化学
过电位
分解水
X射线光电子能谱
电化学
电子顺磁共振
析氧
无机化学
催化作用
物理化学
化学工程
电极
光催化
物理
工程类
生物化学
核磁共振
作者
Amirreza Valizadeh,P. Aleshkevych,Mohammad Mahdi Najafpour
标识
DOI:10.1021/acs.inorgchem.1c03331
摘要
The oxygen-evolution reaction (OER) through water oxidation is an inevitable reaction for water splitting toward storing energy. However, OER is a four-electron and slow reaction, which is also a bottleneck for water splitting. To find the role of Pt and PtO2 on the OER in the presence of Fe, the electrochemistry of Pt foil and PtO2 is investigated in the absence/presence of K2FeO4 as a soluble Fe salt at pH ≈ 13. After the addition of K2FeO4, a remarkable increase in the OER is recorded in the presence of Pt or PtO2. The obtained catalysts were characterized by operando visible spectroscopy, high-resolution transmission electron microscopy, scanning electron microscopy, electron-spin resonance spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, and electrochemical methods. KOH solutions usually contain Fe and/or Ni impurities. It is found that neither Pt nor PtO2 is an OER catalyst in a Ni/Fe-free KOH, and even at an overpotential of 570 mV in purified KOH (pH ≈ 13), no clear OER was observed.
科研通智能强力驱动
Strongly Powered by AbleSci AI