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  • 1
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2018
    In:  ECS Meeting Abstracts Vol. MA2018-02, No. 3 ( 2018-07-23), p. 167-167
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2018-02, No. 3 ( 2018-07-23), p. 167-167
    Kurzfassung: An ever increasing number of electrode materials are nowadays presented as potential candidates for electrochemical capacitor. This includes different forms of carbons (carbon nanotubes, graphene, activated carbon, ...), conducting polymers (PEDOT, PANI, PPy, ...), metal oxides (RuO 2 , MnO 2 , FeWO 4 , ...), or other inorganic materials such as metal nitrides, phosphates, etc... However, most of the reported performance of related electrodes are based on only few mg of active material and/or few mm 2 surface area. Such low values definitely do not enable to upscale the performance using simple multiplying factor. Indeed, several studies have shown that experimental up-scaling of electrodes and devices often leads to quite different values, usually much lower than those reported for small scale electrodes.[1-3] In this manuscript, we will illustrate such discrepancy between small cell and larger cell performance by using commercially available activated carbon in different configurations, including coin-type cells ( 〈 1F) and pouch cells (up to 25 F). The different parameters influencing the electrode preparation (binder, additives, porosity, ...) as well as those related with cell assembly (current collectors, separators, ...) will be detailed as well as their influence on the cell performance. Finally, a practical illustration of symmetrical carbon based EDLC in neutral aqueous electrolyte will be given, namely the internal hybridization of such cell in a PEMFC. Its influence on power capability will be reported and compared with external hybridization using a commercial cylindrical EDLC. [1] True performance metrics in electrochemical energy storage, Y. Gogotsi and P. Simon, Science, 334, 917 (2011). [2] Improving the volumetric energy density of supercapacitors, N. Goubard-Bretesché, O. Crosnier, F. Favier, T. Brousse, Electrochimica Acta 206 (2016) 458–463. [3] A Guideline for Reporting Performance Metrics with Electrochemical Capacitors: From Electrode Materials to Full Devices, A. Balducci, D. Belanger, T. Brousse, J.W. Long, W. Sugimoto, Journal of The Electrochemical Society (2017) 164 (7), A1487-A1488.
    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
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-02, No. 3 ( 2019-09-01), p. 147-147
    Kurzfassung: BSCFs oxides have been prepared by sol-gel process followed by high temperature treatment. The resulting powders show the same perovskite structural arrangement as well as identical morphology characteristics. BSCFs electrodes were tested in 5M LiNO 3 aqueous electrolyte, and have demonstrated promising pseudocapacitive behavior while performances depend on the Co/Fe ratio. A maximum capacitance of 87 F.g -1 was obtained for the electrode based on the BSCF material with x = 0.80. Charge storage mechanism was investigated by in situ X-Ray Absorption Spectroscopy carried out on the ROCK beamline at SOLEIL Synchrotron (France) at both Fe and Co K-edges. Both Co and Fe were found being electrochemically involved in the charge storage mechanism. XAS in situ measurements allow to propose an advanced description of the charge storage mechanism. It shows the involvement of electrolytic cations but also of oxygenated moieties. BSCFs oxides were also investigated in asymmetric devices using FeWO 4 or activated carbon as negative electrode. These two devices were operated between 0 and 1.6 V and have demonstrated a remarkable cycling ability with a high capacitance retention over 45,000 cycles. The advantages and limits of high density oxides with pseudocapacitive behavior operated in devices will also be highlighted in this study.
