低成本全固态电池用焦绿铁(III)羟基氟化阴极与银汞石Li6PS5Cl固态电解质配对的可行性研究

IF 4.7 4区 材料科学 Q2 ELECTROCHEMISTRY
Jaka Sivavec, Julian F. Baumgärtner, Dragos C. Stoian, Matthias Klimpel, Wouter van Beek, Maksym V. Kovalenko, Kostiantyn V. Kravchyk
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引用次数: 0

摘要

随着对低成本、高能量密度全固态电池的需求持续上升,探索由地球上丰富的元素组成的新型阴极势在必行。具有焦绿石结构的羟基氟化铁(Pyr-IHF)由于其组成元素的丰富自然储量、高能量密度和速率能力而成为极具吸引力的正极材料。在这项工作中,我们探索了Pyr-IHF作为全固态电池正极材料与银矾型Li6PS5Cl (LPSCl)固态电解质配对的可行性。我们的研究结果表明,Pyr-IHF/LPSCl阴极在0.1 C倍率下提供了172 mAh g−1的高初始充电容量,在50次循环后容量保持率约为65%。先进的表征技术,包括聚焦离子束扫描电镜,扫描电镜结合能量色散x射线光谱和x射线吸收光谱,表明在电池制备过程中,Pyr-IHF与LPSCl之间发生了明显的氧化还原反应,导致LPSCl分解产物在电化学循环过程中硫氧化还原产生了显著的容量贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

On the Feasibility of Pairing Pyrochlore Iron(III) Hydroxy Fluoride Cathode with Argyrodite Li6PS5Cl Solid-State Electrolyte for Low-Cost All-Solid-State Batteries

On the Feasibility of Pairing Pyrochlore Iron(III) Hydroxy Fluoride Cathode with Argyrodite Li6PS5Cl Solid-State Electrolyte for Low-Cost All-Solid-State Batteries

On the Feasibility of Pairing Pyrochlore Iron(III) Hydroxy Fluoride Cathode with Argyrodite Li6PS5Cl Solid-State Electrolyte for Low-Cost All-Solid-State Batteries

On the Feasibility of Pairing Pyrochlore Iron(III) Hydroxy Fluoride Cathode with Argyrodite Li6PS5Cl Solid-State Electrolyte for Low-Cost All-Solid-State Batteries

On the Feasibility of Pairing Pyrochlore Iron(III) Hydroxy Fluoride Cathode with Argyrodite Li6PS5Cl Solid-State Electrolyte for Low-Cost All-Solid-State Batteries

As demand for low-cost, high-energy-density all-solid-state batteries continues to rise, exploring novel cathodes composed of earth-abundant elements is imperative. Iron hydroxy fluorides with the pyrochlore structure (Pyr-IHF) emerge as compelling cathode materials due to abundant natural reserves of their constituent elements, high energy density, and rate capability. In this work, we explore the viability of Pyr-IHF as a cathode material in all-solid-state batteries when paired with argyrodite-type Li6PS5Cl (LPSCl) solid-state electrolyte. Our findings show that the Pyr-IHF/LPSCl cathode delivers a high initial charge capacity of 172 mAh g−1 at a 0.1 C rate, with ca. 65 % capacity retention after 50 cycles. Advanced characterization techniques, including focused ion beam-scanning electron microscopy, scanning electron microscopy coupled with energy dispersive X-ray spectroscopy, and X-ray absorption spectroscopy, indicate a pronounced redox reaction between Pyr-IHF and LPSCl upon cell preparation, resulting in significant capacity contributions from the sulfur redox of LPSCl decomposition products during electrochemical cycling.

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来源期刊
CiteScore
8.60
自引率
5.30%
发文量
223
期刊介绍: Electrochemical energy storage devices play a transformative role in our societies. They have allowed the emergence of portable electronics devices, have triggered the resurgence of electric transportation and constitute key components in smart power grids. Batteries & Supercaps publishes international high-impact experimental and theoretical research on the fundamentals and applications of electrochemical energy storage. We support the scientific community to advance energy efficiency and sustainability.
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