催化作用
氧还原反应
多孔性
氧气
氮气
化学工程
材料科学
氧还原
还原(数学)
化学
物理化学
有机化学
复合材料
工程类
几何学
数学
电极
电化学
作者
Ji‐Rui Bai,Kai Zhang,Jia‐Yao Gao,Zengyu Han,Yucheng Zhu,Xiaoqi Yuan,Wenfang Cai,Xiaohe Liu,Qing‐Yun Chen,Yun‐Hai Wang
标识
DOI:10.1016/j.jallcom.2024.174599
摘要
Cobalt nitrogen-doped carbon (Co-NC) catalysts are synthesized for oxygen reduction reaction (ORR) via the pyrolysis of zinc-mediated and SiO2-templated 2,6-diaminopyridine (DAP) composites. The resulting Co-NC(Zn12-SiO2[20])-900 demonstrates exceptional ORR activities, with half-wave and onset potentials of 0.835 V and 0.875 V, respectively, which is similar to Pt/C catalyst. In long-term durability test, the Co-NC(Zn12-SiO2[20])-900 catalyst exhibits a negligible E1/2 shift, and in methanol tolerance tests, it displays significantly better performance than commercial Pt/C catalyst. The superior performance can be attributed to the hierarchical porous structure, dense and highly accessible Co-N4 and graphitic nitrogen (g-N) sites. The high content of Co-N4 and g-N sites enhances 3d-orbital filling and reduces the Co centers' on-site magnetic moment, as calculated by density functional theory. This may lead to a decrease in the energy barrier of the rate-determining step (RDS), which in turn enhances the intrinsic activity of the ORR.
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