Electron-Rich Ruthenium on Nitrogen-Doped Carbons Promoting Levulinic Acid Hydrogenation to γ-Valerolactone: Effect of Metal-Support Interaction

被引:69
|
作者
Meng, Zhen [1 ]
Liu, Yong [2 ]
Yang, Guangxing [1 ]
Cao, Yonghai [1 ]
Wang, Hongjuan [1 ]
Peng, Feng [3 ]
Liu, Pengfei [4 ,5 ]
Yu, Hao [1 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
[2] Univ New Hampshire, Dept Chem Engn, Durham, NH 03824 USA
[3] Guangzhou Univ, Sch Chem & Chem Engn, Guangzhou 510006, Guangdong, Peoples R China
[4] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
[5] Spallat Neutron Source Sci Ctr, Dongguan 523803, Peoples R China
基金
中国国家自然科学基金;
关键词
Ruthenium nanoparticle; Electronic state; Levulinic acid; Hydrogenation; Biomass; SELECTIVE HYDROGENATION; RU NANOPARTICLES; CO OXIDATION; CATALYZED HYDROGENATION; PLATINUM NANOPARTICLES; GRAPHITIC-NITROGEN; MESOPOROUS CARBON; FORMIC-ACID; EFFICIENT; CONVERSION;
D O I
10.1021/acssuschemeng.9b03742
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ru has been found to be a highly efficient catalyst for producing gamma-valerolactone from the hydrogenation of levulinic acid. However, the active species on Ru nanoparticles (NPs) are still unclear. Here, we synthesized a series of Ru NPs with tunable chemical states obtained by altering the interaction with carbon-nanotube-based supports, achieved by the strategies of doping carbon nanotubes with N and S atoms, changing the amount of dopants, and varying the loading of Ru. The surface species of the supported Ru NPs, identified by X-ray photoelectron spectroscopy, were linked to the catalytic activities instrinsically. We found that the Ru NPs possessing Ru-0 with lower binding energy (Ru 3p) showed higher activity independent of the parameters of synthesis. Theoretical calculations indicated that the electron-rich Ru-0 enhanced LA hydrogenation through facilitating R-COOH breaking into R-CO and -OH, suggesting a powerful tool modifying the catalytic activity of carbon-supported metals by manipulating the electronic metal-support interaction.
引用
收藏
页码:16501 / 16510
页数:19
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