Architecture of Pd-Au bimetallic nanoparticles in sodium bis(2-ethylhexyl)sulfosuccinate reverse micelles as investigated by X-ray absorption spectroscopy

被引:80
作者
Chen, Ching-Hsiang [1 ,3 ]
Sarma, Loka Subramnanyam [1 ]
Chen, Jiurn-Ming [1 ]
Shih, Shou-Chu [1 ]
Wang, Guo-Rung [1 ]
Liu, Din-Goa [2 ]
Tang, Mau-Tsu [2 ]
Lee, Jyh-Fu [2 ]
Hwang, Bing-Joe [1 ,2 ]
机构
[1] Natl Taiwan Univ Sci & Technol, Dept Chem Engn, Nanoelectrochem Lab, Taipei 106, Taiwan
[2] Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan
[3] Acad Sinica, Inst Atom & Mol Sci, Taipei 115, Taiwan
关键词
bimetallic nanoparticles; X-ray absorption spectroscopy; redox transmetalation reaction; reverse micelles; atomic distribution;
D O I
10.1021/nn700021x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, we demonstrate the unique application of X-ray absorption spectroscopy (XAS) as a fundamental characterization tool to help in designing and controlling the architecture of Pd-Au bimetallic nanoparticles within a water-in-oil microemulsion system of water/sodium bis(2-ethylhexyl)sulfosuccinate (AOT)/n-heptane. Structural insights obtained from the in situ XAS measurements recorded at each step during the formation process revealed that Pd-Au bimetallic clusters with various Pd-Au atomic stackings are formed by properly performing hydrazine reduction and redox transmetalation reactions sequentially within water-in-oil microemulsions. A structural model is provided to explain reasonably each reaction step and to give detailed insight into the nucleation and growth mechanism of Pd-Au bimetallic clusters. The combination of in situ XAS analysis at both the Pd K-edge and the Au L-III-edge and UV-vis absorption spectral features confirms that the formation of Pd-Au bimetallic clusters follows a (Pd-nuclei-Au-stack)-Pd-surf stacking. This result further implies that the thickness of Au-stack and Pd-surf layers may be modulated by varying the dosage of the Au precursor and hydrazine, respectively. In addition, a bimetallic (Pd-Au)(alloy) nanocluster with a (Pd-nuclei-Au-stack)-(Pd-Au-ally)(surf) stacking was also designed and synthesized in order to check the feasibility of Pd,u, layer modification. The result reveals that the Pd-surf layer of the stacked (Pd-nuclei-Au)(stack) bimetallic clusters can be successfully modified to form a (Au-Pd alloy)(surf) layer by a co-reduction of Pd and Au ions by hydrazine. Further, we demonstrate the alloying extent or atomic distribution of Pd and Au in Pd-Au bimetallic nanoparticles, from the derived XAS structural parameters. The complete XAS-based methodology, demonstrated here on the Pd-Au bimetallic system, can easily be extended to design and control the alloying extent or atomic distribution, atomic stacking, and electronic structure to construct many other types of bimetallic systems for interesting applications.
引用
收藏
页码:114 / 125
页数:12
相关论文
共 47 条
  • [1] Limits and advantages of x-ray absorption near edge structure for nanometer scale metallic clusters
    Bazin, D
    Rehr, JJ
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (45) : 12398 - 12402
  • [2] Numerical simulation of the platinum L-III edge white line relative to nanometer scale clusters
    Bazin, D
    Sayers, D
    Rehr, JJ
    Mottet, C
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (27): : 5332 - 5336
  • [3] Anomalous wide angle X-ray scattering (AWAXS) and heterogeneous catalysts
    Bazin, D
    Guczi, L
    Lynch, J
    [J]. APPLIED CATALYSIS A-GENERAL, 2002, 226 (1-2) : 87 - 113
  • [4] Comparison between X-ray absorption spectroscopy, anomalous wide angle X-ray scattering, anomalous small angle X-ray scattering, and diffraction anomalous fine structure techniques applied to nanometer-scale metallic clusters
    Bazin, DC
    Sayers, DA
    Rehr, JJ
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (51): : 11040 - 11050
  • [5] PLATINUM-TIN REFORMING CATALYSTS .2. ACTIVITY AND SELECTIVITY IN HYDROCARBON REACTIONS
    BURCH, R
    GARLA, LC
    [J]. JOURNAL OF CATALYSIS, 1981, 71 (02) : 360 - 372
  • [6] Nucleation and growth mechanism of Pd/Pt bimetallic clusters in sodium bis(2-ethylhexyl)sulfosuceinate (AOT) reverse micelles as studied by in situ X-ray absorption spectroscopy
    Chen, CH
    Hwang, BJ
    Wang, GR
    Sarma, LS
    Tang, MT
    Liu, DG
    Lee, JF
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (46) : 21566 - 21575
  • [7] Formation of bimetallic Ag-Pd nanoclusters via the reaction between ag nanoclusters and Pd2+ ions
    Chen, Ching-Hsiang
    Sarma, Loka Subramanyam
    Wang, Guo-Rung
    Chen, Jiun-Ming
    Shih, Shou-Chu
    Tang, Mau-Tsu
    Liu, Ding-Goa
    Lee, Jyh-Fu
    Chen, Jing-Ming
    Hwang, Bing-Joe
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (21) : 10287 - 10295
  • [8] Structural transformation of PdPt nanoparticles probed with X-ray absorption near edge structure
    Cho, SJ
    Kang, SK
    [J]. CATALYSIS TODAY, 2004, 93-5 : 561 - 566
  • [9] Acetylene hydrogenation on Au-based catalysts
    Choudhary, TV
    Sivadinarayana, C
    Datye, AK
    Kumar, D
    Goodman, DW
    [J]. CATALYSIS LETTERS, 2003, 86 (1-3) : 1 - 8
  • [10] APPLICATION OF ISOTOPIC TRANSIENT KINETICS TO VINYL-ACETATE CATALYSIS
    CRATHORNE, EA
    MACGOWAN, D
    MORRIS, SR
    RAWLINSON, AP
    [J]. JOURNAL OF CATALYSIS, 1994, 149 (02) : 254 - 267