Enhanced methane steam reforming activity and electrochemical performance of Ni 0.9 Fe 0.1 -supported solid oxide fuel cells with infiltrated Ni-TiO 2 particles

21Citations
Citations of this article
29Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Ni 0.9 Fe 0.1 alloy-supported solid oxide fuel cells with NiTiO 3 (NTO) infiltrated into the cell support from 0 to 4 wt.% are prepared and investigated for CH 4 steam reforming activity and electrochemical performance. The infiltrated NiTiO 3 is reduced to TiO 2 -supported Ni particles in H 2 at 650 °C. The reforming activity of the Ni 0.9 Fe 0.1 -support is increased by the presence of the TiO 2 -supported Ni particles; 3 wt.% is the optimal value of the added NTO, corresponding to the highest reforming activity, resistance to carbon deposition and electrochemical performance of the cell. Fueled wet CH 4 at 100 mL min '1, the cell with 3 wt.% of NTO demonstrates a peak power density of 1.20 W cm '2 and a high limiting current density of 2.83 A cm '2 at 650 °C. It performs steadily for 96 h at 0.4 A cm '2 without the presence of deposited carbon in the Ni 0.9 Fe 0.1 -support and functional anode. Five polarization processes are identified by deconvoluting and data-fitting the electrochemical impedance spectra of the cells under the testing conditions; and the addition of TiO 2 -supported Ni particles into the Ni 0.9 Fe 0.1 -support reduces the polarization resistance of the processes ascribed to CH 4 steam reforming and gas diffusion in the Ni 0.9 Fe 0.1 -support and functional anode.

Cite

CITATION STYLE

APA

Li, K., Jia, L., Wang, X., Pu, J., Chi, B., & Li, J. (2016). Enhanced methane steam reforming activity and electrochemical performance of Ni 0.9 Fe 0.1 -supported solid oxide fuel cells with infiltrated Ni-TiO 2 particles. Scientific Reports, 6. https://doi.org/10.1038/srep35981

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free