Heterogeneous Pt and MoOx Co-Loaded TiO2 Catalysts for Low-Temperature CO2 Hydrogenation To Form CH3OH

被引:82
|
作者
Toyao, Takashi [1 ,2 ]
Kayamori, Shingo [1 ]
Maeno, Zen [1 ]
Siddiki, S. M. A. Hakim [1 ]
Shimizu, Ken-ichi [1 ,2 ]
机构
[1] Hokkaido Univ, Inst Catalysis, N-21,W-10, Sapporo, Hokkaido 0010021, Japan
[2] Kyoto Univ, Elements Strategy Initiat Catalysts & Batteries, Kyoto 6158520, Japan
来源
ACS CATALYSIS | 2019年 / 9卷 / 09期
关键词
hydrogenation of CO2; CH3OH synthesis; platinum; MoOx; TiO2; in situ spectroscopy; CARBON-DIOXIDE; SELECTIVE HYDROGENATION; METHANOL SYNTHESIS; CONVERSION; ACID; AMINES; GAS; PERFORMANCE; CHALLENGES; MECHANISM;
D O I
10.1021/acscatal.9b01225
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Efficient conversion of CO2 into useful chemicals, exemplified by the development of methods for low-temperature hydrogenation of CO2 to form methanol (CH3OH), is a highly attractive research target. Herein, we report that Pt nanoparticles, loaded on MoOx/TiO2 as a support (Pt(3)/MoOx(30)TiO2; Pt 3 wt %, MoO3 30 wt %), promote selective hydrogenation of CO2 to produce CH3OH in 73% yield under mild conditions (T = 150 degrees C; t = 48 h; P-CO2 = 1 MPa; P-H2 = 5 MPa). It is significant that the observed yield is almost the equilibrium yield of CH3OH expected under the current reaction conditions. In terms of both the yield and selectivity for CH3OH production, the performance of Pt(3)/MoOx(30)/TiO2 is better than that of other metal catalysts supported on MoOx (30)/TiO2 and of Pt catalysts on other supports. Moreover, the results of an investigation of the reaction mechanism using in situ X-ray absorption fine structure (XAFS) suggest that reduced MoOx species are responsible for the progress of this efficient reaction.
引用
收藏
页码:8187 / 8196
页数:19
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