催化作用
甲醇
X射线光电子能谱
化学
纳米颗粒
部分氧化
甲烷
选择性
密度泛函理论
扫描透射电子显微镜
甲烷厌氧氧化
离子键合
无机化学
吸收光谱法
化学工程
透射电子显微镜
分析化学(期刊)
材料科学
纳米技术
计算化学
离子
有机化学
工程类
物理
量子力学
作者
So-Hwang Kye,Hee Sun Park,Renqin Zhang,Hee Jung Yang,Kyu Hyung Lee,Hoyoung Suh,Jin-Gyu Kim,Min Gyu Kim,Gyeong S. Hwang,Nam Hwi Hur
摘要
Catalytic transformation of methane (CH4) into methanol in a single step is a challenging issue for the utilization of CH4. We present a direct method for converting CH4 into methanol with high selectivity over a Pt/CeO2 catalyst which contains ionic Pt2+ species supported on a CeO2 nanoparticle. The Pt/CeO2 catalyst reproducibly yielded 6.27 mmol/g of Pt with a selectivity of over 95% at 300 °C when CH4 and CO are used as reactants, while the catalyst had a lower activity when using only CH4 without CO. Active lattice oxygen created on the Pt and CeO2 interface provides selective reaction pathways for the conversion of CH4 to methanol. Based on high-angle annular dark-field scanning transmission electron microscopy, x-ray photoelectron spectroscopy, x-ray absorption near-edge structure, extended x-ray absorption fine structure, catalytic studies, and density functional theory calculations, we propose a mechanistic pathway involving CH4 activation at the active site in the vicinity of Pt2+ species.
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