电解
离子键合
氧化物
阴极
吸附
钌
化学
氧气
催化作用
金属
电催化剂
材料科学
无机化学
电化学
物理化学
电极
离子
电解质
有机化学
生物化学
作者
Yuefeng Song,Junyong Min,Yige Guo,Rongtan Li,Geng Zou,Mingrun Li,Yipeng Zang,Weicheng Feng,Xiaoqian Yao,Tianfu Liu,Xiaomin Zhang,Jingcheng Yu,Qingxue Liu,Peng Zhang,Runsheng Yu,Xingzhong Cao,Junfa Zhu,Kun Dong,Guoxiong Wang,Xinhe Bao
标识
DOI:10.1002/ange.202313361
摘要
Abstract Cathodic CO 2 adsorption and activation is essential for high‐temperature CO 2 electrolysis in solid oxide electrolysis cells (SOECs). However, the component of oxygen ionic conductor in the cathode displays limited electrocatalytic activity. Herein, stable single Ruthenium (Ru) atoms are anchored on the surface of oxygen ionic conductor (Ce 0.8 Sm 0.2 O 2‐δ , SDC) via the strong covalent metal‐support interaction, which evidently modifies the electronic structure of SDC surface for favorable oxygen vacancy formation and enhanced CO 2 adsorption and activation, finally evoking the electrocatalytic activity of SDC for high‐temperature CO 2 electrolysis. Experimentally, SOEC with the Ru 1 /SDC‐La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3‐δ cathode exhibits a current density as high as 2.39 A cm −2 at 1.6 V and 800 °C. This work expands the application of single atom catalyst to the high‐temperature electrocatalytic reaction in SOEC and provides an efficient strategy to tailor the electronic structure and electrocatalytic activity of SOEC cathode at the atomic scale.
科研通智能强力驱动
Strongly Powered by AbleSci AI