Gaseous nanobubbles (NBs), with their unique physicochemical properties and promising applications, have become an important research topic. Generation of monodispersed bulk NBs with specified gas content remains a challenge. We developed a simple method for generating bulk NBs, using porous alumina films with ordered straight nano-scaled holes. Different techniques, such as nanoparticle tracking analysis (NTA), atomic force microscopy (AFM), and infrared absorption spectroscopy (IRAS), are used to confirm NB formation. The NTA data demonstrates that the minimum size of the NBs formed is less than 100 nm, which is comparable to the diameter of nanoholes in the porous alumina film. By generating NBs with different gases, including CO2, O2, N2, Ar, and He, we discovered that the minimum size of NBs negatively correlated with the solubility of encapsulated gases in water. Due to the monodispersed size of NBs generated from the highly ordered porous alumina, we determined that NB size is distributed discretely with a uniform increment factor of √2. To explain the observed characteristic size distribution of NBs, we propose a simple model in which two NBs of the same size are assumed to preferentially coalesce. This characteristic bubble size distribution is useful for elucidating the basic characteristics of nanobubbles, such as the long-term stability of NBs. This distribution can also be used to develop new applications of NBs, for example, nano-scaled reaction fields through bubble coalescence.

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Bilayer lipid membranes (BLMs) are used as basic frameworks for biosensors and biohybrid devices due to their unique properties, which include ultrathin thickness, ultrahigh resistivity, and self-assembling ability. However, BLMs can only form and maintain their structure in aqueous environments, which pose significant limitations to their use. In this work, we report on the formation of highly uniform hybrid BLMs at a water/air interface through self-assembly by simply doping the BLMs with a functional organic molecule, copper­(II) 2,9,16,23-tetra-tert-butyl-29H,31H-phthalocyanine (CuPc). By transferring the membrane onto substrates, we were able to produce stable hybrid BLMs under anhydrous conditions. Atomic force microscopy and X-ray diffraction measurements confirmed that the hybrid membranes were composed of single, highly uniform BLMs or stacks of BLMs. Fluorescence resonance energy transfer measurements indicated that the CuPc molecules were located between the hydrophobic tails of lipid molecules, forming a sandwich structure in the hybrid membranes. The hybrid BLMs fabricated by this method substantially expand the range of applications of BLMs to solid-state devices.

We report on a novel lipid bilayer system, in which a lateral bias can be applied in addition to a conventional transmembrane voltage. Freestanding bilayer lipid membranes (BLMs) doped with [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) were formed in a microaperture, around which metal electrodes were deposited. Using this system, it was possible to modulate and amplify photoinduced transmembrane currents by applying a lateral bias along the BLM. The results indicate that the microfabricated Si chip with embedded electrodes is a promising platform for the formation of transistor-like devices based on PCBM-doped BLMs and have potential for use in a wide variety of nanohybrid devices.