Narrowing band gap energy of CeO2 in (Ni/CeO2)@SiO2 catalyst for photothermal methane dry reforming

Thermal catalysis is the most investigated approach for methane dry reforming (MDR) reaction over Ni-based catalysts. However, sintering and carbon deposition in the conventional approach tend to deactivate the Ni catalysts. Developing new technique to resolve the problems is a hot topic for MDR. Herein, we reported a novel (Ni/CeO2)@SiO2 catalyst for MDR by photothermal catalysis. The catalyst was characterized by BET, XRD, TEM and UV-vis diffuse reflectance spectrum to analysis structural and optical properties, which were applied to build relationship with MDR performance. The results revealed that band gap energy of ceria in the catalyst was significantly narrowed by the tiny size of crystal ceria, leading to strong absorbance of visible solar light. The adsorption considerably promoted activations of CH4 on Ni and CO2 on CeO2, and greatly improved gasification of CHx at Ni-CeO2 boundaries. Along with confinement effect from silica shell, sintering and carbon deposition were both resolved for the (Ni/CeO2)@SiO2 catalyst in photothermal MDR. Consequently, photothermal MDR was higher and more stable than thermal MDR over the catalyst. The work provided a new way of photothermal MDR to enhance activity and stability, and simultaneously resolved problems of sintering and carbon deposition.

Automated summary

A novel (Ni/CeO2)@SiO2 catalyst for methane dry reforming (MDR) was investigated using photothermal catalysis to tackle issues of sintering and carbon deposition, leading to higher efficiency and stability in MDR. The band gap energy of ceria was significantly reduced by crystal size, allowing strong absorbance of visible solar light and promoting CH4 and CO2 activation. Additionally, the silica shell confinement effect helped resolve sintering and carbon deposition, ultimately enhancing MDR performance.