X射线吸收精细结构
选择性
催化作用
纳米颗粒
材料科学
电化学
分析化学(期刊)
吸收(声学)
四苯基卟啉
光谱学
无机化学
化学
电极
物理化学
纳米技术
光化学
复合材料
物理
量子力学
生物化学
色谱法
卟啉
作者
Sebastian Kunze,Philipp Grosse,Miguel Bernal,Ilya Sinev,Ioannis Zegkinoglou,Hemma Mistry,Janis Timoshenko,Michael Y. Hu,Jiyong Zhao,E. Ercan,See Wee Chee,Beatriz Roldán Cuenya
标识
DOI:10.1002/anie.202010535
摘要
Abstract Operando nuclear resonant inelastic X‐ray scattering (NRIXS) and X‐ray absorption fine‐structure spectroscopy (XAFS) measurements were used to gain insight into the structure and surface composition of FeCu and FeAg nanoparticles (NPs) during the electrochemical CO 2 reduction (CO 2 RR) and to extract correlations with their catalytic activity and selectivity. The formation of a core–shell structure during CO 2 RR for FeAg NPs was inferred from the analysis of the operando NRIXS data (phonon density of states, PDOS) and XAFS measurements. Electrochemical analysis of the FeAg NPs revealed a faradaic selectivity of 36 % for CO in 0.1 M KHCO 3 at −1.1 V vs. RHE, similar to that of pure Ag NPs. In contrast, a predominant selectivity towards H 2 evolution is obtained in the case of the FeCu NPs, analogous to the results obtained for pure Fe NPs, although small Cu NPs have also been shown to favor H 2 production.
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