双金属片
催化作用
氧气
固态
析氧
化学工程
国家(计算机科学)
材料科学
化学
计算机科学
工程类
物理化学
有机化学
算法
电极
电化学
作者
Ebrahim Sadeghi,Se Yun Kim,Per Morgen,Søren Bredmose Simonsen,Martin A.B. Hedegaard,Raghunandan Sharma,Shuang Ma Andersen
标识
DOI:10.1021/acsaem.5c00307
摘要
Metallic iridium (Ir) and ruthenium (Ru) are among the most active OER electrocatalysts in acidic media. Alloying Ir and Ru can enhance catalytic performance while reducing costs. Here, we introduce a scalable solid-state synthesis method to produce nanostructured IrRu semialloy on a high-porosity carbon substrate for efficient OER. This thermal-based approach offers a straightforward and cost-effective alternative to conventional methods and, therefore, eliminates complex procedures, organic solvents, and capping agents while ensuring fine nanoparticle (NP) dispersion. Electrochemical studies show that Ru-rich samples achieve high initial activity, while Ir-rich samples demonstrate superior stability in 0.1 M HClO 4 . Notably, Ir 0.5 Ru 0.5 /C and Ir 0.25 Ru 0.75 /C electrodes achieved mass activities of 1605 and 2494 A g metal –1 at 1.65 V (versus RHE)., respectively. Among them, Ir 0.5 Ru 0.5 /C retained 70% of its initial OER performance, outperforming commercial IrO 2 (53%) and other as-prepared catalysts in terms of stability. HAADF-STEM analysis revealed that Ir 0.5 Ru 0.5 /C has the finest particle size distribution, with the highest fraction of sub-2 nm NPs. Theoretical calculations confirmed that *–OOH formation is the rate-determining step (RDS) for both catalysts of interest. The highest reaction energy for Ir 0.25 Ru 0.75 /C is 3.94 eV, whereas, for Ir 0.5 Ru 0.5 /C, it is 4.46 eV. This study demonstrates that solid-state synthesis enables the controlled design of highly active and stable IrRu catalysts and offers a promising approach for scalable OER catalyst production.
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