Nanostructured Block Research Articles

Crafting Nanostructured Hybrid Block Copolymer-Gold Nanoparticles by Confined Self-Assembly in Evaporative Droplets.

Hybrid organic-inorganic nanostructures offer significant potential for developing advanced functional materials with numerous technological applications. However, the fabrication process is often tedious and time-consuming. This study presents a facile method for fabricating block copolymer-based photonic microspheres incorporating plasmonic gold nanoparticles. Specifically, the confined self-assembly of poly(styrene)-b-poly(2-vinylpyridine) in emulsion droplets allows the formation of spherical, noniridescent, concentric lamellar structures, i.e., onion-like particles that are subsequently infiltrated with gold salt. Using ethanol as a preferential solvent allows the loading of metal ions exclusively into the poly(2-vinylpyridine) domains, which are subsequently reduced, leading to the in situ, spatially controlled formation of gold nanoparticles. The hybrid structures exhibit a well-defined photonic bandgap and plasmonic resonance at low gold concentrations. These results demonstrate the feasibility of fabricating optically active photonic structures comprising metal nanoparticles in a block copolymer array via a simple two-step fabrication process.

Programmable Analog Circuits with Neuromorphic Nanostructured Platinum Films

AbstractSelf‐assembled nanoparticle or nanowire networks have recently come under the spotlight as systems able to emulate brain‐like data processing performances by exploiting the memristive character and the wiring of the junctions connecting the nanostructured network building blocks. Recently it is demonstrated that nanostructured Au films, fabricated by the assembling of gold clusters produced in the gas phase, have non‐linear and non‐local electric conduction properties caused by the extremely high density of grain boundaries and the resulting complex arrangement of nanojunctions. These observations suggest that nanostructured metallic films can be explored and exploited as a novel class of neuromorphic systems for unconventional electronic devices. Here it is reported that nanostructured cluster‐assembled Pt films show resistive switching activity, negative differential resistance, and reversible memory effects. These properties allow the use of nanostructured Pt films in programmable analog circuits, such as gain amplifiers and relaxation oscillators with fast response.

Lithium iodide transport in double gyroid nanochannels formed by zwitterion‐containing solid polymer electrolytes

AbstractThe fabrication of nanostructured block copolymer (BCP) films endowed with lithium ion‐conducting gyroid (GYR) nanochannels is an appealing solution to build solid polymer electrolytes (SPEs) that combines high ionic conductivity (IC) with suitable mechanical properties. However, the formation of a well‐developed GYR structure remains challenging to achieve from the self‐assembly of polyelectrolyte BCP chains. To overcome this issue, large ion conducting gyroid grains were produced within freestanding polystyrene‐block‐poly(2‐vinylpyridine)‐block‐poly(ethylene oxide) (PS‐b‐P2VP‐b‐PEO) films by combining a solvent vapor annealing (SVA) treatment with an infiltration process. Here, the SVA treatment enabled the manufacture of SPEs entirely composed of a GYR structure while the infiltration process allowed for the incorporation of an appropriate Li salt (i.e., lithium iodoacetate, LiIAc) within the 3D‐interconected nanochannels via a Menshutkin reaction. By using this SVA‐Infiltration strategy, it has been demonstrated that the creation of ion conducting GYR nanochannels enhances the ion transportation capacity of pyridine‐containing SPEs since substantially lower ICs were measured from analog PS‐b‐P2VP‐b‐PEO/LiIAc films having a nominally disordered as‐cast state. Remarkably, zwitterionic pyridinium‐based moieties formed inside the interpenetrated nanochannels enable an efficient migration of Li+ and I3− species, leading to an IC as high as 10−4 S cm−1 at 70°C.

