Liquid Crystal Formation Research Articles

Liquid crystal droplets formation and stabilization during phase transition process

Abstract The study of phase transition processes in liquid crystals (LCs) remains challenging. Most thermotropic LCs exhibit a narrow temperature range and a rapid phase transition from the isotropic (ISO) to the nematic (N) phase, which make it difficult to capture and manipulate the phase transition process. In this study, we observed the evolution of small droplets during the ISO-N phase transition in ferroelectric nematic (NF) LC RM734. After doping with metal nanoparticles (NPs), the temperature range of the phase transition broadened, and the droplets formed during the phase transition remained stable, with their diameter increasing linearly with temperature. In addition, droplets doped with NPs can be well controlled by an external electric field. This discovery not only aids in understanding the fundamental mechanisms of LC phase transitions but also provides a simple alternative method for preparing droplets, which is potentially valuable for applications in optoelectronic devices and sensors.

Formation of Layered Liquid Crystal by Cooperation of Sidechain Array and Rigid Polyacetylene Mainchain

ABSTRACT An acetylene derivative monomer with a pyrimidine – type sidechain with three rings was synthesized by Steglich esterification. Polymerization of the acetylene derivative was then carried out with a rhodium complex. The acetylene monomer and mono-substituted polyacetylene derivative showed liquid crystals (LCs) because their tricyclic parts worked as a mesogenic core. The monomer as an acetylene derivative showed smectic with a tilted structure in the LC aggregation form. The mono-substituted polyacetylene bearing mesogen via short alkyl spacer showed lyotropic and thermotropic LCs of the smectic phase, although generally flexible long alkyl spacer from the main chain connected to sidechain mesogen is required for exhibiting liquid crystal in sidechain type polymer liquid crystals. In the present study, rigid mainchain aligns the sidechain mesogen array to form non-tilted LC. Properties of LCs were evaluated by various analytical techniques, including polarizing optical microscopy. Structural properties were evaluated by nuclear magnetic resonance spectroscopy, gel permeation chromatography, infrared spectroscopy, and ultraviolet – visible absorption spectroscopy.

Efficient preparation of cellulose nanocrystals and regulation of cholesteric liquid crystals for advanced anti‐counterfeiting

AbstractCellulose nanocrystals (CNCs) can self‐assemble to form cholesteric liquid crystal, which make it one of the most promising optical materials at present. CNCs can be produced by sulfuric acid hydrolysis. It is found that hydrolysis conditions influence the existing form of reaction components and their reaction activities, which leads to different reaction routes and mechanisms under varied reaction conditions, with CNCs of varied quality produced. High‐quality CNC with more uniform particle size could be prepared at a critical acid concentration of 64 wt%, which was used to study the formation process of CNC liquid crystal and the structure regulation of cholesteric liquid crystal. By adjusting the drying temperature and adding a small molecule of water‐soluble chitosan (WSC) can well regulate cholesteric liquid crystal and change the pitch of a film, and the reflection wavelength can be redshifted, thus enriching texture patterns and creating distinctive color. Suitable addition of WSC can enhance the multi‐domain effect during liquid crystal formation process and finally creates more colorful film with fine texture. The rich and tunable liquid crystal characteristics endowed by WSC addition is irreplicable and artistic, which helps to realize the great potential application of the composite film in advanced anti‐counterfeiting.

Self-Assembly of Discrete Multi-Chromophoric Systems.

Self-assembly of chromophoric systems is a prerequisite to create well-ordered, processable nanomaterials with multiple functionalities. In the past two decades, the field of functional organic materials has primarily focused on systems featuring only one type of dye/π-conjugated unit. Consequently, many reports with mechanistic insights on the self-assembly of the dyes featuring different molecular packing have been reported. Subsequently, we have witnessed several attempts to organize the multi-chromophoric systems in solution and solid-state via different approaches using self-assembly as a tool. Incorporation of more than one dye is important in creating materials with tuneable optoelectronic properties. Consequently, self-assembly of more than one chromophoric systems have been investigated to some extent. This review aims to discuss the self-assembled materials derived from discrete π-conjugated systems comprising more than one dye units connected through covalent bonding (multi-chromophoric systems). Molecular design of various multi-chromophoric systems leading to the formation of crystals, liquid crystals and supramolecular polymers have been correlated with corresponding properties. We envisage that classification of self-assembled multi-chromophoric systems, with a note on tuneable optoelectronic properties, can provide a deeper understanding on the molecular design strategies, which is important in the fabrication of functional organic materials with optimum performances.

