One-pot synthesis of finely-dispersed Au nanoparticles on ZnO hexagonal sheets for base-free aerobic oxidation of vanillyl alcohol

被引:17
|
作者
Lin, Peng [1 ]
Shang, Rong [1 ]
Zhang, Qizhao [1 ]
Gu, Bang [1 ]
Tang, Qinghu [2 ]
Jing, Fangli [3 ]
Cao, Qiue [1 ]
Fang, Wenhao [1 ]
机构
[1] Yunnan Univ, Natl Demonstrat Ctr Expt Chem & Chem Engn Educ, Sch Chem Sci & Technol, 2 North Cuihu Rd, Kunming 650091, Yunnan, Peoples R China
[2] Henan Normal Univ, Collaborat Innovat Ctr Henan Prov Green Mfg Fine, Sch Chem & Chem Engn, Key Lab Green Chem Media & React,Minist Educ, Xinxiang 453007, Henan, Peoples R China
[3] Southwest Petr Univ, Coll Chem & Chem Engn, 8 Xindu Ave, Chengdu 610500, Peoples R China
基金
中国国家自然科学基金;
关键词
CATALYSTS; GOLD; CO; DEPOSITION; AL2O3; WATER; ACID; AIR;
D O I
10.1039/d2cy00837h
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
Advanced synthesis of highly-dispersed Au nanoparticles is vital to catalysis and green chemistry. In this work, a facile one-pot coordination-calcination method was developed to prepare uniform Au nanoparticles loaded on ZnO using metal ions and the 2-methylimidazole ligand. This Au/ZnO-MZ catalyst was efficient and stable towards sustainable synthesis of vanillin via the base-free aerobic oxidation of vanillyl alcohol. A turnover number of 335 and 100% yield of vanillin were obtained at 120 degrees C and 5 bar of O-2, the best result to date among all the supported noble-metal catalysts. Meanwhile other Au/ZnO catalysts were prepared for comparison by a one-pot precipitation method using ammonia, triethylamine and sodium hydroxide, respectively. The Au/ZnO-MZ catalyst demonstrated unique properties as shown by PXRD, N-2 physisorption, SEM, TEM, H-2-TPR, O-2-TPD, XPS, PL spectroscopy and CO adsorbed DRIFT-IR. Small and metallic-state Au nanoparticles (about 2.2 nm) as active sites were highly dispersed on ZnO hexagonal nanosheets. Sufficient surface oxygen species bearing enhanced oxygen mobility were observed for ZnO carriers. The strong metal-support interaction due to the interfacial electron transfer from Au to ZnO was elucidated. These catalytic features allowed excellent base-free oxidation catalysis by lowering the activation energy. Moreover, the Au/ZnO-MZ catalyst displayed a wide substrate scope of alcohols to produce the corresponding aldehydes. The present findings may probably inspire new preparation methods and applications for Au heterogeneous catalysts.
引用
收藏
页码:4613 / 4623
页数:11
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