Abstract 487: Peptide amphiphiles hitchhike on endogenous biomolecules for enhanced drug delivery

Abstract Peptide amphiphiles (PAs) have been applied as building blocks for self-assembled nanostructures with various morphologies. These self-assembled nanostructures are promising drug delivery platforms as they are naturally biodegradable and biocompatible with low immunogenicity. One primary focus in drug delivery using the PA nanostructures has been to develop strongly assembled structures to avoid disassembly in the blood and allow them to carry payloads to their intended targets. In this work, rather than developing stable self-assembled PA structures, we focused on weakly assembled PA nanostructures to investigate their interactions with blood components and to understand how these interactions affect their biodistribution. We found that weakly assembled PA nanostructures (SA-E) quickly disassembled in plasma and reassembled with lipoproteins (LPs), which significantly prolonged the blood circulation of SA-E in mice. We showed that SA-E crossed the endothelial barriers through transcytosis only when they were assembled with LPs. Cellular uptake studies showed that SA-E accumulated in cancer cells through lipid-raft-mediated uptake. Interestingly, their cellular internalization was independent of LP receptors, suggesting that SA-E assembles with different endogenous biomolecules in vivo. By exploiting these endogenous interactions, SA-E demonstrated high tumor accumulation in a myriad of small animal tumor models of breast, colon, pancreatic, brain, skin, prostate, or lung cancers. SA-E demonstrated large tumor-to-background signal ratios in live animals (>5), extended retention (>2 weeks), and excellent tissue distribution (tumor to liver signal >3) in these tumor models. Encouraged by the excellent tumor accumulation of SA-E, we prepared SA-E drug conjugate using a highly potent and toxic chemotherapeutic agent, Monomethyl auristatin E (MMAE). SA-E-MMAE conjugate demonstrated strong antitumor efficacy in aggressive breast and glioma models in mice with reduced side effects. With its simple and modular design and universal tumor accumulation mechanism, SA-E represents a promising platform for broad applications in cancer therapy. Citation Format: Jared M. Fischer, Morgan Stewart, Mingchong Dai, Samuel Drennan, Sinan Sabuncu, Benjamin Kingston, Isabel Dengos, Li Xiang, Karla Bonic, Xin Yi, Srivathsan Ranganathan, Bruce Branchaud, Adem Yildirim. Peptide amphiphiles hitchhike on endogenous biomolecules for enhanced drug delivery [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2024; Part 1 (Regular Abstracts); 2024 Apr 5-10; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2024;84(6_Suppl):Abstract nr 487.

Toughening epoxy by nano-structured block copolymer to mitigate matrix microcracking of carbon fibre composites at cryogenic temperatures

The incorporation of rigid nanoparticles has proven to enhance microcracking resistance in carbon fibre reinforced polymer (CFRP) composites at cryogenic temperatures, enabling CFRP tanks to store cryogenic liquid like hydrogen without requiring liners. Herein, we investigate efficacy of low-modulus soft nanoparticles in addressing the microcracking challenges inherent in CFRP at cryogenic temperatures. By incorporating a tri-block copolymer (BCP) into an epoxy, nano-structured fillers with an average diameter of approximately 100 nm are formed. Experimental results reveal that, at a 2.5 wt% loading, the BCP significantly increase the fracture energy of the nanocomposite by 392% at −196 °C while maintaining stiffness and strength. More importantly, composite laminates made with the BCP-modified nanocomposite matrix can withstand cryogenic temperatures without matrix microcracking, even when they contain multiple plies with the same orientation, such as [04/904]s, which are known to be highly susceptible to matrix microcracking at cryogenic temperatures. An advanced high-fidelity micromechanical model revealed that the observed toughening effect of nanostructured block copolymer at cryogenic temperatures can be attributed to the increased fracture resistance of the nanocomposite matrix. The findings of this research demonstrate that low concentration of block copolymer can effectively mitigate the initiation and propagation of matrix microcracks in carbon fibre composites at ultra-cold temperatures.

