Elucidating Water Structure with Ultrasensitive Cantilevers
The local hydration structure at the liquid/solid interface influences the function of adsorbed molecules that can range in complexity from a single ion to complex biomolecules. The low damping, high Q, and low force noise that are characteristic of encased cantilevers enable high resolution imaging combined with ultrasensitive force measurement as demonstrated in the high-resolution image shown in (a) that resolves the muscovite mica atomic lattice. Force measurements on the same surface are shown in (b) and schematically in (c) further illustrate the sensitivity of the encased levers. Three distinct oscillations are observed at the mica surface, representing solvent-molecule layers. To date, three structured water layers have been observed in AFM over assembled biomolecules, but only two water layers have been observed on mica. Moreover, the single force curve measured in (b) was taken in only one second and was not averaged, demonstrating one of the most sensitive AFM measurements of water structure to date. Overall, the increased sensitivity offered by encased cantilevers could push AFM to resolve 2D and 3D hydration layers on surfaces in liquid.
Gentle Imaging of Lipid Bilayers with Encased Cantilevers
High viscous damping has limited the AFM’s utility for high resolution imaging of soft materials in solution resulting in sample deformation or damage. Lipid bilayers readily deform under the force applied by the AFM tip. Scuba Probe’s encased cantilevers offer gentler imaging conditions as shown here imaging supported DPPC lipid bilayers (L-αdipalmitoyl-phosphatidylcholine) that were prepared using a Langmuir-Blodgett trough, and transferred onto mica in an aqueous buffer. The softest imaging conditions achieved with (a) conventional silicon nitride cantilevers (Hydra Cantilevers, Applied Nanosciences Inc.) results in a bilayer height of 5.4 nm. In contrast, (b) encased cantilevers reveal a bilayer thickness of 6.5 nm. This bilayer thickness exceeds the highest previously reported thickness using AFM, clearly demonstrating the gentle imaging enabled by the reduced viscous damping.
Encased Cantilevers Make Quantitative Mass Sensing Simple
Cantilever based mass sensors detect minute amounts of material and have the potential to significantly impact biological and chemical diagnostics. Added mass to the cantilever is directly measured through a resonance frequency shift, however the high damping-low Q-factor environment of liquids makes measurements of resonance frequency challenging. The low damping of encased cantilevers enables in-situ mass sensing in liquids that surpasses conventional cantilever based mass sensing, where the uncertainty of the location of the added mass, and the indirect measurement of stress induced bending require various assumptions or models to extract the exact value of the added mass. With encased cantilevers, (a) functionalization and binding of an analyte occur only at the tip and (b) a distinct shift in frequency is easily observed from two consecutive attachment events using 250 nm gold particles. The volume of the gold particles (c) shown in high-angle annular dark field electron microscopy was estimated by projected areas and assuming a spherical form factor (volume estimation in d, green histogram). True mass sensing using encased cantilevers is shown in d (red histogram), where an average mass of 168 fg/nanoparticle is measured. With the potential to reach even attogram sensitivities, encased cantilevers can be used as a sensitive mass sensor for a variety of applications in solution.
Scanning Electrochemical Microscopy using Insulated Cantilevers
Electrochemical processes are central to corrosion, energy storage, catalysis, and biology. Beyond the topography that is measured in atomic force micorscopy, scanning electrochemical microscopy (SECM) measures reaction rates and electrochemically generated species. Here, we demonstrate the capability of Scuba Probe Technologies insulated cantilevers to measure electroactive species being generated at the sample surface. By probing a micro electrode array in hexaammineruthenium (III) chloride operating in sample generation-tip collection mode, we demonstrate that electrical currents on the order of a few pA can be observed. Correlating current (top) with topography (bottom) allows for identification of both active and inactive electrodes.