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通过 operando XAS 和拉曼光谱监测金属碳二亚胺水氧化催化剂的表面转化。

Monitoring surface transformations of metal carbodiimide water oxidation catalysts by operando XAS and Raman spectroscopy.

机构信息

University of Zurich, Department of Chemistry, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.

出版信息

Dalton Trans. 2018 Aug 21;47(31):10759-10766. doi: 10.1039/c8dt01587b. Epub 2018 Jul 6.

Abstract

Transition metal carbodiimides MNCN (M = Co, Ni, CoNi, Mn and Cu), were studied by simultaneous operando Raman and X-ray absorption spectroscopy (XAS) with focus on surface oxide detection during electrocatalytic water oxidation. As a proof of concept, easily modifiable screen-printed electrodes were used in this unified operando synchrotron setup for a trade-off between convenience of electrochemical anodization and spectroscopic data acquisition. Monitoring of chemical and structural transformations at the electrode surface during initial anodic electrode polarization shows stability for MNCN with M = Co, Ni, CoNi and Mn. While MnNCN is inactive, CoNCN emerges as the most active representative of the series. CuNCN displays pronounced side reactions and the formation of a surface copper oxide layer leading to lower current density attributed to water oxidation, as evident from an irreversible variation of the CuNCN redox behaviour in rotating ring-disc voltammetry. Furthermore, the accompanying structural and vibrational spectroscopy properties of the different MNCN compounds were explored with complementary ex situ analytical methods.

摘要

过渡金属碳二亚胺 MNCN(M = Co、Ni、CoNi、Mn 和 Cu)通过同时进行的原位拉曼和 X 射线吸收光谱(XAS)进行了研究,重点是在电催化水氧化过程中检测表面氧化物。作为概念验证,在统一的同步辐射原位设置中使用了易于修饰的丝网印刷电极,在电化学阳极氧化的便利性和光谱数据采集之间进行了权衡。在初始阳极电极极化过程中监测电极表面的化学和结构转化表明,M = Co、Ni、CoNi 和 Mn 的 MNCN 稳定。虽然 MnNCN 不活跃,但 CoNCN 作为该系列中最活跃的代表出现。CuNCN 显示出明显的副反应和表面氧化铜层的形成,导致归因于水氧化的电流密度降低,这从旋转环盘伏安法中 CuNCN 氧化还原行为的不可逆变化中显而易见。此外,还使用互补的非原位分析方法探索了不同 MNCN 化合物的伴随结构和振动光谱特性。

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