SiO2-protected shell mediated templating synthesis of Fe-N-doped carbon nanofibers and their enhanced oxygen reduction reaction performance

被引:216
作者
Hu, Bi-Cheng [1 ]
Wu, Zhen-Yu [1 ]
Chu, Sheng-Qi [2 ]
Zhu, Hong-Wu [1 ]
Liang, Hai-Wei [3 ]
Zhang, Jing [2 ]
Yu, Shu-Hong [1 ,3 ]
机构
[1] Univ Sci & Technol China, Div Nanomat & Chem,CAS Ctr Excellence Nanosci, Hefei Natl Res Ctr Phys Sci Microscale,Dept Chem, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Hefei 230026, Anhui, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, High Field Magnet Lab, Anhui Key Lab Condensed Matter Phys Extreme Condi, Hefei 230031, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH ELECTROCATALYTIC ACTIVITY; METAL-FREE ELECTROCATALYSTS; ORGANIC FRAMEWORK; ACTIVE-SITES; NITROGEN; IRON; CATALYSTS; GRAPHENE; EVOLUTION; ARRAYS;
D O I
10.1039/c8ee00673c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalytic reduction of oxygen plays a crucial role in many energy storage and conversion devices. Currently, the development of high-performance carbon-based non-precious-metal (NPM) oxygen reduction reaction (ORR) catalysts in acidic media still remains a great challenge. Herein, we report a highly active meso/microporous Fe-N-doped carbon nanofiber (Fe-N-CNF) catalyst prepared via a SiO2-protected shell mediated template method. The SiO2-protected shell not only restricts the free migration of iron species but also traps volatile gaseous substances during the pyrolysis process at high temperature, thus leading to a simultaneous optimization of both the surface functionalities and porous structures of the Fe-N-CNF catalysts. Compared to catalysts prepared without a SiO2-protected shell, the Fe-N-CNF catalysts exhibit a much enhanced ORR activity in an acidic medium, along with a superior long-term stability.
引用
收藏
页码:2208 / 2215
页数:8
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