Reverse water-gas shift reaction over Pt/MoOx/TiO2: reverse Mars-van Krevelen mechanism via redox of supported MoOx

被引:40
作者
Mine, Shinya [1 ]
Yamaguchi, Taichi [1 ]
Ting, Kah Wei [1 ]
Maeno, Zen [1 ]
Siddiki, S. M. A. Hakim [1 ]
Oshima, Kazumasa [2 ]
Satokawa, Shigeo [2 ]
Shimizu, Ken-ichi [1 ,3 ]
Toyao, Takashi [1 ,3 ]
机构
[1] Hokkaido Univ, Inst Catalysis, N-21,W-10, Sapporo, Hokkaido 0010021, Japan
[2] Seikei Univ, Fac Sci & Technol, Dept Mat & Life Sci, Musashino, Tokyo 1808633, Japan
[3] Kyoto Univ, Elements Strategy Initiat Catalysts & Batteries, Katsura, Kyoto 6158520, Japan
关键词
HETEROGENEOUS PLATINUM CATALYSTS; TEMPERATURE CO2 HYDROGENATION; CARBON-DIOXIDE; PRODUCT SELECTIVITY; INTERFACIAL SITES; LIQUID FUELS; ACTIVE-SITE; PERFORMANCE; CONVERSION; ACTIVATION;
D O I
10.1039/d1cy00289a
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
The reverse water-gas shift (RWGS) reaction is a promising catalytic route for reducing CO2 emissions because its product, CO, is a key intermediate in various industrialized catalytic processes that produce fuels and chemicals. We describe herein a MoOx/TiO2-supported Pt catalyst (Pt(3)/MoOx(15)/TiO2; Pt loading = 3 wt%, MoO3 loading = 15 wt%) that promotes the RWGS reaction at low temperature (200-300 degrees C) with high activity and selectivity. The catalytic performance for both CO2 conversion and selectivity of Pt(3)/MoOx(15)/TiO2 is better than those of Pt catalysts on other supports and other metal catalysts supported on MoOx(15)/TiO2, as well as Cu- and Fe-Cr-based industrial catalysts. Moreover, results of operando X-ray absorption spectroscopy studies show that the reaction takes place via the reverse Mars-van Krevelen mechanism where H-2 acts as a reducing agent to create oxygen vacancies on the supported Mo oxide species that are filled by CO2 as an oxidizing agent.
引用
收藏
页码:4172 / 4180
页数:9
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