化学
催化作用
四甲基氢氧化铵
热稳定性
煅烧
四方晶系
热液循环
氢氧化物
化学工程
矿物学
无机化学
结晶学
晶体结构
有机化学
工程类
生物化学
作者
Shichao Wang,Hong Xie,Yuyuan Lin,Kenneth R. Poeppelmeier,Tao Li,Randall E. Winans,Yanran Cui,Fabio H. Ribeiro,Christian P. Canlas,Jeffrey W. Elam,Hongbo Zhang,Christopher L. Marshall
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2016-02-15
卷期号:55 (5): 2413-2420
被引量:19
标识
DOI:10.1021/acs.inorgchem.5b02810
摘要
Catalyst support materials of tetragonal ZrO2, stabilized by either La2O3 (La2O3–ZrO2) or CeO2 (CeO2–ZrO2), were synthesized under hydrothermal conditions at 200 °C with NH4OH or tetramethylammonium hydroxide as the mineralizer. From in situ synchrotron powder X-ray diffraction and small-angle X-ray scattering measurements, the calcined La2O3–ZrO2 and CeO2–ZrO2 supports were nonporous nanocrystallites that exhibited rectangular shapes with a thermal stability of up to 1000 °C in air. These supports had an average size of ∼10 nm and a surface area of 59–97 m2/g. The catalysts Pt/La2O3–ZrO2 and Pt/CeO2–ZrO2 were prepared by using atomic layer deposition with varying Pt loadings from 6.3 to 12.4 wt %. Monodispersed Pt nanoparticles of ∼3 nm were obtained for these catalysts. The incorporation of La2O3 and CeO2 into the t-ZrO2 structure did not affect the nature of the active sites for the Pt/ZrO2 catalysts for the water–gas shift reaction.
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