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arXiv:1108.4304 · Physical Review A

Quantum limits for the magnetic sensitivity of a chemical compass

Jianming Cai, Filippo Caruso, Martin Bodo Plenio

Published Apr 11, 2012• 64 citations
arXivHTMLPDF

Abstract

The chemical compass model, based on radical pair reactions, is an idea to explain avian magnetoreception. At present, to the best of our knowledge, questions concerning the key ingredients responsible for the high sensitivity of a chemical compass and the possible role of quantum coherence and decoherence remain unsolved. Here, we investigate the optimized hyperfine coupling for a chemical compass in order to achieve the best magnetic field sensitivity. We show that its magnetic sensitivity limit can be further extended by simple quantum control and may benefit from additional decoherence. With this, we clearly demonstrate how quantum coherence can be exploited in the functioning of a chemical compass. The present results also provide routes toward the design of a biomimetic weak magnetic field sensor.

DOI
10.1103/physreva.85.040304

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The chemical compass model, based on radical pair reactions, is an idea to explain avian magnetoreception. At present, to the best of our knowledge, questions concerning the key ingredients responsible for the high sensitivity of a chemical compass and the possible role of quantum coherence and decoherence remain unsolved. Here, we investigate the optimized hyperfine coupling for a chemical compass in order to achieve the best magnetic field sensitivity. We show that its magnetic sensitivity limit can be further extended by simple quantum control and may benefit from additional decoherence. With this, we clearly demonstrate how quantum coherence can be exploited in the functioning of a chemical compass. The present results also provide routes toward the design of a biomimetic weak magnetic field sensor.
It is known that more than 50 species use the Earth's magnetic field for orientation and navigation. Intensive studies, particularly behavior experiments with birds, provide support for a chemical compass based on magnetically sensitive free radical reactions as a source of this sense. However, the fundamental question of how quantum coherence plays an essential role in such a chemical compass model of avian magnetoreception yet remains controversial. Here, we show that the essence of the chemical compass model can be understood in analogy to a quantum interferometer exploiting global quantum coherence rather than any subsystem coherence. Within the framework of quantum metrology, we quantify global quantum coherence and correlate it with the function of chemical magnetoreception. Our results allow us to understand and predict how various factors can affect the performance of a chemical compass from the unique perspective of quantum coherence assisted metrology. This represents a crucial step to affirm a direct connection between quantum coherence and the function of a chemical compass.
The radical pair mechanism is one of the two main hypotheses to explain the navigability of animals in weak magnetic fields, enabling e.g. birds to see the Earth's magnetic field. It also plays an essential role in the field of spin chemistry. Here, we show how quantum control can be used to either enhance or reduce the performance of such a chemical compass, providing a new route to further study the radical pair mechanism and its applications. We study the role of quantum entanglement in this mechanism, and demonstrate intriguing connections between radical-pair entanglement and the magnetic field sensitivity of the compass. Beyond their immediate application to the radical pair mechanism, these results also demonstrate how state-of-the-art quantum technologies could potentially be used to probe and control biological functions.
The radical-pair mechanism is one of the two main hypotheses to explain the navigability of animals in weak magnetic fields, enabling, e.g., birds to see Earth's magnetic field. It also plays an essential role in spin chemistry. Here, we show how quantum control can be used to either enhance or reduce the performance of such a chemical compass, providing a new route to further study the radical-pair mechanism and its applications. We study the role of radical-pair entanglement in this mechanism, and demonstrate its intriguing connections with the magnetic-field sensitivity of the compass. Beyond their immediate application to the radical-pair mechanism, these results also demonstrate how state-of-the-art quantum technologies could potentially be used to probe and control biological functions.
A radical-pair-based chemical reaction might be used by birds for navigation via the geomagnetic direction. The inherent physical mechanism is that the quantum coherent transition from a singlet state to triplet states of the radical pair could respond to a weak magnetic field and be sensitive to the direction of such a field; this then results in different photopigments to be sensed by the avian eyes. Here, we propose a quantum bionic setup, inspired by the avian compass, as an ultrasensitive probe of a weak magnetic field based on the quantum phase transition of the environments of the two electrons in the radical pair. We prove that the yield of the chemical products via recombination from the singlet state is determined by the Loschmidt echo of the environments with interacting nuclear spins. Thus quantum criticality of environments could enhance the sensitivity of detection of weak magnetic fields.
Chemical reactions involving radical-ion pairs are ubiquitous in biology, since not only are they at the basis of the photosynthetic reaction chain, but are also assumed to underlie the biochemical magnetic compass used by avian species for navigation. Recent experiments with magnetic-sensitive radical-ion-pair reactions provided strong evidence for the radical-ion-pair magnetoreception mechanism, verifying the expected magnetic sensitivities and chemical product yield changes. It is here shown that the theoretical description of radical-ion-pair reactions used since the 70s cannot explain the observed data, because it is based on phenomenological equations masking quantum coherence effects. The fundamental density-matrix equation derived here from basic quantum measurement theory considerations naturally incorporates the quantum Zeno effect and readily explains recent experimental observations on low- and high magnetic-field radical-ion-pair reactions.
Radical-ion pairs and their reactions have triggered the study of quantum effects in biological systems. This is because they exhibit a number of effects best understood within quantum information science, and at the same time are central in understanding the avian magnetic compass and the spin transport dynamics in photosynthetic reaction centers. Here we address radical-pair reactions from the perspective of quantum metrology. Since the coherent spin motion of radical pairs is effected by an external magnetic field, these spin-dependent reactions essentially realize a biochemical magnetometer. Using the quantum Fisher information, we find the fundamental quantum limits to the magnetic sensitivity of radical-pair magnetometers, arriving at a sensitivity $\ensuremath{\delta}B=2\phantom{\rule{0.16em}{0ex}}\mathrm{pT}/\ensuremath{\tau}[1\phantom{\rule{0.16em}{0ex}}\ensuremath{\mu}\text{s}]\sqrt{{\ensuremath{\nu}}_{0}[{10}^{12}]}$, given in terms of radical-pair lifetime $\ensuremath{\tau}$ and number of radical pairs ${\ensuremath{\nu}}_{0}$. We then explore how well the usual measurement scheme considered in radical-pair reactions, the measurement of reaction yields, approaches the fundamental limits. In doing so, we find the optimal hyperfine interaction Hamiltonian that leads to the best magnetic sensitivity as obtained from reaction yields. This is still an order of magnitude smaller than the absolute quantum limit. Finally, we demonstrate that with a realistic quantum reaction control reminding one of Ramsey interferometry, here presented as a quantum circuit involving the spin-exchange interaction and a recently proposed molecular switch, we can approach the fundamental quantum limit within a factor of 2. This work opens the application of well-advanced quantum metrology methods to biological systems.