Co-Sintering of Li1.3Al0.3Ti1.7(PO4)3 and LiFePO4 in Tape-Casted Composite Cathodes for Oxide Solid-State Batteries

IF 4.6 4区 化学 Q2 ELECTROCHEMISTRY Batteries Pub Date : 2023-11-02 DOI:10.3390/batteries9110543
Jean Philippe Beaupain, Katja Waetzig, Henry Auer, Nicolas Zapp, Kristian Nikolowski, Mareike Partsch, Mihails Kusnezoff, Alexander Michaelis
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Abstract

Solid-state batteries (SSBs) with Li-ion conductive electrolytes made from polymers, thiophosphates (sulfides) or oxides instead of liquid electrolytes have different challenges in material development and manufacturing. For oxide-based SSBs, the co-sintering of a composite cathode is one of the main challenges. High process temperatures cause undesired decomposition reactions of the active material and the solid electrolyte. The formed phases inhibit the high energy and power density of ceramic SSBs. Therefore, the selection of suitable material combinations as well as the reduction of the sintering temperatures are crucial milestones in the development of ceramic SSBs. In this work, the co-sintering behavior of Li1.3Al0.3Ti1.7(PO4)3 (LATP) as a solid electrolyte with Li-ion conductivity of ≥0.38 mS/cm and LiFePO4 with a C-coating (LFP) as a Li-ion storage material (active material) is investigated. The shrinkage behavior, crystallographic analysis and microstructural changes during co-sintering at temperatures between 650 and 850 °C are characterized in a simplified model system by mixing, pressing and sintering the LATP and LFP and compared with tape-casted composite cathodes (d = 55 µm). The tape-casted and sintered composite cathodes were infiltrated by liquid electrolyte as well as polyethylene oxide (PEO) electrolyte and electrochemically characterized as half cells against a Li metal anode. The results indicate the formation of reaction layers between LATP and LFP during co-sintering. At Ts > 750 °C, the rhombohedral LATP phase is transformed into an orthorhombic Li1.3+xAl0.3−yFex+yTi1.7−x(PO4)3 (LAFTP) phase. During co-sintering, Fe3+ diffuses into the LATP phase and partially occupies the Al3+ and Ti4+ sites of the NASICON structure. The formation of this LAFTP leads to significant changes in the electrochemical properties of the infiltrated composite tapes. Nevertheless, a high specific capacity of 134 mAh g−1 is measured by infiltrating the sintered composite tapes with liquid electrolytes. Additionally, infiltration with a PEO electrolyte leads to a capacity of 125 mAh g−1. Therefore, the material combination of LATP and LFP is a promising approach to realize sintered ceramic SSBs.
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Li1.3Al0.3Ti1.7(PO4)3和LiFePO4在带铸复合阴极中的共烧结研究
由聚合物、硫代磷酸盐(硫化物)或氧化物代替液体电解质制成的锂离子导电电解质的固态电池(SSBs)在材料开发和制造方面面临着不同的挑战。对于氧化物基固态电池,复合阴极的共烧结是主要挑战之一。较高的工艺温度会导致活性物质和固体电解质发生不希望发生的分解反应。形成的相抑制了陶瓷ssb的高能量和功率密度。因此,选择合适的材料组合以及降低烧结温度是陶瓷ssb发展的关键里程碑。本文研究了Li1.3Al0.3Ti1.7(PO4)3 (LATP)作为锂离子电导率≥0.38 mS/cm的固体电解质和含c涂层的LiFePO4 (LFP)作为锂离子存储材料(活性材料)的共烧结行为。通过混合、压制和烧结LATP和LFP,并与带铸复合阴极(d = 55µm)进行比较,在一个简化的模型系统中表征了在650 ~ 850℃共烧结过程中的收缩行为、晶体学分析和显微组织变化。采用液态电解质和聚氧聚乙烯(PEO)电解质对带铸和烧结复合阴极进行浸渍,并在锂金属阳极上进行了电化学表征。结果表明,在共烧结过程中,LATP和LFP之间形成了反应层。在Ts >750℃时,斜方面体LATP相转变为正交Li1.3+xAl0.3−yFex+yTi1.7−x(PO4)3 (LAFTP)相。在共烧结过程中,Fe3+扩散到LATP相中,部分占据了NASICON结构的Al3+和Ti4+位点。这种LAFTP的形成导致渗透复合带的电化学性能发生显著变化。然而,通过将液体电解质渗透到烧结的复合带中,可以测量到134 mAh g−1的高比容量。此外,PEO电解质的渗透可使电池容量达到125 mAh g−1。因此,LATP和LFP的材料组合是实现烧结陶瓷ssb的一种很有前途的方法。
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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来源期刊
Batteries
Batteries Energy-Energy Engineering and Power Technology
CiteScore
4.00
自引率
15.00%
发文量
217
审稿时长
7 weeks
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