Synergistic Catalysis at the Ni/ZrO2-X Interface toward Low- Temperature Methanation

The CO2 methanation reaction, which achieves the carbon cycle and gains value-added chemicals, has attracted much attention, but the design and exploitation of highly active catalysts remain a big challenge. Herein, zirconium dioxide-supported Ni catalysts toward low-temperature CO2 methanation are obtained via structural topological transformation of NiZrAl-layered double hydroxide (LDH) precursors, which have the feature of an interfacial structure (Ni-O-Zr3+-Vo'') between Ni nanoparticles and ZrO2-x support (0 < x < 1). The optimized catalyst (Ni/ZrO2-x-S2) exhibits exceptional CO2 conversion (similar to 72%) at a temperature as low as 230 degrees C with a similar to 100% selectivity to CH4, without obvious catalyst deactivation within a 110 h reaction at a high gas hourly space velocity of 30,000 mL center dot g-1 center dot h-1. Markedly, the space-time yield of CH4 reaches up to similar to 0.17 molCH4 center dot gcat-1 center dot h-1, which is superior to previously reported Ni catalysts evaluated under similar reaction conditions. Both in situ/operando investigations (diffuse reflectance infrared Fourier transform spectroscopy and X-ray absorption fine structure) and catalytic evaluations substantiate the interfacial synergistic catalysis at the Ni/ZrO2-x interface: the Zr3+-Vo'' facilitates the activation adsorption of CO2, while the H2 molecule experiences dissociation at the metallic Ni sites. This work demonstrates that the metal-support interface effect plays a key role in improving the catalytic behavior toward CO2 methanation, which can be extended to other high-performance heterogeneous catalysts toward structure-sensitive systems.

Automated summary

In this study, zirconium dioxide-supported Ni catalysts were obtained via topological transformation of NiZrAl-layered double hydroxide (LDH) precursors for low-temperature CO2 methanation. The optimized catalyst exhibited exceptional CO2 conversion at a low temperature with high selectivity to CH4, and demonstrated no obvious catalyst deactivation during a long reaction time. The metal-support interface effect was found to play a key role in improving the catalytic behavior for CO2 methanation.