Temperature-dependent elasticity of DNA, RNA, and hybrid double helices

Nucleic acid double helices in their DNA, RNA, and DNA-RNA hybrid form play a fundamental role in biology and are main building blocks of artificial nanostructures, but how their properties depend on temperature remains poorly understood. Here, we report thermal dependence of dynamic bending persistence length, twist rigidity, stretch modulus, and twist-stretch coupling for DNA, RNA, and hybrid duplexes between 7°C and 47°C. The results are based on all-atom molecular dynamics simulations using different force field parameterizations. We first demonstrate that unrestrained molecular dynamics can reproduce experimentally known mechanical properties of the duplexes at room temperature. Beyond experimentally known features, we also infer the twist rigidity and twist-stretch coupling of the hybrid duplex. As for the temperature dependence, we found that increasing temperature softens all the duplexes with respect to bending, twisting, and stretching. The relative decrease of the stretch moduli is 0.003–0.004/°C, similar for all the duplex variants despite their very different stretching stiffness, whereas RNA twist stiffness decreases by 0.003/°C, and smaller values are found for the other elastic moduli. The twist-stretch couplings are nearly unaffected by temperature. The stretching, bending, and twisting stiffness all include an important entropic component. Relation of our results to the two-state model of DNA flexibility is discussed. Our work provides temperature-dependent elasticity of nucleic acid duplexes at the microsecond scale relevant for initial stages of protein binding.

Role of Functionalized Peptides in Nanomedicine for Effective Cancer Therapy.

Peptide-functionalized nanomedicine, which addresses the challenges of specificity and efficacy in drug delivery, is emerging as a pivotal approach for cancer therapy. Globally, cancer remains a leading cause of mortality, and conventional treatments, such as chemotherapy, often lack precision and cause adverse effects. The integration of peptides into nanomedicine offers a promising solution for enhancing the targeting and delivery of therapeutic agents. This review focuses on the three primary applications of peptides: cancer cell-targeting ligands, building blocks for self-assembling nanostructures, and elements of stimuli-responsive systems. Nanoparticles modified with peptides improved targeting of cancer cells, minimized damage to healthy tissues, and optimized drug delivery. The versatility of self-assembled peptide structures makes them an innovative vehicle for drug delivery by leveraging their biocompatibility and diverse nanoarchitectures. In particular, the mechanism of cell death induced by self-assembled structures offers a novel approach to cancer therapy. In addition, peptides in stimuli-responsive systems enable precise drug release in response to specific conditions in the tumor microenvironment. The use of peptides in nanomedicine not only augments the efficacy and safety of cancer treatments but also suggests new research directions. In this review, we introduce systems and functionalization methods using peptides or peptide-modified nanoparticles to overcome challenges in the treatment of specific cancers, including breast cancer, lung cancer, colon cancer, prostate cancer, pancreatic cancer, liver cancer, skin cancer, glioma, osteosarcoma, and cervical cancer.

Autocatalytic DNA circuitries.

Autocatalysis, a self-sustained replication process where at least one of the products functions as a catalyst, plays a pivotal role in life's evolution, from genome duplication to the emergence of autocatalytic subnetworks in cell division and metabolism. Leveraging their programmability, controllability, and rich functionalities, DNA molecules have become a cornerstone for engineering autocatalytic circuits, driving diverse technological applications. In this tutorial review, we offer a comprehensive survey of recent advances in engineering autocatalytic DNA circuits and their practical implementations. We delve into the fundamental principles underlying the construction of these circuits, highlighting their reliance on DNAzyme biocatalysis, enzymatic catalysis, and dynamic hybridization assembly. The discussed autocatalytic DNA circuitry techniques have revolutionized ultrasensitive sensing of biologically significant molecules, encompassing genomic DNAs, RNAs, viruses, and proteins. Furthermore, the amplicons produced by these circuits serve as building blocks for higher-order DNA nanostructures, facilitating biomimetic behaviors such as high-performance intracellular bioimaging and precise algorithmic assembly. We summarize these applications and extensively address the current challenges, potential solutions, and future trajectories of autocatalytic DNA circuits. This review promises novel insights into the advancement and practical utilization of autocatalytic DNA circuits across bioanalysis, biomedicine, and biomimetics.

Effect of Polymer Composition and Morphology on Mechanochemical Activation in Nanostructured Triblock Copolymers.

