Understanding Direct-Ammonia Protonic Ceramic Fuel Cells: High-Performance in the Absence of Precious Metal Catalysts

Ammonia has received considerable attention as a promising carbon-free hydrogen carrier. At temperatures above 400 °C, NH3 is thermodynamically unstable with respect to decomposition into nitrogen and hydrogen and is, thus, suitable for direct use in solid oxide fuel cells (SOFCs) without external reforming. However, poor catalytic activity for ammonia decomposition at the moderate temperatures of protonic ceramic fuel cell (PCFC) operation has resulted in low fuel cell power output relative to operation on hydrogen and likely contributes to reported cell degradation. Here we prepared cells based on a thermodynamically robust electrolyte, a high activity cathode, and an anode with a distinctive structure to overcome challenges of poor activity and stability. The cells delivered peak power densities of 0.59 and 0.44 W cm–2 under H2 and NH3, respectively, at 500 °C, excellent stability over a period of 200 h, and no detectable NOx in the anode exhaust gas.

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Publication Details

Journal
ACS Energy Letters
Published
2024-10-24
DOI
https://doi.org/10.1021/acsenergylett.4c02263
Citations
24
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
Type
article
Field-Weighted Citation Impact
2.57

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article

Understanding Direct-Ammonia Protonic Ceramic Fuel Cells: High-Performance in the Absence of Precious Metal Catalysts

Dylan Bardgett, Sossina Mariam Haile, Sihyuk Choi, Seungchan Kim et al.
24 citations
ACS Energy Letters
Ammonia Synthesis and Nitrogen Reduction
2.57
article

Understanding Direct-Ammonia Protonic Ceramic Fuel Cells: High-Performance in the Absence of Precious Metal Catalysts

Dylan Bardgett, Sossina Mariam Haile, Sihyuk Choi, Seungchan Kim, Grace Xiong, Jiwon Yun
article en
24 citations

Abstract

Ammonia has received considerable attention as a promising carbon-free hydrogen carrier. At temperatures above 400 °C, NH3 is thermodynamically unstable with respect to decomposition into nitrogen and hydrogen and is, thus, suitable for direct use in solid oxide fuel cells (SOFCs) without external reforming. However, poor catalytic activity for ammonia decomposition at the moderate temperatures of protonic ceramic fuel cell (PCFC) operation has resulted in low fuel cell power output relative to operation on hydrogen and likely contributes to reported cell degradation. Here we prepared cells based on a thermodynamically robust electrolyte, a high activity cathode, and an anode with a distinctive structure to overcome challenges of poor activity and stability. The cells delivered peak power densities of 0.59 and 0.44 W cm–2 under H2 and NH3, respectively, at 500 °C, excellent stability over a period of 200 h, and no detectable NOx in the anode exhaust gas.

ACS Energy LettersVol. 9(11)
Northwestern University (US), Kumoh National Institute of Technology (KR), Vaughn College of Aeronautics and Technology (US), Convergence (US), NextGen Aeronautics (United States) (US)
Northwestern University, Korea Institute of Science and Technology, National Research Foundation of Korea, Division of Materials Research, Basic Energy Sciences
Openalex Percentile: Top 9%
Ammonia Synthesis and Nitrogen Reduction
2.57
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