Nanoscale friction varied by isotopic shifting of surface vibrational frequencies

被引:113
作者
Cannara, Rachel J.
Brukman, Matthew J.
Cimatu, Katherine
Sumant, Anirudha V.
Baldelli, Steven
Carpick, Robert W.
机构
[1] Univ Wisconsin, Dept Phys, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Engn Phys, Madison, WI 53706 USA
[3] Univ Houston, Dept Chem, Houston, TX 77004 USA
关键词
D O I
10.1126/science.1147550
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
Friction converts kinetic energy at sliding interfaces into lattice vibrations, but the detailed mechanisms of this process remain unresolved. Atomic force microscopy measurements reveal that changing the mass of the terminating atoms on a surface, and thus their vibrational frequencies, affects nanoscale friction substantially. We compared hydrogen- and deuterium-terminated single-crystal diamond and silicon surfaces, and in all cases the hydrogenated surface exhibited higher friction. This result implies that the lower natural frequency of chemisorbed deuterium reduces the rate at which the tip's kinetic energy is dissipated. This discovery is consistent with a model describing energy transfer to adsorbates from a moving surface.
引用
收藏
页码:780 / 783
页数:4
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