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  • The Electrochemical Society  (6)
  • 1
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2018
    In:  ECS Meeting Abstracts Vol. MA2018-01, No. 8 ( 2018-04-13), p. 785-785
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2018-01, No. 8 ( 2018-04-13), p. 785-785
    Kurzfassung: Lithium-ion battery (LIB) has been a tremendous success for decades. As the demand for rechargeable batteries surges, a need has arisen for low-cost secondary batteries. Among various studies, sodium-ion battery (SIB) is the most promising secondary batteries due to its similar working principles and the abundance of sodium in the natural world. Among many anode materials for SIB, MoS­­ 2 has attracted attention because it can intercalate sodium ions in its layered structure. However, in the repeated intercalation of Na + , MoS 2 suffers from collapse of its layered structure. Herein, we present vertically grown MoS 2 on nitrogenous reduced graphene oxides (N-RGO) with controlled sheet density and height of MoS2 sheets as SIB anode active material. The MoS 2 materials are synthesized by gel-precursor based method. By adjusting the nucleation and growth processes, we controlled the height and density of MoS 2 sheets to find optimal condition that show great performance and high stability. Control of the partial geometry can achieve these improved property because the high sheet density can prevent additional SEI layer and the shortened sheet length reduces the resistance of Na + diffusion. It shows remarkably high reversible discharging capacity of 255mAh/g at 1C and 245mAh/g at 5C discharging with a capacity reduction of 5.35% after 1300 cycles. And closely packed MoS 2 sheets shows specific capacity of 254, 243, 153, 86 mAh/g at 0.2, 2, 10, 50A/g current density, respectively. Furthermore, vertically grown MoS 2 is paired with Na 3 V 2 (PO 4 ) 3 to fabricate SIB full cell, and the full cell shows a specific capacity of 262mAh/g (based on the mass of anode material) during 50 cycles. Figure 1
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2018
    ZDB Id: 2438749-6
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2016
    In:  ECS Meeting Abstracts Vol. MA2016-02, No. 49 ( 2016-09-01), p. 3703-3703
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2016-02, No. 49 ( 2016-09-01), p. 3703-3703
    Kurzfassung: We report the effect of chemical reduction of bismuth vanadate (BiVO 4 ) photoelectrdoe by lithium-based strongly basic solution. Lithium dissolved in ethylenediamine anhydrous rapidly reduces the bismuth vanadate films with momentary immersion in the solution. This chemical reduction could form oxygen vacancies and these defects act as shallow donors for bismuth vanadate and increase the donor densities without trapping. Electrochemical impedance measurements showed that the donor densities of bismuth vanadate films were significantly enhanced. Photoelectrochemical water splitting performance was improved as well with photocurrent increase. The enhanced photoactivities were attributed to increased donor densities of reduced bismuth vanadate, which have effects on the charge transport.
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2016
    ZDB Id: 2438749-6
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2023
    In:  ECS Meeting Abstracts Vol. MA2023-01, No. 36 ( 2023-08-28), p. 2013-2013
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2023-01, No. 36 ( 2023-08-28), p. 2013-2013
    Kurzfassung: Liquid organic hydrogen carrier (LOHC) is a technology that uses renewable energy for hydrogen transportation, storage and utilization. LOHC have advantages that can store and utilize hydrogen rapidly in the lack of transportation infrastructure. A membrane-based LOHC system is a promising technology due to the dynamic operation using electrochemistry. Anion exchange membranes are widely used as electrolyte for electrochemical devices. The performance of LOHC could be determined by the properties of anion exchange membranes. Thus, high anion conducting ionomers must be developed for the superior conversion rates on the electrochemical reduction of liquid toluene to methylcyclohexane. In this study, anion exchangeable polymers containing imidazolium salt as anion-conducting group were synthesized to achieve good conduction of hydroxide ions and their chemical stability. Anion exchange membranes were prepared by a pore-filling method using porous polyethylene substrate. The pore-filling anion exchange membranes were characterized in terms of ion conductivity, areal resistance, ion exchange capacity, water uptake, swelling ratio and mechanical strength. Acknowledgment This research was supported in part by the Korea Institute of Science and Technology (No. 2E31871) and by 2021 Green Convergence Professional Manpower Training Program of the Korea Environmental Industry and Technology Institute funded by the Ministry of Environment.
