Pd-Pd/PdO as active sites on intercalated graphene oxide modified by diaminobenzene: fabrication, catalysis properties, synergistic effects, and catalytic mechanism

被引:14
作者
Li, Zihan [1 ]
Song, Erran [1 ]
Ren, Ruirui [1 ]
Zhao, Wuduo [1 ]
Li, Tiesheng [1 ]
Liu, Minghua [2 ,3 ]
Wu, Yangjie [1 ]
机构
[1] Zhengzhou Univ, Coll Chem & Mol Engn, Kexuedadao 100, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Henan Inst Adv Technol, Kexuedadao 100, Zhengzhou 450001, Henan, Peoples R China
[3] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Zhongguancun North First St 2, Beijing 100190, Peoples R China
关键词
CROSS-COUPLING REACTION; LANGMUIR-BLODGETT-FILMS; PALLADIUM NANOPARTICLES; GREEN SYNTHESIS; C-C; EFFICIENT CATALYST; AEROBIC OXIDATION; HIGHLY EFFICIENT; RATIONAL DESIGN; LEAF EXTRACT;
D O I
10.1039/d2ra00658h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pd-Pd/PdO nanoclusters well dispersed on intercalated graphene oxide (GO) (denoted as GO@PPD-Pd) were prepared and characterized. GO@PPD-Pd exhibited high catalytic activity (a TOF value of 60 705 h(-1)) during the Suzuki coupling reaction, and it could be reused at least 6 times. The real active centre was Pd(200)-Pd(200)/PdO(110, 102). A change in the Pd facets on the surface of PdO was a key factor leading to deactivation, and the aggregation and loss of active centres was also another important reason. The catalytic mechanism involved heterogeneous catalysis, showing that the catalytic processes occurred at the interface, including substrate adsorption, intermediate formation, and product desorption. The real active centres showed enhanced negative charge due to the transfer of electrons from the carrier and ligands, which could effectively promote the oxidative addition reaction, and Pd(200) and the heteroconjugated Pd/PdO interface generated in situ also participated in the coupling process, synergistically boosting activity. Developed GO@PPD-Pd was a viable heterogeneous catalyst that may have practical applications owing to its easy synthesis and stability, and this synergistic approach can be utilized to develop other transition-metal catalysts.
引用
收藏
页码:8600 / 8610
页数:11
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