Highly Efficient Dehydrogenation of Primary Aliphatic Alcohols Catalyzed by Cu Nanoparticles Dispersed on Rod-Shaped La2O2CO3

被引:127
作者
Wang, Fei [1 ]
Shi, Ruijuan [1 ]
Liu, Zhi-Quan [2 ]
Shang, Pan-Ju [2 ]
Pang, Xueyong [2 ]
Shen, Shuai [1 ]
Feng, Zhaochi [1 ]
Li, Can [1 ]
Shen, Wenjie [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
基金
中国国家自然科学基金;
关键词
heterogeneous catalysis; dehydrogenation; primary aliphatic alcohol; reaction coupling; Cu/La2O2CO3; catalyst; crystal-facet selective deposition; active nanoenvironmental; OXIDANT-FREE DEHYDROGENATION; ENVIRONMENTALLY BENIGN OXIDATION; AEROBIC OXIDATION; HETEROGENEOUS CATALYST; SELECTIVE OXIDATION; GOLD NANOPARTICLES; SITES; HYDROTALCITE;
D O I
10.1021/cs400255r
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
Copper nanoparticles dispersed rod-shaped La2O2CO3 efficiently catalyzed transfer dehydrogenation of primary aliphatic alcohols with an aldehyde yield of up to 97%. This high efficiency was achieved by creating a catalytically active nanoenvironement for effective reaction coupling between alcohol dehydrogenation and styrene hydrogenation via hydrogen transfer. The {110} planes on the La2O2CO3 nanorods not only provided substantial amounts of medium-strength basic sites for the activation of alcohol but also directed the selective dispersion of hemispherical Cu particles of about 4.5 mm on their surfaces, which abstracted and transferred hydrogen atoms for styrene hydrogenation. This finding provides a new strategy for developing highly active alcohol-dehydrogenation catalysts by tuning the shape of the oxide support and consequently the metal-oxide interfacial nanostructure.
引用
收藏
页码:890 / 894
页数:5
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