电催化剂
双功能
催化作用
杰纳斯
材料科学
镍
析氧
纳米颗粒
化学工程
合金
电化学
原子单位
碳纤维
无机化学
纳米技术
化学
物理化学
电极
冶金
复合材料
工程类
物理
复合数
量子力学
生物化学
作者
Zehui Li,Hongyan He,Hongbin Cao,Shaoming Sun,Wenlin Diao,Denglei Gao,Peilong Lu,Chun‐yang Zhang,Zhuang Guo,Mingjie Li,Rongji Liu,Dunhao Ren,Chenming Liu,Yi Zhang,Zheng Yang,Jingkun Jiang,Peilong Lu
标识
DOI:10.1016/j.apcatb.2018.08.074
摘要
Single-atom electrocatalysts have attracted board interest in the recent years as they combine the advantages of heterogeneous and homogeneous electrocatalysts. Nevertheless, single-atom electrocatalysts with single metal component cannot further satisfy the demand of catalytic properties. This work developed atomic Co/Ni dual sites in N-doped porous carbon Janus-like frameworks through epitaxial growth of cobalt based MOFs on nickel complexes. Structural characterization and atomic-scale transmission electron microscopy revealed the homogeneously dispersed active sites of Co-Ni alloy and single Co/Ni atoms. Electrochemical data strongly demonstrated the advantages of integrating Co-MOF and Ni complex with different topological structures to form a Janus-like structure. The resultant catalysts afforded onset potential of 0.93 V and half-wave potential of 0.84 V for oxygen reduction reaction in alkaline media, and 0.86 V and 0.73 V in acid media, which is better than single noble-metal-free catalysts, even close to commercial Pt/C. Besides, the catalysts also exhibited good oxygen evolution reaction performance (a current density of 10 mA cm−2 at a potential of 1.59 V) and overvoltage between ORR and OER is 0.78 V. Density functional theory calculations indicated the high electrocatalytic activities are originated from the synergetic effect of atomic Co/Ni-N-C bonds and microstructure of the prepared materials. This work paves a new avenue for the development of multiatomic electrocatalysts for energy conversion.
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