALS International Vol.28 No.8

        To study and understand the solidification behavior of super austenitic stainless steel under different cooling rates and segregationlaws of alloying elements is of great significance to optimize the subsequent diffusion annealing homogenizationtreatment process and improve product quality. According to Thermo-Calc thermodynamic simulation results and combinedwith high temperature laser confocal scanning electron microscope (HT-CSLM), the tissue morphology of 904L superaustenitic stainless steel was observed in-situ during solidification. The solidification path of the test steel was determinedvia calculation with the Scheil-Gulliver model. Microscopy techniques, including true color microscopy, scanning electronmicroscopy (SEM), energy dispersive spectrometer (EDS), and electron probe microanalyzer (EPMA) were used to analyzethe influence of different cooling rates (6 ℃/min, 50 ℃/min, and 100 ℃/min) on the solidification structure and determine themain distribution law of alloying elements. This analysis determined that the solute distribution coefficient (K) of Cr, Mn,Mo, Cu, and Si elements is less than 1 during the solidification process, which means that they will accumulate in the liquidphase. Among them, elemental Mo segregation is the most severe, while elemental Ni hardly segregates. As the cooling rateincreases, the crystallization temperature of the test steel decreases, and the secondary dendrite arm spacing λ2 decreases,the concentration of Mo in the residual liquid phase increases.

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