Observation of the Gold Nanorods/Graphene Composite Formation and Motion with in situ Liquid Cell Transmission Electron Microscopy

被引:4
|
作者
Fang Jiali [1 ]
Chen Xin [1 ]
Li Chang [1 ]
Wu Yulian [1 ]
机构
[1] East China Univ Sci & Technol, Sch Mat Sci & Engn, Shanghai Key Lab Adv Polymer Mat, Key Lab Ultrafine Mat,Minist Educ, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
In situ liquid cell TEM; Self-assembly; Graphene; Gold nanorod; Catalytic performance; AU NANOPARTICLES; CATALYTIC-REDUCTION; GROWTH-MECHANISM; GREEN SYNTHESIS; NANOCRYSTALS; GRAPHENE; 4-NITROPHENOL; HYDROGENATION; FACETS; CARBON;
D O I
10.3866/PKU.WHXB201901035
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
In situ liquid cell transmission electron microscopy (LCTEM) was used to observe the dynamic self-assembly behavior of gold nanorod (AuNR)/graphene (G) composites in real-time. Many important reactions in chemistry, physics, and biology occur in solution and real-time imaging of the reaction objects in a liquid medium can further our understanding of the reaction at the nanoscale. Observations of liquid samples using transmission electron microscopy (TEM) have historically been challenging due to issues with evaporation and difficulty in forming thin liquid layers that are suitable for election beam transmission. In situ LCTEM, as an emerging technology, provides novel opportunities for the real-time and high-resolution observation of dynamic processes in solution. In this communication, we report the use of in situ LCTEM to study the assembly behavior of graphene and AuNRs. By tracking and recording the changes in the positions and shapes of the AuNRs and graphene over time, novel composite formation mechanisms between AuNRs and graphene were observed. The AuNRs tended to approach the graphene edges tip-first due to charge attraction. After the assembled structures were formed, the AuNRs could rotate with the graphene edges, among which the edge-to-edge structure was more stable, without angle changes between the AuNR and graphene edge. Drifting motions of the self-assembled structures were observed. And compared with smaller self-assembled structures, the larger structures seem more effectively resisted pushing by liquid flow. In addition, the motions of the larger structure were more easily slowed due to the drag from the liquid cell window substrate. Graphene folding structures were also observed with LCTEM, suggesting that the folding structure can open and close in the liquid, causing apparent relative position changes between Au and graphene for a fixed AuNR on the graphene layer. Overall, the self-assembled structures are very stable and did not show any disassembly behavior in the liquid. Moreover, the AuNR/graphene composites were used as catalysts and showed improved catalytic performance compared to that of bare AuNRs in 4-nitrophenol reduction experiments. The self-assembled catalyst with a mass composite 1 : 5 AuNRs/G ratio exhibited the best performance with a kapp value of 0.5570 min(-1), 8 times that of the bare AuNRs. This significant improvement is closely related to the optimized and stable structure of the AuNR/graphene composites. In situ LCTEM provided a powerful characterization method for analyzing the complex self-assembly behavior of the composites in a liquid and will be useful for the development of high performance composite catalyst materials.
引用
收藏
页码:808 / 815
页数:8
相关论文
共 36 条
  • [1] Biosensing with plasmonic nanosensors
    Anker, Jeffrey N.
    Hall, W. Paige
    Lyandres, Olga
    Shah, Nilam C.
    Zhao, Jing
    Van Duyne, Richard P.
    [J]. NATURE MATERIALS, 2008, 7 (06) : 442 - 453
  • [2] AuPd bimetallic nanoparticles decorated on graphene nanosheets: their green synthesis, growth mechanism and high catalytic ability in 4-nitrophenol reduction
    Chen, Xiaomei
    Cai, Zhixiong
    Chen, Xi
    Oyama, Munetaka
    [J]. JOURNAL OF MATERIALS CHEMISTRY A, 2014, 2 (16) : 5668 - 5674
  • [3] Recent developments of the in situ wet cell technology for transmission electron microscopies
    Chen, Xin
    Li, Chang
    Cao, Hongling
    [J]. NANOSCALE, 2015, 7 (11) : 4811 - 4819
  • [4] A compartment-less nonenzymatic glucose-air fuel cell with nitrogen-doped mesoporous carbons and Au nanowires as catalysts
    Chu, Mi
    Zhang, Yijia
    Yang, Lu
    Tan, Yueming
    Deng, Wenfang
    Ma, Ming
    Su, Xiaoli
    Xie, Qingji
    Yao, Shouzhuo
    [J]. ENERGY & ENVIRONMENTAL SCIENCE, 2013, 6 (12) : 3600 - 3604
  • [5] Electron microscopy of whole cells in liquid with nanometer resolution
    de Jonge, N.
    Peckys, D. B.
    Kremers, G. J.
    Piston, D. W.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (07) : 2159 - 2164
  • [6] Synergistic Catalysis of Metal-Organic Framework-Immobilized Au-Pd Nanoparticles in Dehydrogenation of Formic Acid for Chemical Hydrogen Storage
    Gu, Xiaojun
    Lu, Zhang-Hui
    Jiang, Hai-Long
    Akita, Tomoki
    Xu, Qiang
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (31) : 11822 - 11825
  • [7] Highly Catalytic Pd-Ag Bimetallic Dendrites
    Huang, Jianfeng
    Vongehr, Sascha
    Tang, Shaochun
    Lu, Haiming
    Meng, Xiangkang
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2010, 114 (35): : 15005 - 15010
  • [8] Synergistic Catalysis of Au@Ag Core-Shell Nanoparticles Stabilized on Metal-Organic Framework
    Jiang, Hai-Long
    Akita, Tomoki
    Ishida, Tamao
    Haruta, Masatake
    Xu, Qiang
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (05) : 1304 - 1306
  • [9] In situ Study of Oxidative Etching of Palladium Nanocrystals by Liquid Cell Electron Microscopy
    Jiang, Yingying
    Zhu, Guomin
    Lin, Fang
    Zhang, Hui
    Jin, Chuanhong
    Yuan, Jun
    Yang, Deren
    Zhang, Ze
    [J]. NANO LETTERS, 2014, 14 (07) : 3761 - 3765
  • [10] Nanoshell-Enabled Photothermal Cancer Therapy: Impending Clinical Impact
    Lal, Surbhi
    Clare, Susan E.
    Halas, Naomi J.
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2008, 41 (12) : 1842 - 1851