Harnessing liquid crystal attributes of near-unit photoluminescent benzothioxanthene photosensitizers: Photophysical profiling in solution, solid state, and polymer matrix embedding

Liquid crystals (LCs) have garnered significant attention for their unique optical and electrical properties, making them promising candidates in various technological applications such as smart displays, sensors, telecommunications, biomedicals or wearable electronics. In this study, we explore the potential of several highly emissive benzothioxanthene imide (BTI) derivatives as LC materials with a focus on their robustness and temperature-stable emission behavior. By tailoring the molecular structure of BTIs, we have accomplished exceptional emissive properties while maintaining the inherent advantages of LCs, such as their self-organizing ability and responsive nature. We describe the formation of enantiotropic liquid crystals whose mesomorphic properties dependent on the nature, length, and position of the side chain. Moreover, we have investigated the thermal stability of their emission spectra over a wide range of temperature, highlighting their potential use in demanding conditions where precise optical performances are critical. Our findings underscore the importance of molecular design in achieving highly emissive LC materials with enhanced robustness and temperature stability, opening new avenues for the use of BTI derivatives.

Time Dependence of Gel Formation in Lyotropic Nematic Liquid Crystals: From Hours to Weeks.

The combination of lyotropic liquid crystals (LLCs) and low-molecular-weight gelators (LMWGs) for the formation of lyotropic liquid crystal gels (LLC gels) leads to a versatile and complex material combining properties of both parent systems. We gelled the calamitic nematic NC phases of a binary and ternary system using the LMWG 3,5-bis-(5-hexylcarbamoyl-pentoxy)-benzoic acid hexyl ester (BHPB-6). This binary system consists of the surfactant N,N-dimethyl-N-ethyl-1-hexadecylammonium bromide (CDEAB) and water, whereas the ternary system consists of the surfactant N,N,N-trimethyl-N-tetradecylammonium bromide (C14TAB), the cosurfactant n-decanol, and water. Though containing similar surfactants, the gelled NC phases of the binary and ternary systems show differences in their visual and gel properties. The gelled NC phase of the binary system remains clear for several days after preparation, whereas the gelled NC phase of the ternary system turns turbid within 24 h. We investigated the time evolution of the gel strength with oscillation rheology measurements (a) within the first 24 h and (b) up to two weeks after gel formation. The shape of the fibers was investigated over different time scales with freeze fracture electron microscopy (FFEM). We demonstrate that despite their similarities, the two LLC gels also have distinct differences.

Stable graphene oxide-based lyotropic liquid crystals for interfacial lubrication

Lyotropic liquid crystals have lubricating properties due to their ordered assembly and fluidity, whose mesogens are often characterized by amphiphilic properties. Despite the attention that graphene oxide (GO) has been studied as a novel amphiphilic lyotropic mesogen this decade, and GO applied as a lubrication additive has been demonstrated in both oil and water-based systems, little research reveals the interfacial lubrication of GO liquid crystals yet. This work reports that GO aqueous dispersion can form lyotropic liquid crystals above a specific critical concentration of 5.00 mg/mL, providing a form of stable water-based lubricant, which can keep stable for several months and can reduce friction by 37.3% and wear by 25.24%. The liquid crystal phase was verified by polarizing microscope and synchrotron radiation small-angle X-ray scattering, and its rheological properties and viscoelasticity were studied by interfacial rheometer. The formation of lyotropic liquid crystals can enhance the stability of GO aqueous dispersions at high density, simultaneously ensuring friction decrease and anti-wear effect. It is attributed to the stable nematic network by the ordered GO sheets. The ordered assembly structure bears vertical shear force, therefore, reducing the wear. It is also assumed that the wide lateral size of graphene oxide promotes the nematic phase thus smoothes the graphene oxide film composed spontaneously under the coincidence of lamellar liquid crystal and 2D layered material. Through this work, the interlayer lubrication of GO was optimized, and the problem of GO dispersion sedimentation was solved by self-assembly. The range of interfacial lubrication of GO aqueous dispersion has been expanded and the synergistic effect is conducive to the environmentally friendly lubricants.

