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Interface-driven boost in the performance and stability of protonic ceramic electrochemical cells

Yoo, Hyun Sik, Lee, Jongseo, Kim, Soyeon, Kim, Joon Gyu, Bang, Sehee, Jung, Yuhan, Kim, Donguk, Wen, Yue, Bae, Min Hyung, Seo, Bong Hyun, Suk, Ji Won, Lee, Wonyoung·2026·Nature Communications

Abstract

Interfacial resistance remains a key challenge in developing high-performance and durable protonic ceramic electrochemical cells (PCECs), especially at low temperatures. Here, we present a systematic interface engineering strategy that quantitatively correlates interfacial contact coverage with electrochemical performance. A thin and dense PrBa 0.5 Sr 0.5 Co 1.5 Fe 0.5 O 5+δ interlayer is fabricated via low-cost and scalable precursor-based electrostatic spray deposition on a BaZr 0.4 Ce 0.4 Y 0.1 Yb 0.1 O 3-δ electrolyte, achieving a nearly complete contact coverage of 92.6 ± 0.6%. Equivalent circuit-based impedance modeling confirms that the improved contact coverage reduced both the interfacial ohmic and polarization resistances. The interface-engineered PCEC achieves a peak power density of 1.01 W/cm 2 in fuel cell mode and a current density of 1.15 A/cm 2 at 1.3 V in electrolysis mode at 500 °C. It also demonstrates improved interfacial mechanical integrity, preventing delamination under harsh thermal cycling, long-term operational stability, and fuel flexibility with direct ammonia and methane.

