1Department of Environment Systems, Graduate School of Frontier Sciences, The University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa, Chiba 277-8563, Japan
2Research Institute of Energy Frontier, Department of Energy and Environment, Research Institute of Energy Frontier, AIST Tuskuba West, 16-1 Onogawa, Tsukuba, Ibaraki 305-8569, Japan
Adv. Mater. Lett., 2019, 10 (8), pp
DOI: 10.5185/amlett.2019.2259
Publication Date (Web): Jan 14, 2019
Copyright © IAAM-VBRI Press
E-mail: otomo@k.u-tokyo.ac.jp
Direct electrochemical synthesis of ammonia was performed using proton-conducting solid oxide fuel cells. In this study, we investigated the effect of electrode potential on the reaction kinetics of ammonia formation with Fe- and Ru-based catalysts in detail. The cell configuration was Pt|BaCe0.9Y0.1O3 (BCY)|K-modified Fe or Ru-BCY. The ammonia formation rate of K-Ru was higher than that of K-Fe at the rest potential. However, the ammonia formation rate significantly increased by cathodic polarization for the Fe catalyst, and it showed a linear increase for the Ru catalyst, i.e., the ammonia formation rate for K-Fe significantly increased from the rest potential by several hundred times to -1.2V at 700oC, but K-Ru showed only a five times increase. The results suggest that the addition of K into Fe-BCY and cathodic polarization can improve the ammonia formation rate because of the promotion of bond dissociation of the N molecule on the Fe catalyst. The present work provides a hint for efficient ammonia formation and contribute to further development of ammonia electrochemical synthesis with proton-conducting solid oxide fuel cells. © VBRI Press.
Ammonia synthesis, proton conductor, electrochemical promotion, energy storage.
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