Effect of glycerol incorporation on the liquid crystal structure of sucrose fatty acid ester in aqueous solution

A series of homogeneous samples with high sugar-surfactant content (sucrose fatty acid ester/water and sucrose fatty acid ester/glycerol/water systems) were prepared with well-controlled processes and investigated by DSC, polarized microscopy, X-ray scattering and rheology. Meanwhile the accuracy of the preparation process is confirmed gas chromatography. The polarized microscopy indicates that the ordering degree of the network structure composed of the liquid crystals may be reduced by the glycerol addition. The results of DSC revealed that 50% glycerol solution could significantly inhibit the crystallization of sucrose fatty acid ester and resulted in a significant widening of the temperature interval for the transformation of the liquid crystal phase into the gel phase. In order to further evaluate the effect of glycerol molecules versus water molecules on the liquid crystal structure of sucrose fatty acid ester, we comparatively analyzed the X-ray scattering data from two perspectives: the mass fraction and molar fraction. It was found that 50% glycerol solution could inhibit the crystallization of sucrose fatty acid ester through changing the water-head group interaction of surfactant, facilitates the integration of sucrose fatty acid ester with different alkyl chain length and may reduce the regularity of liquid crystal, both from the perspective of surfactant mass and molar fraction. Furthermore, the addition of 50% glycerol (w/w) does not significantly impede the liquid crystal formation of sucrose fatty acid ester in aqueous solution. However, from the perspective of surfactant mass fraction, glycerol incorporation could reduce the effective cross-sectional areas of the hydrophilic part of sucrose fatty acid ester in aqueous solution and induce the phase transition of hexagonal liquid crystals to aggregates with less positive curvature, while an opposite tendency could be obtained from the perspective of surfactant molar fraction. The conclusions are also confirmed by subsequent rheological test. Moreover, the results of rheological measurements reveals that the interactions among cylindrical units of the hexagonal liquid crystalline phase become weaker and the surfactant molecules aggregate more loosely in the cylindrical unit with the glycerol incorporation. Moreover, the above-mentioned influence of glycerol on the liquid crystal structure of sucrose fatty acid ester in aqueous solution would be similar but more prominent from the perspective of the molar fraction.

Effect of Functional Group Positional Isomerization on the Mesomorphic Properties and Thermal Stability of Biphenyl Ester Liquid Crystals

AbstractIntermolecular interactions and molecular configurations are of great significance for the formation of liquid crystals. During this study, a series of isomer compounds with biphenyl esters as rigid cores were synthesized, and their mesomorphic properties and thermal stability were investigated. Based on the same rigid core, compounds heptyl 4′‐methoxy‐[1,1′‐biphenyl]‐4‐carboxylate (1OBE7), propyl 4′‐(pentyloxy)‐[1,1′‐biphenyl]‐4‐carboxylate (5OBE3), ethyl 4′‐(hexyloxy)‐[1,1′‐biphenyl]‐4‐carboxylate (6OBE2) and methyl 4′‐(heptyloxy)‐[1,1′‐biphenyl]‐4‐carboxylate (7OBE1) have no mesophase, while compounds hexyl 4′‐ethoxy‐[1,1′‐biphenyl]‐4‐carboxylate (2OBE6), pentyl 4′‐propoxy‐[1,1′‐biphenyl]‐4‐carboxylate (3OBE5) and butyl 4′‐butoxy‐[1,1′‐biphenyl]‐4‐carboxylate (4OBE4) have multiple smectic mesophases, whereas the production of the smectic mesophase is due to the microphase separation between aromatic cores and the alkyl chains. Compound 3OBE5 exhibiting good thermal stability (The value of T5% is 258.3 °C). In addition, with the right shift of the functional group position, compound 4OBE4 formed the widest smectic mesophase. The results show that the mesophase properties and thermal stability of liquid crystals are related to the position of the functional group.

Formation and annihilation of electrically driven defects in nematic liquid crystals with negative dielectric anisotropy

