Synthesizing glassy materials using LiMn2O4 as cathode powder from Li-ion batteries and P2O5

José A. Jiménez
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Abstract

The making of glasses using lithium manganese(III,IV) oxide as cathode-active material of lithium-ion batteries and phosphorus pentoxide as glass former is herein reported for the first time. The raw materials LiMn2O4 and P2O5 were mixed in various proportions and melted in ambient atmosphere directed by xLiMn2O4-(100 − x)P2O5 with x = 15 mol%, 20 mol%, 25 mol%, 30 mol% and 35 mol% nominal compositions. The materials obtained were subsequently characterized by X-ray diffraction (XRD), density, Fourier-transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), optical absorption, and photoluminescence (PL) spectroscopy measurements with decay kinetics analysis. The XRD data supported vitrification in the explored compositional range wherein the density tended to increase with LiMn2O4 concentration. The FT-IR spectra indicated that adding LiMn2O4 at the expense of P2O5 leads to a network depolymerization effect evidenced largely by the upsurge of the vas(PO32) band of end-of-chain PO4 tetrahedra. DSC results showed that the glass transition temperature increased steadily while glass stability decreased with increasing LiMn2O4 content. The optical absorption measurements showed increasingly the presence of both Mn2+ and Mn3+ ions leading to the development of intense purple hues consistent with LiMn2O4 decomposition in the melts. The PL assessment then scrutinized the manifestation of red-emitting Mn2+ ions wherein an emission suppression trend was observed. The decay dynamics evaluation revealed the shortening of the Mn2+ decay times harmonizing with the PL quenching effect. The original work carried out stimulates additional research regarding the potential of vitrification with P2O5 for the management or upcycling of lithium battery components.

Abstract Image

以锂离子电池正极粉LiMn2O4和P2O5合成玻璃材料
本文首次报道了用锰酸锂(III,IV)氧化物作为锂离子电池的阴极活性材料,五氧化二磷作为玻璃原体制备玻璃的方法。采用xLiMn2O4-(100−x)P2O5 (x = 15 mol%、20 mol%、25 mol%、30 mol%和35 mol%标称成分),将原料LiMn2O4和P2O5按不同比例混合,在常温下熔化。随后通过x射线衍射(XRD)、密度、傅里叶变换红外(FT-IR)光谱、差示扫描量热(DSC)、光吸收和光致发光(PL)光谱测量和衰变动力学分析对所获得的材料进行了表征。XRD数据支持在所探索的组成范围内的玻璃化现象,其密度随LiMn2O4浓度的增加而增加。FT-IR光谱表明,以P2O5为代价加入LiMn2O4会导致网络解聚效应,这主要表现在PO4四面体链端vas(PO32−)带的增加。DSC结果表明,随着LiMn2O4含量的增加,玻璃化转变温度稳步升高,玻璃化稳定性下降。光学吸收测量表明,Mn2+和Mn3+离子的存在越来越多,导致熔体中出现与LiMn2O4分解一致的强烈紫色色调。然后,PL评估仔细检查了红色发射Mn2+离子的表现,其中观察到发射抑制趋势。衰减动力学评价表明,Mn2+的衰减时间缩短与PL猝灭效应相一致。最初的工作激发了更多关于P2O5玻璃化在锂电池组件管理或升级回收方面的潜力的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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