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用于钠离子电池的铁掺杂氟磷酸钠钒阴极——发热的电化学表征和原位测量

Iron-Doped Sodium Vanadium Oxyflurophosphate Cathodes for Sodium-Ion Batteries-Electrochemical Characterization and In Situ Measurements of Heat Generation.

作者信息

Essehli R, Maher K, Amin R, Abouimrane A, Mahmoud Abdelfattah, Muralidharan N, Petla Ramesh Kumar, Yahia H B, Belharouak I

机构信息

Energy and Transportation Science Division, Oak Ridge National Laboratory, Oak Ridge Tennessee 37830, United States.

Qatar Environment and Energy Research Institute (QEERI), Hamad Bin Khalifa University, Qatar Foundation, 34110 Doha, Qatar.

出版信息

ACS Appl Mater Interfaces. 2020 Sep 16;12(37):41765-41775. doi: 10.1021/acsami.0c11616. Epub 2020 Sep 3.

Abstract

Sodium-ion batteries (NaIBs) are increasingly being envisioned for grid-scale energy-storage systems because of cost advantages. However, implementation of this vision has been challenged by the low-energy densities delivered by most NaIB cathodes. Toward addressing this challenge, the authors report the synthesis and characterization of a new iron-doped NaFeVO(PO)F cathode using a novel facile hydrothermal route. The synthesized material was characterized using scanning electron microscopy, X-ray diffraction, and Mössbauer spectroscopy techniques. The obtained discharge capacity in the half-cell configuration lies from 119 to 125 to 130 mA h/g at C/10 while tested using three different electrolyte formulations, dimethyl carbonate-ethylene carbonate (EC)-propylene carbonate (PC), diethyl carbonate-EC, and EC-PC, respectively. The synthesized cathodes were also evaluated in full-cell configurations, which delivered an initial discharge capacity of 80 mA h/g with NaTi(PO)MWCNT as the anode. Ionic diffusivity and interfacial charge transfer kinetics were also evaluated as a function of temperature and sodium concentration, which revealed that electrochemical rate performances in this material were limited by charge-transfer kinetics. To understand the heat generation mechanism of the Na/NaFeVO(PO)F half-cell during charge and discharge processes, an electrochemical isothermal calorimetry measurement was carried out at different current rates for two different temperatures (25 and 45 °C). The results showed that the amount of heat generated was strongly affected by the operating charge/discharge state, C-rate, and temperature. Overall, this work provides a new synthesis route for the development of iron-doped NaFeVO(PO)F-based high-performance sodium cathode materials aimed at providing a viable pathway for the development and deployment of large-scale energy-storage based on sodium battery systems.

摘要

由于成本优势,钠离子电池(NaIBs)越来越被视为适用于电网规模储能系统的选择。然而,这一设想的实现受到了大多数NaIB阴极能量密度较低的挑战。为应对这一挑战,作者报告了一种新型简便水热法合成的铁掺杂NaFeVO(PO)F阴极的合成与表征。使用扫描电子显微镜、X射线衍射和穆斯堡尔光谱技术对合成材料进行了表征。在半电池配置中,使用三种不同的电解质配方,即碳酸二甲酯-碳酸乙烯酯(EC)-碳酸丙烯酯(PC)、碳酸二乙酯-EC和EC-PC进行测试时,在C/10下获得的放电容量分别为119至125至130 mA h/g。合成的阴极也在全电池配置中进行了评估,以NaTi(PO)MWCNT作为阳极时,其初始放电容量为80 mA h/g。还评估了离子扩散率和界面电荷转移动力学随温度和钠浓度的变化,结果表明该材料的电化学速率性能受电荷转移动力学限制。为了解Na/NaFeVO(PO)F半电池在充放电过程中的发热机制,在两个不同温度(25和45°C)下以不同电流速率进行了电化学等温量热测量。结果表明,产生的热量受工作充放电状态、C倍率和温度的强烈影响。总体而言,这项工作为开发基于铁掺杂NaFeVO(PO)F的高性能钠阴极材料提供了一条新的合成路线,旨在为基于钠电池系统的大规模储能的开发和部署提供一条可行的途径。

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