自旋态
析氧
溶解度
兴奋剂
材料科学
旋转交叉
自旋(空气动力学)
氧化态
电化学
化学
无机化学
金属
物理化学
热力学
电极
冶金
物理
光电子学
作者
Zhengda He,Rebekka Tesch,Mohammad J. Eslamibidgoli,Michael Eikerling,Piotr M. Kowalski
标识
DOI:10.1038/s41467-023-38978-5
摘要
Doping with Fe boosts the electrocatalytic performance of NiOOH for the oxygen evolution reaction (OER). To understand this effect, we have employed state-of-the-art electronic structure calculations and thermodynamic modeling. Our study reveals that at low concentrations Fe exists in a low-spin state. Only this spin state explains the large solubility limit of Fe and similarity of Fe-O and Ni-O bond lengths measured in the Fe-doped NiOOH phase. The low-spin state renders the surface Fe sites highly active for the OER. The low-to-high spin transition at the Fe concentration of ~ 25% is consistent with the experimentally determined solubility limit of Fe in NiOOH. The thermodynamic overpotentials computed for doped and pure materials, η = 0.42 V and 0.77 V, agree well with the measured values. Our results indicate a key role of the low-spin state of Fe for the OER activity of Fe-doped NiOOH electrocatalysts.
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