A facile approach to tailoring electrocatalytic activities of imine-rich nitrogen-doped graphene for oxygen reduction reaction

被引:25
作者
Lee, Min Seok [1 ]
Whang, Dong Ryeol [2 ]
Choi, Hyun-Jung [3 ]
Yang, Mun Ho [1 ]
Kim, Bong-Gi [4 ]
Baek, Jong-Beom [3 ]
Chang, Dong Wook [1 ]
机构
[1] Pukyong Natl Univ, Dept Ind Chem, Busan 48547, South Korea
[2] Johannes Kepler Univ Linz, Linz Inst Organ Solar Cells LIOS, Inst Phys Chem, A-4040 Linz, Austria
[3] UNIST, Sch Energy & Chem Engn, Ctr Dimens Controllable Organ Frameworks, Ulsan 44919, South Korea
[4] Konkuk Univ, Dept Organ & Nano Syst Engn, Seoul 05029, South Korea
基金
新加坡国家研究基金会;
关键词
Imine; Nitrogen-doped graphene; Oxygen reduction reaction; Electrocatalyst; ENERGY-CONVERSION; NANOPLATELETS; CATALYSTS; OXIDE;
D O I
10.1016/j.carbon.2017.07.001
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
report efficient modulation of the electrocatalytic activity of imine-rich nitrogen-doped graphene nanosheets (IRnGs) in the oxygen reduction reaction (ORR) by chemical functionalization. IRnGs are prepared by a simple acid-catalyzed dehydration reaction between graphene oxide and aniline derivatives. Various electron-donating and electron-withdrawing substituents are introduced in the para-position of aniline to afford diverse IRnG electrocatalysts. Cyclic voltammetry and rotating ring disk electrode measurements show that the electrocatalytic activity of IRnGs for ORR is highly sensitive to the electronic characteristics of functionalities present in their chemical structures. Thus, the above ORR activities are significantly improved by increasing the electron-withdrawing capability of substituents, since this promotes the beneficial polarization of electrocatalytically active imine bond (-C=N-) in IRnGs. In addition, metal-free IRnGs electrocatalysts offer additional advantages of high selectivity, good long-term stability and excellent tolerance to methanol crossover for ORR in alkaline solution. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:515 / 523
页数:9
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