Reactions of size-selected positively charged nickel clusters with carbon monoxide in molecular beams

被引:34
作者
Vajda, S [1 ]
Wolf, S [1 ]
Leisner, T [1 ]
Busolt, U [1 ]
Woste, LH [1 ]
Wales, DJ [1 ]
机构
[1] UNIV CAMBRIDGE, CHEM LABS, CAMBRIDGE CB2 1EW, ENGLAND
关键词
D O I
10.1063/1.474688
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
Reactions of small thermalized positively charged nickel clusters with carbon monoxide were studied in a molecular beam experiment. The nickel clusters were produced in a high intensity cluster ion source and thermalized in a large helium-filled quadrupole ion guide. The clusters were size selected by a quadrupole mass spectrometer. The mass-and charge-selected nickel clusters then passed through a Linear quadrupole drift tube filled with a mixture of helium buffer gas and carbon monoxide. The reaction products were then analyzed by a quadrupole mass-spectrometer, Using this technique, saturation limits for Ni-n(+) clusters with n=4-31 were measured and the competitive reaction channels were identified. Under certain experimental conditions carbide formation was observed in the case of the nickel tetramer, pentamer, and hexamer. The structure of the nickel carbonyl clusters is discussed within the framework of the polyhedral skeletal electron pair theory. The cluster growth may be explained by a pentagonal sequence of structures for n=4-7, capping of the pentagonal bipyramid to buildup an icosahedron at Ni-13(+),and further capping of this icosahedron to form a double icosahedron at Ni-19(+). (C) 1997 American Institute of Physics.
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页码:3492 / 3497
页数:6
相关论文
共 44 条
[1]  
BONACICKOUTECKY V, COMMUNICATION
[2]   LASER-INDUCED MOLECULAR DESORPTION FROM SIZE-SELECTED NICKEL CLUSTER CARBONYL IONS - KINETICS OF THE ADSORPTION DESORPTION EQUILIBRIUM [J].
BRECHIGNAC, C ;
BRECHIGNAC, P ;
FAYET, P ;
SAUNDERS, WA ;
WOSTE, L .
JOURNAL OF CHEMICAL PHYSICS, 1988, 89 (04) :2419-2426
[3]  
BRUCE MI, 1967, ADV ORGANOMET CHEM, V6, P273
[4]   CO CHEMISORPTION ON FREE GAS-PHASE METAL-CLUSTERS [J].
COX, DM ;
REICHMANN, KC ;
TREVOR, DJ ;
KALDOR, A .
JOURNAL OF CHEMICAL PHYSICS, 1988, 88 (01) :111-119
[5]   BONDING CAPABILITIES OF NICKEL CLUSTER IONS - SYNTHETIC CHEMISTRY IN A MOLECULAR-BEAM [J].
FAYET, P ;
MCGLINCHEY, MJ ;
WOSTE, LH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (06) :1733-1738
[6]  
GANTEFOR G, 1988, FARADAY DISCUSS, V86, P197, DOI 10.1039/dc9888600197
[7]   NICKEL GROUP CLUSTER ANION REACTIONS WITH CARBON-MONOXIDE - RATE COEFFICIENTS AND CHEMISORPTION EFFICIENCY [J].
HINTZ, PA ;
ERVIN, KM .
JOURNAL OF CHEMICAL PHYSICS, 1994, 100 (08) :5715-5725
[8]   THE KINETICS OF REACTIONS OF NICKEL CLUSTERS WITH HYDROGEN AND DEUTERIUM [J].
HOFFMAN, WF ;
PARKS, EK ;
NIEMAN, GC ;
POBO, LG ;
RILEY, SJ .
ZEITSCHRIFT FUR PHYSIK D-ATOMS MOLECULES AND CLUSTERS, 1987, 7 (01) :83-89
[9]   Bonding of CO to metal particles: Photoelectron spectra of Ni-n(CO)(m)(-) and Pt-n(CO)(m)(-) clusters [J].
IckingKonert, GS ;
Handschuh, H ;
Gantefor, G ;
Eberhardt, W .
PHYSICAL REVIEW LETTERS, 1996, 76 (07) :1047-1050
[10]   FTMS STUDIES OF SPUTTERED METAL CLUSTER IONS .4. SIZE-SELECTIVE EFFECTS IN THE CHEMISTRY OF FEN+ WITH NH3 AND PDN+ WITH D2 OR C2H4 [J].
IRION, MP ;
SELINGER, A ;
SCHNABEL, P .
ZEITSCHRIFT FUR PHYSIK D-ATOMS MOLECULES AND CLUSTERS, 1991, 19 (1-4) :393-396