Carbon Defects on N-Doped Carbon Promote Catalytic Activity of Pd Nanoparticles for the Selective Hydrogenation of Quinoline

被引:0
|
作者
Zhou, Binghui [1 ]
Ding, Xinlei [1 ]
Chen, Yun [2 ]
Wang, Hanyang [1 ]
Liu, Yadong [1 ]
Wang, Chengfei [1 ]
Bai, Guangmei [1 ]
Qiu, Wenge [1 ]
机构
[1] Beijing Univ Technol, Coll Mat Sci & Engn, Beijing Key Lab Green Catalysis & Separat, Beijing 100124, Peoples R China
[2] Beijing Inst Technol, Sch Chem & Chem Engn, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
N-doped porous carbon; chemicalactivation; hydrothermal carbonization; palladiumcatalyst; selective hydrogenation of quinoline; POROUS CARBON; EFFICIENT; SUPPORT; DECOMPOSITION; COMPOSITES; CHEMISTRY; MILD; GOLD;
D O I
10.1021/acsanm.4c04100
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The activation process is a key step in preparing porous carbon. Herein, three kinds of green activators were separately used to successfully prepare N-doped porous carbons through a two-step strategy: hydrothermal carbonization and chemical activation using microcrystalline cellulose as the carbon source and urea as the nitrogen source. Palladium was deposited on these N-doped microcrystalline cellulose-based carbons (NMC-X, where X represents the activator) via a traditional deposition-precipitation method, and the resulting Pd nanoparticle catalysts (Pd/NMC-X) showed high activity in the selective hydrogenation of quinoline under mild conditions, particularly Pd/NMC-ZC (ZC, zinc carbonate), which achieved complete conversion of quinoline within 100 min at 40 degrees C and 4 atm H-2. Characterization results suggest that the high activity of Pd/NMC-ZC is mainly attributed to the special electronic structure of its Pd species, particularly the distribution of valence states and reducibility of Pd and the high hydrogen spillover capacity between Pd and NMC-ZC. The chemical activation by ZC leads to the formation of multiple defect sites on the carbon skeleton, modifying the carbon surface properties to enhance hydrogen spillover. This also provides an excellent environment for Pd nanoparticle anchoring, thus increasing the Pd-support interactions and regulating the electronic structure of Pd.
引用
收藏
页码:22895 / 22907
页数:13
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