Self-regeneration of supported transition metals by a high entropy-driven principle

The sintering of Supported Transition Metal Catalysts (STMCs) is a core issue during high temperature catalysis. Perovskite oxides as host matrix for STMCs are proven to be sintering-resistance, leading to a family of self-regenerative materials. However, none other design principles for self-regenerative catalysts were put forward since 2002, which cannot satisfy diverse catalytic processes. Herein, inspired by the principle of high entropy-stabilized structure, a concept whether entropy driving force could promote the self-regeneration process is proposed. To verify it, a high entropy cubic Zr-0.5(NiFeCuMnCo)(0.5)O-x is constructed as a host model, and interestingly in situ reversible exsolution-dissolution of supported metallic species are observed in multi redox cycles. Notably, in situ exsolved transition metals from high entropy Zr-0.5(NiFeCuMnCo)(0.5)O-x support, whose entropic contribution (T Delta S-con (R) g = T star 12.7 J mol(-1) K-1) is predominant in increment G, affording ultrahigh thermal stability in long-term CO2 hydrogenation (400 degrees C, >500 h). Current theory may inspire more STWCs with excellent sintering-resistance performance.