Orientationally ordered liquid crystals (LCs) exhibit remarkable physical anisotropy and responsiveness to external fields, which give rise to distinguished physical effects and have led to the emergence of a new generation of electric-optical applications. The LCs are also renowned for their abundance of phases and topological defects, which are of significance in studying both fundamental science and practical technology. One simple approach to generating umbilic defects involves applying an electric field to a homeotropically aligned nematic LC with negative dielectric anisotropy <inline-formula><tex-math id="M8">\begin{document}$\Delta \varepsilon $\end{document}</tex-math><alternatives><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="5-20231655_M8.jpg"/><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="5-20231655_M8.png"/></alternatives></inline-formula>. However, the influence of material properties and external conditions on the dynamic process of nematic LC defects remains unclear. Here, we select seven kinds of nematic LCs with negative dielectrically anisotropy, ranging from –1.1 to –11.5, to explore the dynamics of electric-field-induced umbilics. By using a linearly increasing electric field parallel to the molecular orientation of LC, we systematically investigate the effects of material property (dielectric anisotropy) and external conditions (temperature and electric field parameters) on the formation and annihilation of umbilic defects. The experimental results show that the dynamic process of forming the umbilic defects in nematic LCs is independent of dielectric anisotropy, temperature, and electric field frequency, but follows the Kibble-Zurek mechanism, in which the density of generated umbilic defects exhibits a power-law scaling with the change of the electric field ramp rate, with a scaling exponent of approximately <inline-formula><tex-math id="M9">\begin{document}$1/2$\end{document}</tex-math><alternatives><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="5-20231655_M9.jpg"/><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="5-20231655_M9.png"/></alternatives></inline-formula>. Interestingly, a stronger dielectric anisotropy leads to a higher density of umbilic defects. Additionally, a change in temperature has a significant influence on the density of umbilic defects , in which higher temperature leads to greater defect density under the same external electric field conditions. Furthermore, the annihilation rate of umbilic defects is closely related to the material properties and the ramp of the applied electric field. Specifically, the annihilation rate of umbilic defects becomes faster when dielectric anisotropy is stronger or the electric field ramp is larger. This study provides valuable insights into the relationship between the formation and annihilation of defects, material properties, and external conditions in nematic LCs with dielectrically negative anisotropy, contributing to our comprehensive understanding of the dynamic process of topological defects in soft matter.

Bio-inspired liquid crystal gel induction via nano-hydroxyapatite mesogens: Viscoelastic and hemostasis regulation under bone remodeling pH and temperature control

In this work, a liquid crystal mesophase as a potential bone-repairing booster has been induced from a polyacrylic acid (PAAc) gel loaded with synthetic hydroxyapatite nanoparticles (nHA) under physiological conditions of pH and temperature that resemble the early stages of bone formation. Dynamic processes at the microscale in biological systems require a material capable of behaving following a specific order and fluency. Besides, they must fulfill conditions such as biocompatibility and good mechanical properties. Our study aimed to obtain new data about the safety, hemostasis, biocompatibility (activated partial thromboplastin time (APTT) test, prothrombin time (PT) test, lactate dehydrogenase (LDH) test, red blood cell morphology observation, hemolysis percentage) and physicochemical/mechanical behavior (Attenuated Total Reflection (ATR), Infrared spectroscopy and rheological assays) of nanoparticles, and materials built with them. Both systems have shown biocompatibility with red blood cells and adequate flow properties, demonstrating promising qualities for applicability. The formation of lyotropic liquid crystals at physiological conditions was evaluated with crossed polaroids microscope with a temperature control plate. The formation of these structures under bone remodeling conditions shows the potential application of PAAc-nHA materials. In literature, the study of materials applied as bone fillers is mainly focused on mechanical and osteoblasts compatibility assays. However, the hematological effect, consequences on the coagulation cascade, the integrity of cell membranes, and hemolysis percentage have not been addressed thoroughly. The strength of our work is focused on considering these aspects when tridimensional arrangements essential for bone formation are formed.

The effect of liquid crystal concentration on electrooptical properties of five flexible polymer dispersed liquid crystal formulations

We investigated the effect of concentration on the electro-optical properties of some flexible PDLC formulations with various liquid crystal mixtures. The PDLC films were prepared on flexible ITO-PET supports by UV-PIPS phase separation method and the uniform film thickness was insured by plastic micro-spacers. We found that depending on the type of liquid crystal and PDLC process conditions, the electro-optical properties (off-state and on-state transmissions, switching voltages and response times) provide different concentration dependency with various trends in the studied flexible PDLC formulations.

