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首页> 外文期刊>International journal of hydrogen energy >Ba0.5Sr0.5Fe0.8Sb0.2O3-delta- Sm0.2Ce0.8O2-delta bulk heterostructure composite: A cobalt free Oxygen Reduction Electrocatalyst for low-temperature SOFCs
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Ba0.5Sr0.5Fe0.8Sb0.2O3-delta- Sm0.2Ce0.8O2-delta bulk heterostructure composite: A cobalt free Oxygen Reduction Electrocatalyst for low-temperature SOFCs

机译:Ba0.5Sr0.5Fe0.8Sb0.2O3-delta- Sm0.2Ce0.8O2-delta bulk heterostructure composite: A cobalt free Oxygen Reduction Electrocatalyst for low-temperature SOFCs

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摘要

Low-temperature operated ceramic fuel cells (LT-CFCs 350 degrees to 550 degrees C) hold a great promise than high-temperature solid oxide fuel cells (HT-SOFCs >= 800 degrees C) for numerous large-scale real-application. If a suitable cathode should be developed to overcome the sluggish oxygen reduction activity at low temperatures, the low-temperature operation of ceramic fuel cells could be possible. In this study, we have developed a cobalt-free Ba0.5Sr0.5Fe0.8Sb0.2O3-delta- Sm0.2Ce0.8O2-delta (BSFSb- SDC) a bulk heterostructure composite for efficient ORR electrocatalyst for LT-SOFC cathode. The established BSFSb-SDC bulk heterostructure composite exhibits large lattice parameters, very low-area-specific resistance, and high oxygen reduction reaction (ORR) activity at low operating temperatures. The prepared fuel cell device has demonstrated high-power densities of 890 mW-cm-(2) at 550 degrees C for button-sized SOFC on H-2 and even possible operation at 400 degrees C. It is also found that BSFSb-SDC effectively facilitates small polaron hopping of valence electrons and diffusion of oxygen ions. Various spectroscopic measurements such as X-ray photoelectron, UV-visible, Raman, and Density Functional Theory (DFT) calculations were employed to understand the improved ORR electrocatalyst function of BSFSb-SDC bulk heterostructure composite SOFC cathode. The results can further help to develop functional cobalt-free electro-catalysts for LT-SOFCs and other related applications. (C) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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