Abstract

The planar boron cluster B13+ provides a model to investigate the microscopic origin of the second law of thermodynamics in a small system. It is a molecular rotor with an inner wheel that rotates in an outer bearing. The cyclic reaction path of B13+ passes along thirty equivalent global minimum structures (GMi, i = 1, 2, ..., 30). The GMs are embedded in a cyclic thirty-well potential. They are separated by thirty equivalent transition states with potential barrier Vb. If the boron rotor B13+ is prepared initially in one of the thirty GMs, with energy below Vb, then it tunnels sequentially to its nearest, next-nearest etc. neighbors (520 fs per step) such that all the other GMs get populated. As a consequence, the entropy of occupying the GMs takes about 6 ps to increases from zero to a value close to the maximum value for equi-distribution. Perfect recurrences are practically not observable.

Highlights

  • The importance of molecular rotors has been recognized by the 2016 Nobel Prize in Chemistry awarded to B

  • We use a molecular model rotor to demonstrate the way from molecular quantum dynamics to explicitly time dependent statistical thermodynamics

  • We discover the relation between the tunneling quantum dynamics of a system with cyclic multi-well potential and the time evolution of the entropy of occupying the wells, from zero to close to the maximum value for equidistribution

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Summary

Introduction

The importance of molecular rotors has been recognized by the 2016 Nobel Prize in Chemistry awarded to B. We discover the relation between the tunneling quantum dynamics of a system with cyclic multi-well potential and the time evolution of the entropy of occupying the wells, from zero to close to the maximum value for equidistribution.

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