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二维范德华材料中的离子插层:原位表征和电化学控制黑磷各向异性热导率。

Ionic Intercalation in Two-Dimensional van der Waals Materials: In Situ Characterization and Electrochemical Control of the Anisotropic Thermal Conductivity of Black Phosphorus.

机构信息

Department of Mechanical and Aerospace Engineering, University of California, Los Angeles , Los Angeles, California 90095, United States.

出版信息

Nano Lett. 2017 Mar 8;17(3):1431-1438. doi: 10.1021/acs.nanolett.6b04385. Epub 2017 Feb 27.

Abstract

Two-dimensional van der Waals materials have shown novel fundamental properties and promise for wide applications. Here, we report for the first time an experimental demonstration of the in situ characterization and highly reversible control of the anisotropic thermal conductivity of black phosphorus. We develop a novel platform based on lithium ion batteries that integrates ultrafast optical spectroscopy and electrochemical control to investigate the interactions between lithium ions and the lattices of the black phosphorus electrode. We discover a strong dependence of the thermal conductivity on battery charge states (lithium concentrations) during the discharge/charge process. The thermal conductivity of black phosphorus is reversibly tunable over a wide range of 2.45-3.86, 62.67-85.80, and 21.66-27.58 W·m·K in the cross-plan, zigzag, and armchair directions, respectively. The modulation in thermal conductivity is attributed to phonon scattering introduced by the ionic intercalation in between the interspacing layers and shows anisotropic phonon scattering mechanism based on semiclassical model. At the fully discharged state (x ∼ 3 in LiP), a dramatic reduction of thermal conductivity by up to 6 times from that of the pristine crystal has been observed. This study provides a unique approach to explore the fundamental energy transport involving lattices and ions in the layered structures and may open up new opportunities in controlling energy transport based on novel operation mechanisms and the rational design of nanostructures.

摘要

二维范德华材料表现出新颖的基本性质,并有望得到广泛应用。在这里,我们首次报告了一种原位表征和高度可逆控制黑磷各向异性热导率的实验演示。我们开发了一种基于锂离子电池的新型平台,将超快光学光谱和电化学控制集成在一起,以研究锂离子与黑磷电极晶格之间的相互作用。我们发现,在放电/充电过程中,热导率与电池的荷电状态(锂离子浓度)之间存在强烈的依赖关系。黑磷的热导率在横向上可在 2.45-3.86、62.67-85.80 和 21.66-27.58 W·m·K 的宽范围内可逆调节,分别在交叉平面、锯齿形和扶手椅方向上。热导率的调制归因于层间层之间的离子插层引起的声子散射,并基于半经典模型显示出各向异性的声子散射机制。在完全放电状态(x ∼ 3 在 LiP 中)下,观察到热导率从原始晶体的 6 倍急剧降低。这项研究提供了一种探索涉及层状结构中晶格和离子的基本能量输运的独特方法,并可能基于新的操作机制和纳米结构的合理设计为控制能量输运开辟新的机会。

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