Boosting oxygen reduction activity of spinel CoFe2O4 by strong interaction with hierarchical nitrogen-doped carbon nanocages

• 来源期刊: 科学通报（英文版）
• 年，卷（期）: 2017,（20）
• 页码范围: 1365-1372
• 页数: 8页
• 语种: 英文

摘要

The unique hierarchical nitrogen-doped carbon nanocages (hNCNC) are used as a new support to homogeneously immobilize spinel CoFe2O4 nanoparticles by a facile solvothermal method.The so-constructed hierarchical CoFe204/hNCNC catalyst exhibits a high oxygen reduction activity with an onset potential of 0.966 V and half-wave potential of 0.819 V versus reversible hydrogen electrode,far superior to the corresponding 0.846 and 0.742 V for its counterpart of CoFe2O4/hCNC with undoped hierarchical carbon nanocages (hCNC) as the support,which locates at the top level for spinel-based catalysts to date.Consequently,the CoFe2O4/hNCNC displays the superior performance to the CoFe2O4/hCNC,when used as the cathode catalysts in the home-made Al-air batteries.X-ray photoelectron spectroscopy characterizations reveal the more charge transfer from CoFe2O4 to hNCNC than to hCNC,indicating the stronger interaction between CoFe2O4 and hNCNC due to the nitrogen participation.The enhanced interaction and hierarchical morphology favor the high dispersion and modification of electronic states for the active species as well as the mass transport during the oxygen reduction process,which plays a significant role in boosting the electrocatalytic performances.In addition,we noticed the high sensitivity of O 1 s spectrum to the particle size and chemical environment for spinel oxides,which is used as an indicator to understand the evolution of ORR activities for all the CoFe2O4-related contrast catalysts.Accordingly,the well-defined structure-performance relationship is demonstrated by the combination of experimental characterizations with theoretical calculations.This study provides a promising strategy to develop efficient,inexpensive and durable oxygen reduction electrocatalysts by tuning the interaction between spinel metal oxides and the carbon-based supports.