Selective In Situ Phase Segregation Enabling Efficient and Stable Protonic Ceramic Fuel Cell Cathode Performance
Year: 2025
Type: article
Abstract: Efficient and reliable protonic ceramic fuel cells (PCFCs) necessitate the development of active and durable cathode materials to accelerate the sluggish oxygen reduction reaction (ORR). The most promising PCFC cathode candidates are perovskite‐type structured oxides with mixed oxygen ion, proton, and hole conductivity. However, mixed conductivity often requires materials with alkaline earth elements and the inclusion of these elements in the cathode structure leads to severe degradation in the presence of even small trace amounts of CO 2 in air. Herein, a new approach is presented to address this challenge by inducing selective in situ phase segregation to engineer the cathode surface and bulk separately. This selective phase segregation is achieved via targeted control of the size mismatch of cations in the perovskite‐type structure, enhancing charge transfer in the bulk while improving CO 2 resistance at the surface. By co‐incorporating smaller Li + and larger K + into the model BaCo 0.4 Fe 0.4 Zr 0.1 Y 0.1 O 3−δ cathode material, it is shown that Li + segregates to the surface, protecting it from CO 2 poisoning, while K + remains in the bulk and accelerates proton transport. Consequently, this in situ restructured cathode can boost the PCFC power output by 30% and improve its CO 2 tolerance fivefold in the presence of CO 2 at 600 °C.
Source: Small
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $5,790
Awards: G2105153601, An integrated electrolyser for CO2 conversion from capture media., High Performance Anode for Direct Ammonia Solid Oxide Fuel Cells, Nanoionics: Engineering ion transport with two-dimensional materials, G426999256, G5226692721, G568409692, G5863752249, G6991324060, High performance cathode for protonic ceramic fuel cells
OpenAlex ID: W4411150116
