The authors present a theoretical model to predict the resonance frequency shift due to molecule adsorption on micro- and nanocantilevers. They calculate the frequency shift experienced by cantilevers made of either silicon or the polymer SU-8, when two adsorbates, myosin protein and an alkanethiol, are attached to the cantilever surface. They demonstrate that the effect of the adsorbate stiffness can be comparable or even larger than the mass effect, producing positive frequency shifts. The results provide methods for decoupling both opposite effects and routes for the design of resonators with high sensitivity to molecule adsorption based on either stiffness or mass effects.

We report the selective excitation of the flexural modes of microcantilevers in aqueous solutions, by applying the photothermal excitation technique. The experiments show that a particular vibration mode can be efficiently excited by focusing the intensity-modulated laser beam on regions of high curvature of the vibration shape. In addition, the resulting resonant peaks in liquid appear distorted by an amplitude component that decreases with the frequency. This distortion produces a shift of the resonance to lower frequencies. A theoretical model based on the transformation of optical energy into mechanical energy via an intermediate thermal stage is proposed to interpret the experimental results. The theory shows that the driven oscillation of the cantilever depends on the curvature of the eigenmode at the excitation position and the heating induced by the excitation laser, which decreases with the frequency. The results reported here set the basis for efficient excitation of high vibration modes in liquids and for optimized design of optically driven microresonators.