Integrating photocatalysis and thermocatalysis to enable efficient CO2 reforming of methane on Pt supported CeO2 with Zn doping and atomic layer deposited MgO overcoating

被引:133
|
作者
Pan, Fuping [1 ]
Xiang, Xianmei [1 ]
Du, Zichen [1 ]
Sarnello, Erik [2 ]
Li, Tao [2 ,3 ]
Li, Ying [1 ]
机构
[1] Texas A&M Univ, J Mike Walker 66 Dept Mech Engn, College Stn, TX 77843 USA
[2] Northern Illinois Univ, Dept Chem & Biochem, De Kalb, IL 60115 USA
[3] Argonne Natl Lab, Chem & Mat Sci Grp, Xray Sci Div, Lemont, IL 60439 USA
基金
美国国家科学基金会;
关键词
Dry reforming; Photocatalysis; Stability; Doping; Atomic layer deposition; CARBON-DIOXIDE; NI NANOPARTICLES; TIO2; SURFACE; REDUCTION; CATALYSTS; WATER; NANOCOMPOSITES; PERFORMANCE; CONVERSION;
D O I
10.1016/j.apcatb.2019.118189
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
CO2 reforming or dry reforming of methane (DRM) produces syngas with a low carbon footprint, but the efficiency and stability of DRM remains a challenge. Herein, we report an efficient photo-thereto-chemical DRM (PTC-DRM) process on a Pt supported CeO2 catalyst with Zn doping and surface atomic layer deposition (ALD)-enabled MgO overcoating using concentrated sunlight as the energy input. Under 30 suns irradiation at 600 degrees C, high syngas production rates of 356 and 516 mmol g(-1) h(-1) for H-2 and CO are achieved, which are more than 9 and 3 times larger than those obtained in the thermally driven DRM. Moreover, the light illumination stabilizes the dry reforming process without deactivation, which results from the in situ generation of oxygen vacancy on CeO2 by photo-induced electrons that enables stable CO2 thermo-activation. The ALD coating also reduces surface charge recombination through passivating surface states, thereby enhancing photocatalytic activity.
引用
收藏
页数:9
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