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High-Voltage Stability in KFSI Nonaqueous Carbonate Solutions for Potassium-Ion Batteries: Current Collectors and Coin-Cell Components

机译:KFSI非水碳酸盐溶液中的高压稳定性 - 用于钾离子电池:集电器和硬币细胞组分

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摘要

Cu, Al, and 316L stainless steel are the main components of the current collectors and coin-type cells used in the characterization of potassium-ion battery (KIB) materials and are expected to be electrochemically inactive. Herein, their electrochemical stabilities in a nonaqueous potassium-bis-(fluorosulfonyl)imide (KFSI)-based electrolyte are investigated. In dynamic- and transient-mode polarization, passivation of each metal is observed to occur below 3.9, 3.8, and 4.05 V versus K+/K for Cu, Al, and 316L stainless steel, respectively, which are considered the threshold potentials. The composition of the passive layers of each metal is determined using time-of-flight secondary-ion mass spectrometry. The passive layers of Cu and Al consist of Cu-O (CuO or Cu2O) and Al-O (Al2O3), respectively, and 316L stainless steel is passivated with an outermost Cr-F (CrF3) layer and an inner Cr-O (Cr2O3) layer. Above the threshold potentials, however, severe corrosion of each metal occurs accompanied by the dissolution of metal ions, which could affect the reliability of experimental results for KIBs using KFSI-based electrolytes.
机译:Cu,Al和316L不锈钢是用于钾离子电池(KIB)材料表征的集电器和硬币型电池的主要组成部分,并且预期电化学无效。在此,研究了它们在非水钾 - 双(氟磺酰基)酰亚胺(KFSI)基电解质中的电化学稳定性。在动态和瞬态模式极化中,观察到每种金属的钝化分别观察到Cu,Al和316L不锈钢的3.9,3.8和4.05 V而不是K + / K,这被认为是阈值电位。使用飞行时间二次离子质谱法测定每种金属的被动层的组成。 Cu和Al的被动层分别由Cu-O(CuO或Cu 2 O)和Al-O(Al 2 O 3)组成,并且316L不锈钢钝化,其中最外层CR-F(CRF3)层和内部CR-O( CR2O3)层。然而,在阈值电位之上,每种金属的严重腐蚀伴随金属离子的溶解,这可能影响使用基于KFSI的电解质的KIB的实验结果的可靠性。

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