甲烷化
双金属片
催化作用
化学
格式化
水滑石
合金
漫反射红外傅里叶变换
密度泛函理论
选择性
无机化学
原位
多相催化
傅里叶变换红外光谱
化学工程
光催化
有机化学
计算化学
工程类
作者
Huong Lan Huynh,Jie Zhu,Guanghui Zhang,Yongli Shen,Wakshum Mekonnen Tucho,Yi Ding,Zhixin Yu
标识
DOI:10.1016/j.jcat.2020.10.018
摘要
Bimetallic NiFe catalysts have emerged as a promising alternative to the traditional Ni catalysts for CO2 methanation. However, the promoting effect of Fe on the bimetallic catalysts remains ambiguous. In this study, a series of NiFe catalysts derived from hydrotalcite precursors were investigated. In situ x-ray diffraction (XRD) analysis revealed that small NiFe alloy particles were formed and remained stable during reaction. When Fe/Ni = 0.25, the alloy catalysts exhibited the highest CO2 conversion, CH4 selectivity and stability in CO2 methanation at low temperature of 250–350 °C. The in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) study indicated that the formate pathway was the most plausible reaction scheme on both Ni and NiFe alloy catalysts, while a moderate addition of Fe facilitated the activation of CO2 via hydrogenation to *HCOO. Density functional theory (DFT) calculations further demonstrated that the overall energy barrier for CH4 formation was lower on the alloy surface.
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