Highly Active and Stable Cobalt-Free Hafnium-doped SrFe0.9Hf0.1O3-δ Perovskite Cathode for Solid Oxide Fuel Cells

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

44 Scopus Citations
View graph of relations

Author(s)

  • Zhenbao Zhang
  • Dengjie Chen
  • Shaozao Tan
  • Xiang Yu
  • Zongping Shao

Detail(s)

Original languageEnglish
Pages (from-to)2134-2142
Journal / PublicationACS Applied Energy Materials
Volume1
Issue number5
Publication statusPublished - 29 May 2018
Externally publishedYes

Abstract

Sluggish oxygen reduction reaction (ORR) kinetics and chemical instability of cathode materials hinder the practical application of solid oxide fuel cells (SOFCs). Here we report a Co-free Hf-doped SrFe0.9Hf0.1O3-δ (SFHf) perovskite oxide as a potential cathode focusing on enhancing the ORR activity and chemical stability. We find that SFHf exhibits a high ORR activity, stable cubic crystal structure, and improved chemical stability toward CO2 poisoning compared to undoped SrFeO3-δ. The SFHf cathode has a polarization area-specific resistance as low as 0.193 ω cm2 at 600 °C in a SFHf|Sm0.2Ce0.8O1.9 (SDC)|SFHf symmetrical cell and has a maximum power density as high as 1.94 W cm-2 at 700 °C in an anode-supported fuel cell (Ni+(ZrO2)0.92(Y2O3)0.08 (YSZ)|YSZ|SDC|SFHf). The ORR activity maintains stable for a period of 120 h in air and in CO2-containing atmosphere. The attractive ORR activity is attributed to the moderate concentration of oxygen vacancy and electrical conductivity, as well as the fast oxygen kinetics at the operation temperature. The improved chemical stability is related to the doping of the redox-inactive Hf cation in the Fe site of SrFeO3-δ by decreasing oxygen vacancy concentration and increasing metal-oxygen bond energy. This work proposes an effective strategy in the design of highly active and stable cathodes for SOFCs.

Research Area(s)

  • Co-free, Perovskite cathode, redox-inactive cation, SrFeO3-δ, structure stability

Bibliographic Note

Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].