Combined Electron and Structure Manipulation on Fe-Containing N-Doped Carbon Nanotubes To Boost Bifunctional Oxygen Electrocatalysis

被引:81
作者
Zhao, Lei [1 ]
Wang, Qichen [2 ,3 ]
Zhang, Xinqi [1 ]
Deng, Cheng [1 ]
Li, Zhihong [1 ]
Lei, Yongpeng [2 ,3 ,4 ]
Zhu, Mengfu [1 ]
机构
[1] Chinese PLA, Acad Mil Sci, Inst Med Support Technol, Tianjin 300161, Peoples R China
[2] Cent South Univ, Coll Chem & Chem Engn, State Key Lab Powder Met, Changsha 410083, Hunan, Peoples R China
[3] Cent South Univ, Coll Chem & Chem Engn, Hunan Prov Key Lab Chem Power Sources, Changsha 410083, Hunan, Peoples R China
[4] State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
基金
中国国家自然科学基金;
关键词
bifunctional oxygen electrocatalysts; non-noble-metal; charge transfer; mass transport; Zn-air batteries; METAL-ORGANIC FRAMEWORK; MESOPOROUS CARBON; POROUS CARBON; GRAPHENE; NITROGEN; HYBRIDS; CATALYST; CO; NANOFIBERS;
D O I
10.1021/acsami.8b09197
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
It is a challenge to synthesize highly efficient nonprecious metal electrocatalysts with a well-defined nanostructure and rich active species. Herein, through electron engineering and structure manipulation simultaneously, we constructed Fe-embedded pyridinic-N-dominated carbon nanotubes (CNTs) on ordered mesoporous carbon, showing excellent oxygen reduction reaction activity (half-wave potential, 0.85 V) and an overpotential of 420 mV to achieve 10 mA cm(-2) for oxygen evolution reaction in alkaline media (potential difference, 0.80 V). Density functional theory calculation indicates those Fe@N-4 clusters improve charge transfer and further promote the electrocatalytic reactivity of the functionalized region in CNTs. Rechargeable Zn-air batteries were assembled, displaying robust charging-discharging cycling performance (over 90 h) with voltage gap of only 0.08 V, much lower than that of the Pt/C + Ir/C electrode (0.29 V). This work presents a highly active nonprecious metal-based bifunctional catalyst toward air electrode for energy conversion.
引用
收藏
页码:35888 / 35895
页数:8
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