RESUMEN
Here, we report the effect of Fe(CO)5 additives in the synthesis of branched Pt-CoO nanowires (NWs) and core@shell concave nanocubes (NCs), in a one-pot system. Key to the success of this synthesis is control over the shape of the Pt seeds by controlling the quantity of Fe(CO)5 additive. In the absence of Fe(CO)5, branched Pt-CoO NWs were synthesized through the attachment of small Pt seed particles, followed by the growth of CoO by deposition. On the other hand, Pt@CoO concave NCs were obtained in the presence of Fe(CO)5 because of the stronger adsorption of Co on the Pt (100) surfaces than on the closely packed (111) surfaces. Also, various other conditions including the control of reducing agents, precursor concentrations, and stabilizing agents, were used to verify the effects of reaction kinetics on the synthesis of Pt-CoO nanoparticles. Compared to Pt/graphene oxide (GO) catalyst, branched Pt-CoO NWs supported on GO showed enhanced specific activity toward the oxygen reduction reaction (ORR).
RESUMEN
Since Li4Ti5O12 as a promising anode material in lithium-ion batteries (LIBs) has a poor rate performance due to low electronic conductivity, a doping of Li4Ti5O12 with heterogeneous atoms has been considered to overcome this problem. Herein, we report that there is an upper limit of doping level to maintain the zero strain characteristics of Li4Ti5O12 lattice during charge/discharge process. By using synchrotron studies, it was revealed that the Li+ diffusivity was maximized at a certain doping level for which the conductivity was markedly increased with maintaining the zero strain characteristics. However, with more doses of dopants over the upper limit, the lattice shrank and therefore the Li+ diffusivity decreased, although the electronic conductivity was further increased in comparison with the optimal doping level.
RESUMEN
A simple, inexpensive approach is proposed for enhancing the durability of automotive proton exchange membrane fuel cells by selective promotion of the hydrogen oxidation reaction (HOR) and suppression of the oxygen reduction reaction (ORR) at the anode in startup/shutdown events. Dodecanethiol forms a self-assembled monolayer (SAM) on the surface of Pt particles, thus decreasing the number of Pt ensemble sites. Interestingly, by controlling the dodecanethiol concentration during SAM formation, the number of ensemble sites can be precisely optimized such that it is sufficient for the HOR but insufficient for the ORR. Thus, a Pt surface with an SAM of dodecanethiol clearly effects HOR-selective electrocatalysis. Clear HOR selectivity is demonstrated in unit cell tests with the actual membrane electrode assembly, as well as in an electrochemical three-electrode setup with a thin-film rotating disk electrode configuration.
Asunto(s)
Suministros de Energía Eléctrica , Hidrógeno/química , Catálisis , Electroquímica , Electrodos , Modelos Moleculares , Conformación Molecular , Oxidación-Reducción , Compuestos de Sulfhidrilo/químicaRESUMEN
The production of shape-controlled heterometallic nanoparticles (NPs) consisting of Pt and nonprecious metal oxides is crucial to demonstrate the composition-property relationship of NPs. Herein, we report a facile one-pot approach for the controlled synthesis of dumbbell-like Pt-Fe3O4-MnO x and dendritic Pt-MnO x NPs. The key to the success of this synthesis is in changing the quantity of Fe(CO)5 additive to control the reaction kinetics. In the absence of Fe(CO)5, dendritic Pt-MnO x NPs were synthesized through the assembly of small seed NPs. On the other hand, dumbbell-like Pt-Fe3O4-MnO x NPs were obtained in the presence of Fe(CO)5 through controlling the nucleation and growth of Fe and Mn on the Pt NPs, followed by air oxidation. Compared to a Pt/graphene oxide (GO) catalyst, dumbbell-like Pt-Fe3O4-MnO x NPs on GO showed an enhancement of specific activity toward the oxygen reduction reaction owing to the compressive-strain effect exerted on the Pt lattice.
