Radtke Mariusz, Hess Christian
Eduard Zintl Institute of Inorganic and Physical Chemistry, Technical University of Darmstadt, Darmstadt, Germany.
Front Chem. 2022 Oct 21;10:1038327. doi: 10.3389/fchem.2022.1038327. eCollection 2022.
In this study we report an affordable synthesis and preparation of an electrochemically exfoliated few-layer 2-dimensional (2D) SnS anode material of high cycling durability and demonstrate its performance on the example of alkali metal batteries. The metalation mechanism consists of highly unusual and previously only speculated Sn (III)-state grasped by Raman spectroelectrochemistry aided by symmetry analysis. The prepared 2D material flakes were characterized by high resolution transmission electron microscopy, X-ray photoelectron and Raman spectroscopies. The Raman spectroelectrochemistry was chosen as a dedicated tool for the investigation of alkali-metal-ion intercalation (Li, Na, K), whereby the distortion of the A Raman active mode (out-of-plane S-Sn-S vibration) during battery charging exhibited a substantial dependence on the electrochemically applied potential. As a result of the structural dynamics a considerable Raman red-shift of 17.6 cm was observed during metalation. Linewidth changes were used to evaluate the expansion caused by metalation, which in case of sodium and potassium were found to be minimal compared to lithium. Based on the spectroscopic and electrochemical results, a mechanism for the de-/intercalation of lithium, sodium and potassium is proposed which includes alloying in few-layer 2D SnS materials and the generation of point-defects.
在本研究中,我们报告了一种经济实惠的合成方法,用于制备具有高循环耐久性的电化学剥离少层二维(2D)SnS负极材料,并以碱金属电池为例展示了其性能。金属化机制包括通过对称性分析辅助的拉曼光谱电化学掌握的高度不寻常且此前仅为推测的Sn(III)状态。制备的二维材料薄片通过高分辨率透射电子显微镜、X射线光电子能谱和拉曼光谱进行了表征。拉曼光谱电化学被选为研究碱金属离子嵌入(Li、Na、K)的专用工具,其中电池充电过程中A拉曼活性模式(面外S-Sn-S振动)的畸变表现出对电化学施加电位的显著依赖性。由于结构动力学,在金属化过程中观察到17.6 cm的显著拉曼红移。线宽变化用于评估金属化引起的膨胀,发现钠和钾的膨胀与锂相比最小。基于光谱和电化学结果,提出了锂、钠和钾的脱嵌/嵌入机制,其中包括在少层二维SnS材料中的合金化和点缺陷的产生。