A hierarchical family of three-dimensional potential energy surfaces for He-CO

被引:48
作者
Peterson, KA [1 ]
McBane, GC
机构
[1] Washington State Univ, Dept Chem, Pullman, WA 99164 USA
[2] Grand Valley State Univ, Dept Chem, Allendale, MI 49401 USA
关键词
D O I
10.1063/1.1947194
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
A hierarchical family of five three-dimensional potential energy surfaces has been developed for the benchmark He-CO system. Four surfaces were obtained at the coupled cluster singles and doubles level of theory with a perturbational estimate of triple excitations, CCSD(T), and range in quality from the doubly augmented double-zeta basis set to the complete basis set (CBS) limit. The fifth corresponds to an approximate CCSDT/CBS surface (CCSD with iterative triples/CBS, denoted CBS+corr). The CBS limit results were obtained by pointwise basis set extrapolations of the individual counterpoise-corrected interaction energies. For each surface, over 1000 interaction energies were accurately interpolated using a reproducing kernel Hilbert space approach with an R-6+R-7 asymptotic form. In each case, both three-dimensional and effective two-dimensional surfaces were developed. In standard Jacobi coordinates, the final CBS+corr surface has a global minimum at r(CO)=2.1322a(0),R=6.418a(0), and gamma=70.84 degrees with a well depth of -22.34 cm(-1). The other four surfaces have well depths ranging from -14.83 cm(-1) [CCSD(T)/d-aug-cc-pVDZ] to -22.02 cm(-1) [CCSD(T)/CBS]. For each of these surfaces the infrared spectrum has been accurately calculated and compared to experiment, as well as to previous theoretical and empirical surfaces. The final CBS+corr surface exhibits root-mean-square and maximum errors compared to experiment (He-4) of just 0.03 and 0.04 cm(-1), respectively, for all 42 transitions and is the most accurate ab initio surface to date for this system. Other quantities investigated include the interaction second virial coefficient, the integral cross sections, and thermal rate coefficients for rotational relaxation of CO by He, and rate coefficients for CO vibrational relaxation by He. All the observable quantities showed a smooth convergence with respect to the quality of the underlying interaction surface. (c) 2005 American Institute of Physics.
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页数:15
相关论文
共 85 条
[1]   A STABLE LINEAR REFERENCE POTENTIAL ALGORITHM FOR SOLUTION OF THE QUANTUM CLOSE-COUPLED EQUATIONS IN MOLECULAR-SCATTERING THEORY [J].
ALEXANDER, MH ;
MANOLOPOULOS, DE .
JOURNAL OF CHEMICAL PHYSICS, 1987, 86 (04) :2044-2050
[2]   LOW-TEMPERATURE VIBRATIONAL-RELAXATION OF CARBON-MONOXIDE BY LIGHT MASS SPECIES [J].
ALLEN, DC ;
PRICE, TJ ;
SIMPSON, CJSM .
CHEMICAL PHYSICS, 1979, 41 (03) :449-460
[3]  
[Anonymous], ACES
[4]   State to state He-CO rotationally inelastic scattering [J].
Antonova, S ;
Lin, A ;
Tsakotellis, AP ;
McBane, GC .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (05) :2384-2390
[5]   Vibrational relaxation of CO by collisions with 4He at ultracold temperatures [J].
Balakrishnan, N ;
Dalgarno, A ;
Forrey, RC .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (02) :621-627
[6]   VIBRATIONAL-RELAXATION OF N-2 BY COLLISION WITH HE ATOMS [J].
BANKS, AJ ;
CLARY, DC ;
WERNER, HJ .
JOURNAL OF CHEMICAL PHYSICS, 1986, 84 (07) :3788-3797
[7]   CALCULATION OF SMALL MOLECULAR INTERACTIONS BY DIFFERENCES OF SEPARATE TOTAL ENERGIES - SOME PROCEDURES WITH REDUCED ERRORS [J].
BOYS, SF ;
BERNARDI, F .
MOLECULAR PHYSICS, 1970, 19 (04) :553-&
[8]  
BREWER J, 1967, MRL2915C AFOSR
[9]   QUALITATIVE ASPECTS OF QUANTUM MECHANICAL SECOND VIRIAL COEFFICIENT [J].
BRUCH, LW .
JOURNAL OF CHEMICAL PHYSICS, 1971, 54 (10) :4281-&