石墨烯
氮化硼
原子单位
六方氮化硼
分子动力学
原子力显微镜
化学物理
硼
共价键
凝聚态物理
材料科学
化学
纳米技术
计算化学
物理
有机化学
量子力学
作者
Da Wu,Zhengpu Zhao,Bo Lin,Yizhi Song,Jiajie Qi,Jian Jiang,Z. X. Yuan,Bowei Cheng,Mengze Zhao,Ye Tian,Zhichang Wang,Muhong Wu,Ke Bian,Kaihui Liu,Limei Xu,Xiao Cheng Zeng,Enge Wang,Ying Jiang
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2024-06-13
卷期号:384 (6701): 1254-1259
标识
DOI:10.1126/science.ado1544
摘要
Low-dimensional water transport can be drastically enhanced under atomic-scale confinement. However, its microscopic origin is still under debate. In this work, we directly imaged the atomic structure and transport of two-dimensional water islands on graphene and hexagonal boron nitride surfaces using qPlus-based atomic force microscopy. The lattice of the water island was incommensurate with the graphene surface but commensurate with the boron nitride surface owing to different surface electrostatics. The area-normalized static friction on the graphene diminished as the island area was increased by a power of ~-0.58, suggesting superlubricity behavior. By contrast, the friction on the boron nitride appeared insensitive to the area. Molecular dynamic simulations further showed that the friction coefficient of the water islands on the graphene could reduce to <0.01.
科研通智能强力驱动
Strongly Powered by AbleSci AI