Hybrid Structure of TiO2-Graphitic Carbon as a Support of Pt Nanoparticles for Catalyzing Oxygen Reduction Reaction

The durability of catalysts in fuel cells is a longstanding issue that needs to be resolved. Catalyst stability of the fuel cell has always been a problem, studies are underway to address them. Herein, to address this issue, we synthesize a hybrid structure consisting of SP carbon (SP) as the graphitic carbon and TiO2 as the metal oxide using a microwave method for use as a support for Pt nanoparticles. Anatase TiO2 and Pt nanoparticles with sizes of ~5 and 3.5 ± 1.4 nm, respectively, are uniformly dispersed on a modified graphitic SP carbon support (Pt-TiO2-SP). This supported Pt catalyst exhibits significantly improves durability in the oxygen reduction reaction (ORR). Furthermore, the Pt-TiO2-SP carbon hybrid catalyst manifests superior electrocatalytic stability and higher onset potential in ORR than those exhibited by Pt-SP carbon without TiO2. Pt-TiO2-SP exhibits an activity loss of less than 68 mV after 5000 electrochemical cycles, whereas an activity loss of ~100 mV is observed for Pt-SP carbon in a stability test. These results suggest that the strong metal–support interaction in TiO2-supported Pt catalyst significantly enhances the activity of Pt nanocatalyst.

Influence of Lattice Oxygen on the Catalytic Activity of Blue Titania Supported Pt Catalyst under CO oxidation

Despite enormous research into understanding the reaction mechanism for CO oxidation over transition metal supported TiO2, the active species for oxidation remains controversial. Herein, characteristics of active oxygen species of...

Ordered SnO2@C Flake Array as Catalyst Support for Improved Electrocatalytic Activity and Cathode Durability in PEMFCs

Pt-SnO2@C-ordered flake array was developed on carbon paper (CP) as an integrated cathode for proton exchange membrane fuel cell through a facile hydrothermal method. In the integrated cathode, Pt nanoparticles were deposited uniformly with a small particle size on the SnO2@C/CP support. Electrochemical impedance spectroscopy analysis revealed lower impedance in a potential range of 0.3–0.5 V for the ordered electrode structure. An electrochemically active surface area and oxygen reduction peak potential determined by cyclic voltammetry measurement verified the synergistic effect between Pt and SnO2, which enhanced the electrochemical catalytic activity. Besides, compared with the commercial carbon-supported Pt catalyst, the as-developed SnO2@C/CP-supported Pt catalyst demonstrated better stability, most likely due to the positive interaction between SnO2 and the carbon coating layer.