Synergistic effect in bimetallic copper-silver (CuxAg) nanoparticles enhances silicon conversion in Rochow reaction

被引:38
作者
Zhang, Zailei [1 ]
Ji, Yongjun [1 ]
Li, Jing [1 ]
Zhong, Ziyi [2 ]
Su, Fabing [1 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
[2] ASTAR, Inst Chem Engn & Sci, Singapore 627833, Singapore
来源
RSC ADVANCES | 2015年 / 5卷 / 67期
基金
中国国家自然科学基金;
关键词
SOLVOTHERMAL SYNTHESIS; CATALYTIC PERFORMANCE; ALLOY NANOPARTICLES; MESOPOROUS CARBON; CUO MICROSPHERES; REDUCTION; NI; MICROPARTICLES; HYDROGENATION; OXIDATION;
D O I
10.1039/c5ra04575d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The oleylamine thermal reduction process was employed to prepare bimetallic copper-silver (CuxAg (0 <= x <= 50)) nanoparticles, such as Cu, Cu50Ag, Cu20Ag, Cu10Ag, Cu5Ag, CuAg, CuAg2, and Ag, by using Cu(CH3COO)(2) and AgNO3 as the precursors. The samples were characterized by X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, and X-ray photoelectron spectroscopy. The CuxAg hybrid nanostructure showed good particle dispersion, and Cu and Ag metals were well mixed. The catalytic properties of these bimetallic CuxAg nanoparticles as model catalysts for the Rochow reaction were explored. Compared to monometallic Cu and Ag nanoparticles, bimetallic CuxAg nanoparticles resulted in a much higher silicon conversion, which is attributed to the synergistic electronic effect between Cu and Ag metals. For example, the Cu atom was observed to have a lower electron density in the CuxAg bimetallic nanoparticle than that in monometallic Cu nanoparticles, which enhanced the formation of methylchlorosilanes on the silicon surface with chloromethane, demonstrating the significance of the CuxAg bimetallic catalysts in catalytic reactions during organosilane synthesis. The insights gained in this study should be conducive to the design of good Cubased catalysts for the Rochow reaction.
引用
收藏
页码:54364 / 54371
页数:8
相关论文
共 52 条
  • [1] Thermodynamic assessment of the copper catalyzed direct synthesis of methylchlorosilanes
    Acker, Joerg
    Bohmhammel, Klaus
    [J]. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2008, 693 (15) : 2483 - 2493
  • [2] Bimetallic Cyanide-Bridged Coordination Polymers as Lithium Ion Cathode Materials: Core@Shell Nanoparticles with Enhanced Cyclability
    Asakura, Daisuke
    Li, Carissa H.
    Mizuno, Yoshifumi
    Okubo, Masashi
    Zhou, Haoshen
    Talham, Daniel R.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (07) : 2793 - 2799
  • [3] Effect of low aluminum silicon on the direct process
    Bablin, JM
    Crawford, AC
    DeMoulpied, DC
    Lewis, LN
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2003, 42 (15) : 3555 - 3565
  • [4] CHARACTERIZATION OF REACTIVE AREAS IN THE DIRECT PROCESS FOR THE PRODUCTION OF METHYLCHLOROSILANES
    BANHOLZER, WF
    BURRELL, MC
    [J]. JOURNAL OF CATALYSIS, 1988, 114 (02) : 259 - 270
  • [5] ACTIVE-SITE FORMATION IN THE DIRECT PROCESS FOR METHYLCHLOROSILANES
    BANHOLZER, WF
    LEWIS, N
    WARD, W
    [J]. JOURNAL OF CATALYSIS, 1986, 101 (02) : 405 - 415
  • [6] Banin U, 2007, NAT MATER, V6, P625, DOI 10.1038/nmat1993
  • [7] EXAFS as a tool to interrogate the size and shape of mono and bimetallic catalyst nanoparticles
    Beale, Andrew M.
    Weckhuysen, Bert M.
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2010, 12 (21) : 5562 - 5574
  • [8] RuCu nanoparticles supported on graphene: A highly efficient catalyst for hydrolysis of ammonia borane
    Cao, Nan
    Hu, Kai
    Luo, Wei
    Cheng, Gongzhen
    [J]. JOURNAL OF ALLOYS AND COMPOUNDS, 2014, 590 : 241 - 246
  • [9] Silver nanoparticles capped by oleylamine: Formation, growth, and self-organization
    Chen, Meng
    Feng, Yong-Gang
    Wang, Xia
    Li, Ting-Cheng
    Zhang, Jun-Yan
    Qian, Dong-Jin
    [J]. LANGMUIR, 2007, 23 (10) : 5296 - 5304
  • [10] Size-Controlled Synthesis of Platinum-Copper Hierarchical Trigonal Bipyramid Nanoframes
    Chen, Sheng
    Su, Hongyang
    Wang, Youcheng
    Wu, Wenlong
    Zeng, Jie
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (01) : 108 - 113