Prediction of the Structural Color of Liquid Crystals via Machine Learning

Materials that generate structural color may be promising alternatives to dyes and pigments due to their relative long-term stability and environmentally benign properties. Liquid crystal (LC) mixtures of cholesteryl esters demonstrate structural color due to light reflected from the helical structure of the self-assembled molecules. The apparent color depends on the pitch length of the liquid crystal. While a wide range of colors have been achieved with such LC formulations, the nature of the pitch–concentration relationship has been difficult to define. In this work, various machine learning approaches to predict the reflected wavelength, i.e., the position of the selective reflection band, based on LC composition are compared to a Scheffe cubic model. The neural network regression model had a higher root mean squared error (RMSE) than the Scheffe cubic model with improved predictions for formulations not included in the dataset. Decision tree regression provided the best overall performance with the lowest RMSE and predicted position of the selective reflection band within 0.8% of the measured values for LC formulations not included in the dataset. The predicted values using the decision tree were over two-fold more accurate than the Scheffe cubic model. These results demonstrate the utility of machine learning models for predicting physical properties of LC formulations.

Low-Frequency Ultrasound Effects on Cellulose Nanocrystals for Potential Application in Stabilizing Pickering Emulsions.

Cellulose, in the form of cellulose nanocrystals (CNCs), is a promising biomaterial for stabilizing Pickering emulsions (PEs). PEs are commonly formed using low-frequency ultrasound (LFU) treatment and impact CNC properties. The present study investigated the specific effects of LFU treatment on CNCs' chemical and physical properties. CNCs were characterized using dynamic light scattering, ζ;-potential determination, Fourier transform infrared spectroscopy, X-ray diffraction, and contact angle measurement. CNC suspensions were studied using rheological analysis and static multiple light scattering. LFU treatment broke CNC aggregates and modified the rheological behavior of CNC suspensions but did not affect the CNCs' chemical or crystallographic structures, surface charge, or hydrophilic properties. During the storage of CNC suspensions and PEs, liquid crystal formation was observed with cross-polarized light. Hypotheses related to the impact of liquid crystal CNCs on PE stability were proposed.

Anticancer Potential of Novel Nanoemulgel Formulations in Melanoma

Melanoma is classified as one of the most common cancers with an increasing incidence rate and the conventional treatment options that come with undesirable effects decrease the life quality of patients. Herein, as an alternative therapy option for systemic administration, Carbopol-based nanoemulgel formulations for local delivery were designed. Topical drug delivery systems containing Oxaliplatin, a cisplatin derivative anticancer drug used in the treatment of colorectal cancers, were evaluated for their potential for melanoma treatment. Nanoemulgel formulations with particle size under 300 nm were prepared and characterized in terms of droplet size, zeta potential and liquid crystal formation. The viscosity, as a critical attribute for topical drug delivery systems, was also evaluated, and pseudoplastic behavior of these novel drug delivery systems were confirmed. The controlled drug release pattern was shown with in vitro drug release studies with a significant difference from oxaliplatin when applied in solution. In vitro cell viability evaluation with L929 mouse fibroblast cell line confirmed the biocompatibility of prepared formulations, and the anticancer effect of novel nanoemulgel formulations were presented in B16-F10 mouse melanoma cell line. In conclusion, the anticancer potential of Oxaliplatin nanoemulgels were shown in vitro as a therapy option for melanoma, and the advantages of emulsion and gel-based drug delivery systems were combined in a nanotechnology platform for effective and patient-friendly application of an anticancer therapy for melanoma.

Particle Size Controlled Chiral Structural Color of Monodisperse Cholesteric Liquid Crystals Particles

AbstractCholesteric liquid crystals (CLCs) are becoming increasingly popular due to their unique chiral structural color. Unlike ordinary CLCs materials, CLCs particles exhibit angle‐independence, making them particularly noteworthy. However, currently, there are limited effective methods for controlling the structural color of CLCs particles, other than adjusting the concentration of chiral dopants or introducing stimuli‐responsive groups. Here, a scalable and cost‐effective process for preparing monodisperse CLCs particles via dispersion polymerization is reported. By making CLCs into micrometer‐sized monodisperse spheres, the helical pitch of CLCs can be varied according to its particle size, and the resulting structural color hue due to Bragg reflection can also be changed. Covering the CLCs particles with polydimethylsiloxane results in the formation of a polymer dispersed liquid crystals–like structure, which enhances the structural color appearance and thermal stability of the CLCs particles. Additionally, a simple strategy to produce chiral anti‐counterfeiting QR codes is developed. By combining CLCs particles with commercially available pigments, an anti‐counterfeiting QR code that can only be displayed under a specific circular polarizer is created. This approach and resulting CLCs particles expand the modulation of CLCs structural color and enrich the application of structural color in the field of chiral optical anti‐counterfeiting.

