水煤气变换反应
氢氧化物
催化作用
扩展X射线吸收精细结构
材料科学
空位缺陷
X射线光电子能谱
无机化学
镍
氧化物
纳米颗粒
化学工程
化学
金属
吸收光谱法
结晶学
纳米技术
冶金
工程类
生物化学
量子力学
物理
作者
Ming Xu,Shan He,Hao Chen,Guoqing Cui,Lirong Zheng,Bin Wang,Min Wei
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2017-09-25
卷期号:7 (11): 7600-7609
被引量:352
标识
DOI:10.1021/acscatal.7b01951
摘要
The modulation of strong metal–support interaction (SMSI) plays a key role and remains a challenge in achieving the desired catalytic performance in many important chemical reactions. Herein, we report a TiO2–x-modified Ni nanocatalyst with tunable Ni–TiO2–x interaction via a two-step procedure: preparation of Ni/Ti mixed metal oxide (NiTi–MMO) from NiTi-layered double hydroxide (NiTi–LDH) precursor, followed by a further reduction treatment at different temperatures. A combination study (XRD, TEM, H2-TPR, XPS, and in situ EXAFS) verifies that a high reduction temperature enhances the Ni–TiO2–x interaction, which results in an increased coverage degree of Ni nanoparticles by TiO2–x as well as electron density of interfacial Ni (Niδ−). Moreover, the creation of a Niδ−–Ov–Ti3+ interface site (Ov denotes oxygen vacancy) induced by strong Ni–TiO2–x interaction serves as dual-active site to efficiently catalyze the water–gas shift reaction (WGSR). The optimized catalyst (Ni@TiO2–x(450)) via tuning Ni–TiO2–x interaction gives a TOF value of 3.8 s–1, which is ∼7 times larger than the conventional 15%Ni/TiO2(450) catalyst. Such a high catalytic efficiency is attributed to the interfacial site (Niδ−–Ov–Ti3+) with medium strength of metal–support interaction, as revealed by in situ diffuse reflectance Fourier transform infrared spectroscopy (in situ DRIFTS), which promotes the synergic catalysis between Niδ− and oxygen vacancy toward WGSR.
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