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Critical role of intercalated water for electrocatalytically active nitrogen-doped graphitic systems
Author(s) -
Ulises Martinez,
Joseph H. Dumont,
Edward F. Holby,
Kateryna Artyushkova,
Geraldine M Purdy,
Akhilesh Kumar Singh,
Nathan H. Mack,
Plamen Atanassov,
David A. Cullen,
Karren L. More,
Manish Chhowalla,
Piotr Zelenay,
Andrew M. Dattelbaum,
Aditya D. Mohite,
Gautam Gupta
Publication year - 2016
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.1501178
Subject(s) - catalysis , nitrogen , doping , oxygen reduction reaction , materials science , oxygen , chemical engineering , water splitting , oxygen reduction , nanotechnology , chemistry , electrochemistry , photocatalysis , organic chemistry , optoelectronics , engineering , electrode
Graphitic materials are essential in energy conversion and storage because of their excellent chemical and electrical properties. The strategy for obtaining functional graphitic materials involves graphite oxidation and subsequent dissolution in aqueous media, forming graphene-oxide nanosheets (GNs). Restacked GNs contain substantial intercalated water that can react with heteroatom dopants or the graphene lattice during reduction. We demonstrate that removal of intercalated water using simple solvent treatments causes significant structural reorganization, substantially affecting the oxygen reduction reaction (ORR) activity and stability of nitrogen-doped graphitic systems. Amid contrasting reports describing the ORR activity of GN-based catalysts in alkaline electrolytes, we demonstrate superior activity in an acidic electrolyte with an onset potential of ~0.9 V, a half-wave potential (E½) of 0.71 V, and a selectivity for four-electron reduction of >95%. Further, durability testing showed E½ retention >95% in N2- and O2-saturated solutions after 2000 cycles, demonstrating the highest ORR activity and stability reported to date for GN-based electrocatalysts in acidic media.

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