Simple coordination complex-derived Ni NP anchored N-doped porous carbons with high performance for reduction of nitroarenes

被引:18
|
作者
Xu, Dan [1 ,2 ]
Pan, Ying [1 ]
Zhu, Liangkui [1 ]
Yusran, Yusran [1 ]
Zhang, Daliang [1 ]
Fang, Qianrong [1 ]
Xue, Ming [1 ]
Qiu, Shilun [1 ]
机构
[1] Jilin Univ, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Jilin, Peoples R China
[2] Hainan Med Coll, Coll Pharm, Haikou 571119, Hainan, Peoples R China
来源
CRYSTENGCOMM | 2017年 / 19卷 / 44期
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; EXCELLENT CATALYTIC PERFORMANCE; SITU HOT STAGE; NANOPOROUS CARBONS; RATIONAL DESIGN; NANOPARTICLES; NITROGEN; HYDROGENATION; GRAPHENE; CARBONIZATION;
D O I
10.1039/c7ce01571b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Coordination complexes are ideal sacrificial templates for fabricating their respective derivatives by changing the thermal conditions. In this study, nitrogen-doped hierarchical porous carbons anchored with nickel nanoparticles (Ni NPs) were prepared by using rod-like nickel dimethylglyoximate [Ni(dmg)(2)] as a sacrificial template under nitrogen flow at different temperatures. The structure, morphology and properties of the products were characterised by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), N-2 adsorption-desorption measurements and ultraviolet-visible (UV-vis) spectrophotometry. The optimised Ni@NC-700 sample exhibited an excellent ability to reduce 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) by NaBH4 in an aqueous solution, which shortened the reduction time to 3.0 min with a conversion of nearly 100%. In addition, Ni@NC-700 possessed magnetic properties, which provided efficient separation by an external magnetic field. The present report may provide a potential and favourable method for preparing magnetically reusable Ni NP anchored N-doped porous carbon catalysts derived from a simple coordination complex.
引用
收藏
页码:6612 / 6619
页数:8
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