Dynamic Structure Evolution of Composition Segregated Iridium-Nickel Rhombic Dodecahedra toward Efficient Oxygen Evolution Electrocatalysis
Yecan Pi, Qi Shao, Xing Zhu, Xiaoqing Huang
Abstract
Yecan Pi, Qi Shao, Xing Zhu, Xiaoqing Huang
Abstract
The anodic oxygen evolution reaction (OER) is central to various energy conversion devices, but the investigation of the dynamic evolution of catalysts in different OER conditions remains quite limited, which is unfavorable for the understanding of the actual structure–activity relationship and catalyst optimization. Herein, we constructed monodispersed IrNi x nanoparticles (NPs) with distinct composition-segregated features and captured their structural evolution in various OER environments. We decoded the interesting self-reconstruction of IrNi x NPs during the OER, in which an Ir-skin framework is generated in an acidic electrolyte, while a Ni-rich surface layer is observed in an alkaline electrolyte owing to Ni migration. Benefiting from such self-reconstruction, considerable OER enhancements are achieved under both acidic and alkaline conditions. For comparison, IrNi x nanoframes with Ir skins prepared by chemical etching show a similar structural evolution result in the acidic electrolyte, but a total different phenomenon in the alkaline electrolyte. By tracking the structural evolution of IrNi x catalysts and correlating them with OER activity trajectories, the present work provides a significant understanding for designing efficient OER catalysts with controlled compositional distributions.
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The anodic oxygen evolution reaction (OER) is central to various energy conversion devices, but the investigation of the dynamic evolution of catalysts in different OER conditions remains quite limited, which is unfavorable for the understanding of the actual structure–activity relationship and catalyst optimization. Herein, we constructed monodispersed IrNi x nanoparticles (NPs) with distinct composition-segregated features and captured their structural evolution in various OER environments. We decoded the interesting self-reconstruction of IrNi x NPs during the OER, in which an Ir-skin framework is generated in an acidic electrolyte, while a Ni-rich surface layer is observed in an alkaline electrolyte owing to Ni migration. Benefiting from such self-reconstruction, considerable OER enhancements are achieved under both acidic and alkaline conditions. For comparison, IrNi x nanoframes with Ir skins prepared by chemical etching show a similar structural evolution result in the acidic electrolyte, but a total different phenomenon in the alkaline electrolyte. By tracking the structural evolution of IrNi x catalysts and correlating them with OER activity trajectories, the present work provides a significant understanding for designing efficient OER catalysts with controlled compositional distributions.
Key concepts: Oxygen evolution, Electrocatalyst, Electrolyte, Catalysis, Materials science, Iridium, Nickel, Chemical engineering