Enhancing the Electrochemical Performance in Symmetrical Solid Oxide Cells through Nanoengineered Redox-Stable Electrodes with Exsolved Nanoparticles

Abstract

Symmetrical solid oxide cells (SSOCs) have recently gained significant attention for their potential in energy conversion due to their simplified cell configuration, cost-effectiveness, and excellent reversibility. However, previous research efforts have mainly focused on improving the electrode performance of perovskite-type electrodes through different doping strategies, neglecting microstructural optimization. This work presents novel approaches for the nanostructural tailoring of (La 0.8 Sr 0.2 ) 0.95 Fe 1−x Ti x O 3−δ (LSFT x , x = 0.2 and 0.4) electrodes using a single-step spray-pyrolysis deposition process. By incorporating these electrodes into a Ce 0.9 Gd 0.1 O 1.95 (CGO) porous backbone or employing a nanocomposite architecture with nanoscale particle size, we achieved significant improvements in the polarization resistance (R p ) compared with traditional screenprinted electrodes. To further boost the fuel oxidation performance, a Ni-doping strategy, coupled with meticulous microstructural optimization, was implemented. The exsolution of Ni nanoparticles under reducing conditions resulted in remarkable R p values as low as 0.34 and 0.11 Ω cm 2 in air and wet H 2 at 700 °C, respectively. Moreover, an electrolyte-supported cell with symmetrical electrodes demonstrated a stable maximum power density of 617 mW cm −2 at 800 °C. These findings highlight the importance of combining electrode composition optimization with advanced morphology control in the design of highly efficient and durable SSOCs.

Enhanced Cathode Performance in Pr0.5Sr0.5FeO3−δ of Perovskite Catalytic Materials via Doping with VB Subgroup Elements (V, Nb, and Ta)

“…Solid oxide fuel cells (SOFCs) perform coordinated work using various components [1][2][3][4][5][6][7][8][9]. The basic components of a battery include three parts.…”