催化作用
双金属片
密度泛函理论
化学
X射线吸收精细结构
电催化剂
氧还原反应
氧气
扩展X射线吸收精细结构
材料科学
无机化学
计算化学
物理化学
电极
吸收光谱法
电化学
生物化学
物理
量子力学
光谱学
有机化学
作者
Zhiran Sun,Shuhua Liu,Yajie Guo,Fuxian Zheng,Bing Nan,Wenjun Kang,Konggang Qu,Lei Wang,Rui Li,Zongge Li,Lile Dong,Haibo Li
标识
DOI:10.1016/j.electacta.2024.143857
摘要
The sluggish reaction kinetics of oxygen reduction reactions (ORR), combined with a long-standing dependence on expensive and unstable platinum-based catalysts, has significantly hindered the progress of sustainable energy solutions. Here, we have developed an atomically dispersed bimetallic FeCu-loaded N-doped porous carbon (Fe1Cu1-NC) catalyst for remarkable ORR efficiency. X-ray absorption fine structure (XAFS) analysis accurately determines that the coordination state of atomically dispersed Fe-Cu sites is a two-N-bridged with N6 ligand. Fe1Cu1-NC has demonstrated superior ORR performance in alkaline environments when compared to commercial Pt/C catalysts. Notably, Fe1Cu1-NC exhibits a higher power density and specific capacity than Pt/C in zinc-air batteries. Density functional theory (DFT) calculations further confirm that the improved performance is due to the combined action of Cu and Fe single atoms, which results in a negative shift of the d-band center energy of Fe and facilitates activation of ORR intermediates.
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