Can optical spectroscopy directly elucidate the ground state of C20?

被引:54
作者
Castro, A [1 ]
Marques, MAL
Alonso, JA
Bertsch, GF
Yabana, K
Rubio, A
机构
[1] Univ Valladolid, Dept Fis Teor, E-47011 Valladolid, Spain
[2] Univ Basque Country, Fac Quim, Dept Fis Mat, Ctr Mixto CSIC,UPV,EHU, E-20080 San Sebastian, Spain
[3] Donostia Int Phys Ctr, San Sebastian 20080, Spain
[4] Univ Valladolid, Dept Fis Teor, E-47011 Valladolid, Spain
[5] Univ Washington, Dept Phys, Seattle, WA 98195 USA
[6] Univ Washington, Inst Nucl Theory, Seattle, WA 98195 USA
[7] Univ Tsukuba, Inst Phys, Tsukuba, Ibaraki 3058571, Japan
关键词
D O I
10.1063/1.1430737
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
The optical response of the lowest energy isomers of the C-20 family is calculated using time-dependent density functional theory within a real-space, real-time scheme. Significant differences are found among the spectra of the different isomers, and thus we propose optical spectroscopy as a tool for experimental investigation of the structure of these important clusters. (C) 2002 American Institute of Physics.
引用
收藏
页码:1930 / 1933
页数:4
相关论文
共 30 条
[1]   Electron-vibration coupling in time-dependent density-functional theory: Application to benzene [J].
Bertsch, GF ;
Schnell, A ;
Yabana, K .
JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (09) :4051-4054
[2]   PRECURSORS TO C-60 FULLERENE FORMATION [J].
BRABEC, CJ ;
ANDERSON, EB ;
DAVIDSON, BN ;
KAJIHARA, SA ;
ZHANG, QM ;
BERNHOLC, J ;
TOMANEK, D .
PHYSICAL REVIEW B, 1992, 46 (11) :7326-7328
[3]   LDA predictions of C-20 isomerizations: Neutral and charged species [J].
Bylaska, EJ ;
Taylor, PR ;
Kawai, R ;
Weare, JH .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (17) :6966-6972
[4]   3-DIMENSIONAL TIME-DEPENDENT HARTREE-FOCK CALCULATIONS - APPLICATION TO O-16+O-16 COLLISIONS [J].
FLOCARD, H ;
KOONIN, SE ;
WEISS, MS .
PHYSICAL REVIEW C, 1978, 17 (05) :1682-1699
[5]   Mechanism of fullerene formation [J].
Goroff, NS .
ACCOUNTS OF CHEMICAL RESEARCH, 1996, 29 (02) :77-83
[6]   STRUCTURE AND STABILITY OF MOLECULAR CARBON - IMPORTANCE OF ELECTRON CORRELATION [J].
GROSSMAN, JC ;
MITAS, L ;
RAGHAVACHARI, K .
PHYSICAL REVIEW LETTERS, 1995, 75 (21) :3870-3873
[7]   An efficient method for calculating molecular excitation energies by time-dependent density-functional theory [J].
Heinze, HH ;
Görling, A ;
Rösch, N .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (06) :2088-2099
[8]   ANNEALING CARBON CLUSTER IONS - A MECHANISM FOR FULLERENE SYNTHESIS [J].
HUNTER, JM ;
FYE, JL ;
ROSKAMP, EJ ;
JARROLD, MF .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (07) :1810-1818
[9]   Chemistry - The smallest fullerene [J].
Jarrold, MF .
NATURE, 2000, 407 (6800) :26-27
[10]   Density functional study of carbon clusters C2n (2≤n≤16).: I.: Structure and bonding in the neutral clusters [J].
Jones, RO .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (11) :5189-5200