Interference much like that observed in two-slit experiments can be seen in the outcomes of chemical processes in which multiple reaction mechanisms lead to the same final state.
This paper explores the concept of reaction pathway interference, extending the principles observed in quantum mechanics to the realm of chemical reactions. While quantum mechanical systems exhibit interference due to superposition and multiple pathways, this work posits that even in the absence of quantum coherence between reaction pathways, statistical interactions between them can lead to observable macroscopic "path interference." This phenomenon, termed Reaction Pathway Interference, offers a novel framework for understanding and describing complex reaction networks, particularly those involving multiple steps and competing pathways. The theoretical framework presented here focuses on the statistical relationships and correlations between reaction rates, proposing that these can generate interference patterns analogous to those observed in wave phenomena. The core idea involves quantifying the degree of overlap in the rate distributions of competing pathways and demonstrating how this overlap can lead to deviations from expected statistical behavior. This work lays the groundwork for a more nuanced understanding of reaction dynamics and provides a potential explanation for observed complexities in chemical systems.
Laser light has been used as a probe of atoms, molecules, and solids since the invention of the laser. The use of laser light in a more active role, to modify and process surfaces, and initiate chemical reactions, followed shortly thereafter. But usually it is the intensity and the directionality of the laser light that is employed, not necessarily its coherence, and not particularly the fact that it has a well-defined phase. 'Coherence control' can be broadly understood as the set of processes whereby light modifies matter in a way that is critically dependent on the incident light beams possessing well-defined phases. While in a laser matter is manipulated to produce light of the desired properties, in coherent control light is manipulated -- in particular, its phase and intensity is adjusted -- to produce a material response of the desired type. Of the various coherent control processes that are currently being investigated, some involve a transition in the material medium from an initial state to a final state by two or more possible processes. With each of these is associated a quantum mechanical amplitude, and hence the probability for the transition can show interference effects between the two amplitudes, just as in the familiar two-slit interference experiment the probability for the electron to be observed at a given position involves a probability that is the square of the sum of two amplitudes. In quantum interference control (QUIC), the relative phase of the two amplitudes is adjusted by adjusting the relative phase of two polarizations of a single beam, or the relative phase of two beams at different frequencies. It is this particular type of coherent control that is of interest in this communication.
Constructive Quantum Interference in a Photo-Chemical Reaction of 87Rb Bose Einstein Condensate
Interferences emerge when multiple pathways coexist together leading towards the same result. A Recent study by Blasing and coworkers [PRL 121(7):073202] showed that in a photo-association reaction of Raman dressed spin orbit coupled 87Rb Bose Einstein Condensate when the reactant spin state is prepared in a coherent superposition of multiple bare spin states it leads to a destructive interference between reaction pathways. Here we report a theoretical study for a reaction scheme which leads to constructive quantum interference. This is achieved by changing the reactive scattering channel in the reaction. As the origin of coherent control comes from the spin part of the wavefunction it is sufficient to use radio frequency coupling to achieve the superposition state. Our results show that interferences can be used as a resource for the coherent control of photo-chemical reactions. The approach is general and can be employed to study a wide spectra of chemical reactions in the ultracold regime.