The effect of composition and morphology on mechanochemical activation in nanostructured block copolymers was investigated in a series of poly(methyl methacrylate)-block-poly(n-butyl acrylate)-block-poly(methyl methacrylate) (PMMA-b-PnBA-b-PMMA) triblock copolymers containing a force-responsive spiropyran unit in the center of the rubbery PnBA midblock. Triblock copolymers with identical PnBA midblocks and varying lengths of PMMA end-blocks were synthesized from a spiropyran-containing macroinitiatior via atom transfer radical polymerization, yielding polymers with volume fractions of PMMA ranging from 0.21 to 0.50. Characterization by transmission electron microscopy revealed that the polymers self-assembled into spherical and cylindrical nanostructures. Simultaneous tensile tests and optical measurements revealed that mechanochemical activation is strongly correlated to the chemical composition and morphologies of the triblock copolymers. As the glassy (PMMA) block content is increased, the overall activation increases, and the onset of activation occurs at lower strain but higher stress, which agrees with predictions from our previous computational work. These results suggest that the self-assembly of nanostructured morphologies can play an important role in controlling mechanochemical activation in polymeric materials and provide insights into how polymer composition and morphology impact molecular-scale force distributions.

Developing Quantitative Nondestructive Characterization of Nanomaterials: A Case Study on Sequential Infiltration Synthesis of Block Copolymers.

The sequential infiltration synthesis (SIS) of inorganic materials in nanostructured block copolymer templates has rapidly progressed in the last few years to develop functional nanomaterials with controllable properties. To assist this rapid evolution, expanding the capabilities of nondestructive methods for quantitative characterization of the materials properties is required. In this paper, we characterize the SIS process on three model polymers with different infiltration profiles through ex situ quantification by reference-free grazing incidence X-ray fluorescence. More qualitative depth distribution results were validated by means of X-ray photoelectron spectroscopy and scanning transmission electron microscopy combined with energy-dispersive X-ray spectroscopy.

Controlled Orientation of Silicon-Containing Diblock Copolymer Thin Films by Substrate Functionalization Under Vacuum

This work demonstrates a simple approach to control the orientation of the self-assembled nanostructured block copolymer thin films of polystyrene-block-polydimethylsiloxane (PS-b-PDMS) by functionalization of the oxide layer (SiO2) on the Si substrate followed by thermal annealing under low-pressure environmental conditions. The substrate can be functionalized through two-step grafting of hydroxy-terminated polystyrene brush (PS–OH brush) followed by hydroxy-terminated polydimethylsiloxane brush (PDMS–OH brush) onto the wafer substrate. By controlling the grafting ratio of PS–OH and PDMS–OH brushes, the affinities of the PS and PDMS blocks with the substrates can be fine-tuned to provide a neutral substrate in order to form perpendicular cylinders from the bottom after thermal annealing. Owing to the vacuum-driven orientation [i.e., thermal annealing under low-pressure environment conditions (∼10–4 Pa)], the orientation of the cylinders can be controlled at the air/polymer interface. Interestingly, by combining the vacuum-driven approach with substrate functionalization, perpendicular cylinders from the air/polymer interface and substrate/polymer interface can be generated, respectively. Consequently, well-aligned perpendicular cylinders with long-range ordering can be fabricated by the self-alignment process.

Improving the Photoresponse of Transistor Memory Using Self-Assembled Nanostructured Block Copolymers as a Photoactive Electret

Improving the Photoresponse of Transistor Memory Using Self-Assembled Nanostructured Block Copolymers as a Photoactive Electret

Nanostructured block copolymer muscles.

High-performance actuating materials are necessary for advances in robotics, prosthetics and smart clothing. Here we report a class of fibre actuators that combine solution-phase block copolymer self-assembly and strain-programmed crystallization. The actuators consist of highly aligned nanoscale structures with alternating crystalline and amorphous domains, resembling the ordered and striated pattern of mammalian skeletal muscle. The reported nanostructured block copolymer muscles excel in several aspects compared with current actuators, including efficiency (75.5%), actuation strain (80%) and mechanical properties (for example, strain-at-break of up to 900% and toughness of up to 121.2 MJ m-3). The fibres exhibit on/off rotary actuation with a peak rotational speed of 450 r.p.m. Furthermore, the reported fibres demonstrate multi-trigger actuation (heat and hydration), offering switchable mechanical properties and various operating modes. The versatility and recyclability of the polymer fibres, combined with the facile fabrication method, opens new avenues for creating multifunctional and recyclable actuators using block copolymers.

