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Controllable synthesis of oxygenated carbon supported palladium nanodendrites for highly efficient nitroaromatics reduction
被引:5
|作者:
Zhao, Wen
[1
]
Wang, Tianlong
[1
]
Wang, Baoan
[1
]
Wang, Ran
[1
]
Xia, Yu
[1
]
Liu, Mengping
[1
]
Tian, Lihong
[1
]
机构:
[1] Hubei Univ, Hubei Collaborat Innovat Ctr Adv Organochem Mat, Key Lab Synth & Applicat Organ Funct Mol, Minist Educ, Wuhan 430062, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Carbon dots;
Palladium nanodendrites;
Nitroaromatics;
Hydrogenation;
MESOPOROUS CARBON;
QUANTUM DOTS;
CATALYTIC-ACTIVITY;
AROMATIC NITRO;
PHOTOCATALYTIC PERFORMANCE;
SELECTIVE HYDROGENATION;
SILVER NANOPARTICLES;
ACTIVATED CARBONS;
PD NANOPARTICLES;
GRAPHENE;
D O I:
10.1016/j.colsurfa.2022.130677
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:
Palladium nanodendrites supported on oxygenated carbon layer (Pd/ O-carbon) have been prepared herein through modulating the mass ratio of Pd (II) precursor and carbon dots derived from sucrose without additional reducing agent. Characterizations of FT-IR, XPS spectra and TEM graphs reveal that oxygen-bearing groups on carbon dots play important role in reducing Pd(II) into Pd(0), controlling nanoparticle growth and stabilizing Pd nanodendrites. The as-prepared Pd/ O-carbon presents size-dependent activity on catalytic p-nitrophenol (4-NP) reduction using NaBH4 as hydrogen donor. The reaction rate constant of 4-NP on Pd/ O-carbon with Pd particle size of 4-7 nm almost triples that on catalyst with Pd nanoparticles of 6-10 nm. Pd / O-carbon can be reused for 10 times without obvious decreased activity, showing a long-term chemical stability in 4-NP reduction reaction. In addition, Pd / O-carbon achieves similar to 100% selectivity on nitrobenzene conversion and > 95% selectivity for the hydrogenation of substituted nitrobenzene compounds with methyl-, chloro- and amino- groups to corresponding aniline through tandem reaction with NH3BH3 as hydrogen donor in methanol/ water solvent (volume ratio of 1:3).
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页数:9
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