Glory scattering in deeply inelastic molecular collisions

被引:19
作者
Besemer, Matthieu [1 ]
Tang, Guoqiang [1 ]
Gao, Zhi [1 ,2 ]
van der Avoird, Ad [1 ]
Groenenboom, Gerrit C. [1 ]
van de Meerakker, Sebastiaan Y. T. [1 ]
Karman, Tijs [1 ]
机构
[1] Radboud Univ Nijmegen, Inst Mol & Mat, Nijmegen, Netherlands
[2] Huazhong Univ Sci & Technol, Key Lab Fundamental Phys Quant Measurement, Sch Phys, Minist Educ, Wuhan, Peoples R China
基金
欧洲研究理事会;
关键词
JZ-PRESERVING PROPENSITIES; VT-RATE COEFFICIENTS; SEMICLASSICAL CALCULATIONS; KINEMATIC APSE; CROSS-SECTIONS; NO RADICALS; DEPENDENCE; ENERGY; VV;
D O I
10.1038/s41557-022-00907-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For molecular collisions, the deflection of a molecule's trajectory provides one of the most sensitive probes of the interaction potential and there are general rules of thumb that relate the direction of deflection to precollision conditions. Following intuition, forward scattering results from glancing collisions, whereas near head-on collisions result in back scattering. Here we present the observation of forward scattering in inelastic processes that defies this common wisdom. For deeply inelastic collisions between NO radicals and CO or HD molecules, we observed forward scattering in fully resolved pair-correlated differential cross-sections, despite the low impact parameters that are needed to induce a sufficient energy transfer. We rationalized these findings by extending the textbook model of hard-sphere scattering-taking inelastic energy transfer into account-and attribute the forward scattering to glory-type trajectories caused by attractive forces. This phenomenon, which we refer to as hard-collision glory scattering, is predicted to be ubiquitous. We derive under which conditions hard-collision glory scattering occurs and retrospectively identify such behaviour in previously studied systems.
引用
收藏
页码:664 / +
页数:7
相关论文
共 35 条
[1]   Dynamics of the simplest chlorine atom reaction: An experimental and theoretical study [J].
Alagia, M ;
Balucani, N ;
Cartechini, L ;
Casavecchia, P ;
vanKleef, EH ;
Volpi, GG ;
Aoiz, FJ ;
Banares, L ;
Schwenke, DW ;
Allison, TC ;
Mielke, SL ;
Truhlar, DG .
SCIENCE, 1996, 273 (5281) :1519-1522
[2]   A quantum mechanical and quasi-classical trajectory study of the Cl+H2 reaction and its isotopic variants:: Dependence of the integral cross section on the collision energy and reagent rotation [J].
Aoiz, FJ ;
Bañares, L ;
Castillo, JF ;
Menéndez, M ;
Skouteris, D ;
Werner, HJ .
JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (05) :2074-2081
[3]   VV-RATE AND VT-RATE COEFFICIENTS IN N2 BY A QUANTUM-CLASSICAL MODEL [J].
BILLING, GD ;
FISHER, ER .
CHEMICAL PHYSICS, 1979, 43 (03) :395-401
[4]   SEMICLASSICAL CALCULATIONS OF ROTATIONAL-VIBRATIONAL TRANSITIONS IN HE-H2 [J].
BILLING, GD .
CHEMICAL PHYSICS, 1975, 9 (03) :359-369
[5]   APPLICABILITY OF CLASSICAL TRAJECTORY EQUATIONS IN INELASTIC-SCATTERING THEORY [J].
BILLING, GD .
CHEMICAL PHYSICS LETTERS, 1975, 30 (03) :391-393
[6]   Rotational alignment effects in NO(X) plus Ar inelastic collisions: An experimental study [J].
Brouard, M. ;
Chadwick, H. ;
Eyles, C. J. ;
Hornung, B. ;
Nichols, B. ;
Aoiz, F. J. ;
Jambrina, P. G. ;
Stolte, S. .
JOURNAL OF CHEMICAL PHYSICS, 2013, 138 (10)
[7]   SEMI-CLASSICAL CALCULATION OF VV AND VT RATE COEFFICIENTS IN CO [J].
CACCIATORE, M ;
BILLING, GD .
CHEMICAL PHYSICS, 1981, 58 (03) :395-407
[8]  
Child MS., 1974, Molecular Collision Theory
[9]  
Clausius R., 1857, Annalen der Physik und Chemie, V176, P353