氧化物
电解
阴极
材料科学
电化学
电流密度
极化(电化学)
密度泛函理论
无机化学
阴极保护
化学工程
电导率
催化作用
氧气
离子
电极
功率密度
分析化学(期刊)
傅里叶变换红外光谱
化学
聚合物电解质膜电解
电子
电解水
电子密度
化学物理
电流(流体)
作者
Yixin Li,Chenglin Cai,Jun Tong,Longkai Xiang,Xing Zhou,Lei Zhu,Ying Li,Liang Qiu,Baowen Zhou,Zhen Huang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-12-19
卷期号:16 (1): 670-679
标识
DOI:10.1021/acscatal.5c07349
摘要
The Ni-based cathode is central to the performances of solid oxide electrolysis cells (SOECs), yet it suffers from poor oxygen ion conductivity, sluggish electron transport, and inefficient CO2/H2O activation. This study explores a heteroatom-doping strategy to comprehensively address the ionic, electronic, and molecular issues in solid oxide cells. When operated in SOEC mode, the maximum power density of the N-doped Ni/CGO (NiO/CGON) cathode achieved a 29.6% improvement over its undoped Ni/CGO, along with a 27.3% reduction in polarization resistance. Moreover, a 31.3% increase in maximum current density was obtained along with considerable stable operation over 150 h at an industrial-scale current density of 0.5 A/cm2. Combined electrochemical measurements, in situ diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy, and density functional theory (DFT) simulations reveal that N-doped-induced local covalency elevation via the formation of Ce–O/N bonds substantially promotes the oxygen ion and electron conductivity and creates the synergistic Lewis acid–base sites for simultaneous activation of both CO2 and H2O, thereby collectively addressing the ionic, electronic, and molecular issues in SOCs in one simple method.
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