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二硫化钛纳米薄片钠化的电子显微镜研究

Electron Microscopy Investigation of Sodiation of Titanium Disulfide Nanoflakes.

作者信息

Wang Xiuzhen, Yao Zhenpeng, Hwang Sooyeon, Pan Ying, Dong Hui, Fu Maosen, Li Na, Sun Ke, Gan Hong, Yao Yan, Aspuru-Guzik Alán, Xu Qingyu, Su Dong

机构信息

School of Physics , Southeast University , Nanjing 211189 , China.

Center for Functional Nanomaterials , Brookhaven National Laboratory , Upton , New York 11973 , United States.

出版信息

ACS Nano. 2019 Aug 27;13(8):9421-9430. doi: 10.1021/acsnano.9b04222. Epub 2019 Aug 12.

Abstract

Two-dimensional (2D) metal sulfides show great promise for their potential applications as electrode materials of sodium ion-batteries because of the weak interlayer van der Waals interactions, which allow the reversible accommodation and extraction of sodium ions. The sodiation of metal sulfides can undergo a distinct process compared to that of lithiation, which is determined by their metal and structural types. However, the structural and morphological evolution during their electrochemical sodiation is still unclear. Here, we studied the sodiation reaction dynamics of TiS by employing transmission electron microscopy and first-principles calculations. During the sodium-ion intercalation process, we observed multiple intermediate phases (phase II, phase Ib, and phase Ia), different from its lithiation counterpart, with varied sodium occupation sites and interlayer stacking sequences. Further insertion of Na ions prompted a multistep extrusion reaction, which led to the phase separation of Ti metal from the NaS matrix, with its 2D morphology expanded to a 3D morphology. In contrast to regular conversion electrodes, TiS still maintained a compact structure after a full sodiation. First-principles calculations reveal that the as-identified phases are thermodynamically preferred at corresponding intercalation/extrusion stages compared to other possible phases. The present work provides the fundamental mechanistic understanding of the sodiation process of 2D transition metal sulfides.

摘要

二维(2D)金属硫化物因其层间范德华相互作用较弱,有望成为钠离子电池的电极材料,这种弱相互作用使得钠离子能够可逆地嵌入和脱出。与锂化过程相比,金属硫化物的钠化过程可能会经历不同的过程,这取决于它们的金属和结构类型。然而,其电化学钠化过程中的结构和形态演变仍不清楚。在此,我们通过透射电子显微镜和第一性原理计算研究了TiS的钠化反应动力学。在钠离子嵌入过程中,我们观察到多个中间相(II相、Ib相和Ia相),这与锂化过程不同,其钠占据位点和层间堆积序列各不相同。进一步插入钠离子引发了多步挤出反应,导致Ti金属与NaS基体发生相分离,其二维形态扩展为三维形态。与常规转换电极不同,TiS在完全钠化后仍保持紧密结构。第一性原理计算表明,与其他可能的相相比,所确定的相在相应的嵌入/挤出阶段在热力学上更占优势。本工作为二维过渡金属硫化物的钠化过程提供了基本的机理认识。

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