尖晶石
析氧
纳米颗粒
原子单位
材料科学
氧化物
纳米尺度
化学工程
氧气
纳米技术
化学
物理化学
冶金
物理
有机化学
电极
量子力学
工程类
电化学
作者
Weikai Xiang,Nating Yang,Xiaopeng Li,Julia Linnemann,Ulrich Hagemann,Olaf Ruediger,Markus Heidelmann,Tobias Falk,Matteo Aramini,Serena DeBeer,Martin Muhler,Kristina Tschulik,Tong Li
标识
DOI:10.1038/s41467-021-27788-2
摘要
The three-dimensional (3D) distribution of individual atoms on the surface of catalyst nanoparticles plays a vital role in their activity and stability. Optimising the performance of electrocatalysts requires atomic-scale information, but it is difficult to obtain. Here, we use atom probe tomography to elucidate the 3D structure of 10 nm sized Co2FeO4 and CoFe2O4 nanoparticles during oxygen evolution reaction (OER). We reveal nanoscale spinodal decomposition in pristine Co2FeO4. The interfaces of Co-rich and Fe-rich nanodomains of Co2FeO4 become trapping sites for hydroxyl groups, contributing to a higher OER activity compared to that of CoFe2O4. However, the activity of Co2FeO4 drops considerably due to concurrent irreversible transformation towards CoIVO2 and pronounced Fe dissolution. In contrast, there is negligible elemental redistribution for CoFe2O4 after OER, except for surface structural transformation towards (FeIII, CoIII)2O3. Overall, our study provides a unique 3D compositional distribution of mixed Co-Fe spinel oxides, which gives atomic-scale insights into active sites and the deactivation of electrocatalysts during OER.
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