Oxygen Species on Nitrogen-Doped Carbon Nanosheets as Efficient Active Sites for Multiple Electrocatalysis

被引:60
|
作者
Lv, Jing-Jing [1 ,2 ]
Li, Yanle [2 ,3 ]
Wu, Shaojun [1 ,2 ]
Fang, Hua [1 ,2 ]
Li, Ling-Ling [1 ,2 ]
Song, Rong-Bin [1 ,2 ]
Ma, Jing [2 ,3 ]
Zhu, Jun-Jie [1 ,2 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Collaborat Innovat Ctr Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
[3] Nanjing Univ, Sch Chem & Chem Engn, MOE, Key Lab Mesoscop Chem, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
g-C3N4; template; oxygen-modified nitrogen-doped carbon nanosheets; multifunctional electrocatalysis; Zn-air batteries; water-splitting cells; METAL-FREE ELECTROCATALYSTS; POROUS CARBON; TOPOLOGICAL DEFECTS; ALLOY NANOPARTICLES; REDUCTION; GRAPHENE; CATALYSTS; NANOTUBES; OXIDATION; ENERGY;
D O I
10.1021/acsami.8b00240
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Designing and synthesizing nanomaterials with high coverages of active sites is one of the most-pivotal factors in the construction of state-of-the-art electrocatalysts with high performance. Herein, we proposed a facile in situ templated method for the fabrication of oxygen-species-modified nitrogen doped carbon nanosheets (O-N-CNs). The epoxy oxygen and ketene oxygen combined with graphitic-nitrogen defects in O-N-CNs gave more active sites for the oxygen-reduction reaction (ORR) and the oxygen-evolution reaction (OER), as proven via theoretical and experimental results, while the carbonyl-oxygen and epoxy-oxygen species showed more efficient electrocatalytic activity for the hydrogen evolution reaction (HER). Hence, the O-N-CNs showed highly active electrocatalytic performance toward ORR, OER, and HER More importantly, the superior multifunctional electrocatalytic activity of O-N-CNs allowed their use in the construction of Zn-air batteries to power the corresponding water-splitting cells. This work can offer an understanding of underlying mechanisms of oxygen species on N-doped carbon materials toward multiple electrocatalysis and facilitate the engineering of electrocatalysts for energy-storage and-conversion devices.
引用
收藏
页码:11678 / 11688
页数:11
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