Microtubular Fuel Cell with Ultrahigh Power Output per Footprint.

A novel realization of microtubular direct methanol fuel cells (µDMFC) with ultrahigh power output is reported by using "rolled-up" nanotechnology. The microtube (Pt-RuO2 -RUMT) is prepared by rolling up Ru2 O layers coated with magnetron-sputtered Pt nanoparticles (cat-NPs). The µDMFC is fabricated by embedding the tube in a fluidic cell. The footprint of per tube is as small as 1.5 × 10-4 cm2 . A power density of ≈257 mW cm-2 is obtained, which is three orders of magnitude higher than the present microsized DFMCs. Atomic layer deposition technique is applied to alleviate the methanol crossover as well as improve stability of the tube, sustaining electrolyte flow for days. A laminar flow driven mechanism is proposed, and the kinetics of the fuel oxidation depends on a linear-diffusion-controlled process. The electrocatalytic performance on anode and cathode is studied by scanning both sides of the tube wall as an ex situ working electrode, respectively. This prototype µDFMC is extremely interesting for integration with micro- and nanoelectronics systems.

Conformational change of bovine serum albumin molecules at neutral pH in ultra-diluted aqueous solutions.

Surface chemical and electrochemical techniques were applied to reveal the unfolding of bovine serum albumin (BSA) molecules induced by concentrations in aqueous solution. Real-time surface pressures vs time (π-t) kinetic curves were recorded over an aqueous subphase (190 mL) by spreading BSA solutions of different concentrations but of the same amount (8.0 × 10(-4) mg) at the air/water (A/W) interface. A critical concentration (∼1.0 ppm) was discovered below which the surface pressure declines with time and the BSA is totally solubilized in the water subphase. Above this critical concentration (e.g., 8.0 ppm), the surface pressure goes up and the protein molecules assemble into a Langmuir monolayer at the A/W interface. These findings demonstrate that the BSA molecules have different conformations in the spreading protein solutions. The conformational transition in BSA molecules induced by concentrations was also confirmed by spectroscopy means and the catalytic hydrogen evolution reaction on a silver amalgam electrode by using constant current chronopotentiometric stripping. This discovery fills in gaps of Foster's N (normal) → F (fast) model, in which the unfolding of BSA molecules occurs at neutral pH values (8.0-4.3).

Ultrasmall SnO2 nanocrystals: hot-bubbling synthesis, encapsulation in carbon layers and applications in high capacity Li-ion storage.

Ultrasmall SnO2 nanocrystals as anode materials for lithium-ion batteries (LIBs) have been synthesized by bubbling an oxidizing gas into hot surfactant solutions containing Sn-oleate complexes. Annealing of the particles in N2 carbonifies the densely packed surface capping ligands resulting in carbon encapsulated SnO2 nanoparticles (SnO2/C). Carbon encapsulation can effectively buffer the volume changes during the lithiation/delithiation process. The assembled SnO2/C thus deliver extraordinarily high reversible capacity of 908 mA·h·g(-1) at 0.5 C as well as excellent cycling performance in the LIBs. This method demonstrates the great potential of SnO2/C nanoparticles for the design of high power LIBs.