Abstract
Defect engineering is a key chemical tool to modulate the electronic structure and reactivity of nanostructured catalysts. Here, we report how engineering defects in a palladium metallene nanostructure results in a highly active catalyst for the alkaline oxygen reduction reaction (ORR). A defect-rich WOx and MoOx modified Pd metallene (denoted as D-Pd M) was synthesized by a facile wet-chemical method. Detailed structural analyses reveal the presence of three distinct atomic-scale defects, that is pores, concave surfaces, and surface-anchored individual WOx and MoOx sites. The presence of this combination of defects results in excellent catalytic ORR activity with a half-wave potential of 0.93 V vs. RHE and a mass activity of 1.3 A·mgPd-1 at 0.9 V vs. RHE, outperforming the commercial references Pt/C and Pd/C by factors of 6.5 and 3.9, respectively. The practical usage of the compound is demonstrated by integration into a custom-designed Zn-air battery. At notably low D-Pd M loading (26 μgPd·cm-2), the system achieves a high specific capacity (809 mAh·gZn-1) together with excellent discharge potential stability. In sum, this study provides a blueprint for the targeted introduction of distinct defect sites into metallene ORR catalysts, leading to materials with outstanding performance metrics.
Supplementary materials
Title
Supplementary Information
Description
The supplementary information contains supporting experimental procedures, characterizations, electrochemical measurements, computational details, Zn-air battery meansurement details, supplementary figures, and author contributions.
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