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2023
    ZDB Id: 2438749-6
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2023
    In:  ECS Meeting Abstracts Vol. MA2023-01, No. 36 ( 2023-08-28), p. 2009-2009
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2023-01, No. 36 ( 2023-08-28), p. 2009-2009
    Kurzfassung: Water electrolyzer is a device that converts renewable electrical energy into environmentally friendly chemical energy, hydrogen. Water electrolysis is mainly categorized into proton exchange membrane water electrolysis (PEMWE) and anion exchange membrane water electrolysis (AEMWE). Non-precious electrocatalysts and hydrocarbon-based polymeric membranes are used for two different systems. It is advantageous for AEMWE in terms of cost. However, low current density and chemical stability for current anion exchange membrane technology (AEM) restricts early market penetration. Thus, thedevelopment of low resistance and high durable AEMs is of importance. In this study, superior ion conductivity and high durable pore-filling AEMs were developed for AEMWE. Pore-filling AMEs with different contents of crosslinking monomers were prepared by the monomers using chemically stable anion exchangeable functional groups in a porous polyethylene(PE) substrate. Properties of the AEMs were characterized through areal resistance, ionic conductivity, ion exchange capacity, water uptake, swelling ratio, mechanical strength and hydrogen crossover. In addition, AEMWE performance and durability tests were also conducted. Acknowledgments This research was supported in part by Cooperative Research Program for Agriculture Science and Technology Development (Project No. PJ016253), Rural Development Administration, Republic of Korea and by 2021 Green Convergence Professional Manpower Training Program of the Korea Environmental Industry and Technology Institute funded by the Ministry of Environment.
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2023
    ZDB Id: 2438749-6
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 5
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2020
    In:  ECS Meeting Abstracts Vol. MA2020-01, No. 2 ( 2020-05-01), p. 359-359
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2020-01, No. 2 ( 2020-05-01), p. 359-359
    Kurzfassung: Graphite, which is commercially used as anode material in lithium-ion battery (LIB), has a low theoretical capacity of 372 mAh/g, and therefore should be replaced by alternative material with high capacity for the toward vehicles and other applications. Not only that, the cost and environmental issues should be considered in the production of alternative materials. In this regard, silicon materials have received the extensive research interest due to their high specific capacity of 3579 mAh/g, a low lithiation reaction voltage plateau (vs. Li/Li + ) and abundant sources. Unfortunately, Si electrode typically suffers from irreversible capacity fading during cycling from their volume expansion and low intrinsic electronic conductivity. Recently, development of nanostructural design with various morphologies, Si nanowires, Si nanoparticles, and porous structures has received attention as a promising way to solve these problems. Nanostructural design largely improve cycle life by providing a sufficient free volume to accommodate silicon electrode expansion. However, commercially utilization of Si electrode is still insurmountable owing to some critical issues such as high costs, poor scalability and hazardous precursors. Furthermore, nanostructure Si includes severe side reactions due to a large surface area, low tap density. Here, we simply use the SiO 2 +Graphite mixture as the starting material and synthesize Si@SiC@Graphite composite material through electro-deoxidation method applied with the FFC Cambridge process, a simple approach for the high-purity extraction of metals from solid oxides via molten salt electrolysis that is known to be energy-saving and environmentally friendly. The electro-deoxidation was carried out in a molten CaCl 2 at 1123 K in cell voltage of 2.6 V and 2.9 V. As an anode material, the prepared Si@SiC@graphite composite resolves all of the aforementioned critical issues and shows 900 mAh/g after 300 cycles without capacity fading. Furthermore, we fabricated high tap-density Si@SiC@graphite powder (~ 0.76 g/ml) using a mechanical pressing method, resulting in a high capacity ( 〉 3.0 mAh/cm 2 ) at the large loading of cathode, verifying the successful design of stable electron transfer and high dense structure.
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2020
    ZDB Id: 2438749-6
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 6
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2008
    In:  Journal of The Electrochemical Society Vol. 155, No. 1 ( 2008), p. J1-
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 155, No. 1 ( 2008), p. J1-
    Materialart: Online-Ressource
    ISSN: 0013-4651
    RVK:
    Sprache: Englisch
    Verlag: The Electrochemical Society
    Publikationsdatum: 2008
    Standort Signatur Einschränkungen Verfügbarkeit
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