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Pyridinic-N-Doped Graphene Paper from Perforated Graphene Oxide for Efficient Oxygen Reduction
Author(s) -
Gyeong Sook Bang,
Gi Woong Shim,
Gwang Hyuk Shin,
Dae Yool Jung,
Hamin Park,
Won G. Hong,
Jinseong Choi,
JaeSeung Lee,
SungYool Choi
Publication year - 2018
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.8b00400
Subject(s) - graphene , oxide , doping , materials science , hydrogen peroxide , oxygen , diffusion , limiting current , electrode , etching (microfabrication) , chemical engineering , electron transfer , perforation , inorganic chemistry , chemistry , nanotechnology , electrochemistry , photochemistry , composite material , optoelectronics , organic chemistry , metallurgy , physics , punching , layer (electronics) , engineering , thermodynamics
We report a simple approach to fabricate a pyridinic-N-doped graphene film (N-pGF) without high-temperature heat treatment from perforated graphene oxide (pGO). pGO is produced by a short etching treatment with hydrogen peroxide. GO perforation predominated in a short etching time (∼1 h), inducing larger holes and defects compared to pristine GO. The pGO is advantageous to the formation of a pyridinic N-doped graphene because of strong NH 3 adsorption on vacancies with oxygen functional groups during the nitrogen-doping process, and the pyridinic-N-doped graphene exhibits good electrocatalytic activity for oxygen reduction reaction (ORR). Using rotating-disk electrode measurements, we confirm that N-pGF undergoes a four-electron-transfer process during the ORR in alkaline and acidic media by possessing sufficient diffusion pathways and readily available ORR active sites for efficient mass transport. A comparison between Pt/N-pGF and commercial Pt/C shows that Pt/N-pGF has superior performance, based on its more positive onset potential and higher limiting diffusion current at -0.5 V.

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