Synthesis and Electrochemical Characterization of N-Doped Partially Graphitized Ordered Mesoporous Carbon-Co Composite

被引:103
|
作者
Tang, Jing [1 ]
Wang, Tao [1 ,2 ]
Pan, Xuchen [1 ]
Sun, Xin [1 ]
Fan, Xiaoli [1 ]
Guo, Yunxia [1 ]
Xue, Hairong [1 ]
He, Jianping [1 ]
机构
[1] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Technol, Nanjing 210016, Peoples R China
[2] Natl Inst Mat Sci, Int Ctr Mat Nanoarchitecton WPI MANA, Tsukuba, Ibaraki 3050044, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2013年 / 117卷 / 33期
基金
中国国家自然科学基金;
关键词
HIGH ELECTROCATALYTIC ACTIVITY; CATALYTIC GRAPHITIZATION; PLATINUM NANOPARTICLES; TRANSITION-METAL; FACILE SYNTHESIS; NITROGEN; PERFORMANCE; NANOTUBES; ARRAYS; NANOCOMPOSITE;
D O I
10.1021/jp405775x
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
N-doped ordered mesoporous carbon-Co composites (Co-N-OMC) with 2D hexagonal structure, uniform pore size (4.4 nm), high surface area (550 m(2) g(-1)), and medium pore volume (0.61 cm(3) g(-1)) were successfully fabricated through facile one-step template method. We employed resol as the carbon precursor, triblock copolymer as the template agent, and cobaltous acetate and urea as additives. XPS analysis revealed that nitrogen was successfully doped in ordered mesoporous carbon and existed in the form of pyridine-like and quaternary-N nitrogen atoms. More importantly, metallic Co nanoparticles with uniform diameter around 15 nm highly dispersed in carbon matrix without adding any dispersion agent, which was probably due to the confinement effect of mesoporous structure. It was unambiguously demonstrated by HRTEM analysis that there were layered graphitic sheets present around Co particles, resulting from in situ catalytic graphitization of amorphrous carbon by Co species. Pt catalyst deposited on Co-N-OMC composite showed an excellent electrocatalytic activity for both methanol oxidation and oxygen reduction reaction, which was probably due to its suitable pore structure, improved degree of graphitization, presence of nitrogen, and high dispersion of Pt nanoparticles.
引用
收藏
页码:16896 / 16906
页数:11
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