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2022 Fiscal Year Research-status Report

Development of efficient low-cost SOFC/SOEC protonic cathodes for reliable energy distribution

Research Project

Project/Area Number 19K05672
Research InstitutionKyushu University

Principal Investigator

Kwati Leonard  九州大学, カーボンニュートラル・エネルギー国際研究所, 助教 (70734391)

Project Period (FY) 2019-04-01 – 2025-03-31
Keywordsprotonic air electrode / catalytic activity / steam electrolysis / fuel cell / hydration / ionic transport / mixed conductivity
Outline of Annual Research Achievements

Proton-conducting solid-oxide electrolysis and fuel cells represent viable, intermediate-temperature green energy conversion and storage technologies. However, their commercial viability has been hindered, in part, by the development of corresponding single-phase electrode components with mixed proton-electron conductivity (MPEC) and effective catalytic activity toward oxygen reduction and evolution reactions (ORR/OER). Also, the basic principles required to achieve high electronic conductivity accompanied by proton and oxygen-ion conduction are
poorly understood. This section of the work aims to understand the fundamental properties of these electrodes, like hydration, electronic
structure, conductivity, and catalytic activity. So far, the origin of catalytic activity in LnCo0.5Ni0.5O3-δ (Ln=La, Pr and Nd) perovskites
"positrodes" (positive electrode) were investigated by low energy-ion scattering (LEIS), hydration and DFT studies. LEIS results reveal that La, Pr, Nd, and Pr cations dominate the outer atomic layer, with profound implications for catalytic activity. Whereas the First principal calculations performed using the plane-wave DFT method and hybrid HSE06 functional suggest the catalytic activity and electronic properties depend on the valence shell structure of the Ln-site cation and their redox properties.

Current Status of Research Progress
Current Status of Research Progress

3: Progress in research has been slightly delayed.

Reason

Proton kinetics studies and computational studies in some materials were delayed due to the COVID-19 Pandemic.

Strategy for Future Research Activity

By employing deuterium as a tracer indicator, proton formation and transport were observed on the surface and bulk of some materials like BaGd0.8La0.2Co2O6-δ (BGLC), La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF) and Ba0.5La0.5CoO3-δ (BLC). However, to fully understand the underlying principles of ionic transport in these oxides, additional spectroscopic studies are required to reveal their electronic properties, the spin state of constituent cations, their coordination, and changes while the oxide is being exposed to water vapor. From now on, I will focus on using X-ray absorption spectroscopy (XAS) realized in both near-edge and extended ranges (if possible) to further understand the dependence between elemental compositions and their electron configuration. Detailed near-edge feature analysis will be performed to obtain
information on the oxidation state and changes in the electronic structure of all elements upon hydration.

Causes of Carryover

The present amount is what was left over and carried forward due to project extension and will be used for research expenditure, beam line
payment.
The purchase of items such as, high-grade chemical reagents for material synthesis, High purity gases, platinum lead wires, equipment
maintenance

  • Research Products

    (2 results)

All 2022

All Presentation (2 results) (of which Int'l Joint Research: 2 results)

  • [Presentation] Understanding the Origin of Enhanced Catalytic Activity inLnCo0.5Ni0.5O3-δ (Ln = Pr, La) Perovskites Type Oxides on Protonic Electrochemical Device2022

    • Author(s)
      Kwati Leonard (PI)
    • Organizer
      23rd International Conference on Solid State Ionics (SSI 23)
    • Int'l Joint Research
  • [Presentation] Investigating the Origin of Enhanced Catalytic Activity in LnCo0.5Ni0.5O3-δ (Ln = La, Pr, Nd) "Positrodes" on Ceramic Protonic electrolytes2022

    • Author(s)
      Kwati Leonard (PI)
    • Organizer
      第48回 固体イオニクス討論会
    • Int'l Joint Research

URL: 

Published: 2024-12-25  

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