ABSTRACT
Metal-support interaction strongly influences the catalytic properties of metal-based catalysts. Here, titanium nitride (TiN) nanospheres are shown to be an outstanding support, for tuning the electronic property of platinum (Pt) nanoparticles and adjusting the morphology of indium sulfide (In2S3) active components, forming flower-like core-shell nanostructures (TiN-Pt@In2S3). The strong metal-support interaction between Pt and TiN through the formation of Pt-Ti bonds favors the migration of charge carriers and leads to the easy reducibility of TiN-Pt, thus improving the photocatalytic atom efficiency of Pt. The TiN-Pt@In2S3 composite shows reduction of Pt loading by 70% compared to the optimal Pt-based system. In addition, the optimal TiN-Pt@In2S3 composite exhibits a H2 evolution rate 4 times that of a Pt reference. This increase outperforms all other supports reported thus far.
ABSTRACT
As sustainable energy becomes a major concern for modern society, renewable and clean energy systems need highly active, stable, and low-cost catalysts for the oxygen evolution reaction (OER). Mesoporous materials offer an attractive route for generating efficient electrocatalysts with high mass transport capabilities. Herein, we report an efficient hard templating pathway to design and synthesize three-dimensional (3-D) mesoporous ternary nickel iron nitride (Ni3FeN). The as-synthesized electrocatalyst shows good OER performance in an alkaline solution with low overpotential (259 mV) and a small Tafel slope (54 mV dec-1), giving superior performance to IrO2 and RuO2 catalysts. The highly active contact area, the hierarchical porosity, and the synergistic effect of bimetal atoms contributed to the improved electrocatalytic performance toward OER. In a practical rechargeable Zn-air battery, mesoporous Ni3FeN is also shown to deliver a lower charging voltage and longer lifetime than RuO2. This work opens up a new promising approach to synthesize active OER electrocatalysts for energy-related devices.
