催化作用
纳米颗粒
材料科学
氧还原
电催化剂
兴奋剂
碳纤维
联轴节(管道)
氧气
氧还原反应
无机化学
化学工程
纳米技术
物理化学
化学
电极
电化学
有机化学
光电子学
复合数
工程类
复合材料
冶金
作者
Yuan Pan,Xuelu Ma,Minmin Wang,Xuan Yang,Shoujie Liu,Hsiao‐Chien Chen,Zeweng Zhuang,Yanhui Zhang,Weng‐Chon Cheong,Chao Zhang,Xing Cao,Rongan Shen,Qian Xu,Wei Zhu,Yunqi Liu,Xingdong Wang,Xuejiang Zhang,Wensheng Yan,Jun Li,Hao Chen,Chen Chen,Yadong Li
标识
DOI:10.1002/adma.202203621
摘要
A coupling catalyst of highly dispersed N, P co-doped carbon frames (NPCFs) anchored with Fe single atoms (SAs) and Fe2 P nanoparticles (NPs) is synthesized by a novel in situ doping-adsorption-phosphatization strategy for the electrocatalytic oxygen reduction reaction (ORR). The optimized Fe SAs-Fe2 P NPs/NPCFs-2.5 catalyst shows a superior ORR activity and stability in 0.5 m H2 SO4 and 0.1 m KOH, respectively. Theoretical calculations reveal a synergistic effect, in that the existence of Fe2 P weakens the adsorption of ORR intermediates on active sites and lowers the reaction free energy. The doped P atoms with a strong electron-donating ability elevate the energy level of Fe-3d orbitals and facilitate the adsorption of O2 . The active Fe atoms exist in a low oxidation state and are less positively charged, and they serve as an electron reservoir capable of donating and releasing electrons, thus improving the ORR activity. Operando and in situ characterization results indicate that the atomically dispersed FeN4 /FeP coupled active centers in the Fe SAs-Fe2 P NPs/NPCFs-2.5 catalyst are characteristic of the different catalytic mechanisms in acidic and alkaline media. This work proposes a novel idea for constructing coupling catalysts with atomic-level precision and provides a strong reference for the development of high-efficiency ORR electrocatalysts for practical application.
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