Understanding the fate of an electronically excited molecule constitutes an important task for theoretical chemistry, and practical implications range from the interpretation of atto- and femtosecond spectroscopy to the development of light-driven molecular machines, the control of photochemical reactions, and the possibility of capturing sunlight energy. However, many challenging conceptual an...

Multiple vibrational mode coupling that induces the missing mode effect and Duschinsky rotation on the potential energy surface of the S(1) state in the Cy3 molecule was clarified by real-time ultrafast spectroscopy with a few-cycle laser pulse. The contributions of homogeneous and inhomogeneous dephasing to the total dephasing time were found to be 55% and 45%, respectively.

Experiments on gels have provided contradictory results concerning the relation between correlation and response functions during aging. To clarify this puzzle, we numerically investigate the fluctuation-dissipation plot in equilibrium polymers and in network forming gels employing two distinct observables, (i) the density Fourier transform and (ii) the single-particle potential energy, to prob...

We present an exact decomposition of the complete wave function for a system of nuclei and electrons evolving in a time-dependent external potential. We derive formally exact equations for the nuclear and electronic wave functions that lead to rigorous definitions of a time-dependent potential energy surface (TDPES) and a time-dependent geometric phase. For the H(2)(+) molecular ion exposed to ...

In an attempt to extend the range of model jamming transitions, we simulate systems of athermal particles which attract when slightly overlapping. Following from recent work on purely repulsive systems, dynamics are neglected and relaxation performed via a potential energy minimisation algorithm. Our central finding is of a transition to a low-density tensile solid which is sharp in the limit o...

The potential energy surface (PES) of the [C, N, F, S] system was investigated by quantum chemical and experimental methods. Seven minima were located on the ground state PES by density functional and ab initio electronic structure calculations. Four of these isomers, FSCN, FSNC, FCNS and FNCS, have an acyclic structure, while the other three, FC(NS), FS(CN) and FN(SC), form a three-membered fl...

The three adiabatic potential surfaces of the Cl(2P)-HF complex that correlate with the 2P ground state of the Cl atom were calculated with the ab initio RCCSD(T) method (partially spin-restricted coupled cluster theory including single and double excitations and perturbative correction for the triples). With the aid of a geometry-dependent diabatic mixing angle, calculated by the complete acti...

Instantaneous (laser-field-dependent) potential energy curves leading to neutral fragmentations of methane were calculated at several laser intensities from 1.4 × 10(13) to 1.2 × 10(14) W/cm(2) (from 1.0 × 10(10) to 3.0 × 10(10) V/m) using ab initio molecular orbital (MO) methods to validate the observation of neutral fragmentations induced by intense femtosecond IR pulses (Kong et al. J. Chem....

A method is presented that can find the global minimum of very complex condensed matter systems. It is based on the simple principle of exploring the configurational space as fast as possible and of avoiding revisiting known parts of this space. Even though it is not a genetic algorithm, it is not based on thermodynamics. The efficiency of the method depends strongly on the type of moves that a...

Quasi-classical trajectories have been integrated to study the vibrational relaxation of the O + NO(v) process as a function of the initial vibrational quantum number for T = 298 K, 1500 K, and 3000 K. Two reliable potential energy surfaces have been employed for the A' and A'' doublet states of NO2. The calculated vibrational relaxation rate constants show a nearly v-independent behavior at ro...