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2019
    ZDB Id: 2438749-6
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  • 3
    In: Electrochimica Acta, Elsevier BV, Vol. 271 ( 2018-05), p. 677-684
    Materialart: Online-Ressource
    ISSN: 0013-4686
    Sprache: Englisch
    Verlag: Elsevier BV
    Publikationsdatum: 2018
    ZDB Id: 1483548-4
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  • 4
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-04, No. 5 ( 2019-06-30), p. 286-286
    Kurzfassung: Supercapacitors are attractive electrochemical energy storage devices for high power applications. However, volumetric energy density is the main limitation for their integration in such applications as terrestrial transport systems. The use of high density pseudocapacitive oxides as electrode material could lead to a volumetric energy density improvement. With this aim, materials from Ba 0,5 Sr 0,5 Co x Fe 1-x O 3-δ family, so called BSCFs, have been studied. Several compositions have been prepared and evaluated as positive electrode materials in aqueous neutral electrolyte. Volumetric capacitances have shown to be greater than those of activated carbons, already used in commercialized supercapacitors. Their electrochemical properties are strongly related to the cobalt to iron ratio, to the charging rate, to the electrolyte composition, and other key parameters. The study of the charge storage mechanism occuring in these materials has been investigated thanks to in situ X-Ray absorption spectroscopy and operando X-Ray diffraction performed at SOLEIL (France) and SPring-8 (Japan) synchrotron facilities respectively. Devices coupling BSCF based positive electrode with activated carbon or FeWO 4 based negative electrode have demonstrated the added value of such materials to improve the volumetric energy density of supercapacitors.
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2019
    ZDB Id: 2438749-6
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  • 5
    Online-Ressource
    Online-Ressource
    Royal Society of Chemistry (RSC) ; 2021
    In:  CrystEngComm Vol. 23, No. 41 ( 2021), p. 7298-7304
    In: CrystEngComm, Royal Society of Chemistry (RSC), Vol. 23, No. 41 ( 2021), p. 7298-7304
    Kurzfassung: Iron tungstate, Fe 2 WO 6 , is a promising photocatalytic, thermoelectric and electrochemically active material for energy storage devices. However, its structure is poorly described in the literature reporting on these applications. For the first time, we solved the crystal structure of its high temperature form using powder X-ray diffraction and the incommensurately modulated structural model. The structure adopts a (3 + 1)-dimensional Pbcn (0 β 0)000 superspace group with the cell parameters a = 4.57964(7) Å, b = 5.58662(8) Å, and c = 4.96920(7) Å and the modulation vector q = 0.6687(4) b *, close to the commensurate case q = 2/3 b *. The first-order satellite reflections visible in the powder diffraction patterns show, compared to the main reflections, a substantial broadening of the diffraction lines, caused by the small size of the ordered domains. This broadening has been successfully described using a line-broadening model, designed for incommensurately modulated structures, and confirms the incommensurate structural description. Such findings can be of great help to further understand the reported physical and electrochemical properties.
    Materialart: Online-Ressource
    ISSN: 1466-8033
    Sprache: Englisch
    Verlag: Royal Society of Chemistry (RSC)
    Publikationsdatum: 2021
    ZDB Id: 2025075-7
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  • 6
    In: Nature Communications, Springer Science and Business Media LLC, Vol. 15, No. 1 ( 2024-02-07)
    Kurzfassung: In recent decades, more than 100,000 scientific articles have been devoted to the development of electrode materials for supercapacitors and batteries. However, there is still intense debate surrounding the criteria for determining the electrochemical behavior involved in Faradaic reactions, as the issue is often complicated by the electrochemical signals produced by various electrode materials and their different physicochemical properties. The difficulty lies in the inability to determine which electrode type (battery vs. pseudocapacitor) these materials belong to via simple binary classification. To overcome this difficulty, we apply supervised machine learning for image classification to electrochemical shape analysis (over 5500 Cyclic Voltammetry curves and 2900 Galvanostatic Charge-Discharge curves), with the predicted confidence percentage reflecting the shape trend of the curve and thus defined as a manufacturer. It’s called “capacitive tendency”. This predictor not only transcends the limitations of human-based classification but also provides statistical trends regarding electrochemical behavior. Of note, and of particular importance to the electrochemical energy storage community, which publishes over a hundred articles per week, we have created an online tool to easily categorize their data.
