Sunlight Powered Continuous Flow Reverse Water Gas Shift Process Using a Plasmonic Au/TiO2 Nanocatalyst

被引:9
|
作者
Molina, Pau Martinez [1 ]
Bossers, Koen W. [1 ]
Wienk, Jelle D. [1 ]
Rohlfs, Jelle [1 ]
Meulendijks, Nicole [1 ]
Verheijen, Marcel A. [2 ,3 ]
Buskens, Pascal [1 ,4 ]
Sastre, Francesc [1 ]
机构
[1] Netherlands Org Appl Sci Res TNO, High Tech Campus 25, NL-5656 AE Eindhoven, Netherlands
[2] Eurofins Mat Sci, High Tech Campus 11, NL-5656 AE Eindhoven, Netherlands
[3] Eindhoven Univ Technol, Dept Appl Phys, NL-5600 MB Eindhoven, Netherlands
[4] Hasselt Univ, Inst Mat Res, Design & Synth Inorgan Mat DESINe, Agoralaan Bldg D, B-3590 Diepenbeek, Belgium
关键词
Carbon dioxide; photochemistry; reverse Water gas Shift flow; solar light; surface plasmon resonance; PHOTOCATALYTIC REDUCTION; CATALYZED CONVERSION; CO2; NANOPARTICLES; METHANE; HYDROGENATION; PERFORMANCE; MECHANISM; SYNGAS; DRIVEN;
D O I
10.1002/asia.202300405
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The continuous flow reverse water gas shift (rWGS) process was efficiently catalyzed by a plasmonic Au/TiO2 nanocatalyst using sunlight as sole and sustainable energy source. The influence of the catalyst bed thickness on the CO production rate was studied, and three different catalytic regimes were identified as direct plasmon catalysis (DPC), shielded plasmon catalysis (SPC) and unused plasmon catalysis (UPC). The CO2:H-2 ratio was optimized to 4:1 and a maximum CO production rate of 7420 mmol.m(-2).h(-1) was achieved under mild reaction conditions (p=3.5 bar, no external heating, E-e=14.0 kW.m(-2)), corresponding to an aparent quantum efficiency of 4.15%. The stability of the Au/TiO2 catalyst was studied for 110 h continuous operation, maintaining more than 82% of the initial CO production rate. On/off experiments mimicking discontinuous sunlight powered processing furthermore showed that the Au/TiO2 catalyst was stable for 8 consecutive runs.
引用
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页数:7
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