TY - JOUR
T1 - Multistep Lithiation of Tin Sulfide
T2 - An Investigation Using in Situ Electron Microscopy
AU - Hwang, Sooyeon
AU - Yao, Zhenpeng
AU - Zhang, Lei
AU - Fu, Maosen
AU - He, Kai
AU - Mai, Liqiang
AU - Wolverton, Chris
AU - Su, Dong
N1 - Funding Information:
Electron microscopy work was performed at the Center for Functional Nanomaterials, Brookhaven National Laboratory, which is supported by the U.S. Department of Energy (DOE), Office of Basic Energy Science, under contract DE-SC0012704. DFT calculations were supported by the Center for Electrochemical Energy Science, an Energy Frontier Research Center funded by the US Department of Energy, Office of Science, Office of Basic Energy Sciences under award number DEAC02-06CH11357. We thank Dr. Peng Gao for helpful discussion.
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/4/24
Y1 - 2018/4/24
N2 - Two-dimensional (2D) metal sulfides have been widely explored as promising electrodes for lithium-ion batteries since their two-dimensional layered structure allows lithium ions to intercalate between layers. For tin disulfide, the lithiation process proceeds via a sequence of three different types of reactions: intercalation, conversion, and alloying, but the full scenario of reaction dynamics remains nebulous. Here, we investigate the dynamical process of the multistep reactions using in situ electron microscopy and discover the formation of an intermediate rock-salt phase with the disordering of Li and Sn cations after initial 2D intercalation. The disordered cations occupy all the octahedral sites and block the channels for intercalation, which alter the reaction pathways during further lithiation. Our first-principles calculations of the nonequilibrium lithiation of SnS2 corroborate the energetic preference of the disordered rock-salt structure over known layered polymorphs. The in situ observations and calculations suggest a two-phase reaction nature for intercalation, disordering, and following conversion reactions. In addition, in situ delithiation observation confirms that the alloying reaction is reversible, while the conversion reaction is not, which is consistent with the ex situ analysis. This work reveals the full lithiation characteristic of SnS2 and sheds light on the understanding of complex multistep reactions in 2D materials.
AB - Two-dimensional (2D) metal sulfides have been widely explored as promising electrodes for lithium-ion batteries since their two-dimensional layered structure allows lithium ions to intercalate between layers. For tin disulfide, the lithiation process proceeds via a sequence of three different types of reactions: intercalation, conversion, and alloying, but the full scenario of reaction dynamics remains nebulous. Here, we investigate the dynamical process of the multistep reactions using in situ electron microscopy and discover the formation of an intermediate rock-salt phase with the disordering of Li and Sn cations after initial 2D intercalation. The disordered cations occupy all the octahedral sites and block the channels for intercalation, which alter the reaction pathways during further lithiation. Our first-principles calculations of the nonequilibrium lithiation of SnS2 corroborate the energetic preference of the disordered rock-salt structure over known layered polymorphs. The in situ observations and calculations suggest a two-phase reaction nature for intercalation, disordering, and following conversion reactions. In addition, in situ delithiation observation confirms that the alloying reaction is reversible, while the conversion reaction is not, which is consistent with the ex situ analysis. This work reveals the full lithiation characteristic of SnS2 and sheds light on the understanding of complex multistep reactions in 2D materials.
KW - density functional theory
KW - in situ transmission electron microscopy
KW - lithium-ion batteries
KW - multistep lithiation
KW - tin disulfide
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U2 - 10.1021/acsnano.8b00758
DO - 10.1021/acsnano.8b00758
M3 - Article
C2 - 29613765
AN - SCOPUS:85045918456
SN - 1936-0851
VL - 12
SP - 3638
EP - 3645
JO - ACS nano
JF - ACS nano
IS - 4
ER -