    Materialart: Online-Ressource
    ISSN: 2041-1723
    Sprache: Englisch
    Verlag: Springer Science and Business Media LLC
    Publikationsdatum: 2024
    ZDB Id: 2553671-0
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  • 7
    Online-Ressource
    Online-Ressource
    Elsevier BV ; 2018
    In:  Electrochimica Acta Vol. 287 ( 2018-10), p. 161-162
    In: Electrochimica Acta, Elsevier BV, Vol. 287 ( 2018-10), p. 161-162
    Materialart: Online-Ressource
    ISSN: 0013-4686
    Sprache: Englisch
    Verlag: Elsevier BV
    Publikationsdatum: 2018
    ZDB Id: 1483548-4
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 8
    In: Nanomaterials, MDPI AG, Vol. 11, No. 6 ( 2021-05-26), p. 1405-
    Kurzfassung: The stability upon cycling of Fe2WO6 used as a negative electrode material for electrochemical capacitors was investigated. The material was synthesized using low temperature conditions for the first time (220 °C). The electrochemical study of Fe2WO6 in a 5 M LiNO3 aqueous electrolyte led to a specific and volumetric capacitance of 38 F g−1 and 240 F cm−3 when cycled at 2 mV·s−1, respectively, associated with a minor capacitance loss after 10,000 cycles. In order to investigate this very good cycling stability, both surface and bulk characterization techniques (such as Transmission Electron Microscopy, Mössbauer spectroscopy, and magnetization measurements) were used. Only a slight disordering of the Fe3+ cations was observed in the structure, explaining the good stability of the Fe2WO6 upon cycling. This study adds another pseudocapacitive material to the short list of compounds that exhibit such a behavior up to now.
    Materialart: Online-Ressource
    ISSN: 2079-4991
    Sprache: Englisch
    Verlag: MDPI AG
    Publikationsdatum: 2021
    ZDB Id: 2662255-5
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  • 9
    Online-Ressource
    Online-Ressource
    Walter de Gruyter GmbH ; 2021
    In:  Open Chemistry Vol. 19, No. 1 ( 2021-04-12), p. 432-441
    In: Open Chemistry, Walter de Gruyter GmbH, Vol. 19, No. 1 ( 2021-04-12), p. 432-441
    Kurzfassung: Energy storage is an integral part of the modern world. One of the newest and most interesting concepts is the internal hybridization achieved in metal-ion capacitors. In this study, for the first time we used sodium borohydride (NaBH 4 ) as a sacrificial material for the preparation of next-generation sodium-ion capacitors (NICs). NaBH 4 is a material with large irreversible capacity of ca. 700 mA h g −1 at very low extraction potential close to 2.4 vs Na + /Na 0 . An assembled NIC cell with the composite-positive electrode (activated carbon/NaBH 4 ) and hard carbon as the negative one operates in the voltage range from 2.2 to 3.8 V for 5,000 cycles and retains 92% of its initial capacitance. The presented NIC has good efficiency 〉 98% and energy density of ca. 18 W h kg −1 at power 2 kW kg −1 which is more than the energy (7 W h kg −1 at 2 kW kg −1 ) of an electrical double-layer capacitor (EDLC) operating at voltage 2.7 V with the equivalent components as in NIC. Tin phosphide (Sn 4 P 3 ) as a negative electrode allowed the reaching of higher values of the specific energy density 33 W h kg −1 (ca. four times higher than EDLC) at the power density of 2 kW kg −1 , with only 1% of capacity loss upon 5,000 cycles and efficiency 〉 99%.
    Materialart: Online-Ressource
    ISSN: 2391-5420
    Sprache: Englisch
    Verlag: Walter de Gruyter GmbH
    Publikationsdatum: 2021
    ZDB Id: 2825411-9
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  • 10
    Online-Ressource
    Online-Ressource
    The Electrochemical Society ; 2011
    In:  ECS Transactions Vol. 35, No. 32 ( 2011-10-11), p. 91-98
    In: ECS Transactions, The Electrochemical Society, Vol. 35, No. 32 ( 2011-10-11), p. 91-98
    Kurzfassung: Sodium ion batteries represent an interesting alternative to lithium ion batteries for large scale energy storage, due to the inexpensive and massive sources of sodium. Moreover, the incertitude related to lithium resources and their suppliers could become a major problem in the coming years. In this study, synthesis and electrochemical analyses were performed to examine TiO2 (B) and Na2Ti6O13's potential as negative electrode materials in sodium ion batteries. These materials were selected due to their well-known small cation insertion redox reactions.
    Materialart: Online-Ressource
    ISSN: 1938-5862 , 1938-6737
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2011
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