@article {1062,
	title = {Cobalt-substituted SrTi0.3Fe0.7O3-δ: a stable high-performance oxygen electrode material for intermediate-temperature solid oxide electrochemical cells},
	journal = {Energy \& Environmental Science},
	volume = {11},
	year = {2018},
	month = {07/2018},
	pages = {1870-1879},
	abstract = {<p><span style="color: $\#$111111; font-family: -apple-system, system-ui, {\textquoteright}Segoe UI{\textquoteright}, {\textquoteright}Helvetica Neue{\textquoteright}, Helvetica, Arial, sans-serif; font-size: 13px; white-space: pre-wrap; background-color: $\#$fafafa;">Published on July 11th, 2018. A key need in the development of solid oxide cells (SOCs) is for electrodes that promote fast oxygen reduction and oxygen evolution reactions at reduced operating temperature (<=700 {\textdegree}C), with sufficient durability to allow operation over desired 40 000 h lifetimes. A wide range of electrode materials have been investigated, with some providing resistance low enough for cell operation below 700 {\textdegree}C, but it is generally found that the electrode performance degrades over time. Here we demonstrate an oxygen electrode material, Sr(Ti0.3Fe0.7-xCox)O3-δ (STFC), that provides a unique combination of excellent oxygen electrode performance and long-term stability. The addition of a relatively small amount of Co to Sr(Ti0.3Fe0.7)O3-δ, e.g., x = 0.07, reduces the electrode polarization resistance by \&gt;2 times. The STFC electrode yields stable performance in both fuel cell and electrolysis modes at 1 A cm-2. The fundamental oxygen diffusion and surface exchange coefficients of STFC are determined, and shown to be substantially better than those of La0.6Sr0.4Co0.2Fe0.8O3-δ, the most widely used SOC oxygen electrode material. While other electrode materials have been shown to exhibit better oxygen transport coefficients than STFC, they do not match its stability.</span></p>},
	doi = {10.1039/C8EE00449H},
	url = {https://pubs.rsc.org/en/content/articlelanding/2018/ee/c8ee00449h},
	author = {Shan-Lin Zhang and Hongqian Wang and Matthew Y. Lu and Ai-Ping Zhang and Liliana V. Mogni and Qinyuan Liu and Cheng-Xin Li and Chang-Jiu Li and Scott A. Barnett}
}