Synthesis of block copolymers containing 3-chloro-2-hydroxypropyl methacrylate by NMP – a versatile platform for functionalization

This study highlights the potential of 3-chloro-2-hydroxypropyl methacrylate (ClHPMA) as a functional building block in nanostructured block copolymer architectures.

Coupling of Planar Waveguide Modes in All-Dielectric Multilayer Structures: Monitoring the Dependence of Local Electric Fields on the Coupling Strength

Except for a few cases to which sophisticated techniques are applicable, it is difficult to observe experimentally local electric fields or near fields associated with excitation of electromagnetic modes supported by building blocks of nanostructures. Although elucidating the behavior of the local electric fields or near fields is very useful to develop potential applications of the nanostructures, in many cases, their behaviors have been only speculated from simulations based on the electromagnetic theory. Here, we develop a simple technique that allows us to study experimentally the average behavior of the local electric fields inside two planar waveguide layers interacting with each other in all-dielectric multilayer structures. The study is made possible by doping the two waveguide layers with two different fluorophores. Fluorescence intensities detected at two different wavelengths allow us to study separately the behaviors of the local electric fields inside each waveguide layer. Angle-scan fluorescence excitation spectra are measured for two different series of multilayer samples by exciting the samples in an attenuated total reflection geometry. The line shapes observed are in good agreement with theoretical ones calculated based on the electromagnetic theory, confirming that the experimental fluorescence excitation spectra reflect well the average behaviors of the local electric fields. Applying the developed technique, we investigate systematically the changes in the local electric fields inside the waveguide layers caused by the change in the strength of coupling between the two waveguide modes. In one series of the samples, a gradual transition in the behavior of the local electric fields, from a Fano-resonant behavior to a double-peak behavior, is demonstrated with increasing the coupling strength. In another series of the samples, the coupling strength is widely changed and the formation of the coupled modes in a strong coupling regime is clearly observed. The observed changes in the local electric fields can be reproduced very well by simple analytical calculations based on a coupled oscillator model. The model is helpful to gain physical insights into the coupling of the waveguide modes, which cannot be obtained by the electromagnetic calculations.

Inception of Carbonaceous Nanostructures via Hydrogen-Abstraction Phenylacetylene-Addition Mechanism.

Sufficient experimental evidence has suggested that polycyclic aromatic hydrocarbons are the building blocks of carbonaceous nanostructures in combustion and circumstellar envelops of carbon-rich stars, but their fundamental formation mechanisms remain elusive. By exploring the reaction kinetics of phenylacetylene with 1-naphthyl/4-phenanthryl radicals, we provide compelling theoretical and experimental evidence for a novel and self-consistent hydrogen-abstraction phenylacetylene-addition (HAPaA) mechanism. HAPaA operates efficiently at both low and high temperatures, leading to the formation, expansion, and nucleation of peri-condensed aromatic hydrocarbons (PCAHs), which are otherwise difficult to synthesis via traditional hydrogen-abstraction acetylene/vinylacetylene-addition pathways. The HAPaA mechanism can be generalized to other α-alkynyl PCAHs and thus provides an alternative covalent bond bridge for PCAH combination via an acetylene linker. The proposed HAPaA mechanism may contribute toward a comprehensive understanding of soot formation, carbonaceous nanomaterials synthesis, and the origin and evolution of carbon in our galaxy.

