Search NASA⌕ Search

DOE OSTI · 1865182

Nanostructured Cathodes for Solid Oxide Fuel Cells by a Solution Spray-Coating Process

Abstract

Composite nano-cathodes containing Sr-doped LaMnO 3 (LSM) and Gd 2 O 3 -doped CeO 2 (GDC) were deposited on yttria-stabilized zirconia (YSZ) discs and YSZ/NiO + YSZ bi-layer discs using an aqueous solution. The samples were heated over a range of temperatures from 700°C to 1200°C to form LSM + GDC porous films. The crystallite size was estimated using X-ray diffraction (XRD) Scherrer formula. The crystallite size was in the ~3 nm to ~80 nm range. Polarization resistance was measured by electrochemical impedance spectroscopy (EIS) from 400°C to 700°C. Nano-cathodes of ~70 nm thickness fired at 700°C exhibited polarization resistance of ~0.23 Ωcm 2 at 700°C. By contrast, LSM + YSZ cathodes made by a conventional process exhibited polarization resistance of ~2 Ωcm 2 . Fuel cell tests were conducted at 700°C on cells with nano-cathodes and conventional LSM + YSZ cathode. The maximum power density was ~0.51 Wcm –2 with nano-cathodes. By contrast, the corresponding power density with conventional LSM + YSZ cathodes was ~0.11 Wcm –2 . Here, the present work shows that very thin cathode functional layers can be deposited on sintered YSZ/NiO + YSZ bi-layer discs by using an aqueous solution. This approach in principle could be extended to large area cells.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Zhang, Lei, Zhu, Liangzhu, Virkar, Anil V.. 2016-09-21. Nanostructured Cathodes for Solid Oxide Fuel Cells by a Solution Spray-Coating Process. https://doi.org/10.1149/2.0541613jes

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related reports

Cyclic moisture reactivation of calcium sorbents for long duration thermochemical energy storage

The transition to a flexible and reliable energy infrastructure, using electro-thermal energy generation technologies such as geothermal, concentrated solar power, and nuclear, usually demands simultaneous advancement of thermal energy storage (TES) to support on-demand electricity generation and industrial applications while mitigating the inherent intermittency of renewable energy sources and power outages from direct energy generation. Among TES technologies, thermochemical energy storage (TCES) based on calcium looping emerges as a compelling high-power energy storage candidate due to its high reaction enthalpy, compatibility with elevated operating temperatures, and abundance of low-cost materials. However, the long-term durability of calcium-based sorbents for TCES is hindered by surface sintering and particle aggregation, leading to performance degradation over repeated thermal cycles. This study explores a moisture hydration-based strategy to regenerate a degraded calcium sorbent and mitigate performance degradation for long duration TCES. The addition of moisture transforms calcium oxide into calcium hydroxide and produces intercalation water layers, associated with a regenerated surface area and reduced calcium oxide crystallite size. Both these effects are beneficial in restoring the sorbents' reactivity for carbonization. Additionally, an optimized hydration-assisted reactivation protocol balances the recovered energy storage capacity with heating penalty required for moisture removal from hydrated samples, resulting in an enhanced energy storage capacity up to 176% compared to benchmark sorbents that undergo cycling without reactivation after 60 cycles. In conclusion, these results highlight the potential of hydration-assisted reactivation to enhance the long-term performance of TCES, providing an effective pathway to advancing electro-thermal storage technologies.

36 MATERIALS SCIENCE↗