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Hauptverfasser: Xue, Chaowu, Sun, Mengzhao, Zhou, Zixuan, Yao, Zhuoran, Shen, Li-Qun, Kong, Xiao, Zhao, Honglong, Ding, Feng, Willinger, Marc, Liu, Zhongkai, Wang, Zhu-Jun
Format: Preprint
Veröffentlicht: 2026
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Online-Zugang:https://arxiv.org/abs/2604.15639
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author Xue, Chaowu
Sun, Mengzhao
Zhou, Zixuan
Yao, Zhuoran
Shen, Li-Qun
Kong, Xiao
Zhao, Honglong
Ding, Feng
Willinger, Marc
Liu, Zhongkai
Wang, Zhu-Jun
author_facet Xue, Chaowu
Sun, Mengzhao
Zhou, Zixuan
Yao, Zhuoran
Shen, Li-Qun
Kong, Xiao
Zhao, Honglong
Ding, Feng
Willinger, Marc
Liu, Zhongkai
Wang, Zhu-Jun
contents Twisted graphene layers (TGLs) provide a powerful platform for investigating multiple quantum phenomena, yet their scalable deployment is hindered by the lack of reliable synthesis with precise angle. Here, benefited from a deeper understanding of the interplay between grain index and graphene growth kinetics, we report a scalable strategy to grow TGLs with pre-designed twist angles on platinum (Pt) via chemical vapor deposition (CVD), Through a combination of complementary in situ methods, we identified the activity sequence of different Pt grains and attributed it to the area ratio of exposed (110) facets during graphene-induced surface reconstruction. Moreover, we revealed that CVD-grown graphene orientation is determined by the grain-orientation-dependent surface morphology. By leveraging the so-established correlations between grain index with both graphene growth priority and its orientation, we achieve controlled folding and tearing of graphene overlayer using a pair of adjacent grains with dramatically different catalytical activity and kink-free atomic steps. We reveal that overlayer-induced step bunching and terrace reconfiguration critically govern the domain morphology and folding direction. Building on this mechanistic insight, we demonstrate a substrate-engineering framework where specific platinum grains are rationally selected to yield TGLs with pre-designed twist angles, including magic angle with flat band dispersion. This work not only highlights fundamental kinetics of Pt catalyzed graphene CVD growth, but also offers a generalizable methodology for manipulating foldable two-dimensional materials via dynamic substrate reconstruction, exampled by programmable growth of high-quality TGLs on open surfaces.
format Preprint
id arxiv_https___arxiv_org_abs_2604_15639
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Facet-dependent Chemical Kinetics Governed Growth of Twisted Graphene Layers with Pre-designed Angles
Xue, Chaowu
Sun, Mengzhao
Zhou, Zixuan
Yao, Zhuoran
Shen, Li-Qun
Kong, Xiao
Zhao, Honglong
Ding, Feng
Willinger, Marc
Liu, Zhongkai
Wang, Zhu-Jun
Materials Science
Chemical Physics
Twisted graphene layers (TGLs) provide a powerful platform for investigating multiple quantum phenomena, yet their scalable deployment is hindered by the lack of reliable synthesis with precise angle. Here, benefited from a deeper understanding of the interplay between grain index and graphene growth kinetics, we report a scalable strategy to grow TGLs with pre-designed twist angles on platinum (Pt) via chemical vapor deposition (CVD), Through a combination of complementary in situ methods, we identified the activity sequence of different Pt grains and attributed it to the area ratio of exposed (110) facets during graphene-induced surface reconstruction. Moreover, we revealed that CVD-grown graphene orientation is determined by the grain-orientation-dependent surface morphology. By leveraging the so-established correlations between grain index with both graphene growth priority and its orientation, we achieve controlled folding and tearing of graphene overlayer using a pair of adjacent grains with dramatically different catalytical activity and kink-free atomic steps. We reveal that overlayer-induced step bunching and terrace reconfiguration critically govern the domain morphology and folding direction. Building on this mechanistic insight, we demonstrate a substrate-engineering framework where specific platinum grains are rationally selected to yield TGLs with pre-designed twist angles, including magic angle with flat band dispersion. This work not only highlights fundamental kinetics of Pt catalyzed graphene CVD growth, but also offers a generalizable methodology for manipulating foldable two-dimensional materials via dynamic substrate reconstruction, exampled by programmable growth of high-quality TGLs on open surfaces.
title Facet-dependent Chemical Kinetics Governed Growth of Twisted Graphene Layers with Pre-designed Angles
topic Materials Science
Chemical Physics
url https://arxiv.org/abs/2604.15639