ABSTRACT
One-dimensional iron-oxide/carbon hybrid nano tubular structures were synthesized via anodic aluminium oxide (AAO) template method. Highly unform iron oxide nanoparticles and carbon structures were formed simultaneously on the wall surface of the AAO template from an iron-oleate precursor by solventless thermal decomposition method. The 1D iron-oxide/carbon nanostructures were obtained after removing the AAO template. The typical size of the iron oxide nanoparticles was - 6 nm, and the nanoparticles had a crystalline structure of maghemite (γ-Fe2O3), which was determined from the HRTEM and X-ray diffraction (XRD). This nanocrystalline spinel structure could provide more active sites for oxygen reduction reaction (ORR) catalysis due to the higher specific surface area and numerous defects. As an ORR catalyst, the hybrid nanotubes showed higher limiting mass activity (8.8 A/g) and a more positive onset potential (-0.241 V, vs. Hg/HgCl) than iron oxide nanoparticles in alkaline media. This electrocatalytic activity of the nanocomposites is mainly attributed to the synergetic effects of the iron oxide nanoparticles and carbon matrix in the one-dimensional nanostructure.
Subject(s)
Carbon/chemistry , Ferric Compounds/chemistry , Nanocomposites/chemistry , Nanotubes/chemistry , Oxygen/chemistry , Hydrogen-Ion Concentration , Nanotechnology , Oxidation-ReductionABSTRACT
A poly(p-phenylene)-based multiblock polymer is developed with an oligomeric chain extender and cerium (CE-sPP-PPES + Ce3+) to realize better performance and durability in proton exchange membrane fuel cells. The membrane performance is evaluated in single cells at 80 °C and at 100% and 50% relative humidity (RH). The accelerated stability test is conducted 90 °C and 30% RH, during which linear sweep voltammetry and hydrogen permeation detection are monitored periodically. Results demonstrate that the proton conductivity of the pristine hydrocarbon membranes is superior to that of PFSA membranes, and the hydrogen crossover is significantly lower. In addition, a composite membrane containing cerium performs similarly to a pristine membrane, particularly at low RH levels. Adding cerium to CE-sPP-PPES + Ce3+ membranes improves their chemical durability significantly, with an open circuit voltage decay rate of only 89 µV/h for 1000 h. The hydrogen crossover is maintained across accelerated stability tests, as confirmed by hydrogen detection and crossover current density. The short-circuit resistance indicates that membrane thinning is less likely to occur. Collectively, these results demonstrate that a hydrocarbon membrane with cerium is a potential alternative for fuel cell applications.
ABSTRACT
Carbon-supported Pd electrocatalyst is prepared by an improved aqueous impregnation method applying a reducing agent of HCHO and an acidic sedimentation promoter of HCl. We investigate the effect of a solution pH on the zeta potential of both Pd particles and carbon support. The opposite sign of zeta potential results in uniform dispersion of Pd on carbon surface without aggregation problem. TEM analysis shows that optimal solution pH of 4.27 adjusted by NaOH provides a mean particle diameter of 3.2 nm with narrow size distribution. Cyclic voltammograms indicate that home-made Pd/C catalyst exhibits significantly higher electrochemical active surface area and better stability compared with commercial 40 wt.% Pd/C in a formic acid oxidation.
ABSTRACT
We report a novel method for the synthesis of a self-reducible (thermally reducible without a reducing atmosphere) and alcohol-soluble copper-based metal-organic decomposition (MOD) ink for printed electronics. Alcohol-solvent-based conductive inks are necessary for commercial printing processes such as reverse offset printing. We selected copper(II) formate as a precursor and alkanolamine (2-amino-2-methyl-1-propanol) as a ligand to make an alcohol-solvent-based conductive ink and to assist in the reduction reaction of copper(II) formate. In addition, a co-complexing agent (octylamine) and a sintering helper (hexanoic acid) were introduced to improve the metallic copper film. The specific resistivity of copper-based MOD ink (Cuf-AMP-OH ink) after heat treatment at 350 °C is 9.46 µΩ·cm, which is 5.5 times higher than the specific resistivity of bulk copper. A simple stamping transfer was conducted to demonstrate the potential of our ink for commercial printing processes.
ABSTRACT
We introduce a simple process to synthesize few-layered MoS(2) nanosheets supported on coaxial carbon nanotubes through an L-cysteine-assisted hydrothermal route, in which L-cysteine, a cheap and ordinary amino acid, plays a fundamental role in controlling the morphology of the hybrid material and the binder to help the growth of MoS(2) nanosheets on the surface of the carbon nanotubes. It is also demonstrated that the polypeptide formed by L-cysteine can be transformed into amorphous carbon by heat treatment under an inert atmosphere. The materials exhibit high capacity and excellent cycling performance when used as anode materials for lithium ion batteries. The specific capacity of a composite with 1 : 4 molar ratio of MoS(2) to carbon nanotubes is 736.5 mAh g(-1) after the first cycle, increased for several initial cycles, and remains at 823.4 mAh g(-1) even after 30 cycles, when cycled at a current density of 100 mA g(-1). At a very high current density of 1600 mA g(-1), the material shows a stable capacity of approximately 530 mAh g(-1) after 30 cycles. The noteworthy improvement in the electrochemical performance of the material can be attributed to their unique structure and the synergistic effects of amorphous carbon and few-layered MoS(2).