Alkaline Leaching: A Facile Surface Activation Strategy to Improve the Reactivity of Air Electrodes for Solid Oxide Fuel Cells

Y Yeongtaek Hong (Department of Materials Science and Engineering Seoul National University (SNU) Seoul Republic of Korea) H Hyunseung Kim (Research Institute of Advanced Materials) S Sang Won Lee (Korea Institute of Ceramic Engineering and Technology (KICET) Jinju Republic of Korea) Y Yong Beom Kim S SungHyun Jeon (Research Institute of Advanced Materials Seoul National University Seoul Republic of Korea) S Sangwoo Kim H Hainan Sun (School of Chemistry and Chemical Engineering Nantong University Jiangsu P. R. China) J Jeongah Lee (Department of Materials Science and Engineering Seoul National University (SNU) Seoul Republic of Korea) S Seongwoo Nam (Research Institute of Advanced Materials (RIAM) Seoul National University (SNU) Seoul Republic of Korea) S Seungwoo Roh (Department of Materials Science and Engineering Seoul National University (SNU) Seoul Republic of Korea) T Tae Ho Shin (Korea Institute of Ceramic Engineering and Technology (KICET) Jinju Republic of Korea) W WooChul Jung (Research Institute of Advanced Materials)

Abstract

ABSTRACT The energy conversion efficiency of solid oxide fuel cells is primarily governed by the performance of their air electrodes. Several surface modification techniques, including nanocatalyst decoration, surface coating, and acid etching, have been reported to enhance the performance of air electrodes. However, these approaches often face limitations in cost and time efficiency. In this study, we propose alkaline leaching as a straightforward and innovative strategy to activate the surface of mixed‐conducting oxides by selectively dissolving the A‐site cation during bias application in an alkaline solution. After 10 min of alkaline leaching, the surface of the PrBa 0.8 Ca 0.2 Co 2 O 5+δ electrode becomes cobalt‐rich and amorphous, recognized for its favorable impact on reactivity. As a result, when the surface‐modified electrode is used as the air electrode in a solid oxide fuel cell, it exhibits a 5.6 fold enhancement in catalytic activity, achieving an area‐specific resistance of 0.019 Ω cm 2 . Single cell measurements further demonstrate a 33 % increase in maximum power density, reaching 2.10 W cm −2 at 650°C. This work provides a strategic approach for engineering highly active oxide surfaces, leveraging a straightforward system operable at ambient pressure and room temperature, with broad applicability across diverse devices.

Article Details

Volume / Issue Vol. 38, Issue 33
Published June 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (12)

Y

Yeongtaek Hong

Department of Materials Science and Engineering Seoul National University (SNU) Seoul Republic of Korea

H

Hyunseung Kim

Research Institute of Advanced Materials

S

Sang Won Lee

Korea Institute of Ceramic Engineering and Technology (KICET) Jinju Republic of Korea

Y

Yong Beom Kim

S

SungHyun Jeon

Research Institute of Advanced Materials Seoul National University Seoul Republic of Korea

S

Sangwoo Kim

H

Hainan Sun

School of Chemistry and Chemical Engineering Nantong University Jiangsu P. R. China

J

Jeongah Lee

Department of Materials Science and Engineering Seoul National University (SNU) Seoul Republic of Korea

S

Seongwoo Nam

Research Institute of Advanced Materials (RIAM) Seoul National University (SNU) Seoul Republic of Korea

S

Seungwoo Roh

Department of Materials Science and Engineering Seoul National University (SNU) Seoul Republic of Korea

T

Tae Ho Shin

Korea Institute of Ceramic Engineering and Technology (KICET) Jinju Republic of Korea

W

WooChul Jung

Research Institute of Advanced Materials