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Strategic atomic trapping at heterointerfaces for protonic ceramic cells.

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Area of Science:

  • Materials Science and Engineering
  • Electrochemistry
  • Sustainable Energy Technologies

Background:

  • Reversible protonic ceramic electrochemical cells (PCECs) are crucial for sustainable energy conversion.
  • Minimizing precious metal usage in composite electrodes is essential for cost-effective PCECs.
  • Precisely engineered heterointerfaces are key to unlocking PCEC potential.

Purpose of the Study:

  • To introduce an atomic trapping strategy for restructuring interfacial chemistry in perovskite/fluorite heteroelectrodes.
  • To achieve catalytic synergy by manipulating the ruthenium (Ru) coordination environment.
  • To develop a universal strategy for next-generation solid-state energy devices.

Main Methods:

  • Atomic trapping strategy applied to Ba$_{0.5}$Sr$_{0.5}$Co$_{0.8}$Fe$_{0.2}$O$_{3-δ}$ (BSCF) perovskite and Ru@CeO$_{2-δ}$ fluorite heteroelectrodes.
  • Scalable co-sintering protocol to induce thermodynamically driven Ru migration.
  • Analysis of interfacial electron redistribution, oxygen vacancies, and triple conductivity.

Main Results:

  • Coupled interfaces formed by Ru migration into the perovskite matrix.
  • Optimized interfacial properties, including enhanced electron redistribution and oxygen vacancy generation.
  • Low Ru loading electrode demonstrated bifunctionality: 1.51 W cm$^{-2}$ (peak power density) and -2.21 A cm$^{-2}$ (electrolysis current density) at 650 °C.
  • Notable durability with minimal degradation (0.09 mV h$^{-1}$) over 400 h at 600 °C.

Conclusions:

  • The atomic trapping strategy effectively engineers dynamic heterointerfaces with atomic precision.
  • This approach optimizes interfacial chemistry, leading to improved catalytic synergy and PCEC performance.
  • The developed method offers a promising universal strategy for advanced solid-state energy devices.