High-Resolution Tracking Asymmetric Lithium Insertion and Extraction and Local Structure Ordering in SnS2

被引:54
作者
Gao, Peng [1 ,2 ]
Wang, Liping [3 ]
Zhang, Yu-Yang [4 ]
Huang, Yuan [5 ]
Liao, Lei [6 ,7 ]
Sutter, Peter [8 ]
Liu, Kaihui [2 ,9 ]
Yu, Dapeng [2 ,9 ]
Wang, En-Ge [2 ,10 ]
机构
[1] Peking Univ, Sch Phys, Electron Microscopy Lab, Beijing 100871, Peoples R China
[2] Collaborat Innovat Ctr Quantum Matter, Beijing 100871, Peoples R China
[3] Univ Elect Sci & Technol China, State Key Lab Elect Thin Films & Integrated Devic, Chengdu 610054, Peoples R China
[4] Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
[5] Brookhaven Natl Lab, Upton, NY 11973 USA
[6] Wuhan Univ, Dept Phys, Wuhan 430072, Peoples R China
[7] Wuhan Univ, Key Lab Artificial Micro & Nanostruct, Minist Educ, Wuhan 430072, Peoples R China
[8] Univ Nebraska, Dept Elect & Comp Engn, Lincoln, NE 68588 USA
[9] Peking Univ, Sch Phys, State Key Lab Mesoscop Phys, Beijing 100871, Peoples R China
[10] Peking Univ, Sch Phys, Int Ctr Quantum Mat, Beijing 100871, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
Lithitim ion battery; in situ TEM; first-principles calculation; intermediate phase; electrochemistry dynamics; IN-SITU OBSERVATION; ELECTROCHEMICAL LITHIATION; CONVERSION REACTION; ELECTRODE MATERIALS; HIGH-CAPACITY; ION; INTERCALATION; HYSTERESIS; COMPOSITE; MECHANISM;
D O I
10.1021/acs.nanolett.6b02136
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the rechargeable lithium ion batteries, the rate capability and energy efficiency are largely governed by the lithium ion transport dynamics and phase transition pathways in electrodes. Real-time and atomic-scale tracking of fully reversible lithium insertion and extraction processes in electrodes, which would ultimately lead to mechanistic understanding of how the electrodes function and why they fail, is highly desirable but very challenging. Here, we track lithium insertion and extraction in the van der Waals interactions dominated SnS2 by in situ high-resolution TEM method. We find that the lithium insertion occurs via a fast two-phase reaction to form expanded and defective LiSnS2, while the lithium extraction initially involves heterogeneous nucleation of intermediate superstructure Li0.5SnS2 domains with a 14 nm size. Density functional theory calculations indicate that the Li0.5SnS2 is kinetically favored and structurally stable. The asymmetric reaction pathways may supply enlightening insights into the mechanistic understanding of the underlying electrochemistry in the layered electrode materials and also suggest possible alternatives to the accepted explanation of the origins of voltage hysteresis in the intercalation electrode materials.
引用
收藏
页码:5582 / 5588
页数:7
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