Details
Original language | English |
---|---|
Pages (from-to) | 47-54 |
Number of pages | 8 |
Journal | International Journal of Mass Spectrometry |
Volume | 202 |
Issue number | 1-3 |
Publication status | Published - 27 Nov 2000 |
Externally published | Yes |
Abstract
Multicollision-induced dissociation (MCID) has been applied to gold clusters, Au(n)/2+ (n = 7-35) and Au(n)/3+ (n = 19-35) stored in a Penning trap. By application of ion cyclotron resonance excitation and pulses of argon collision gas, fragmentation yields have been measured as a function of the clusters' kinetic energy. The corresponding dissociation energies have been determined by use of the impulsive collision theory and the quantum Rice-Ramsperger-Kassel (RRK) model for the energy transfer to internal cluster modes and for delayed dissociation, respectively. As compared to earlier measurements of singly charged gold clusters the variation of the stability as a function of cluster size is reduced. The doubly charged clusters show an odd-even effect that is reversed with respect to that of singly charged gold clusters. This is similar to findings by electron impact ionization/dissociation and in line with the expectations for simple metal clusters, where the structure and stability is governed by the number of atomic valence electrons. However, no cluster sizes of particular stability (magic numbers) are observed. In general, the dissociation energy of small clusters is smaller than that of the larger ones because of the influence of the Coulomb force. In contrast to the singly charged gold clusters the odd-even effect of Au(n)/2+ disappears at small cluster sizes n < 11; explained as a consequence of the dominance of trimer fission in that size region. (C) 2000 Elsevier Science B.V.
Keywords
- Cluster fission, Collision induced dissociation, Dissociation energies, Gold clusters, Multiply charged clusters
ASJC Scopus subject areas
- Physics and Astronomy(all)
- Instrumentation
- Physics and Astronomy(all)
- Condensed Matter Physics
- Chemistry(all)
- Spectroscopy
- Chemistry(all)
- Physical and Theoretical Chemistry
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In: International Journal of Mass Spectrometry, Vol. 202, No. 1-3, 27.11.2000, p. 47-54.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Multicollision-induced dissociation of multiply charged gold clusters, Au(n)/2+, n = 7-35, and Au(n)/3+, n = 19-35
AU - Ziegler, J.
AU - Dietrich, G.
AU - Krückeberg, S.
AU - Lützenkirchen, K.
AU - Schweikhard, L.
AU - Walther, Clemens
N1 - Funding information: This work was financed in part by the Deutsche Forschungsgemeinschaft (Schw 401/7) and also supported by the Materials Science Research Center at Mainz and the Fonds der Chemischen Industrie. Furthermore, S.K. thanks the Studienstiftung des deutschen Volkes, and C.W. thanks the Graduiertenkolleg Physik und Chemie Supramolekularer Systeme for their support.
PY - 2000/11/27
Y1 - 2000/11/27
N2 - Multicollision-induced dissociation (MCID) has been applied to gold clusters, Au(n)/2+ (n = 7-35) and Au(n)/3+ (n = 19-35) stored in a Penning trap. By application of ion cyclotron resonance excitation and pulses of argon collision gas, fragmentation yields have been measured as a function of the clusters' kinetic energy. The corresponding dissociation energies have been determined by use of the impulsive collision theory and the quantum Rice-Ramsperger-Kassel (RRK) model for the energy transfer to internal cluster modes and for delayed dissociation, respectively. As compared to earlier measurements of singly charged gold clusters the variation of the stability as a function of cluster size is reduced. The doubly charged clusters show an odd-even effect that is reversed with respect to that of singly charged gold clusters. This is similar to findings by electron impact ionization/dissociation and in line with the expectations for simple metal clusters, where the structure and stability is governed by the number of atomic valence electrons. However, no cluster sizes of particular stability (magic numbers) are observed. In general, the dissociation energy of small clusters is smaller than that of the larger ones because of the influence of the Coulomb force. In contrast to the singly charged gold clusters the odd-even effect of Au(n)/2+ disappears at small cluster sizes n < 11; explained as a consequence of the dominance of trimer fission in that size region. (C) 2000 Elsevier Science B.V.
AB - Multicollision-induced dissociation (MCID) has been applied to gold clusters, Au(n)/2+ (n = 7-35) and Au(n)/3+ (n = 19-35) stored in a Penning trap. By application of ion cyclotron resonance excitation and pulses of argon collision gas, fragmentation yields have been measured as a function of the clusters' kinetic energy. The corresponding dissociation energies have been determined by use of the impulsive collision theory and the quantum Rice-Ramsperger-Kassel (RRK) model for the energy transfer to internal cluster modes and for delayed dissociation, respectively. As compared to earlier measurements of singly charged gold clusters the variation of the stability as a function of cluster size is reduced. The doubly charged clusters show an odd-even effect that is reversed with respect to that of singly charged gold clusters. This is similar to findings by electron impact ionization/dissociation and in line with the expectations for simple metal clusters, where the structure and stability is governed by the number of atomic valence electrons. However, no cluster sizes of particular stability (magic numbers) are observed. In general, the dissociation energy of small clusters is smaller than that of the larger ones because of the influence of the Coulomb force. In contrast to the singly charged gold clusters the odd-even effect of Au(n)/2+ disappears at small cluster sizes n < 11; explained as a consequence of the dominance of trimer fission in that size region. (C) 2000 Elsevier Science B.V.
KW - Cluster fission
KW - Collision induced dissociation
KW - Dissociation energies
KW - Gold clusters
KW - Multiply charged clusters
UR - http://www.scopus.com/inward/record.url?scp=0034675876&partnerID=8YFLogxK
U2 - 10.1016/S1387-3806(00)00207-4
DO - 10.1016/S1387-3806(00)00207-4
M3 - Article
AN - SCOPUS:0034675876
VL - 202
SP - 47
EP - 54
JO - International Journal of Mass Spectrometry
JF - International Journal of Mass Spectrometry
SN - 1387-3806
IS - 1-3
ER -