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  1. Choi, S., Davenport, T. C. & Haile, S. M. Protonic ceramic electrochemical cells for hydrogen production and electricity generation: exceptional reversibility, stability, and demonstrated faradaic efficiency. Energy Environ. Sci. 12, 206–215 (2019). · DOI
  2. Hong, K. et al. Direct methane protonic ceramic fuel cells with self-assembled Ni-Rh bimetallic catalyst. Nat. Commun. 14, 7485 (2023). · DOI
  3. Kim, D. et al. Advances and challenges in developing protonic ceramic cells. Mater. Today Energy 36, 101365 (2023). · DOI
  4. Yang, L. et al. Enhanced sulfur and coking tolerance of a mixed ion conductor for SOFCs: BaZr0.1Ce0.7Y0.2–xYbxO3–δ. Science 326, 126–129 (2009). · DOI
  5. Liu, F. et al. Lowering the operating temperature of protonic ceramic electrochemical cells to <450 °C. Nat. Energy 8, 1145–1157 (2023). · DOI
  6. Choi, S. et al. Exceptional power density and stability at intermediate temperatures in protonic ceramic fuel cells. Nat. Energy 3, 202–210 (2018). · DOI
  7. Duan, C. et al. Highly efficient reversible protonic ceramic electrochemical cells for power generation and fuel production. Nat. Energy 4, 230–240 (2019). · DOI
  8. Kim, J. H. et al. A universal oxygen electrode for reversible solid oxide electrochemical cells at reduced temperatures. Energy Environ. Sci. 16, 3803–3814 (2023). · DOI
  9. Saqib, M. et al. Transition from perovskite to misfit-layered structure materials: a highly oxygen-deficient and stable oxygen electrode catalyst. Energy Environ. Sci. 14, 2472–2484 (2021). · DOI
  10. Seong, A. et al. Electrokinetic proton transport in triple (H+/O2−/e−) conducting oxides as a key descriptor for highly efficient protonic ceramic fuel cells. Adv. Sci. 8, 2004099 (2021). · DOI
  11. Choi, M. et al. Interface engineering to operate reversible protonic ceramic electrochemical cells below 500 °C. Adv. Energy Mater. 15, 2400124 (2025). · DOI
  12. Bian, W. et al. Revitalizing the interface in protonic ceramic cells by acid etch. Nature 604, 479–485 (2022). · DOI · Paper page
  13. Zhang, Y. et al. Thermal-expansion offset for high-performance fuel cell cathodes. Nature 591, 246–251 (2021). · DOI
  14. Lee, J. et al. Enhanced interface reactivity by a nanowrinkled functional layer for intermediate-temperature solid oxide fuel cells. J. Mater. Chem. A 7, 21120–21127 (2019). · DOI
  15. Li, C. et al. Electrolyte-electrode interface: a key factor for advanced protonic ceramic electrochemical cells. Ceram. Int. 50, 4656–4664 (2024). · DOI
  16. Xu, K. et al. A universal interfacial-engineering strategy for the air electrodes of reversible protonic ceramic electrochemical cells. Energy Environ. Sci. 18, 6722–6731 (2025). · DOI
  17. Zhou, T. et al. Significantly enhanced performance of protonic ceramic fuel cells by laser engineering the electrolyte/cathode interface. ACS Energy Lett. 9, 4557–4563 (2024). · DOI
  18. Hwang, S. et al. A hydrogel-assisted GDC chemical diffusion barrier for durable solid oxide fuel cells. J. Mater. Chem. A 9, 11683–11690 (2021). · DOI
  19. Kim, D. et al. Quantitative interface engineering framework for high-performance and durable protonic ceramic electrochemical cells. Adv. Energy Mater. https://doi.org/10.1002/aenm.202505277 (2026). · DOI
  20. Yoo, H. S. et al. Interface engineering to improve electrochemical performance of intermediate-temperature solid oxide fuel cells. Appl. Surf. Sci. 639, 158188 (2023). · DOI
  21. Lee, J., Kim, S. Y., Yoo, H. S. & Lee, W. Pd-WO3 chemiresistive sensor with reinforced self-assembly for hydrogen detection at room temperature. Sens. Actuators, B 368, 132236 (2022). · DOI
  22. Sharma, R. K. et al. An innovative architectural design to enhance the electrochemical performance of La2NiO4+δ cathodes for solid oxide fuel cell applications. J. Power Sources 316, 17–28 (2016). · DOI
  23. Yoo, H. S. et al. Conformal nanocoating at the electrode–electrolyte interface for active and durable solid oxide electrochemical cells. ACS Nano 20, 5918–5927 (2026). · DOI
