Solid-supported lipid membranes are popular models that connect biological and artificial materials used in bio-technological applications. Controlling the lipid organization and the related functions of these model systems entails understanding and characterizing their phase behavior. Quartz crystal microbalance with dissipation monitoring (QCM-D) is an acoustic-based surface-sensitive technique which is widely used in bio-interfacial science of solid-supported lipid membranes. Its sensitivity to mass and energy dissipation changes at the solid-lipid layer-liquid interface allows the detection of phase transformations of solid-supported membrane geometries. In this perspective, we highlight this valuable feature and its related methodology, review current advances and briefly discuss future perspectives. Furthermore, a specific example is also provided on the ability of QCM-D to detect changes in lipid organization of cholesterol containing solid-supported lipid vesicle layers (SVLs) upon the addition of aspirin.

The authors report on the effect of ionic strength on the formation of supported vesicle layers of anionic phospholipids 1,2-dimyristoyl-sn-glycero-3-phospho-rac-glycerol (DMPG) and dimyristoylphosphatidylserine (DMPS) onto gold. Using quartz crystal microbalance with dissipation monitoring the authors show that vesicle adsorption is mainly governed by NaCl concentration, reflecting the importance of electrostatic interactions in anionic lipids, as compared to zwitterionic 1,2-dimyristoyl-sn-glycero-3-phosphocholine. At low ionic strength, low or no adsorption is observed as a result of vesicle–vesicle electrostatic repulsion. At medium ionic strength, the negative charges of DMPG and DMPS are screened resulting in larger adsorption and a highly dissipative intact vesicle layer. In addition, DMPS exhibits a peculiar behavior at high ionic strength that depends on the temperature of the process.

In this study, we report on a combined approach to preparing an active electrode material for supercapattery application by making nanocomposites of Polyaniline/Cerium (PANI/Ce) with different weight percentages of magnetite (Fe₃O₄). Fourier-transform infrared spectroscopy (FTIR) and x-ray diffraction (XRD) analyses supported the interaction of PANI with Ce and the formation of the successful nanocomposite with magnetite nanoparticles. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses showed the uniform and porous morphology of the composites. Cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) were used to test the supercapattery behavior of the nanocomposite electrodes in 1.0 M H₂SO₄. It was found that the supercapattery electrode of PANI/Ce+7 wt.% Fe₃O₄ exhibited a specific capacity of 171 mAhg⁻¹ in the potential range of −0.2 to 1.0 V at the current density of 2.5 Ag⁻¹. Moreover, PANI/Ce+7 wt.% Fe₃O₄ revealed a power density of 376.6 Wkg⁻¹ along with a maximum energy density of 25.4 Whkg⁻¹ at 2.5 Ag⁻¹. Further, the cyclic stability of PANI/Ce+7 wt.% Fe₃O₄ was found to be 96.0% after 5,000 cycles. The obtained results suggested that the PANI/Ce+Fe₃O₄ nanocomposite could be a promising electrode material candidate for high-performance supercapattery applications.