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One-step green synthesis of Au@Pd concave nanocubes in deep eutectic solvents and their highly catalytic activities for selective hydrogenation
被引:0
|作者:
Liu, Tianhang
[1
]
Yao, Kaisheng
[1
]
Li, Shuaibo
[2
]
Li, Hang
[1
]
Wang, Qi
[1
]
Han, Tianhang
[1
]
Wang, Aozhou
[1
]
Zhao, Haili
[3
]
机构:
[1] Henan Univ Sci & Technol, Sch Chem & Chem Engn, Luoyang 471023, Henan, Peoples R China
[2] Xian Jiaotong Liverpool Univ, Sch Sci, Xian 215028, Jiangsu, Peoples R China
[3] Henan Univ Sci & Technol, Sch Phys & Engn, Luoyang 471023, Henan, Peoples R China
关键词:
Deep eutectic solvents;
green synthesis;
Au@Pd concave nanocubes;
selective hydrogenation;
SHAPE-CONTROLLED SYNTHESIS;
CHEMOSELECTIVE HYDROGENATION;
ELECTROCATALYTIC ACTIVITY;
GOLD NANOPARTICLES;
NANOCRYSTALS;
TEMPERATURE;
WATER;
MICROSTRUCTURES;
OCTAHEDRON;
DYNAMICS;
D O I:
10.1016/j.jallcom.2024.177027
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:
Concave nanomaterials possess superior properties, but their synthesis usually requires complicated steps, specific conditions and additional reagents (surfactants, capping agents, seeds, etc.). Herein, the well-defined Au@Pd concave nanocubes (CNCs) is facile one-step fabricated in a deep eutectic solvent (DES, named reline) composed of choline chloride (ChCl) and urea. It is found that the reline is crucial to the formation of Au@Pd CNCs. Owing to the concave core-shell structures, and electronic effects between Au core and Pd shell, Au@Pd CNCs exhibited excellent catalytic performance, and recovery convenience in the selective hydrogenation of 4nitrostyrene. Specifically, under normal temperature and pressure conditions (25 degrees C, 0.1 MPa), 4-nitrostyrene can be completely hydrogenated to 4-nitroethylbenzene within 7.0 min. After five cycles, Au@Pd CNCs still maintain the highly catalytic activity and 100 % selectivity toward 4-nitroethylbenzene. It is expected that wellconstructed Au@Pd CNCs also display advanced potentials in other applications.
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