摘要
Nonprecious metal electrocatalysts (NPMEs) have been recognized as highly promising oxygen electroreduction catalysts, but improving their activity and stability in acidic electrolyte remains critical. Here, we integrated self-assembly technology induced by rotary evaporation with the hard-template method to synthesize Fe–N-codoped NPMEs with large specific surface areas and hierarchical pore structure. The presence of Fe3+ assisted complete removal of the ZnO hard template at a relatively low temperature, which is beneficial for both the in situ growth of micropores/mesopores within the carbon layers and the retention of more nitrogen-containing groups. The obtained Fe–N–C/ZnO porous carbon material exhibited outstanding oxygen reduction reaction catalytic activity, along with respectable electrochemical stability in a perchloric acid electrolyte. Applied in fuel cells, the electrocatalyst loading was reduced to 2.0 mg/cm2 because of increased mass transfer arising from the hierarchical porous structure and resulting in a power density of 700 mW/cm2.
危险品化学品经营许可证(带存储)