The stationary point used by Sherrington and Kirkpatrick in their evaluation of the free energy of a spin glass by the method of steepest descent is examined carefully. It is found that, although this point is a maximum of the integrand at high temperatures, it is not a maximum in the spin glass phase nor in the ferromagnetic phase at low temperatures. The instability persists in the presence of a magnetic field. Results are given for the limit of stability both for a partly ferromagnetic interaction in the absence of an external field and for a purely random interaction in the presence of a field.

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We demonstrate that the coupling of excitonic and vibrational motion in biological complexes can provide mechanisms to explain the long-lived oscillations that have been obtained in non linear spectroscopic signals of different photosynthetic pigment protein complexes and we discuss the contributions of excitonic versus purely vibrational components to these oscillatory features. Considering a dimer model coupled to a structured spectral density we exemplify the fundamental aspects of the electron-phonon dynamics, and by analyzing separately the different contributions to the non linear signal, we show that for realistic parameter regimes purely electronic coherence is of the same order as purely vibrational coherence in the electronic ground state. Moreover, we demonstrate how the latter relies upon the excitonic interaction to manifest. These results link recently proposed microscopic, non-equilibrium mechanisms to support long lived coherence at ambient temperatures with actual experimental observations of oscillatory behaviour using 2D photon echo techniques to corroborate the fundamental importance of the interplay of electronic and vibrational degrees of freedom in the dynamics of light harvesting aggregates.

We exploit the geometry of a zig-zag cold-ion crystal in a linear trap to propose the quantum simulation of a paradigmatic model of long-ranged magnetic frustration. Such a quantum simulation would clarify the complex features of a rich phase diagram that presents ferromagnetic, dimerized antiferromagnetic, paramagnetic, and floating phases, together with previously unnoticed features that are hard to assess by numerics. We analyze in detail its experimental feasibility, and provide supporting numerical evidence on the basis of realistic parameters in current ion-trap technology.Comment: replaced with published versio

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