z-logo
open-access-imgOpen Access
Sub‐50 nm Iron–Nitrogen‐Doped Hollow Carbon Sphere‐Encapsulated Iron Carbide Nanoparticles as Efficient Oxygen Reduction Catalysts
Author(s) -
Tan Haibo,
Li Yunqi,
Kim Jeonghun,
Takei Toshiaki,
Wang Zhongli,
Xu Xingtao,
Wang Jie,
Bando Yoshio,
Kang YongMook,
Tang Jing,
Yamauchi Yusuke
Publication year - 2018
Publication title -
advanced science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.388
H-Index - 100
ISSN - 2198-3844
DOI - 10.1002/advs.201800120
Subject(s) - catalysis , materials science , nanoparticle , carbide , carbon fibers , electrolyte , mesoporous material , oxygen , styrene , ethylene glycol , nitrogen , inorganic chemistry , chemical engineering , nuclear chemistry , copolymer , chemistry , nanotechnology , composite number , organic chemistry , electrode , metallurgy , composite material , engineering , polymer
Sub‐50 nm iron–nitrogen‐doped hollow carbon sphere‐encapsulated iron carbide nanoparticles (Fe 3 C‐Fe,N/C) are synthesized by using a triblock copolymer of poly(styrene‐ b ‐2‐vinylpyridine‐ b ‐ethylene oxide) as a soft template. Their typical features, including a large surface area (879.5 m 2 g −1 ), small hollow size (≈16 nm), and nitrogen‐doped mesoporous carbon shell, and encapsulated Fe 3 C nanoparticles generate a highly active oxygen reduction reaction (ORR) performance. Fe 3 C‐Fe,N/C hollow spheres exhibit an ORR performance comparable to that of commercially available 20 wt% Pt/C in alkaline electrolyte, with a similar half‐wave potential, an electron transfer number close to 4, and lower H 2 O 2 yield of less than 5%. It also shows noticeable ORR catalytic activity under acidic conditions, with a high half‐wave potential of 0.714 V, which is only 59 mV lower than that of 20 wt% Pt/C. Moreover, Fe 3 C‐Fe,N/C has remarkable long‐term durability and tolerance to methanol poisoning, exceeding Pt/C regardless of the electrolyte.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here