I. K. Kominis

Quantum measurement corrections to CIDNP in photosynthetic reaction centers

Chemically induced dynamic nuclear polarization is a signature of spin order appearing in many photosynthetic reaction centers. Such polarization, significantly enhanced above thermal equilibrium, is known to result from the nuclear spin sorting inherent in the radical pair mechanism underlying long-lived charge-separated states in photosynthetic reaction centers. We will show here that the recently understood fundamental quantum dynamics of radical-ion-pair reactions open up a new and completely unexpected pathway toward obtaining chemically induced dynamic nuclear polarization signals. The fundamental decoherence mechanism inherent in the recombination process of radical pairs is shown to produce nuclear spin polarizations of the order of 104 times (or more) higher than the thermal equilibrium value at the Earths magnetic field relevant to natural photosynthesis. This opens up the possibility of a fundamentally new exploration of the biological significance of high nuclear polarizations in photosynthesis.

Coherent triplet excitation suppresses the heading error of the avian compass

Radical-ion pair reactions are currently understood to underlie the biochemical magnetic compass of migratory birds. It was recently shown that radical-ion pair reactions form a rich playground for the application of quantum-information-science concepts and effects. We will show here that the intricate interplay between the quantum Zeno effect and the coherent excitation of radical-ion pairs leads to an exquisite angular sensitivity of the reaction yields. This results in a significant and previously unanticipated suppression of the avian compass heading error, opening the way to quantum engineering precision biological sensors.

Sub-shot-noise magnetometry with a correlated spin-relaxation dominated alkali-metal vapor.

Spin noise sets fundamental limits to the precision of measurements using spin-polarized atomic vapors, such as performed with sensitive atomic magnetometers. Spin squeezing offers the possibility to extend the measurement precision beyond the standard quantum limit of uncorrelated atoms. Contrary to current understanding, we show that, even in the presence of spin relaxation, spin squeezing can lead to a significant reduction of spin noise, and hence an increase in magnetometric sensitivity, for a long measurement time. This is the case when correlated spin relaxation due to binary alkali-atom collisions dominates independently acting decoherence processes, a situation realized in thermal high atom-density magnetometers and clocks.

Comment on ‘Spin-selective reactions of radical pairs act as quantum measurements’ (Chemical Physics Letters 488 (2010) 90–93)

Abstract It is shown that the master equation introduced by Jones and Hore and purported to describe radical–ion pair reactions is not self-consistent.

Magnetic sensitivity and entanglement dynamics of the chemical compass

Abstract We present the quantum limits to the magnetic sensitivity of a new kind of magnetometer based on biochemical reactions. Radical-ion-pair reactions, the biochemical system underlying the chemical compass, are shown to offer a new and unique physical realization of a magnetic field sensor competitive to modern atomic or condensed matter magnetometers. We elaborate on the quantum coherence and entanglement dynamics of this sensor, showing that they provide the physical basis for testing our understanding of the fundamental quantum dynamics of radical-ion-pair reactions.

Photon statistics as an experimental test discriminating between theories of spin-selective radical–ion-pair reactions

Abstract Radical–ion-pair reactions were recently shown to represent a rich biophysical laboratory for the application of quantum measurement theory methods and concepts. We here propose a concrete experimental test that can clearly discriminate among the fundamental master equations currently attempting to describe the quantum dynamics of these reactions. The proposed measurement based on photon statistics of fluorescing radical pairs is shown to be molecular-model-independent and capable of elucidating the singlet–triplet decoherence inherent in the radical–ion-pair recombination process.

The radical-pair mechanism as a paradigm for the emerging science of quantum biology

The radical-pair mechanism was introduced in the 1960s to explain anomalously large EPR and NMR signals in chemical reactions of organic molecules. It has evolved to the cornerstone of spin chemistry, the study of the effect electron and nuclear spins have on chemical reactions, with the avian magnetic compass mechanism and the photosynthetic reaction center dynamics being prominent biophysical manifestations of such effects. In recent years the radical-pair mechanism was shown to be an ideal biological system where the conceptual tools of quantum information science can be fruitfully applied. We will here review recent work making the case that the radical-pair mechanism is indeed a major driving force of the emerging field of quantum biology.

Collision kernels from velocity-selective optical pumping with magnetic depolarization

Weexperimentallydemonstratehowmagneticdepolarizationofvelocity-selectiveopticalpumpingcanbeused to single out the collisional cusp kernel best describing spin- and velocity-relaxing collisions between potassium atoms and low-pressure helium. The range of pressures and transverse fields used simulate the optical pumping regime pertinent to sodium guidestars employed in adaptive optics. We measure the precession of spin-velocity modes under the application of transverse magnetic fields, simulating the natural configuration of mesospheric sodium optical pumping in the geomagnetic field. We also provide a full theoretical account of the experimental data using the recently developed cusp kernels, which realistically quantify velocity damping collisions in this optical pumping regime. A single cusp kernel with a sharpness s = 13 ± 2 provides a global fit to the K-He data.

Quantum Zeno effect in atomic spin-exchange collisions

The suppression of spin-exchange relaxation in dense alkali-metal vapors discovered in 1973 and governing modern atomic magnetometers is here reformulated in terms of quantum measurement theory and the quantum Zeno effect. This provides a new perspective of understanding decoherence in spin-polarized atomic vapors.