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Journal of Chemical Theory and Computation

Constructive Quantum Interference in Photochemical Reactions

Sumit Suresh Kale, Yong P. Chen, Sabre Kais

Published Nov 17, 2021• 5 citations
Publisher

Abstract

Interferences emerge when multiple pathways coexist together, leading toward the same result. Here, we report a theoretical study for a reaction scheme that leads to constructive quantum interference in a photoassociation (PA) reaction of a 87 Rb Bose–Einstein condensate where the reactant spin state is prepared in a coherent superposition of multiple bare spin states. This is achieved by changing the reactive scattering channel in the PA reaction. As the origin of coherent control comes from the spin part of the wavefunction, we show that it is sufficient to use radio frequency (RF) coupling to achieve the superposition state. We simulate the RF coupling on a quantum processor (IBMQ Lima), and our results show that interferences can be used as a resource for the coherent control of photochemical reactions. The approach is general and can be employed to study a wide spectrum of chemical reactions in the ultracold regime.

DOI
10.1021/acs.jctc.1c00826

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Interferences emerge when multiple pathways coexist together, leading toward the same result. Here, we report a theoretical study for a reaction scheme that leads to constructive quantum interference in a photoassociation (PA) reaction of a 87 Rb Bose–Einstein condensate where the reactant spin state is prepared in a coherent superposition of multiple bare spin states. This is achieved by changing the reactive scattering channel in the PA reaction. As the origin of coherent control comes from the spin part of the wavefunction, we show that it is sufficient to use radio frequency (RF) coupling to achieve the superposition state. We simulate the RF coupling on a quantum processor (IBMQ Lima), and our results show that interferences can be used as a resource for the coherent control of photochemical reactions. The approach is general and can be employed to study a wide spectrum of chemical reactions in the ultracold regime.
Constructive Quantum Interference in a Photo-Chemical Reaction of 87^{87}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 87^{87}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.
Coherent control of reactants remains a long-standing challenge in quantum chemistry. In particular, we have studied laser-induced molecular formation (photoassociation) in a Raman-dressed spin-orbit-coupled ^{87}Rb Bose-Einstein condensate, whose spin quantum state is a superposition of multiple bare spin components. In contrast to the notably different photoassociation-induced fractional atom losses observed for the bare spin components of a statistical mixture, a superposition state with a comparable spin composition displays the same fractional loss on every spin component. We interpret this as the superposition state itself undergoing photoassociation. For superposition states induced by a large Raman coupling and zero Raman detuning, we observe a nearly complete suppression of the photoassociation rate. This suppression is consistent with a model based upon quantum destructive interference between two photoassociation pathways for colliding atoms with different spin combinations. This model also explains the measured dependence of the photoassociation rate on the Raman detuning at a moderate Raman coupling. Our work thus suggests that preparing atoms in quantum superpositions may represent a powerful new technique to coherently control photochemical reactions.
Coherent superpositions and entanglement are hallmarks of quantum mechanics, but they are fragile and can easily be perturbed by their environment. Selected isolated physical systems can maintain coherence and generate entanglement using well-controlled interactions. Chemical reactions, where bonds break and form, are highly dynamic quantum processes. A fundamental question is whether coherence can be preserved in chemical reactions and then harnessed to generate entangled products. Here we investigate this question by studying the 2KRb →\rightarrow→ K2_22​ + Rb2_22​ reaction at 500 nK, focusing on the the nuclear spin degrees of freedom. We prepare the initial nuclear spins in KRb in an entangled state and characterize the preserved coherence in nuclear spin wavefunction after the reaction. The data are consistent with full coherence at the end of the reaction. This suggests that entanglement can be prepared within the reactants, followed by a chemical reaction that produces separate, entangled molecules. We additionally demonstrate control of the reaction product state distribution by deliberately decohering the reactants.
Entanglement is a crucial resource for achieving quantum advantages in quantum computation, quantum sensing, and quantum communication. As shown in this Letter, entanglement is also a valuable resource for the coherent control of the large class of bimolecular chemical reactions. We utilize an entanglement-enhanced coherent control scheme, in which the initial preparation of the superposition state is divided into two steps: the first entangles the reactants, and the second is responsible for coherent control. This approach can overcome the limitations of traditional coherent control of scattering caused by noninterfering pathways, known as satellite terms. By tuning the amount of entanglement between reactants, the visibility of coherent control in chemical reactions can be modulated and optimized. Significantly, there exists an optimal amount of entanglement, which ensures complete indistinguishability of the reaction pathways, maximizing the extent of control. This entanglement-enhanced coherent control scheme is computationally illustrated using the ultracold KRb + KRb reaction, where perfect control over the parity of the product rotational states is achieved.
We show that the photoassociation of an atomic Bose-Einstein condensate to form condensed molecules is a chemical process which not only does not obey the Arrhenius rules for chemical reactions, but that it can also depend on the quantum statistics of the reactants. Comparing the predictions of a truncated Wigner representation for different initial quantum states, we find that, even when the quantum prediction for an initial coherent state is close to the Gross-Pitaevskii prediction, other quantum states may result in very different dynamics.
Abstract Quantum effects in chemical reactions are most pronounced at ultracold temperatures, where only a few partial waves contribute. While interference among many partial waves is theoretically expected to persist at higher temperatures, direct evidence for such quantum effects in reactive processes has been lacking. Here, we report signatures of quantum interference suppressing a chemical reaction in the multi-partial-wave regime: resonant charge exchange between a single 87 Rb + ion and its parent atom 87 Rb. Using quantum-logic detection on a single atom-ion pair and a calibrated in-situ measurement of Langevin collision probabilities, we benchmark the thermally averaged reaction rate against both classical and quantum predictions. We find that the reaction rate is suppressed by over an order of magnitude relative to the classical expectation, despite occurring in the millikelvin temperature regime (more than three orders of magnitude above the s -wave threshold), where more than a dozen partial waves contribute. These results suggest quantum interference as a key mechanism in chemical reactivity beyond the ultracold limit and offer a platform for probing coherent quantum effects in atom-ion reactions where ab initio methods remain intractable.