Switchable friction enabled by nanoscale self-assembly on graphene

被引:72
作者
Gallagher, Patrick [1 ]
Lee, Menyoung [1 ]
Amet, Francois [2 ,3 ]
Maksymovych, Petro [4 ]
Wang, Jun [4 ]
Wang, Shuopei [5 ]
Lu, Xiaobo [5 ]
Zhang, Guangyu [5 ]
Watanabe, Kenji [6 ]
Taniguchi, Takashi [6 ]
Goldhaber-Gordon, David [1 ]
机构
[1] Stanford Univ, Dept Phys, Stanford, CA 94305 USA
[2] Duke Univ, Dept Phys, Durham, NC 27708 USA
[3] Appalachian State Univ, Dept Phys & Astron, Boone, NC 28608 USA
[4] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
[5] Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
[6] Natl Inst Mat Sci, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan
基金
中国国家自然科学基金;
关键词
ATOMIC-FORCE MICROSCOPY; HEXAGONAL BORON-NITRIDE; MONOLAYER GRAPHENE; WATER INTERFACE; ANISOTROPY; DOMAINS; ORGANIZATION; SULFATE; SURFACE; AIR;
D O I
10.1038/ncomms10745
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Graphene monolayers are known to display domains of anisotropic friction with twofold symmetry and anisotropy exceeding 200%. This anisotropy has been thought to originate from periodic nanoscale ripples in the graphene sheet, which enhance puckering around a sliding asperity to a degree determined by the sliding direction. Here we demonstrate that these frictional domains derive not from structural features in the graphene but from self-assembly of environmental adsorbates into a highly regular superlattice of stripes with period 4-6 nm. The stripes and resulting frictional domains appear on monolayer and multilayer graphene on a variety of substrates, as well as on exfoliated flakes of hexagonal boron nitride. We show that the stripe-superlattices can be reproducibly and reversibly manipulated with submicrometre precision using a scanning probe microscope, allowing us to create arbitrary arrangements of frictional domains within a single flake. Our results suggest a revised understanding of the anisotropic friction observed on graphene and bulk graphite in terms of adsorbates.
引用
收藏
页数:7
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