Icosahedral gold cage clusters:: M@Au12- (M = V, Nb, and Ta)

被引:134
作者
Zhai, HJ [1 ]
Li, J
Wang, LS
机构
[1] Washington State Univ, Dept Phys, Richland, WA 99352 USA
[2] Pacific NW Natl Lab, WR Wiley Environm Mol Sci Lab, Richland, WA 99352 USA
关键词
D O I
10.1063/1.1799574
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
We report the observation and characterization of a series of stable bimetallic 18-valence-electron clusters containing a highly symmetric 12-atom icosahedral Au cage with an encapsulated central heteroatom of Group VB transition metals, M@Au-12(-) (M=V,Nb,Ta). Electronic and structural properties of these clusters were probed by anion photoelectron spectroscopy and theoretical calculations. Characteristics of the M@Au-12(-) species include their remarkably high binding energies and relatively simple spectral features, which reflect their high symmetry and stability. The adiabatic electronic binding energies of M@Au-12(-) were measured to be 3.70+/-0.03, 3.77+/-0.03, and 3.76+/-0.03 eV for M=V, Nb, and Ta, respectively. Comparison of density-functional calculations with experimental data established the highly symmetric icosahedral structures for the 18-electron cluster anions, which may be promising building blocks for cluster-assembled nanomaterials in the form of stoichiometric [M@Au-12(-)]X+ salts. (C) 2004 American Institute of Physics.
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收藏
页码:8369 / 8374
页数:6
相关论文
共 42 条
[1]   ENERGY-ADJUSTED ABINITIO PSEUDOPOTENTIALS FOR THE 2ND AND 3RD ROW TRANSITION-ELEMENTS [J].
ANDRAE, D ;
HAUSSERMANN, U ;
DOLG, M ;
STOLL, H ;
PREUSS, H .
THEORETICA CHIMICA ACTA, 1990, 77 (02) :123-141
[2]   Properties of WAu12 [J].
Autschbach, J ;
Hess, BA ;
Johansson, MP ;
Neugebauer, J ;
Patzschke, M ;
Pyykkö, P ;
Reiher, M ;
Sundholm, D .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2004, 6 (01) :11-22
[3]   A NEW MIXING OF HARTREE-FOCK AND LOCAL DENSITY-FUNCTIONAL THEORIES [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (02) :1372-1377
[4]   SYNTHESIS AND X-RAY STRUCTURAL CHARACTERIZATION OF THE CENTERED ICOSAHEDRAL GOLD CLUSTER COMPOUND [AU13(PME2PH)10CL2](PF6)3 - THE REALIZATION OF A THEORETICAL PREDICTION [J].
BRIANT, CE ;
THEOBALD, BRC ;
WHITE, JW ;
BELL, LK ;
MINGOS, DMP ;
WELCH, AJ .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1981, (05) :201-202
[5]   Molecular excitation energies to high-lying bound states from time-dependent density-functional response theory: Characterization and correction of the time-dependent local density approximation ionization threshold [J].
Casida, ME ;
Jamorski, C ;
Casida, KC ;
Salahub, DR .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (11) :4439-4449
[6]   Asymptotic correction approach to improving approximate exchange-correlation potentials: Time-dependent density-functional theory calculations of molecular excitation spectra [J].
Casida, ME ;
Salahub, DR .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (20) :8918-8935
[7]   ENERGY-ADJUSTED ABINITIO PSEUDOPOTENTIALS FOR THE 1ST-ROW TRANSITION-ELEMENTS [J].
DOLG, M ;
WEDIG, U ;
STOLL, H ;
PREUSS, H .
JOURNAL OF CHEMICAL PHYSICS, 1987, 86 (02) :866-872
[8]   The structures of small gold cluster anions as determined by a combination of ion mobility measurements and density functional calculations [J].
Furche, F ;
Ahlrichs, R ;
Weis, P ;
Jacob, C ;
Gilb, S ;
Bierweiler, T ;
Kappes, MM .
JOURNAL OF CHEMICAL PHYSICS, 2002, 117 (15) :6982-6990
[9]  
GU X, IN PRESS PHYS REV B
[10]   Towards an order-N DFT method [J].
Guerra, CF ;
Snijders, JG ;
te Velde, G ;
Baerends, EJ .
THEORETICAL CHEMISTRY ACCOUNTS, 1998, 99 (06) :391-403