Issue 14, 2012

Phase transition between cubic and monoclinic polymorphs of the tetracyanoethylene crystal: the role of temperature and kinetics

Abstract

Prediction of the relative stabilities and phase transition behavior of molecular crystalline polymorphs is highly coveted as distinct phases can possess different physical and chemical properties while having similar energies. Crystalline tetracyanoethylene (TCNE, C6N4) is known to exhibit rich solid state phase behavior under different thermodynamic conditions, as demonstrated by a wealth of experimental studies on this system. Despite this fact, the role of temperature and kinetics on the phase diagram of TCNE remains poorly understood. Here, first-principles calculations and high-resolution Fourier-transformed infrared (HR-FTIR) spectroscopy experiments are used to study the relative stabilities of the cubic and monoclinic phases of TCNE as a function of temperature. Specifically, density-functional theory with the van der Waals interactions method of Tkatchenko and Scheffler (DFT+vdW) is employed. The accuracy of this approach is demonstrated by the excellent agreement between the calculated and experimental structures. We find that the cubic phase is the most stable polymorph at 0 K, but becomes less favorable than the monoclinic phase at 160 K. This temperature-induced phase transition is explained on the basis of varying close contacts and vibrational entropies as a function of temperature. These findings are supported by a temperature-dependent HR-FTIR linewidth study of the C[triple bond, length as m-dash]N vibrons.

Graphical abstract: Phase transition between cubic and monoclinic polymorphs of the tetracyanoethylene crystal: the role of temperature and kinetics

Supplementary files

Article information

Article type
Paper
Submitted
06 Mar 2012
Accepted
20 Apr 2012
First published
24 May 2012

CrystEngComm, 2012,14, 4656-4663

Phase transition between cubic and monoclinic polymorphs of the tetracyanoethylene crystal: the role of temperature and kinetics

B. Schatschneider, J. Liang, S. Jezowski and A. Tkatchenko, CrystEngComm, 2012, 14, 4656 DOI: 10.1039/C2CE25321F

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