AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (7.7 MB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Research Article | Open Access

Kinetically-controlled wafer-scale synthesis of quasi-one-dimensional W6Te6 via a WS2 template anion-exchange strategy

Mingzhu Xu1Shuangquan Qu1,2Mengting Huang1Yiming Ding1Binbin Zhang1Shibo Wang1Wenlei Fu1Shiqi Yang3,4Huixia Yang1Yu Zhang1,5Yuanxiao Ma1Yu Ye3Ruiwen Shao2Xiaolong Xu1 ( )Yeliang Wang1 ( )
School of Integrated Circuits and Electronics, MIIT Key Laboratory for Low-Dimensional Quantum Structure and Devices, Beijing Institute of Technology, Beijing 100081, China
Beijing Advanced Innovation Center for Intelligent Robots and Systems, School of Medical Technology, Beijing Institute of Technology, Beijing 100081, China
State Key Laboratory for Mesoscopic Physics and Frontiers Science Center for Nano-optoelectronics, School of Physics, Peking University, Beijing 100871, China
School of Physics and Optoelectronic Engineering, Beijing University of Technology, Beijing 100124, China
Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing 100081, China
Show Author Information

Abstract

Quasi-one-dimensional (quasi-1D) van der Waals (vdW) materials represent an emerging frontier in nanoscience, yet the synthesis of their metastable phases remains a significant challenge, as exemplified by W6Te6, whose formation is precluded by the thermodynamically favored growth of the stable WTe2 phase. Here, we report a robust, kinetically-controlled anion-exchange (KCAE) strategy, involving a two-step process: A sputtered tungsten (W) film is converted into a stable, vertically-grained 2H-WS2 template, followed by controlled tellurization. The high activation energy required to break the W–S bonds acts as a kinetic barrier that inhibits the formation of the WTe2 phase, enabling the precise isolation of the metastable W6Te6 phase. Mechanistic studies indicate that the conversion initiates via heterogeneous nucleation at the exposed edges of the vertical WS2 grains. This KCAE framework enables the first-ever synthesis of uniform, 1-inch wafer-scale W6Te6 films. Furthermore, this template-based method is fully compatible with standard photolithography, allowing for the pre-patterning of complex W6Te6 nanostructures. Our work establishes a generalizable platform for the wafer-scale synthesis of metastable vdW materials previously inaccessible by conventional methods.

Graphical Abstract

This work introduces a kinetically-controlled anion-exchange (KCAE) strategy that utilizes a vertically-oriented 2H-WS2 film as a template to selectively synthesize the metastable W6Te6 phase, achieving the wafer-scale synthesis of uniform W6Te6 films.

Electronic Supplementary Material

Download File(s)
8711_ESM.pdf (825.8 KB)

References

【1】
【1】
 
 
Nano Research
Article number: 94908711

{{item.num}}

Comments on this article

Go to comment

< Back to all reports

Review Status: {{reviewData.commendedNum}} Commended , {{reviewData.revisionRequiredNum}} Revision Required , {{reviewData.notCommendedNum}} Not Commended Under Peer Review

Review Comment

Close
Close
Cite this article:
Xu M, Qu S, Huang M, et al. Kinetically-controlled wafer-scale synthesis of quasi-one-dimensional W6Te6 via a WS2 template anion-exchange strategy. Nano Research, 2026, 19(9): 94908711. https://doi.org/10.26599/NR.2026.94908711
Topics:

382

Views

65

Downloads

0

Crossref

0

Web of Science

0

Scopus

0

CSCD

Received: 14 January 2026
Revised: 09 March 2026
Accepted: 06 April 2026
Published: 04 July 2026
© The Author(s) 2026. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).