Research group · MME
Soft Matter & Self-Assembly Group
Investigating the principles by which soft materials — polymers, colloids, liquid crystals, and biological macromolecules — organize into ordered structures, and exploiting those principles to design materials with programmed function.
Overview
Self-assembly is one of nature's most powerful design strategies: under the right conditions, disordered components spontaneously organize into structures with precisely defined symmetry, geometry, and function. The Soft Matter & Self-Assembly Group works to understand and control this process — both to predict when and why it occurs, and to harness it for the rational design of new materials.
Our research combines experiment and theory. On the experimental side, we synthesize and characterize soft material systems: block copolymers, colloidal suspensions, lyotropic liquid crystals, peptide amphiphiles, and DNA-coated nanoparticles. On the theoretical side, we develop coarse-grained models and free-energy landscapes that capture the essential physics of assembly transitions. We use cryo-TEM and confocal microscopy to image assembled structures in situ, and small-angle X-ray scattering to resolve structural order at sub-nanometer resolution.
Practical applications motivate much of our work. Controlled self-assembly underlies the design of drug-delivery vesicles, anti-fouling surface coatings, structurally colored photonic materials, and responsive hydrogels for sensing and actuation. We maintain active applied collaborations through VIAS Scientific Services and contribute to graduate training across the MME doctoral track.
Research themes
- Block copolymer microphase separation and templating
- Colloidal assembly: entropy-driven, depletion-driven, and DNA-mediated
- Liquid crystal order in biological and synthetic amphiphile systems
- Free-energy calculations and coarse-grained molecular dynamics
- Stimuli-responsive soft materials: pH, temperature, light, ionic strength
- Self-assembly for drug delivery: vesicles, micelles, and hydrogel matrices
- Structural color from colloidal photonic crystals
Current projects
Active · 2023–2026
ProgramAssembly
Encoding structural information in DNA-coated colloids to direct assembly into prescribed three-dimensional architectures. Develops design rules for addressable self-assembly with 12–24 distinct particle species, validated by cryo-TEM and supported by free-energy simulations.
Funded by Veyra Strategic Research Fund · 440,000 cr
Active · 2022–2025
SmartHydrogel
Thermoresponsive hydrogel matrices for controlled drug release. Synthesizes and characterizes poly(N-isopropylacrylamide) copolymers with tunable lower critical solution temperatures, enabling programmable release profiles triggered by body-temperature thresholds.
Funded by VIAS Applied Research Fund · 310,000 cr
Active · 2024–2027
PhotonicSoft
Structural color in colloidal photonic crystals assembled from monodisperse silica and polymer spheres. Explores routes to crack-free large-area films with iridescent, angle-dependent reflectance for decorative and security coating applications.
Funded by VIAS Core Grants Programme · 185,000 cr
Active · 2023–2025
LiquidCrystalBio
Lyotropic liquid crystal phases in concentrated solutions of cellulose nanocrystals and polypeptides. Maps the phase diagram and develops scalable casting methods to produce birefringent optical films with programmable optical axes for polarization optics.
Funded by VIAS MME Division Initiative · 210,000 cr
Selected publications
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Lindqvist, D., Marín-Torres, E., & Okonkwo, S. (2024). Addressable self-assembly of DNA-functionalized colloids into prescribed three-dimensional architectures. Veyra Technical Reports. VEYRA-DOI:10.veyra/2024-smsa-002
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Lindqvist, D. & Habib, R. (2023). Thermoresponsive copolymer hydrogels with tunable LCST for burst-modulated drug release. Veyra Preprint Series. VEYRA-DOI:10.veyra/2023-smsa-007
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Okonkwo, S., Vogt, N., & Lindqvist, D. (2022). Free-energy barriers in colloidal crystal nucleation from suspension: a coarse-grained simulation study. Veyra Technical Reports. VEYRA-DOI:10.veyra/2022-smsa-004
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Marín-Torres, E. & Lindqvist, D. (2021). Structural color in crack-free colloidal films: substrate adhesion and drying-rate effects. Veyra Preprint Series. VEYRA-DOI:10.veyra/2021-smsa-003
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Lindqvist, D., Zeng, H., & Habib, R. (2019). Block copolymer thin-film phase diagrams under confinement: a combined GISAXS and simulation study. Veyra Technical Reports. VEYRA-DOI:10.veyra/2019-smsa-001
People
Led by Prof. Davor Lindqvist. Postdoctoral researchers: Elena Marín-Torres, Rashida Habib, and Sina Vogt. Doctoral students: Samuel Okonkwo, Haoran Zeng, Britta Holm, Valentin Petrescu, Ananya Chakraborty, Osamu Iida, Fiona Lester, Katarzyna Wiśniewska, Mireille Barbé, and Liam Farquhar. Three laboratory technicians maintain synthesis and characterization equipment. Contact smsa@veyra.example regarding open positions or collaboration.