4.7 Article

Operational Aspects of a Perovskite Chromite-Based Fuel Electrode in Solid Oxide Electrolysis Cells (SOEC)

Journal

ACS APPLIED ENERGY MATERIALS
Volume 5, Issue 7, Pages -

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.2c00680

Keywords

high-temperature electrolysis; solid oxide electrolysis cell; green hydrogen; fuel electrode; perovskite; chromite; p-type; conductivity

Funding

  1. German Academic Exchange Service (DAAD)
  2. German Federal Ministry of Education and Research (BMBF) [n03SFKE20]

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This study investigates the performance of lanthanum strontium chromite perovskite as a fuel electrode in steam electrolysis. The perovskite fuel electrode exhibits comparable performance to state-of-the-art Ni-CGO-based cells at higher temperatures, and even better performance at lower temperatures. The reaction mainly occurs on the oxygen vacancy sites on the perovskite surface, with the assistance of exsolved metallic Ni nanoparticles. However, a decrease in conductivity is observed over time, likely due to diffusion limitations. The lower activation energy of the perovskite fuel electrode holds promise for green hydrogen production via steam electrolysis at reduced temperatures.
The lanthanum strontium chromite perovskite La0.65Sr0.3Cr0.85Ni0.15O3-delta (L6SSCrN) was implemented as fuel electrode in electrolyte-supported cells (ESC). The electrochemical cell performance in steam electrolysis operation with a fuel gas mixture of 80% H2O-20% H-2 was demonstrated to be comparable to that of Ni-CGO-based state of the art cells at 860 degrees C. At 830, 800, and 770 degrees C, the perovskite fuel electrode exhibited a gain in performance. Lower apparent activation energy barrier values were calculated for the L6SSCrN in symmetrical and full cell configurations, in contrast to Ni-CGO fuel electrodes. A reaction model is proposed, where the water-splitting reaction mainly occurs on the oxygen vacancy sites on the L65SCrN surface and where the exsolved metallic Ni nanoparticles assist the catalytic activity of the electrode with hydrogen spillover and H-2 desorption. We observed a voltage degradation of similar to 48 mV/kh during 1000 h of operation under steam electrolysis conditions at 860 degrees C close to the thermoneutral voltage. van der Pauw conductivity measurements corroborated this degradation with a decrease of the perovskite's p-type conductivity, which appeared to be a diffusion-limited phenomenon. Nevertheless, the lower activation energy of the perovskite-based fuel electrode for solid oxide cells (SOCs) is promising for green hydrogen production via steam electrolysis at a reduced temperature (below 860 degrees C) and without the need of a hydrogen sweep.

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