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Generating giant and tunable nonlinearity in a macroscopic mechanical resonator from a single chemical bond

Nonlinearity in macroscopic mechanical systems may lead to abundant phenomena for fundamental studies and potential applications. However, it is difficult to generate nonlinearity due to the fact that macroscopic mechanical systems follow Hooke's law and respond linearly to external force, unle...

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Detalles Bibliográficos
Autores principales: Huang, Pu, Zhou, Jingwei, Zhang, Liang, Hou, Dong, Lin, Shaochun, Deng, Wen, Meng, Chao, Duan, Changkui, Ju, Chenyong, Zheng, Xiao, Xue, Fei, Du, Jiangfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894958/
https://www.ncbi.nlm.nih.gov/pubmed/27225287
http://dx.doi.org/10.1038/ncomms11517
Descripción
Sumario:Nonlinearity in macroscopic mechanical systems may lead to abundant phenomena for fundamental studies and potential applications. However, it is difficult to generate nonlinearity due to the fact that macroscopic mechanical systems follow Hooke's law and respond linearly to external force, unless strong drive is used. Here we propose and experimentally realize high cubic nonlinear response in a macroscopic mechanical system by exploring the anharmonicity in chemical bonding interactions. We demonstrate the high tunability of nonlinear response by precisely controlling the chemical bonding interaction, and realize, at the single-bond limit, a cubic elastic constant of 1 × 10(20) N m(−3). This enables us to observe the resonator's vibrational bi-states transitions driven by the weak Brownian thermal noise at 6 K. This method can be flexibly applied to a variety of mechanical systems to improve nonlinear responses, and can be used, with further improvements, to explore macroscopic quantum mechanics.