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The Pt/g-C3N4-CNS catalyst via in situ synthesis process with excellent performance for methanol electrocatalytic oxidation reaction
被引:6
作者:
Liang, Xiaolong
[1
,2
,3
]
Dong, Fang
[1
,2
]
Tang, Zhicheng
[1
,2
]
Wang, Qingchun
[3
]
机构:
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, Natl Engn Res Ctr Fine Petrochem Intermediates, Lanzhou 730000, Peoples R China
[3] Inner Mongolia Univ Sci & Technol, Coll Mat & Met Engn, Baotou 014010, Peoples R China
关键词:
GRAPHITIC CARBON NITRIDE;
REDUCED GRAPHENE OXIDE;
FACILE SYNTHESIS;
NANOSHEET;
SUPPORT;
HYBRID;
D O I:
10.1039/d1nj05858d
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
This study reports the preparation of a graphite carbon nitride (C3N4) and carbon nanosheet (CNS) composite support (g-C3N4-CNS) by in situ synthesis (IS), and the effect of the Pt-based catalyst on methanol electrocatalytic oxidation (MOR) was investigated. The experiment proved that Pt/IS-g-C3N4-CNS has higher MOR catalytic performance and stability than Pt/MS-g-C3N4-CNS, which was prepared by mechanical synthesis. Notably, the Pt/IS-g-C3N4-CNS catalyst has the best electrocatalytic activity. The current density of the Pt/IS-g-C3N4-CNS catalyst is 105.1 mA cm(-2), and its chronoamperometry current loss rate is 66.4%, which is much higher than that of Pt/MS-g-C3N4-CNS. Through BET, TEM, XRD, and XPS characterization, it was found that the in situ synthesized g-C3N4-CNS composite support has stronger interaction, larger specific surface area, and higher pyridine nitrogen and pyrrole nitrogen content, which jointly promote the dispersion of Pt nanoparticles and present superior electrocatalytic performance for the MOR reaction.
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页码:3121 / 3129
页数:9
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