Abstract

Perovskites with in situ exsolved metal nanoparticles have been extensively studied for CO2 electrolysis in solid oxide electrolysis cell. However, exsolution process is strongly governed by the sluggish diffusion rate of cations and poor structural stability issues. Here we present a new exsolution process on redox stable Pr0.7Sr0.3Cr0.9Ni0.1O3−δ (PSCN) perovskite by topotactic exsolution. This process tends to generate host stoichiometric Pr0.7Sr0.3Cr0.9(FeNi)0.1O3−δ perovskite, triggering Ni cations segregation from the host while maintaining structural stability via supplement of Fe guest cations. The FeNi alloy nanoparticles decorated cathode showed a current density of 1.49 A cm−2 at 800 °C and 1.6 V for CO2 electrolysis, demonstrating over 62.0 % improvement compared to the primitive PSCN cathode. Experimental studies and density functional theory calculations revealed that the activity originated from the unique ability to adsorb and activate CO2 at the metal/perovskite interfaces. This cation supplement strategy may expand the frontiers in the evolution of exsolution on perovskite catalysts for CO2 utilization and other heterogeneous catalytic reactions.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call