Photoswitching between Water-Tolerant Adhesion and Swift Release by Inverting Liquid Crystal Fingerprint Topography.

Although switchable adhesive surfaces are important and desirable for soft robotics, it is still challenging to replicate nature's switchable adhesion capability on artificial surfaces, especially for underwater applications. Here polymeric coatings with fingerprint topographies that are capable of switching the surface adhesion upon light illumination are reported. This is achieved via a synergistic combination of surface topographical inversion and spatially selective distribution of adhesive polymers. The surface topographical inversion is accomplished by the anisotropic deformation of the fingerprint-configured liquid crystal network (LCN) coating upon light-controlled order parameter modulation. Adhesive and nonadhesive polymers are spatial-selectively arranged on top of the LCN coating following the alternating homeotropic and planar domains, respectively, where liquid crystal mesogens are orthogonally aligned. The adhesive part is composed of a water-tolerant adhesive polymer with 3,4-dihydroxy-l-phenylalanine (catechol) groups inspired by mussel byssus. This report presents a dynamic surface with locally alternating nonadhesive indented areas and adhesive elevated areas where the topographical positions can be dynamically changed with light illumination which can serve as smart skins for robotic applications.

Calibrating lateral displacement sensitivity of AFM by stick-slip on stiff, amorphous surfaces.

We calibrate the lateral mode AFM (LFM) by determining the position-sensitive photodetector (PSPD) signal dependency on the lateral tip displacement, which is analogous to the constant-compliance region in normal-force calibration. By stick-slip on stiff, amorphous surfaces (silica or glass), the lateral tip displacement is determined accurately using the feedback loop control of AFM system. The sufficiently high contact stiffness between the Si AFM tip and stiff, amorphous surfaces substantially reduces the error of PSPD signal dependency on the lateral tip displacement. No damage or modification of the AFM probe is involved and only a clean silicon or glass wafer is needed.

Molecular-Scale Hybrid Membranes Derived from Metal-Organic Polyhedra for Gas Separation.

The preparation and the performance of mixed matrix membranes based on metal-organic polyhedra (MOPs) are reported. MOP fillers can be dispersed as discrete molecular units (average 9 nm in diameter) when low filler cargos are used. In spite of the low doping amount (1.6 wt %), a large performance enhancement in permeability, aging resistance, and selectivity can be achieved. We rationalize this effect on the basis of the large surface to volume ratio of the filler, which leads to excellent dispersion at low concentrations and thus alters polymer packing. Although membranes based only on the polymer component age quickly with time, the performance of the resulting MOP-containing membranes meets the commercial target for postcombustion CO2 capture for more than 100 days.

Enhanced vapour sensing using silicon nanowire devices coated with Pt nanoparticle functionalized porous organic frameworks.

Recently various porous organic frameworks (POFs, crystalline or amorphous materials) have been discovered, and used for a wide range of applications, including molecular separations and catalysis. Silicon nanowires (SiNWs) have been extensively studied for diverse applications, including as transistors, solar cells, lithium ion batteries and sensors. Here we demonstrate the functionalization of SiNW surfaces with POFs and explore its effect on the electrical sensing properties of SiNW-based devices. The surface modification by POFs was easily achieved by polycondensation on amine-modified SiNWs. Platinum nanoparticles were formed in these POFs by impregnation with chloroplatinic acid followed by chemical reduction. The final hybrid system showed highly enhanced sensitivity for methanol vapour detection. We envisage that the integration of SiNWs with POF selector layers, loaded with different metal nanoparticles will open up new avenues, not only in chemical and biosensing, but also in separations and catalysis.

Fast and controlled fabrication of porous graphene oxide: application of AFM tapping for mechano-chemistry.

This paper describes a novel method to fabricate porous graphene oxide (PGO) from GO by exposure to oxygen plasma. Compared to other methods to fabricate PGO described so far, e.g. the thermal and steam etching methods, oxygen plasma etching method is much faster. We studied the development of the porosity with exposure time using atomic force microscopy (AFM). It was found that the development of PGO upon oxygen-plasma exposure can be controlled by tapping mode AFM scanning using a Si tip. AFM tapping stalls the growth of pores upon further plasma exposure at a level that coincides with the fraction of sp2 carbons in the GO starting material. We suggest that AFM tapping procedure changes the bond structure of the intermediate PGO structure, and these stabilized PGO structures cannot be further etched by oxygen plasma. This constitutes the first report of tapping AFM as a tool for local mechano-chemistry.