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Study of Catalytic Reaction at Electrode-Electrolyte Interfaces by a CV-XAFS Method

机译:CV-XAFs方法研究电极 - 电解质界面催化反应

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A method combining cyclic voltammetry (CV) with x-ray absorption fine structure (XAFS) spectroscopy, viz. CV-XAFS, has been developed to enable in situ real-time investigation of atomic and electronic structures related to electrochemical reactions. We use this method to study the reaction of a Pt/C cathode catalyst in the oxygen reduction reaction (ORR) in an alkaline electrolyte, using x-ray energies near the Pt L-III edge for XAFS measurements. It was found that the current induced by the ORR was first observed at approximately 0.08 V versus Hg/HgO, although the Pt valence, which is reflected in the oxidation states, remained almost unchanged. The electronic structure of the catalytic surface in the ORR was observed to be different in the negative and positive scan directions of CV measurements. Hydrogen adsorption is also discussed on the basis of the observation of this spectral change. We have demonstrated that CV-XAFS provides dynamical structural and electronic information related to electrochemical reactions and can be used for in situ real-time measurements of a catalyst.
机译:一种方法将循环伏安法(CV)与X射线吸收细结构(XAFS)光谱,VIZ。已经开发了CV-XAFS,以便原位实时调查原子和电子结构与电化学反应相关的原子和电子结构。我们使用该方法使用Pt L-III边缘附近的X射线能量来研究Pt / C阴极催化剂在碱性电解质中的氧还原反应(ORR)中的反应。发现由ORR引起的电流在约0.08V与HG / HGO中观察到,尽管在氧化态中反射的PT价几乎保持不变。观察到ORR中的催化表面的电子结构在CV测量的阴性和正扫描方向上不同。还基于观察该光谱变化的氢吸附。我们已经证明CV-XAFS提供与电化学反应相关的动态结构和电子信息,并且可以用于原位的催化剂的实时测量。

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