Self-Assembly Dual Active Site Nanocomposite Anode Ce0.6Mn0.3Fe0.1O2−δ/NiFe/MnOx for Electrooxidative Dehydrogenation of Ethane to Ethylene

Shixian Zhang, Chunming Xu*, Rongzheng Ren, Jinshuo Qiao, Zhenhua Wang, Wang Sun*, Kening Sun*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

As the demand for ethylene grows continuously in industry, conversion of ethane to ethylene has become more and more important; however, it still faces fundamental challenges of low ethane conversion, low ethylene selectivity, overoxidation, and instability of catalysts. Electrooxidative dehydrogenation of ethane (EODHE) in a solid oxide electrolysis cell (SOEC) is an alternative process. Here, a multiphase oxide Ce0.6Mn0.3Fe0.1O2−δ-NiFe-MnOx has been fabricated by a self-assembly process and utilized as the SOEC anode material for EODHE. The highest ethane conversions reached 52.23% with 94.11% ethylene selectivity at the anode side and CO with 10.9 mL min-1 cm-2 at the cathode side, at 1.8 V at 700 °C. The remarkable electrooxidative performance of CMF-NiFe-MnOx is ascribed to the NiFe alloy and MnOx nanoparticles and improvement of the concentration of oxygen vacancies within the fluorite substrate, generating dual active sites for C2H6 adsorption, dehydrogenation, and selective transformation of hydrogen without overoxidizing the ethylene generated. Such a tailored strategy achieves no significant degradation observed after 120 h of operation and constitutes a promising basis for EODHE.

Original languageEnglish
Pages (from-to)3451-3459
Number of pages9
JournalACS applied materials & interfaces
Volume16
Issue number3
DOIs
Publication statusPublished - 24 Jan 2024

Keywords

  • CMF/NiFe/MnO anode
  • CO utilization
  • SOEC
  • electrooxidative dehydrogenation
  • ethane to ethylene

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