材料科学
范德瓦尔斯力
拉曼光谱
铟
插层(化学)
纳米技术
石墨烯
纳米线
化学气相沉积
纳米尺度
化学物理
光电子学
无机化学
分子
化学
光学
物理
有机化学
作者
Ryusuke Natsui,Hiroshi Shimizu,Yusuke Nakanishi,Zheng Liu,Akito Shimamura,Nguyen Tuan Hung,Yung-Chang Lin,Takahiko Endo,Jiang Pu,Iori Kikuchi,Taishi Takenobu,Susumu Okada,Kazu Suenaga,Riichiro Saito,Yasumitsu Miyata
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-02-23
卷期号:17 (6): 5561-5569
被引量:1
标识
DOI:10.1021/acsnano.2c10997
摘要
One-dimensional (1D) conducting materials are of great interest as potential building blocks for integrated nanocircuits. Ternary 1D transition-metal chalcogenides, consisting of M6X6 wires with intercalated A atoms (M = Mo or W; X = S, Se, or Te; A = alkali or rare metals, etc.), have attracted much attention due to their 1D metallic behavior, superconductivity, and mechanical flexibility. However, the conventional solid-state reaction usually produces micrometer-scale bulk crystals, limiting their potential use as nanoscale conductors. Here we demonstrate a versatile method to fabricate indium (In)-intercalated W6Te6 (In–W6Te6) bundles with a nanoscale thickness. We first prepared micrometer-long, crystalline bundles of van der Waals W6Te6 wires using chemical vapor deposition and intercalated In into the crystal via a vapor-phase reaction. Atomic-resolution electron microscopy revealed that In atoms were surrounded by three adjacent W6Te6 wires. First-principles calculations suggested that their wire-by-wire stacking can transform through postgrowth intercalation. Individual In–W6Te6 bundles exhibited metallic behavior, as theoretically predicted. We further identified the vibrational modes by combining polarized Raman spectroscopy and nonresonant Raman calculations.
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