Certification of qubits in the prepare-and-measure scenario with large input alphabet and connections with the Grothendieck constant.

We address the problem of testing the quantumness of two-dimensional systems in the prepare-and-measure (PM) scenario, using a large number of preparations and a large number of measurement settings, with binary outcome measurements. In this scenario, we introduce constants, which we relate to the Grothendieck constant of order 3. We associate them with the white noise resistance of the prepared qubits and to the critical detection efficiency of the measurements performed. Large-scale numerical tools are used to bound the constants. This allows us to obtain new bounds on the minimum detection efficiency that a setup with 70 preparations and 70 measurement settings can tolerate.

Reciprocity in the degeneracies of some tetra-atomic molecular ions.

Various ab initio computations, as, e.g., in G. J. Halász and Á. Vibók, Int. J. Quantum Chem. 111, 342 (2011), have shown that in molecules of the type (HCCH)(+), when the extremal H atoms are distorted from a linear form but maintain a planar geometry, a pair of conical intersections (ci) occur at such positions that the ratios of the distortional coordinates of the two atoms are in the two ci's reciprocals of each other. These computations have here been extended to locate the ci's also for HCNH. The two groups of results are explained by simple analytic perturbational expressions for the energy differences of the lowest adjacent electronic states, with inclusion of excited state effects.

Theoretical study of the reaction of H atoms with vibrationally highly excited HF molecules.

Vibrationally highly excited molecules react extremely fast with atoms and probably with radicals. The phenomenon can be utilized for selectively enhancing the rate of reactions of specific bonds. On the basis of quasiclassical trajectory calculations, the paper analyzes mechanistic details of a prototype reaction, H + HF(v). At vibrational quantum numbers v above 2, the reaction exhibits capture-type behavior, that is, the reactive cross section diverges as the relative translational energy of the partners decreases, both for the abstraction and for the exchange channel. The mechanism of the reaction for both channels is different at low and at high translational energy. At low vibrational energy, the reaction is activated, which is switched to capture-type at high excitation. The reason is an attractive potential that acts on the attacking H atom when the HF molecule is stretched. In contrast to the 6-SEC potential surface of Mielke et al., the switch cannot be observed on the Stark-Werner potential surface, due to a small artificial barrier at high H-HF separation, preventing the reactants from obeying the attractive potential and also proving the importance of the latter. The exchange reaction can be observed even when the total energy available for the partners is below the exchange barrier, because at low translational energies the product F atom of a successful abstraction step can re-abstract that H atom from the intermediate product H2 molecule that was originally the attacker.

Dynamics of bimolecular reactions of vibrationally highly excited molecules: quasiclassical trajectory studies.

Excitation functions from quasiclassical trajectory calculations on the H + H2O --> OH + H2, H + HF --> F + H2, and H + H'F --> H' + HF reactions indicate a different behavior at low and high vibrational excitation of the breaking bond. When the reactant tri- or diatomic molecule is in vibrational ground state or in a low vibrationally excited state, all these reactions are activated; i.e., there is a nonzero threshold energy below which there is no reaction. In contrast, at high-stretch excited-states capture-type behavior is observed; i.e., with decreasing translational energy the reactive cross-section diverges. The latter induces extreme vibrational enhancement of the thermal rate consistent with the experiments. The results indicate that the speed-up observed at high vibrational excitation is beyond the applicability of Polanyi's rules in their common form; instead, it can be interpreted in terms of an attractive potential acting on the attacking H atom when it approaches the reactant with a stretched X-H bond.