Theory and simulations of light-induced self-assembly in colloids with quantum chemistry derived empirical potentials.

Abstract

Light-induced self-assembly (LISA) is a non-invasive method for tuning material properties. Photoresponsive ligands coated on the surfaces of nanoparticles are often used to achieve LISA. We report simulation studies for a photoresponsive ligand, azobenzene dithiol (ADT), which switches from a <i>trans</i>-to-<i>cis</i> configuration on exposure to ultraviolet light, allowing self-assembly in ADT-coated gold nanoparticles (NPs). This is attributed to a higher dipole moment of <i>cis</i>-ADT over <i>trans</i>-ADT which leads to a dipole-dipole attraction facilitating self-assembly. Singh and Jha [<i>Comput. Theor. Chem.</i>, 2021, <b>1206</b>, 113492] used quantum-chemistry calculations to quantify the interaction energy of a pair of ADT ligands in their <i>cis</i> and <i>trans</i> conformations. The interaction energy between ligands was fit to a potential energy function of the Lennard-Jones (LJ) form having distinct exponents for attractive and repulsive contributions. Using this generalized equation for the ligand-ligand interaction energy, we calculated the total effective interaction energy between a pair of <i>cis</i> as well as <i>trans</i> ADT-coated NPs. Specifically, we calculated the effective interaction energies between <i>cis</i>/<i>trans</i>-NPs using discrete as well as continuous approaches. Given the limitations of experiments in probing individual ligand conformations, we also studied the effect of varying the functional ligand length on the interaction energy between NPs and identified the optimal functional ligand length to capture the steric and conformational effects. Finally, using the effective interaction energy, we obtained a generalized potential energy function, which was applied in Langevin dynamics simulations to capture self-assembly in NPs.