Micelle structure of nonionic surfactants containing carbon dioxide moieties in protic ionic liquids

Partial substitution of ethylene oxide with carbon dioxide moieties can yield greener nonionic surfactants with comparable functionalities. In water, studies showed that the incorporation of CO2 moieties suppresses the formation of liquid crystalline phases at high concentrations. A similar reduction in solvation and suppression of liquid crystal formation is observed here in the ionic liquids ethylammonium nitrate and propylammonium nitrate. Small-angle neutron scattering is used to study the solvation and packing of micelles in ionic liquids as functions of temperature, concentration, and content of CO2 moieties. By comparing with aqueous solutions, this work shows that while the nature of surfactant-solvent interaction is comparable among water and alkylammonium nitrate ILs, their behaviours in the solvated micelle shell are different. The lack of liquid crystalline phases should be attributed to the small excluded volume of micelles, which can be fine-tuned via ion design and choice of solvent.Graphical

Preparation and Physicochemical Evaluation of Injectable Sustained-Release Risperidone by Lipid Liquid Crystal Vehicle

Introduction: Risperidone is a highly effective medicine in patients with mental disorders. Since maintaining blood concentrations of risperidone within the therapeutic index is pivotal during treatment, these patients should receive medication daily and continuously. Method: In this study, an optimal lipid liquid crystal was designed according to the maximum release for 60 days based on different ratios of phosphatidylcholine (PC) to sorbitan monooleate (PC:SMO), tween 80 (w/w%), and tocopherol acetate (w/w%) using Design Expert software with the Central Composite Design (CCD) method. Release evaluations were conducted in vitro to compare the effects of lipid liquid crystal and Risperdal CONSTA®. The structure evaluation was also tested using polarized electron microscopy and in vitro assessment via cell culture. Results: The optimal formulation was selected based on the maximum release (100%) of the drug obtained within 2 months with a PC: SMO ratio of 58.6%, tween 0.82% (w/w), and tocopherol acetate 3.6% (w/w). A hexagonal mesophase with a dihedral structure was observed in the liquid crystal structure. No toxicity was observed in the cell culture test. Conclusion: The comparison of the results of in vitro studies of the liquid crystal formulation containing risperidone and the commercial formulation, Risperdal CONSTA®, showed that the liquid crystal system provides better and more uniform drug release for 60 days. Therefore, it can increase patient compliance and ease the problems of oral administration

Anisotropic Frictional Properties Induced by Cellulose Nanofibril Assembly.

The alignment of geometrically anisotropic nanomaterials regulates their functions. Self-ordering of rod-like cellulose nanocrystals (CNCs) results in liquid-crystal formation, and the ordering of the CNCs exhibits unique optical properties. Native cellulose nanofibrils (CNFs) are considered to be oriented, and thus the orientation is correlated with their functions, such as their mechanical strength and cell responses. In contrast, the ordering of artificially pulverized CNFs with high aspect ratios is restricted by their long fibrous shape. Here, we propose a facile fabrication method for non-uniaxial, fingerprint-like alignment of CNFs using the Langmuir-Blodgett technique. The obtained Langmuir-Blodgett films of CNFs exhibited anisotropic frictional properties depending on the orientation direction. This process for fabrication of CNF ultrathin films is expected to be used for novel surface design with desired structure-function correlations, which provides anisotropic surface properties to the material surface.

Nematic to Cholesteric Transformation in the Cellulose Nanocrystal Droplet Phase

Nucleation, growth, and transformation of chirality in nanomaterial systems is a growing research topic with broad interest in tunable and configurable chiroptical materials. Similar to other one-dimensional nanomaterials, cellulose nanocrystals (CNCs), which are nanorods of naturally abundant biopolymer cellulose, display chiral or cholesteric liquid crystal (LC) phases in the form of tactoids. However, the nucleation and growth of the cholesteric CNC tactoids to equilibrium chiral structures and their morphological transformations are yet to be critically assessed. We noticed that the onset of liquid crystal formation in CNC suspensions is characterized by the nucleation of a nematic tactoid that grows in volume and spontaneously transforms into a cholesteric tactoid. The cholesteric tactoids merge with the neighboring tactoids to form bulk cholesteric mesophases with various configurational palettes. We applied scaling laws from the energy functional theory and found suitable agreement with the morphological transformation of the tactoid droplets monitored for their fine structure and orientation by quantitative polarized light imaging.