  24. Lee, J., Bang, S. & Lee, W. Sol-gel combustion-assisted electrostatic spray deposition for durable solid oxide fuel cell cathodes. Front. Chem. 10, 873758 (2022). · DOI
  25. Choi, M., Lee, J. & Lee, W. Fluid mechanical approaches for rational design of infiltrated electrodes of solid oxide fuel cells. Int. J. Precis. Eng. Manuf. - Green. Technol. 6, 53–61 (2019). · DOI
  26. Choi, S. et al. Highly efficient and robust cathode materials for low-temperature solid oxide fuel cells: PrBa0.5Sr0.5Co2−xFexO5+δ. Sci. Rep. 3, 2426 (2013). · DOI · Paper page
  27. Kane, N. et al. Durable and high-performance thin-film BHYb-coated BZCYYb bilayer electrolytes for proton-conducting reversible solid oxide cells. ACS Appl. Mater. Interfaces 15, 32395–32403 (2023). · DOI
  28. Luo, Z. et al. Harnessing high-throughput computational methods to accelerate the discovery of optimal proton conductors for high-performance and durable protonic ceramic electrochemical cells. Adv. Mater. 36, 2311159 (2024). · DOI · Paper page
  29. Bang, S., Lee, J. & Lee, W. Highly connected oxygen ion conduction pathways in anode functional layer for high-performance solid oxide fuel cells. J. Power Sources 553, 232290 (2023). · DOI
  30. Bang, S. et al. Sequential core–shell-to-alloy evolution enables the structural stabilization and catalytic activation of solid oxide electrolysis cells. Adv. Funct. Mater. https://doi.org/10.1002/adfm.202525596 (2026). · DOI
  31. Zheng, H., Riegraf, M., Sata, N. & Costa, R. A double perovskite oxygen electrode in Zr-rich proton conducting ceramic cells for efficient electricity generation and hydrogen production. J. Mater. Chem. A 11, 10955–10970 (2023). · DOI
  32. Zheng, S., Bian, W. & Ding, H. A robust protonic ceramic fuel cell with a triple conducting oxygen electrode under accelerated stress tests. Mater. Adv. 5, 2296–2305 (2024). · DOI
  33. Zheng, S. et al. Enhancing surface activity and durability in a triple conducting electrode for protonic ceramic electrochemical cells. Nat. Commun. 16, 4146 (2025). · DOI
  34. Choi, S. M. et al. Electrochemical analysis of high-performance protonic ceramic fuel cells based on a columnar-structured thin electrolyte. Appl. Energy 233, 29–36 (2019). · DOI
  35. Choi, M., Lee, J. & Lee, W. Nano-film coated cathode functional layers towards high performance solid oxide fuel cells. J. Mater. Chem. A 6, 11811–11818 (2018). · DOI
  36. An, H. et al. A 5 × 5 cm2 protonic ceramic fuel cell with a power density of 1.3 W cm–2 at 600 °C. Nat. Energy 3, 870–875 (2018). · DOI
  37. Choi, M. et al. Exceptionally high performance of protonic ceramic fuel cells with stoichiometric electrolytes. Energy Environ. Sci. 14, 6476–6483 (2021). · DOI
  38. Ding, H. et al. Self-sustainable protonic ceramic electrochemical cells using a triple conducting electrode for hydrogen and power production. Nat. Commun. 11, 1907 (2020). · DOI · Paper page
  39. Duan, C. et al. Highly durable, coking and sulfur-tolerant, fuel-flexible protonic ceramic fuel cells. Nature 557, 217–222 (2018). · DOI
  40. Luo, Z. et al. Critical role of acceptor dopants in designing highly stable and compatible proton-conducting electrolytes for reversible solid oxide cells. Energy Environ. Sci. 15, 2992–3003 (2022). · DOI
  41. Park, K. et al. Understanding the highly electrocatalytic active mixed triple conducting NaxCa3–xCo4O9–δ oxygen electrode materials. Adv. Energy Mater. 13, 2202999 (2023). · DOI
  42. Pei, K. et al. Surface restructuring of a perovskite-type air electrode for reversible protonic ceramic electrochemical cells. Nat. Commun. 13, 2207 (2022). · DOI
  43. Wu, W. et al. 3D Self-architectured steam electrode enabled efficient and durable hydrogen production in a proton-conducting solid oxide electrolysis cell at temperatures lower than 600 °C. Adv. Sci. 5, 1800360 (2018). · DOI
  44. Liu, Z. et al. Strategic atomic trapping at heterointerfaces for protonic ceramic cells. Nat. Commun. 16, 10405 (2025). · DOI
  45. Rehman, S. U. et al. Designing the nano-scale architecture of the air electrode for high-performance and robust reversible solid oxide cells. Appl. Catal. B Environ. Energy 333, 122784 (2023). · DOI
