TY - JOUR
T1 - Force-Field Benchmark for Polydimethylsiloxane
T2 - Density, Heat Capacity, Isothermal Compressibility, Viscosity and Thermal Conductivity
AU - Xiang, Zhirui
AU - Gao, Chao
AU - Long, Teng
AU - Ding, Lifeng
AU - Zhou, Tianhang
AU - Wu, Zhenghao
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society.
PY - 2025/2/13
Y1 - 2025/2/13
N2 - Polysiloxanes are versatile polymeric materials with widespread applications in industries ranging from electronics to biomedical devices because of their unique thermal and viscoelastic properties. Accurate molecular simulations of polysiloxanes are essential for understanding their broad applications from a microscopic perspective. However, the accuracy of these simulations is highly dependent on the quality of the force fields used. In this work, we present a comprehensive benchmark and development of force fields tailored for polydimethylsiloxane, which is one of the most widely used polysiloxane materials. Our focus is on their performance in predicting key thermophysical properties including density, heat capacities, isothermal compressibility, and transport properties such as viscosity and thermal conductivity. Experimental measurements are performed in parallel to rigorously validate simulation outcomes. Existing force fields for polydimethylsiloxane, including those derived for organic and inorganic systems, are systematically evaluated against experimental data to identify limitations in accuracy and transferability. Simulation results are compared extensively with experimental observations across a range of temperatures and pressures, revealing the strengths and shortcomings of these commonly utilized force fields for polydimethylsiloxane. Discrepancies between force field predictions and experimental measurements are analyzed in detail for thermodynamic and transport properties of polydimethylsiloxane. This benchmark study serves as a critical assessment of current force fields for polydimethylsiloxane and offers guidelines for their further development, enabling more reliable simulations of polysiloxane-based materials for various industrial applications. (Figure presented.)
AB - Polysiloxanes are versatile polymeric materials with widespread applications in industries ranging from electronics to biomedical devices because of their unique thermal and viscoelastic properties. Accurate molecular simulations of polysiloxanes are essential for understanding their broad applications from a microscopic perspective. However, the accuracy of these simulations is highly dependent on the quality of the force fields used. In this work, we present a comprehensive benchmark and development of force fields tailored for polydimethylsiloxane, which is one of the most widely used polysiloxane materials. Our focus is on their performance in predicting key thermophysical properties including density, heat capacities, isothermal compressibility, and transport properties such as viscosity and thermal conductivity. Experimental measurements are performed in parallel to rigorously validate simulation outcomes. Existing force fields for polydimethylsiloxane, including those derived for organic and inorganic systems, are systematically evaluated against experimental data to identify limitations in accuracy and transferability. Simulation results are compared extensively with experimental observations across a range of temperatures and pressures, revealing the strengths and shortcomings of these commonly utilized force fields for polydimethylsiloxane. Discrepancies between force field predictions and experimental measurements are analyzed in detail for thermodynamic and transport properties of polydimethylsiloxane. This benchmark study serves as a critical assessment of current force fields for polydimethylsiloxane and offers guidelines for their further development, enabling more reliable simulations of polysiloxane-based materials for various industrial applications. (Figure presented.)
UR - http://www.scopus.com/inward/record.url?scp=85216894139&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcb.4c08471
DO - 10.1021/acs.jpcb.4c08471
M3 - Article
C2 - 39895120
AN - SCOPUS:85216894139
SN - 1520-6106
VL - 129
SP - 1864
EP - 1873
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 6
ER -