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    Effect of Phosphate Additive for Thermal Stability in a Vanadium Redox Flow Battery

    Source: Journal of Electrochemical Energy Conversion and Storage:;2017:;volume( 014 ):;issue: 004::page 41007
    Author:
    Yeon
    ,
    Sun-Hwa;So
    ,
    Jae Young;Yun
    ,
    Jin Hee;Park
    ,
    Se-Kook;Shin
    ,
    Kyoung-Hee;Jin
    ,
    Chang-Soo;Lee
    ,
    Yun Jung
    DOI: 10.1115/1.4038019
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Organic/inorganic materials are investigated as additives to improve the stability of a vanadium electrolyte for a vanadium redox flow battery (VRFB) at operating temperatures of 25 °C and 40 °C. Among these materials, the most effective additive is chosen based on the thermal stability and electrochemical performance with a long inhibition time. Through precipitation time and electrochemical measurements, the results show that the best inhibition effect is achieved by adding sodium pyrophosphate dibasic (SPD, H2Na2O7P2) as an additive at a considerably high H2SO4 concentration (3M) electrolyte, indicating an improved redox reversibility and electrochemical activity. Nonflow cell assembled with the SPD additive exhibits larger discharge capacity retentions of 40% than a blank solution with the retentions of 2% at 600 cycles at 40 °C. In the case of flow cell, the capacity retention on the SPD additive shows 55.4%, which is 5.3% higher than the blank solution at 40 °C and 180 cycles. The morphology of the precipitation is investigated by SEM, which exhibits more severe V2O5 precipitation amount on the carbon felt electrode used in the blank electrolyte at 40 °C, which causes larger capacity losses compared to cells assembled with the SPD additive electrolyte.
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      Effect of Phosphate Additive for Thermal Stability in a Vanadium Redox Flow Battery

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    https://yetl.yabesh.ir/yetl1/handle/yetl/4242987
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    • Journal of Electrochemical Energy Conversion and Storage

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    contributor authorYeon
    contributor authorSun-Hwa;So
    contributor authorJae Young;Yun
    contributor authorJin Hee;Park
    contributor authorSe-Kook;Shin
    contributor authorKyoung-Hee;Jin
    contributor authorChang-Soo;Lee
    contributor authorYun Jung
    date accessioned2017-12-30T11:44:07Z
    date available2017-12-30T11:44:07Z
    date copyright10/17/2017 12:00:00 AM
    date issued2017
    identifier issn2381-6872
    identifier otherjeecs_014_04_041007.pdf
    identifier urihttp://138.201.223.254:8080/yetl1/handle/yetl/4242987
    description abstractOrganic/inorganic materials are investigated as additives to improve the stability of a vanadium electrolyte for a vanadium redox flow battery (VRFB) at operating temperatures of 25 °C and 40 °C. Among these materials, the most effective additive is chosen based on the thermal stability and electrochemical performance with a long inhibition time. Through precipitation time and electrochemical measurements, the results show that the best inhibition effect is achieved by adding sodium pyrophosphate dibasic (SPD, H2Na2O7P2) as an additive at a considerably high H2SO4 concentration (3M) electrolyte, indicating an improved redox reversibility and electrochemical activity. Nonflow cell assembled with the SPD additive exhibits larger discharge capacity retentions of 40% than a blank solution with the retentions of 2% at 600 cycles at 40 °C. In the case of flow cell, the capacity retention on the SPD additive shows 55.4%, which is 5.3% higher than the blank solution at 40 °C and 180 cycles. The morphology of the precipitation is investigated by SEM, which exhibits more severe V2O5 precipitation amount on the carbon felt electrode used in the blank electrolyte at 40 °C, which causes larger capacity losses compared to cells assembled with the SPD additive electrolyte.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleEffect of Phosphate Additive for Thermal Stability in a Vanadium Redox Flow Battery
    typeJournal Paper
    journal volume14
    journal issue4
    journal titleJournal of Electrochemical Energy Conversion and Storage
    identifier doi10.1115/1.4038019
    journal fristpage41007
    journal lastpage041007-11
    treeJournal of Electrochemical Energy Conversion and Storage:;2017:;volume( 014 ):;issue: 004
    contenttypeFulltext
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