镍
5-羟甲基糠醛
动力学
催化作用
过渡金属
无定形固体
化学
相(物质)
化学动力学
无机化学
材料科学
化学工程
光化学
有机化学
物理
量子力学
工程类
作者
Juhyung Choi,Suhwan Yoo,Phuong Minh Nguyen,Eunchong Lee,Hyeyoung Shin,Yun Jeong Hwang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-04-14
卷期号:15 (9): 6906-6917
被引量:23
标识
DOI:10.1021/acscatal.4c06419
摘要
Nickel-based electrocatalysts have been studied for the electrochemical 5-hydroxymethylfurfural oxidation reaction (HMFOR) to produce 2,5-furan-dicarboxylic acid. Their catalytic activity is suggested to be related to structural changes and hydrogen atom transfer pathways. Here, we developed an efficient electrocatalyst by introducing amorphous NiOOH through electro-driven dual-ion leaching from phosphorized nickel–molybdenum oxide nanoarrays. Operando X-ray absorption spectroscopy and Raman spectroscopy reveal that the amorphous NiOOH catalyst undergoes a rapid phase transformation to form Ni(OH)2 states during the HMFOR, whereas a conventional NiOOH catalyst transitions to Ni(OH)2 via a mixed phase of NiOOH/Ni(OH)2. Operando infrared spectroscopy analysis under chronopotentiometry additionally provides insights into the electro-kinetics, supporting the generation of water through the combination of OH– and released proton during HMFOR. This indicates that the coordination environments near the active Ni element influence the dehydrogenation kinetics of the active nickel species. This study provides insights into the kinetics of HMFOR associated with the structural transition for the design of Ni-based electrocatalysts.
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