scholarly journals Direct observation of bimolecular reactions of ultracold KRb molecules

Science ◽  
2019 ◽  
Vol 366 (6469) ◽  
pp. 1111-1115 ◽  
Author(s):  
M.-G. Hu ◽  
Y. Liu ◽  
D. D. Grimes ◽  
Y.-W. Lin ◽  
A. H. Gheorghe ◽  
...  

Femtochemistry techniques have been instrumental in accessing the short time scales necessary to probe transient intermediates in chemical reactions. In this study, we took the contrasting approach of prolonging the lifetime of an intermediate by preparing reactant molecules in their lowest rovibronic quantum state at ultralow temperatures, thereby markedly reducing the number of exit channels accessible upon their mutual collision. Using ionization spectroscopy and velocity-map imaging of a trapped gas of potassium-rubidium (KRb) molecules at a temperature of 500 nanokelvin, we directly observed reactants, intermediates, and products of the reaction 40K87Rb + 40K87Rb → K2Rb2* → K2 + Rb2. Beyond observation of a long-lived, energy-rich intermediate complex, this technique opens the door to further studies of quantum-state–resolved reaction dynamics in the ultracold regime.

2006 ◽  
Vol 125 (2) ◽  
pp. 021101 ◽  
Author(s):  
Alexander M. Zolot ◽  
Warren W. Harper ◽  
Bradford G. Perkins ◽  
Paul J. Dagdigian ◽  
David J. Nesbitt

2020 ◽  
Vol 71 (1) ◽  
pp. 289-313 ◽  
Author(s):  
Bhumika Jayee ◽  
William L. Hase

Nonstatistical dynamics is important for many chemical reactions. The Rice-Ramsperger-Kassel-Marcus (RRKM) theory of unimolecular kinetics assumes a reactant molecule maintains a statistical microcanonical ensemble of vibrational states during its dissociation so that its unimolecular dynamics are time independent. Such dynamics results when the reactant's atomic motion is chaotic or irregular. Intrinsic non-RRKM dynamics occurs when part of the reactant's phase space consists of quasiperiodic/regular motion and a bottleneck exists, so that the unimolecular rate constant is time dependent. Nonrandom excitation of a molecule may result in short-time apparent non-RRKM dynamics. For rotational activation, the 2J + 1 K levels for a particular J may be highly mixed, making K an active degree of freedom, or K may be a good quantum number and an adiabatic degree of freedom. Nonstatistical dynamics is often important for bimolecular reactions and their intermediates and for product-energy partitioning of bimolecular and unimolecular reactions. Post–transition state dynamics is often highly complex and nonstatistical.


2016 ◽  
Vol 45 (13) ◽  
pp. 3576-3594 ◽  
Author(s):  
Helen Chadwick ◽  
Rainer D. Beck

This tutorial review provides an introduction and overview of quantum state resolved reactivity measurements for methane chemisorption on transition metal surfaces.


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