Measurement of the Dewetting, Nucleation, and Deactivation Kinetics of Carbon Nanotube Population Growth by Environmental Transmission Electron Microscopy

被引:44
作者
Bedewy, Mostafa [1 ,2 ,3 ,6 ]
Viswanath, B. [1 ,2 ,7 ]
Meshot, Eric R. [4 ]
Zakharov, Dmitri N. [5 ]
Stach, Eric A. [5 ]
Hart, A. John [1 ,2 ,3 ]
机构
[1] MIT, Dept Mech Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] MIT, Lab Mfg & Prod, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] Univ Michigan, Dept Mech Engn, 2350 Hayward St, Ann Arbor, MI 48109 USA
[4] Lawrence Livermore Natl Lab, Phys & Life Sci Directorate, Livermore, CA 94550 USA
[5] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[6] Univ Pittsburgh, Swanson Sch Engn, Pittsburgh, PA 15261 USA
[7] Indian Inst Technol, Mandi 175005, India
关键词
CHEMICAL-VAPOR-DEPOSITION; IN-SITU MEASUREMENTS; X-RAY-DIFFRACTION; CATALYST NANOPARTICLES; CARPET GROWTH; ARRAYS; STATE; SPECTROSCOPY; DYNAMICS; DENSITY;
D O I
10.1021/acs.chemmater.6b00798
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
Understanding the collective growth of carbon nanotube (CNT) populations is key to tailoring their properties for many applications. During the initial stages of CNT growth by chemical vapor deposition, catalyst nanoparticle formation by thin-film dewetting and the subsequent CNT nucleation processes dictate the CNT diameter distribution, areal density, and alignment. Herein, we use in situ environmental transmission electron microscopy (E-TEM) to observe the catalyst annealing, growth, and deactivation stages for a population of CNTs grown from a thin-film catalyst. Complementary in situ electron diffraction and TEM imaging show that, during the annealing step in hydrogen, reduction of the iron oxide catalyst is concomitant with changes in the thin-film morphology; complete dewetting and the formation of a population of nanoparticles is only achieved upon the introduction of the carbon source, acetylene. The dewetting kinetics, i.e., the appearance of distinct nanoparticles, exhibits a sigmoidal (autocatalytic) curve with 95% of all nanoparticles appearing within 6 s. After nanoparticles form, they either nucleate CNTs or remain inactive, with incubation times measured to be as small as 3.5 s. Via E-TEM we also directly observe the crowding and self-alignment of CNTs after dewetting and nucleation. In addition, in situ electron energy loss spectroscopy reveals that the collective rate of carbon accumulation decays exponentially. We conclude that the kinetics of catalyst formation and CNT nucleation must both be addressed in order to achieve uniform and high CNT density, and their transient behavior may be a primary cause of the well-known nonuniform density of CNT forests.
引用
收藏
页码:3804 / 3813
页数:10
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