Enhancing Ni Exsolution by Nonmetal B-Site Substituents (Si and P) in SrTiO3-Based Solid Oxide Fuel Cell Anodes

In situ nanoparticle exsolution is an excellent strategy to enhance the electrocatalytic activity of solid oxide fuel cell (SOFC) electrodes. Herein, we report that Si and P can be used as B-site nonmetal substituents to improve the electrochemical performance of the model SOFC anode SrTiO 3−δ after testing different Si- and P-substitution levels. First-principles calculations show that Si- or P-substitution promotes the Ni diffusion as well as its segregation toward the surface. Related experiments show that the area-specific resistance (ASR) measured at 800 °C in 3% humidified H 2 improves upon Si- and P-substitution from 0.600 Ω cm 2 for Sr 0.8 Ti 0.9 Ni 0.1 O 3−δ (STN) to 0.061 Ω cm 2 for Sr 0.8 Ti 0.85 Ni 0.1 Si 0.05 O 3−δ and 0.056 Ω cm 2 for Sr 0.8 Ti 0.85 Ni 0.1 P 0.05 O 3−δ . Moreover, the P-substituted material shows excellent stability with a symmetric cell, retaining its ASR for 70 h in 3% humidified H 2 . X-ray photoelectron spectroscopy measurements reveal that even a slight nonmetal substitution can reduce Ni to a lower oxidation state than STN before exsolution. In turn, this promotes the reduction of Ni during exsolution, which improves the ASR. For the first time, nonmetal substituents in perovskite oxides are utilized to aid Ni exsolution from the host lattice, opening new avenues to improve the electrochemical activity.