  46. Bang, S. et al. Heterostructured electrodes for Cr-tolerant solid oxide fuel cells. J. Mater. Chem. A 12, 24103–24113 (2024). · DOI
  47. Choi, M., Kim, S. J. & Lee, W. Effects of water atmosphere on chemical degradation of PrBa0.5Sr0.5Co1.5Fe0.5O5+δ electrodes. Ceram. Int. 47, 7790–7797 (2021). · DOI
  48. Choi, M. & Lee, W. Tuning the oxygen vacancy concentration in a heterostructured electrode for high chemical and electrochemical stabilities. Chem. Eng. J. 431, 134345 (2022). · DOI
  49. Lee, W. et al. Cation size mismatch and charge interactions drive dopant segregation at the surfaces of manganite perovskites. J. Am. Chem. Soc. 135, 7909–7925 (2013). · DOI
  50. Graves, C. et al. Eliminating degradation in solid oxide electrochemical cells by reversible operation. Nat. Mater. 14, 239–244 (2015). · DOI · Paper page
  51. Park, B.-K., Zhang, Q., Voorhees, P. W. & Barnett, S. A. Conditions for stable operation of solid oxide electrolysis cells: oxygen electrode effects. Energy Environ. Sci. 12, 3053–3062 (2019). · DOI
  52. Bang, S. et al. Equalized oxygen partial pressure for carbon coking-free dry reforming of methane in intermediate temperature solid oxide fuel cells. Chem. Eng. J. https://doi.org/10.1016/j.cej.2025.163163 (2025). · DOI
  53. Chen, Y. et al. A robust fuel cell operated on nearly dry methane at 500 °C enabled by synergistic thermal catalysis and electrocatalysis. Nat. Energy 3, 1042–1050 (2018). · DOI
  54. Duan, C. et al. Readily processed protonic ceramic fuel cells with high performance at low temperatures. Science 349, 1321–1326 (2015). · DOI
  55. Zhang, H. et al. An efficient and durable anode for ammonia protonic ceramic fuel cells. Energy Environ. Sci. 15, 287–295 (2022). · DOI
  56. Aoki, Y. et al. High-efficiency direct ammonia fuel cells based on BaZr0.1Ce0.7Y0.2O3−δ/Pd oxide-metal junctions. Glob. Chall. 2, 1700088 (2018). · DOI
  57. He, F. et al. A new Pd-doped proton-conducting perovskite oxide with multiple functionalities for efficient and stable power generation from ammonia at reduced temperatures. Adv. Energy Mater. 11, 2003916 (2021). · DOI
  58. Lin, Y. et al. Proton-conducting fuel cells operating on hydrogen, ammonia and hydrazine at intermediate temperatures. Int. J. Hydrog. Energy 35, 2637–2642 (2010). · DOI
  59. Miyazaki, K., Muroyama, H., Matsui, T. & Eguchi, K. Impact of the ammonia decomposition reaction over an anode on direct ammonia-fueled protonic ceramic fuel cells. Sustain. Energy Fuels 4, 5238–5246 (2020). · DOI
  60. Takagi, Y., Lai, B.-K., Kerman, K. & Ramanathan, S. Low temperature thin film solid oxide fuel cells with nanoporous ruthenium anodes for direct methane operation. Energy Environ. Sci. 4, 3473–3478 (2011). · DOI
  61. Zha, S., Moore, A., Abernathy, H. & Liu, M. GDC-based low-temperature SOFCs powered by hydrocarbon fuels. J. Electrochem. Soc. 151, A1128 (2004). · DOI
  62. Zhang, L. & Yang, W. Direct ammonia solid oxide fuel cell based on thin proton-conducting electrolyte. J. Power Sources 179, 92–95 (2008). · DOI

Metadata

Authors
Yoo, H. S., Lee, J., Kim, S., Kim, J. G., Bang, S., Jung, Y., Kim, D., Wen, Y., Bae, M. H., Seo, B. H., Suk, J. W., & Lee, W.
Venue
Nature Communications
Published
2026-09-17
Volume
17
Issue
1
ISSN
2041-1723
Cited by
0
Language
en
Licence
Funders
  • National Research Foundation of Korea (2022R1A2C3012372, RS-2024-00448287, RS-2026-25501632)
  • Korea Research Institute of Chemical Technology (KK2513-30)

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CoChat. (2026). Citation check: Interface-driven boost in the performance and stability of protonic ceramic electrochemical cells. https://app.cochat.ai/papers/10.1038/s41467-026-77561-6
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Yoo, H. S., Lee, J., Kim, S., Kim, J. G., Bang, S., Jung, Y., Kim, D., Wen, Y., Bae, M. H., Seo, B. H., Suk, J. W., & Lee, W. (2026). Interface-driven boost in the performance and stability of protonic ceramic electrochemical cells. Nature Communications. https://doi.org/10.1038/s41467-026-77561-6

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