Stabilizing Catalytic Performance in Dry Reforming of Methane via Surface-Engineered Intermetallic Carbide Nanoparticles
Olusola Johnson, Yang He, Jillian R. Richter, Isabella St. Pierre-Charles, Babu Joseph, John N. Kuhn
Abstract
Intermetallic Ni 3 ZnC 0.7 catalysts were synthesized and demonstrated for the stable low-temperature CO 2 reforming of methane. Annealing of silica-supported Ni 3 Zn nanoparticles with CO 2 /CH 4 formed an intermetallic ordered Ni 3 ZnC 0.7 phase with interstitial subsurface carbon atoms, and Ni δ- -Zn δ+ paired active sites. The intermetallic carbide exhibited exceptional 160 h stability with negligible deactivation, contrasted with severe deactivation in the monometallic Ni catalyst due to coking. The critical roles of carbon diffusion, local structural and electronic modulation, and intermetallic bonding in stabilizing the optimal surface structure in intermetallic carbide nanocatalysts were revealed through in situ XPS, HS-LEIS, XAS, neutron PDF analysis, and performance testing. The controlled synthesis of these intermetallic carbide nanoparticles provides insights into designing the next generation of high performing nanocatalysts.