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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Influence of Electrolyte Composition on the Electrochemical Reaction Mechanism of Bismuth Fluoride Electrode in Fluoride Shuttle Battery
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Influence of Electrolyte Composition on the Electrochemical Reaction Mechanism of Bismuth Fluoride Electrode in Fluoride Shuttle Battery

机译:电解质组合物对氟化氟化电池氟化铋电极电化学反应机理的影响

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Fluoride shuttle battery (FSB) is a promising next-generation battery candidate. In the FSB, metal fluoride and organic solvent containing supporting electrolyte salt and anion acceptor were used as active material and electrolyte. In this study, using bis[2-(2-methoxyethoxy)ethyl] ether (tetraglyme: G4) containing cesium fluoride (CsF; 0.45 mol dm(-3) or saturated) and triphenylboroxine (TPhBX; 0.50 mol dm(-3)) as electrolyte (CsF(0.45)-TPhBX(0.50)-G4 and CsF(sat.)-TPhBX(0.50)-G4), the electrochemical performance of bismuth fluoride (BiF3) was assessed. Although the discharge and charge reactions of BiF3 electrode proceeded in both electrolytes, the cycling performance of BiF3 electrode in CsF(0.45)-TPhBX(0.50)-G4 was poorer than that in CsF(sat.)-TPhBX(0.50)-G4. The cause of differences in the electrochemical properties was investigated using atomic absorption spectrometry (AAS), X-ray photoelectron spectroscopy (XPS), cross-sectional scanning electron microscopy (SEM)/energy dispersive X-ray spectroscopy (EDX). The AAS results indicate that the poor cycling performance with CsF(0.45)-TPhBX(0.50)-G4 was due to the dissolution of active material during charging. The XPS and cross-sectional SEM/EDX results indicate that the formation state of Bi, and the progress of electrolyte decomposition during discharging were affected by the CsF/TPhBX ratio in the electrolyte.
机译:氟化物梭电池(FSB)是一个有前途的下一代电池候选者。在FSB中,使用含有支持电解质盐和阴离子受体的金属氟化物和有机溶剂作为活性材料和电解质。在该研究中,使用含氟化铯(CSF; 0.45mol DM(-3)或饱和的)和三苯基硼氧胺(TPHBX; 0.50mol DM(-3) )作为电解质(CSF(0.45)-TPHBX(0.50)-G4和CSF(饱和) - TPHBX(0.50)-G4),评估氟化铋(BIF 3)的电化学性能。尽管BIF3电极的放电和充电反应在两个电解质中进行,但是在CSF(0.45) - -Thbx(0.50)-G4中的BIF 3电极的循环性能比CSF(SAT。) - TPHBX(0.50)-G4中较差。研究了电化学性质的差异的原因,使用原子吸收光谱法(AAS),X射线光电子能谱(XPS),横截面扫描电子显微镜(SEM)/能量分散X射线光谱(EDX)进行横截面扫描电子显微镜(EDX)。 AAS结果表明,具有CSF(0.45)-TPHBX(0.50)-G4的循环性能差是由于活性物质在充电期间的溶解。 XPS和横截面SEM / EDX结果表明Bi的形成状态,放电过程中的电解质分解的进展受电解质中的CSF / TPHBX比的影响。

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