Exsolution trends and co-segregation aspects of self-grown catalyst nanoparticles in perovskites

Abstract

In perovskites, exsolution of transition metals has been proposed as a smart catalyst design for energy applications. Although there exist transition metals with superior catalytic activity, they are limited by their ability to exsolve under a reducing environment. When a doping element is present in the perovskite, it is often observed that the surface segregation of the doping element is changed by oxygen vacancies. However, the mechanism of co-segregation of doping element with oxygen vacancies is still an open question. Here we report trends in the exsolution of transition metal (Mn, Co, Ni and Fe) on the PrBaMn ₂O _{5+ δ} layered perovskite oxide related to the co-segregation energy. Transmission electron microscopic observations show that easily reducible cations (Mn, Co and Ni) are exsolved from the perovskite depending on the transition metal-perovskite reducibility. In addition, using density functional calculations we reveal that co-segregation of B-site dopant and oxygen vacancies plays a central role in the exsolution.

Abstract

Exsolution of transition metals from perovskites provides an effective route to useful catalysts, but the underlying factors governing exsolution remain poorly understood. Here, the authors find trends in exsolution in layered perovskites, showing that co-segregation of B-site dopant and oxygen vacancies plays a central role.