Nitrogen-doped carbon nanotubes and graphene composite structures for energy and catalytic applications

被引:426
|
作者
Lee, Won Jun [1 ]
Maiti, Uday Narayan [1 ]
Lee, Ju Min [1 ]
Lim, Joonwon [1 ]
Han, Tae Hee [2 ]
Kim, Sang Ouk [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Ctr Nanomat & Chem React, Inst Basic Sci, Taejon 305701, South Korea
[2] Hanyang Univ, Dept Organ & Nano Engn, Seoul 133791, South Korea
关键词
OXYGEN-REDUCTION REACTION; HIGH ELECTROCATALYTIC ACTIVITY; HETEROJUNCTION SOLAR-CELLS; CHEMICAL-VAPOR-DEPOSITION; PLATINUM NANOPARTICLES; LITHIUM-STORAGE; CNX NANOTUBES; TRANSPORT ENHANCEMENT; ELECTRONIC-STRUCTURE; GOLD NANOPARTICLES;
D O I
10.1039/c4cc00146j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Substitutional heteroatom doping is a promising route to modulate the outstanding material properties of carbon nanotubes and graphene for customized applications. Recently, (nitrogen-) N-doping has been introduced to ensure tunable work-function, enhanced n-type carrier concentration, diminished surface energy, and manageable polarization. Along with the promising assessment of N-doping effects, research on the N-doped carbon based composite structures is emerging for the synergistic integration with various functional materials. This invited feature article reviews the current research progress, emerging trends, and opening opportunities in N-doped carbon based composite structures. Underlying basic principles are introduced for the effective modulation of material properties of graphitic carbons by N-doping. Composite structures of N-doped graphitic carbons with various functional materials, including (i) polymers, (ii) transition metals, (iii) metal oxides, nitrides, sulphides, and (iv) semiconducting quantum dots are highlighted. Practical benefits of the synergistic composite structures are investigated in energy and catalytic applications, such as organic photovoltaics, photo/electro-catalysts, lithium ion batteries and supercapacitors, with a particular emphasis on the optimized interfacial structures and properties.
引用
收藏
页码:6818 / 6830
页数:13
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