4.8 Article

Atomic Co/Ni dual sites and Co/Ni alloy nanoparticles in N-doped porous Janus-like carbon frameworks for bifunctional oxygen electrocatalysis

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 240, 期 -, 页码 112-121

出版社

ELSEVIER
DOI: 10.1016/j.apcatb.2018.08.074

关键词

Atomic; Dual sites; Electrocatalysts; Oxygen reduction reaction; Oxygen evolution reaction

资金

  1. National Natural Science Foundation of China [91545125, U1662121, 51425405, 51402298, 51608509]
  2. National High Technology Research and Development Program of China (863 Program) [2014AA06A513]
  3. Youth Innovation Promotion Association of CAS
  4. Postdoctoral Science Foundation [2016M590670]
  5. Natural Science Foundation of Shandong Province [ZR2016EEB25]
  6. Alexander von Humboldt Foundation Postdoctoral Research Fellowship [1186323]
  7. Beijing Municipal Commission Educationand Cross training plan for high level talents in Beijing colleges and universities [KM201710015009]
  8. Tsinghua Qingfeng Scholarship [THQF2018-16]

向作者/读者索取更多资源

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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