材料科学
催化作用
非阻塞I/O
制作
合金
氧化物
化学工程
燃料电池
烧结
电化学
电解
铂金
电解水
氢
电催化剂
制氢
纳米技术
原子层沉积
固体氧化物燃料电池
电解质
分解
电流密度
沉积(地质)
相(物质)
复合数
氢燃料
分解水
双金属片
过程(计算)
析氧
作者
Sehee Bang,Hyun Sik Yoo,Joon Gyu Kim,Jae Hoon Jung,Dongjin Kim,Jungdeok Park,Wonyoung Lee
标识
DOI:10.1002/adfm.202525596
摘要
Abstract Solid oxide electrolysis cells (SOECs) offer high efficiency and scalability in green hydrogen production. However, improving their electrochemical performance within conventional fabrication processes is limited because of the substantial structural changes that occur during high‐temperature sintering and the subsequent reduction of the fuel electrode. Herein, sintering‐resistant and spontaneously alloyed NiO@CoO core–shell catalysts fabricated by powder atomic layer deposition (ALD) are presented. The conformal CoO shell suppresses NiO coarsening during sintering, thereby enlarging the triple phase boundary network in the fuel electrode. During subsequent reduction, the core–shell structure spontaneously transforms into a homogeneous NiCo alloy without an additional post‐processing step, enhancing the catalytic activity for the hydrogen evolution reaction. As a result, the ALD‐modified cell exhibits a ≈2 times higher current density of 2.30 A cm −2 at 1.3 V and 750 °C compared to the reference cell. This sequential structural stabilization and catalytic activation within a single fabrication process offers a practical and scalable pathway for realizing high‐performance SOECs.
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