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Cobalt Sulfide Nanowires Core Encapsulated by a N, S Codoped Graphitic Carbon Shell for Efficient Oxygen Reduction Reaction
Author(s) -
Han Ce,
Li Qun,
Wang Dewen,
Lu Qingqing,
Xing Zhicai,
Yang Xiurong
Publication year - 2018
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.201703642
Subject(s) - cobalt sulfide , materials science , mesoporous material , nanowire , cobalt , nanotechnology , sulfide , nanomaterials , calcination , oxygen reduction reaction , chemical engineering , catalysis , carbon fibers , electrocatalyst , chemistry , composite number , electrode , electrochemistry , composite material , organic chemistry , engineering , metallurgy
Exploration of economical electrocatalysts for highly efficient and stable oxygen reduction reaction (ORR) is believed to be essential for diverse future renewable energy applications. Herein, cobalt sulfide nanowire core encapsulated in a N, S codoped graphitic carbon shell (CoS NWs@NSC) is successfully fabricated via the calcination of polydopamine‐coated Co(CO 3 ) 0.5 (OH) 0.11 H 2 O NWs with sulfur powder under argon atmosphere. The uniform encapsulation of CoS core by N, S codoped graphitic carbon shell favors the interaction of the core–shell structure for generating stable and numerous ORR active sites homogeneously dispersed throughout the materials. Meanwhile, the wire‐like CoS NWs@NSC stacks to form 3D mesoporous conductive networks, which improves the mass and charge transport capability of catalyst. Accordingly, the resultant CoS NWs@NSC electrocatalysts possess excellent ORR activity through the four‐electron pathway with superior stability and methanol tolerance over the Pt/C in 0.1 m KOH. This strategy can offer inspiration for designing and fabricating novel core–shell‐structured nanomaterials with active sites derived from uniform morphology as potential electrocatalysts for various vital renewable energy devices.