Anharmonic magnetic deformation of self-assembled molecular nanocapsules
O.V. Manyuhina, I.O. Shklyarevskiy, P. Jonkheijm, P.C.M. Christianen,, A. Fasolino, M.I. Katsnelson, A.P.H.J. Schenning, E.W. Meijer, O. Henze,, A.F.M. Kilbinger, W.J. Feast, and J.C. Maan

TL;DR
This study investigates how high magnetic fields deform self-assembled molecular nanocapsules, confirming theoretical predictions at low fields and proposing a new model to explain high-field behavior.
Contribution
The paper experimentally confirms the quadratic scaling of deformation with magnetic field and capsule size, and introduces a modified free energy model for high-field behavior.
Findings
Deformation scales quadratically with magnetic field and capsule radius at low fields.
Bending rigidity of capsules determined as (2.6±0.8)×10^{-21} J.
High-field behavior indicates increased rigidity not explained by Helfrich model.
Abstract
High magnetic fields were used to deform spherical nanocapsules, self-assembled from bola-amphiphilic sexithiophene molecules. At low fields the deformation -- measured through linear birefringence -- scales quadratically with the capsule radius and with the magnetic field strength. These data confirm a long standing theoretical prediction (W. Helfrich, Phys. Lett. {\bf 43A}, 409 (1973)), and permits the determination of the bending rigidity of the capsules as (2.60.8) J. At high fields, an enhanced rigidity is found which cannot be explained within the Helfrich model. We propose a complete form of the free energy functional that accounts for this behaviour, and allows discussion of the formation and stability of nanocapsules in solution.
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