Insight by In Situ Gas Electron Microscopy on the Thermal Behaviour and Surface Reactivity of Cobalt Nanoparticles

被引:19
作者
Dembele, Kassioge [1 ,2 ]
Bahri, Mounib [1 ]
Melinte, Georgian [1 ]
Hirlimann, Charles [1 ]
Berliet, Adrien [2 ]
Maury, Sylvie [2 ]
Gay, Anne-Sophie [2 ]
Ersen, Ovidiu [1 ,3 ,4 ]
机构
[1] IPCMS, 23 Rue Loess, F-67034 Strasbourg, France
[2] IFP Energies Nouvelles, Rond Point 8, F-69360 Changeur De Solaize, France
[3] Univ Strasbourg, Inst Adv Studies USIAS, 5 Allee Gen Rouvillois, F-67083 Strasbourg, France
[4] Inst Univ France, 1 Rue Descartes, F-75231 Paris, France
关键词
insitu TEM; cobalt catalyst; encapsulation; carbon nanotubes; FISCHER-TROPSCH SYNTHESIS; CARBON-MONOXIDE DISPROPORTIONATION; CATALYSTS; CO; DEACTIVATION; NANOTUBES; GROWTH; REGENERATION; HYDROCARBONS; NUCLEATION;
D O I
10.1002/cctc.201800854
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
Here the thermal behaviour and the surface reactivity of cobalt catalysts supported by alumina-silica and promoted by platinum were investigated by insitu transmission electron microscopy (insitu TEM) in a syngas environment. At the standard operating temperature of 220 degrees C, atomic diffusion and sintering processes onto the support are quite limited on the time scale of the TEM experiment. At temperatures between 350 and 450 degrees C, particles encapsulation occurred due to a higher CO dissociation and conversion into graphitic layers. Beyond 500 degrees C, carbon nanotubes (CNTs) growth is activated and the particles undergo (i) morphological changes through continuous elongation and contraction; and (ii) microstructural changes with the appearance of cobalt carbide. By comparing reactions under pure CO and a mixture CO-H-2, it was shown that the addition of dihydrogen to CO increased the rate of CNTs growth and modified the structure of the nanotubes. These results clearly demonstrate the strong ability of the insitu TEM to provide the main lines of the reactivity synopsis of nanocatalysts at a nanometric scale under temperature and reactive gas.
引用
收藏
页码:4004 / 4009
页数:6
相关论文
共 43 条
[1]   Mechanisms for catalytic carbon nanofiber growth studied by ab initio density functional theory calculations [J].
Abild-Pedersen, F ;
Norskov, JK ;
Rostrup-Nielsen, JR ;
Sehested, J ;
Helveg, S .
PHYSICAL REVIEW B, 2006, 73 (11)
[2]   Catalyst deactivation by carbon formation during CO hydrogenation to hydrocarbons on mesoporous Co3O4 [J].
Ahn, Chang-Il ;
Koo, Hyun Mo ;
Jin, Mingshi ;
Kim, Ji Man ;
Kim, Taegyu ;
Suh, Young-Woong ;
Yoon, Ki June ;
Bae, Jong Wook .
MICROPOROUS AND MESOPOROUS MATERIALS, 2014, 188 :196-202
[3]   Micro-fabricated channel with ultra-thin yet ultra-strong windows enables electron microscopy under 4-bar pressure [J].
Alan, Tuncay ;
Yokosawa, Tadahiro ;
Gaspar, Joao ;
Pandraud, Gregory ;
Paul, Oliver ;
Creemer, Fredrik ;
Sarro, Pasqualina M. ;
Zandbergen, Henny W. .
APPLIED PHYSICS LETTERS, 2012, 100 (08)
[4]   Novel MEMS-Based Gas-Cell/Heating Specimen Holder Provides Advanced Imaging Capabilities for In Situ Reaction Studies [J].
Allard, Lawrence F. ;
Overbury, Steven H. ;
Bigelow, Wilbur C. ;
Katz, Michael B. ;
Nackashi, David P. ;
Damiano, John .
MICROSCOPY AND MICROANALYSIS, 2012, 18 (04) :656-666
[5]   NUCLEATION AND GROWTH OF CARBON DEPOSITS FROM NICKEL CATALYZED DECOMPOSITION OF ACETYLENE [J].
BAKER, RTK ;
BARBER, MA ;
WAITE, RJ ;
HARRIS, PS ;
FEATES, FS .
JOURNAL OF CATALYSIS, 1972, 26 (01) :51-&
[6]   CONTROLLED ATMOSPHERE ELECTRON-MICROSCOPY [J].
BAKER, RTK ;
HARRIS, PS .
JOURNAL OF PHYSICS E-SCIENTIFIC INSTRUMENTS, 1972, 5 (08) :793-&
[7]   CONTROLLED ATMOSPHERE ELECTRON-MICROSCOPY OF GAS-SOLID INTERACTIONS [J].
BAKER, RTK .
CRC CRITICAL REVIEWS IN SOLID STATE AND MATERIALS SCIENCES, 1976, 6 (04) :375-399
[8]   Mechanisms of catalyst deactivation [J].
Bartholomew, CH .
APPLIED CATALYSIS A-GENERAL, 2001, 212 (1-2) :17-60
[9]   Visualising reacting single atoms under controlled conditions: Advances in atomic resolution in situ Environmental (Scanning) Transmission Electron Microscopy (E(S)TEM) [J].
Boyes, Edward D. ;
Gai, Pratibha L. .
COMPTES RENDUS PHYSIQUE, 2014, 15 (2-3) :200-213
[10]   How does activation affect the cobalt crystallographic structure? An in situ XRD and magnetic study [J].
Braconnier, L. ;
Landrivon, E. ;
Clemencon, I. ;
Legens, C. ;
Diehl, F. ;
Schuurman, Y. .
CATALYSIS TODAY, 2013, 215 :18-23