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Electrocatalytically Active Hollow Carbon Nanospheres Derived from PS‐ b ‐P4VP Micelles
Author(s) -
Cao Shubo,
Qu Ting,
Li Yayuan,
Zhang Ang,
Xue Longfei,
Zhao Yongbin,
Zheng Lirong,
Chen Aihua,
Shui Jianglan
Publication year - 2018
Publication title -
particle and particle systems characterization
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.877
H-Index - 56
eISSN - 1521-4117
pISSN - 0934-0866
DOI - 10.1002/ppsc.201700404
Subject(s) - electrocatalyst , micelle , copolymer , polystyrene , chemical engineering , materials science , methanol , carbon fibers , reversible hydrogen electrode , tetrahydrofuran , electrode , electrolyte , chemistry , composite number , organic chemistry , working electrode , electrochemistry , solvent , polymer , composite material , engineering , aqueous solution
A facile method using polystyrene‐ b ‐poly(4‐vinyl pyridine) (PS‐ b ‐P4VP) micelles is demonstrated to synthesize N/FeN 4 ‐doped hollow carbon nanospheres (N/FeN 4 ‐CHNS) with high electrocatalytic activity for oxygen reduction reactions (ORRs). Uniform spherical micelles with PS core and P4VP shell are prepared by exposing PS‐ b ‐P4VP in a mixture of ethanol/tetrahydrofuran. Pyridinic N in shell cooperates with Fe 3+ to induce an in situ polymerization of pyrrole. Tuning molecular composition of PS‐ b ‐P4VP can form hollow carbon spheres with controlled size down to sub‐100 nm that remains challenge using traditional hard template strategies. N/FeN 4 ‐CHNS possesses a series of desirable properties as electrode materials, including easy fabrication, high reproducibility, large surface area, and highly accessible porous surface. This electrocatalyst exhibits excellent ORR activity (onset potential of 0.976 V vs reversible hydrogen electrode (RHE) and half‐wave potential of 0.852 V vs RHE), higher than that of commercial Pt/C (20 wt%) in an alkaline media, and shows a good activity in an acidic media as well. In addition to its higher stability and methanol tolerance than Pt/C in both alkaline and acidic electrolytes, highly competitive single cell performance is achieved in a proton exchange membrane fuel cell. This work provides a general approach to preparing functionalized small hollow nanospheres based on self‐assembly of block copolymers.