Probing into the multifunctional role of copper species and reaction pathway on copper-cerium-zirconium catalysts for CO2 hydrogenation to methanol using high pressure in situ DRIFTS
发表时间：2020-04-15
点击次数：
- 论文类型：
- 期刊论文
- 第一作者：
- Wang, Weiwei
- 通讯作者：
- Qu, ZP (reprint author), Dalian Univ Technol, Sch Environm Sci & Technol, Key Lab Ind Ecol & Environm Engn, Dalian 116029, Peoples R China.; Fu, Q (reprint author), Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China.
- 合写作者：
- Qu, Zhenping,Song, Lixin,Fu, Qiang
- 发表时间：
- 2020-02-01
- 发表刊物：
- JOURNAL OF CATALYSIS
- 收录刊物：
- EI、SCIE
- 文献类型：
- J
- 卷号：
- 382
- 页面范围：
- 129-140
- ISSN号：
- 0021-9517
- 关键字：
- Methanol synthesis; CO2 hydrogenation; Surface CuO; Cu-Ce-Zr; In situ DRIFTS
- 摘要：
- A series of ternary copper-cerium-zirconium catalysts containing two kinds of copper species, surface CuO and Cu-Ce-Zr solid solution, are prepared and studied for catalytic properties of CO2 hydrogenation to methanol. The copper-cerium-zirconium catalyst calcined at 450 degrees C (CCZ-450) is much more favorable for improving the nature of surface CuO species and forming Cu-Ce-Zr solid solution than others. The best catalytic behavior in terms of methanol selectivity (T = 280 C, SCH3OH = 71.8%), turnover frequency (TOFCO2 =13.4 x 10(-2) s(-1)) and activation energy (E-a = 28.5 kJ/mot) are achieved using CCZ-450. The excellent catalytic performance of CCZ-450 is attributed to the stronger H2 adsorption ability arising from highly dispersed surface CuO specie with higher copper surface area and higher concentration of active bi/m-HCOO* intermediate caused by the formation of Cu-Ce-Zr solid solution. Both the dispersion and surface area of active sites and the activation abilities of CO2 are critical for catalyst activity and product selectivity. In situ diffuse reflectance infrared fourier transform spectroscopy (DRIFTS) experiments at 3 MPa confirm that both bi-HCOO* and m-HCOO* are the active intermediates for CO2 hydrogenation to methanol. The accumulation of m-HCOO on the catalyst surface is the crucial step of CO2 hydrogenation to methanol. (C) 2019 Elsevier Inc. All rights reserved.
- 是否译文：
- 否
