CO2-Selective Nanoporous Metal-Organic Framework Microcantilevers.

Nanoporous anodic aluminum oxide (AAO) microcantilevers are fabricated and MIL-53 (Al) metal-organic framework (MOF) layers are directly synthesized on each cantilever surface by using the aluminum oxide as the metal ion source. Exposure of the MIL53-AAO cantilevers to various concentrations of CO2, N2, CO, and Ar induces changes in their deflections and resonance frequencies. The results of the resonance frequency measurements for the different adsorbed gas molecules are almost identical when the frequency changes are normalized by the molecular weights of the gases. In contrast, the deflection measurements show that only CO2 adsorption induces substantial bending of the MIL53-AAO cantilevers. This selective deflection of the cantilevers is attributed to the strong interactions between CO2 and the hydroxyl groups in MIL-53, which induce structural changes in the MIL-53 layers. Simultaneous measurements of the resonance frequency and the deflection are performed to show that the diffusion of CO2 into the nanoporous MIL-53 layers occurs very rapidly, whereas the binding of CO2 to hydroxyl groups occurs relatively slowly, which indicates that the adsorption of CO2 onto the MIL-53 layers and the desorption of CO2 from the MIL-53 layers are reaction limited.

Adsorption and desorption characteristics of alcohol vapors on a nanoporous ZIF-8 film investigated using silicon microcantilevers.

Zinc oxide nanorods were synthesized directly on a silicon microcantilever and converted into a nanoporous ZIF-8 film via a solvothermal reaction. The simultaneous measurements of the resonance frequency and deflection of the cantilever revealed that the adsorption of alcohol vapors induced a structural change in the ZIF-8 framework.

Communication: anti-icing characteristics of superhydrophobic surfaces investigated by quartz crystal microresonators.

We investigated the anti-icing characteristics of superhydrophobic surfaces with various morphologies by using quartz crystal microresonators. Anodic aluminum oxide (AAO) or ZnO nanorods were synthesized directly on gold-coated quartz crystal substrates and their surfaces were rendered hydrophobic via chemical modifications with octyltrichlorosilane (OTS), octadecyltrichlorosilane (ODS), or octadecanethiol (ODT). Four different hydrophobic nanostructures were prepared on the quartz crystals: ODT-modified hydrophobic plain gold (C18-Au), an OTS-modified AAO nanostructure (C8-AAO), an ODS-modified AAO nanostructure (C18-AAO), and ODT-modified ZnO nanorods (C18-ZnO). The water contact angles on the C18-Au, C8-AAO, C18-AAO, and C18-ZnO surfaces were measured to be 91.4°, 147.2°, 156.3°, and 157.8°, respectively. A sessile water droplet was placed on each quartz crystal and its freezing temperature was determined by monitoring the drastic changes in the resonance frequency and Q-factor upon freezing. The freezing temperature of a water droplet was found to decrease with decreases in the water contact radius due to the decreases in the number of active sites available for ice nucleation.

Characterization of underwater stability of superhydrophobic surfaces using quartz crystal microresonators.

We synthesized porous aluminum oxide nanostructures directly on a quartz crystal microresonator and investigated the properties of superhydrophobic surfaces, including the surface wettability, water permeation, and underwater superhydrophobic stability. After increasing the pore diameter to 80 nm (AAO80), a gold film was deposited onto the AAO80 membrane, and the pore entrance size was reduced to 30 nm (AAO30). The surfaces of the AAO80 and AAO30 were made to be hydrophobic through chemical modification by incubation with octadecanethiol (ODT) or octadecyltrichlorosilane (OTS), which produced three different types of superhydrophobic surfaces on quartz microresonators: OTS-modified AAO80 (OTS-AAO80), ODT-modified AAO30 (ODT-AAO30), and ODT-OTS-modified AAO30 (TS-AAO30). The loading of a water droplet onto a microresonator or the immersion of a resonator into water induced changes in the resonance frequency that corresponded to the water permeation into the nanopores. TS-AAO30 exhibited the best performance, with a low degree of water permeation, and a high stability. These features were attributed to the presence of sealed air pockets and the narrow pore entrance diameter.

Photoacoustic spectroscopy of surface adsorbed molecules using a nanostructured coupled resonator array.

A rapid method of obtaining photoacoustic spectroscopic signals for trace amounts of surface adsorbed molecules using a nanostructured coupled resonator array is described. Explosive molecules adsorbed on a nanoporous anodic aluminum oxide cantilever, which has hexagonally ordered nanowells with diameters and well-to-well distances of 35 nm and 100 nm, respectively, are excited using pulsed infrared (IR) light with a frequency matching the common mode resonance frequency of the coupled resonator. The common mode resonance amplitudes of the coupled resonator as a function of illuminating IR wavelength present a photoacoustic IR absorption spectrum representing the chemical signatures of the adsorbed explosive molecules. In addition, the mass of the adsorbed molecules as an orthogonal signal for quantitative analysis is determined by measuring the variation of the localized, individual mode resonance frequency of a cantilever on the array. The limit of detection of the ternary mixture of explosive molecules (1:1:1 of trinitrotoluene (TNT), cyclotrimethylene trinitramine (RDX) and pentaerythritol tetranitrate (PETN)) is estimated to be ~ 100 ng cm(-2). These multi-modal signals enable us to perform quantitative and rapid chemical sensing and analysis in ambient conditions.

Electronic nose based on multipatterns of ZnO nanorods on a quartz resonator with remote electrodes.

An electrodeless monolithic multichannel quartz crystal microbalance (MQCM) sensor was developed via the direct growth of ZnO nanorod patterns of various sizes onto an electrodeless quartz crystal plate. The patterned ZnO nanorods acted as independent resonators with different frequencies upon exposure to an electric field. The added mass of ZnO nanostructures was found to significantly enhance the quality factor (QF) of the resonator in electrodeless QCM configuration. The QF increased with the length of the ZnO nanorods; ZnO nanorods 5 µm in length yielded a 7-fold higher QF compared to the QF of a quartz plate without ZnO nanorods. In addition, the ZnO nanorods offered enhanced sensitivity due to the enlarged sensing area. The developed sensor was used as an electronic nose for detection of vapor mixtures with impurities.