TY - JOUR
T1 - Self-Assembly Dual Active Site Nanocomposite Anode Ce0.6Mn0.3Fe0.1O2−δ/NiFe/MnOx for Electrooxidative Dehydrogenation of Ethane to Ethylene
AU - Zhang, Shixian
AU - Xu, Chunming
AU - Ren, Rongzheng
AU - Qiao, Jinshuo
AU - Wang, Zhenhua
AU - Sun, Wang
AU - Sun, Kening
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/1/24
Y1 - 2024/1/24
N2 - 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.
AB - 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.
KW - CMF/NiFe/MnO anode
KW - CO utilization
KW - SOEC
KW - electrooxidative dehydrogenation
KW - ethane to ethylene
UR - http://www.scopus.com/inward/record.url?scp=85182557653&partnerID=8YFLogxK
U2 - 10.1021/acsami.3c16107
DO - 10.1021/acsami.3c16107
M3 - Article
C2 - 38194627
AN - SCOPUS:85182557653
SN - 1944-8244
VL - 16
SP - 3451
EP - 3459
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 3
ER -