过电位
析氧
塔菲尔方程
X射线光电子能谱
催化作用
材料科学
X射线吸收光谱法
价(化学)
物理化学
吸收光谱法
电化学
化学
核磁共振
物理
电极
光学
生物化学
有机化学
作者
Wei Sun,Ya Song,Xue‐Qing Gong,Limei Cao,Ji Yang
标识
DOI:10.1021/acsami.5b10159
摘要
Oxygen evolution reaction (OER) catalysts with high activity are of particular importance for renewable energy production and storage. Here, we prepare Kx≈0.25IrO2 catalyst that exhibits an excellent OER activity compared to IrO2, which is univerally acknoweledged as a state-of-the-art OER catalyst. The prepared catalyst reflects a small overpotential 0.35 V at a current density of 10 mA cm–2 and a lower Tafel slope (65 mV dec–1) compared to that for IrO2 (74 mV dec–1). The performed X-ray photoelectron spectroscopy (XPS) and X-ray adsorption (XAS) experiments indicate that the Ir-site of Kx≈0.25IrO2 has a lower valence and more Ir-5d occupied states, suggesting more electrons on the Ir site. The extra electrons located on the Ir site and distorted IrO6 octahedral symmetry have a significant effect on the 5d orbital energy distribution which is verified by our DOS calculation. The performed DFT calculations state that the Kx≈0.25IrO2 essentially obtains good OER performance because it has a lower theoretical overpotential (0.50 V) compared to IrO2 (0.61 V).
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