Flexible and Extensive Platinum Ion Gel Condensers for Programmable Catalysis

Catalytic condensers comprised of ion gels separating a metal electrode from a platinum-on-carbon active layer were fabricated and characterized to achieve more powerful, high surface area dynamic heterogeneous catalyst surfaces. Ion gels comprised of PVDF/ [EMIM]+[TFSI]- were spin coated as a 3.8 μm film on a Au surface, after which carbon sputtering of a 1.8 nm carbon film and electron-beam evaporation of 2 nm Pt clusters created an active surface exposed to reactant gases. Electronic characterization indicated that most charge condensed within the Pt nanoclusters upon application of a potential bias, with the condenser device achieving a capacitance of ~20 μF/cm^2 at applied frequencies up to 120 Hz. Maximum charge of ~10^14 |e-| cm^(-2) was condensed under stable device conditions at 200 °C on catalytic films with ~10^15 sites cm^(-2). Grazing incidence infrared spectroscopy measured carbon monoxide adsorption isobars indicating a change in CO* binding energy of ~16 kJ/mol over an applied potential bias of only 1.25 V. Condensers were also fabricated on flexible, large area Kapton substrates allowing stacked or tubular form factors that facilitate high volumetric active site densities, ultimately enabling a fast and powerful catalytic condenser that can be fabricated for programmable catalysis applications

Alumina Graphene Catalytic Condenser for Programmable Solid Acids

Precise control of electron density at catalyst active sites enables regulation of surface chemistry for optimal rate and selectivity to products. Here, an ultrathin catalytic film of amorphous alumina (4 nm) was integrated into a catalytic condenser device that enabled tunable electron depletion from the alumina active layer and correspondingly stronger Lewis acidity. The catalytic condenser had the following structure: amorphous alumina/graphene/HfO2 dielectric (70 nm)/p-type Si. Application of positive voltages up to +3 V between graphene and the p-type Si resulted in electrons flowing out of the alumina; positive charge accumulated in the catalyst. Temperature programmed surface reaction of thermocatalytic isopropanol dehydration to propene on the charged alumina surface revealed a shift in the propene formation peak temperature of up to ΔT(peak)~50 ⁰C relative to the uncharged film, consistent with a 16 kJ/mol (0.17 eV) reduction in the apparent activation energy. Electrical characterization of the thin amorphous alumina film by ultraviolet photoelectron spectroscopy (UPS) and scanning tunneling microscopy (STM) indicates the film is a defective semiconductor with an appreciable density of in-gap electronic states. Density functional theory calculations of isopropanol binding on the pentacoordinate aluminum active sites indicate significant binding energy changes (ΔBE) up to 60 kJ/mol (0.62 eV) for 0.125 e- depletion per active site, supporting the experimental findings. Overall, the results indicate that continuous and fast electronic control of thermocatalysis can be achieved with the catalytic condenser device