Three-point functions in ABJM and Bethe Ansatz

We develop an integrability-based framework to compute structure constants of two sub-determinant operators and a single-trace non-BPS operator in ABJM theory in the planar limit. In this first paper, we study them at weak coupling using a relation to an integrable spin chain. We first develop a nested Bethe ansatz for an alternating SU(4) spin chain that describes single-trace operators made out of scalar fields. We then apply it to the computation of the structure constants and show that they are given by overlaps between a Bethe eigenstate and a matrix product state. We conjecture that the determinant operator corresponds to an integrable matrix product state and present a closed-form expression for the overlap, which resembles the so-called Gaudin determinant. We also provide evidence for the integrability of general sub-determinant operators. The techniques developed in this paper can be applied to other quantities in ABJM theory including three-point functions of single-trace operators.

Energy transport in Z3 chiral clock model

We characterize the energy transport in a one dimensional Z3 chiral clock model. The model generalizes the Z2 symmetric transverse field Ising model (TFIM). The model is parametrized by a chirality parameter Θ, in addition to f and J which are analogous to the transverse field and the nearest neighbour spin coupling in the TFIM. Unlike the well studied TFIM and XYZ models, does not transform to a fermionic system. We use a matrix product states implementation of the Lindblad master equation to obtain the non-equilibrium steady state (NESS) in systems of sizes up to 48. We present the estimated NESS current and its scaling exponent γ as a function of Θ at different f/J. The estimated γ(f/J,Θ) point to a ballistic energy transport along a line of integrable points f=Jcos{3Θ} in the parameter space; all other points deviate from ballistic transport. Analysis of finite size effects within the available system sizes suggest a diffusive behavior away from the integrable points.

Ultrafast carrier dynamics at organic donor-acceptor interfaces - A quantum-based assessment of the hopping model

We investigate the charge transfer dynamics of photogenerated excitons at the donor-acceptor interface of an organic solar cell blend under the influence of molecular vibrations. This is examined using an effective Hamiltonian, parametrized by density functional theory calculations, to describe the full quantum behaviour of the relevant molecular orbitals, which are electronically coupled with each other and coupled to over one hundred vibrations (via Holstein coupling). This electron-phonon system is treated in a numerically quasi-exact fashion using the matrix-product-state ansatz. We provide insight into different mechanisms of charge separation and their relation to the electronic driving energy for the separation process. We find ultrafast electron transfer, which for small driving energy is dominated by kinetic processes and at larger driving energies by dissipative phonon emission connected to the prevalent vibration modes. Using this fully quantum mechanical model we perform a benchmark comparison to a recently developed semi-classical hopping approach, which treats the hopping and vibration time scales consistently. We find qualitatively and quantitatively good agreement between the results of the sophisticated matrix-product-state based quantum dynamics and the simple and fast time-consistent-hopping approach.