单层
材料科学
锂(药物)
插层(化学)
扫描透射电子显微镜
储能
纳米技术
透射电子显微镜
基质(水族馆)
原子单位
双层
光电发射电子显微术
化学物理
化学工程
无机化学
电子显微镜
膜
化学
光学
内分泌学
功率(物理)
工程类
地质学
物理
海洋学
医学
量子力学
生物化学
作者
Seung‐Ho Yu,Michael J. Zachman,Kibum Kang,Hui Gao,Xin Huang,Francis J. DiSalvo,Jiwoong Park,Lena F. Kourkoutis,Héctor D. Abruña
标识
DOI:10.1002/aenm.201902773
摘要
Abstract While lithium ion batteries with electrodes based on intercalation compounds have dominated the portable energy storage market for decades, the energy density of these materials is fundamentally limited. Today, rapidly growing demand for this type of energy storage is driving research into materials that utilize alternative reaction mechanisms to enable higher energy densities. Transition metal compounds are one such class of materials, with storage enabled by “conversion” reactions, where the material is converted to new compound upon lithiation. MoS 2 is one example of this type of material that has generated a large amount of interest recently due to its high theoretical lithium storage capacity compared to graphite. Here, cryogenic scanning transmission electron microscopy techniques are used to reveal the atomic‐scale processes that occur during reaction of a model monolayer MoS 2 system by enabling the unaltered atomic structure to be determined at various levels of lithiation. It is revealed that monolayer MoS 2 can undergo a conversion reaction even with no substrate, and that the resulting particles are smaller than those that form in bulk MoS 2 , likely due to the more limited 2D diffusion. Additionally, while bilayer MoS 2 undergoes intercalation with a corresponding phase transition before conversion, monolayer MoS 2 does not.
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