How a family of nanostructured amphiphilic block copolymers synthesized by RAFT-PISA take advantage of thiol groups to direct the in situ assembly of high luminescent CuNCs within their thermo-responsive core

• Multithiolated block copolymer nanoparticles (P-NPs) were synthesized by RAFT-PISA. • Monodisperse P-NPs with tunable size are formed under uncontrolled RAFT polymerization. • P-NPs with thermo-responsive core and hydrophilic shell exhibit high water stability. • Thiolated P-NPs serve as template for in situ assembly of luminescent CuNCs in water. • Fluorescent nanohybrids exhibit pH/thermo-response, photostability and oxidation resistance. The development of fluorescent water stable copper nanoclusters (CuNCs) deserves the scientific interest due to their outstanding properties and low-cost. These fluorescent CuNCs can be synthesized using natural or synthetic polymers with thiol groups. Herein, for the first time, we propose the use of novel amphiphilic block copolymer nano-objects, synthesized by polymerization induced self-assembly (PISA) via reversible-addition fragmentation chain transfer (RAFT), as templates for the synthesis and water stabilization of CuNCs. The polymeric NPs provide water-stability due to the poly(hydroxyethyl acrylate) corona and the thermos-responsive core, based on 2-(2-methoxyethoxy) ethyl methacrylate (MEO 2 MA) and 2-(acetylthio) ethyl methacrylate (AcSEMA) decorated with protected thiol groups, drive the “ in situ ” reduction of copper ions into copper nanocrystals and their assembling in high luminescent nanohybrids in water. In order to optimize the fluorescence properties a methodical study was carried out varying polymers composition and architecture, thiol content and nanoparticle size. All the polymeric nanoparticles synthesized by PISA and decorated with thiol groups induce the formation of luminescent CuNCs in their hydrophobic core. The sizes of the hydrophilic/hydrophobic block, as well as, thiol content are key factors in the emission properties of the CuNC nanohybrids that offer high colloidal stability in water, pH- and thermo-response, significance photostability and strong resistance to oxidation.

Evolution of sub-surface microstructure under linear reciprocating wear of nanostructured bainitic steel

Nanostructured bainitic steels have high strength as well as a combination of significant ductility, fracture toughness and sub-critical fatigue crack growth life. Hence, they can be potentially useful in structures suffering rolling and/or sliding fatigue e.g. rails, mining components, bearings and shafts. However, such applications require high wear resistance which is not solely dependent on the initial strength since repetitive sliding often leads to sub-surface microstructural evolution that alters the tribological response with time. In the current study, three nanostructured bainitic blocks with lath thickness of 45, 54 and 77 nm have been made from steel of composition: Fe-0.86C-1.45Si-1.8Mn-0.47Al-1.88Co-0.23Mo (wt%) by austempering at 250, 300 and 350 °C respectively. We have investigated the friction and microstructural evolution under reciprocating sliding motion of a 10 mm spherical tungsten carbide indenter at 10 kN load and correlated the findings with the initial morphology of bainite. All specimens exhibited hardening after multiple cycles of deformation. However, the steel austempered at the lowest temperature showed the highest sub-surface hardness and lowest friction coefficient and was the most resistant to wear when tested under sliding fatigue for up to 500 cycles. Repeated sliding resulted in formation of two kinds of layers: white etching layer (WEL) and severely deformed layer (SDL). WEL exhibited very fine microstructure whereas the SDL showed alignment of retained austenite and bainitic laths along the direction of highest shear stress. There was a predominant presence of WEL in the specimens austempered at the lowest temperature and SDL in the specimens transformed at the highest temperature. Atomic probe tomography (APT) was used to investigate the distribution of carbon in the deformed layers just below the wear track after 500 sliding cycles for 250 and 350 °C austempered condition. No significant change in carbon has been detected in any of the austempered specimens after wear.

Limiting Current in Nanostructured Block Copolymer Electrolytes

Next-generation electrolytes for lithium batteries must be able to conduct ions at sufficiently high current densities; yet this regime is rarely studied directly. The limiting current density of an electrolyte quantifies the highest possible rate of ion transport under an applied dc potential. Herein, we report on the limiting current density in twelve nanostructured polystyrene-block-poly(ethylene oxide) (PS-b-PEO, or SEO) copolymer electrolytes. We find that the limiting current at a given salt concentration increases systematically with increasing volume fraction of the PEO block (φEO). In contrast, the effective-medium theory, commonly used to analyze conductivity in block copolymer electrolytes, predicts that limiting current is independent of φEO. To resolve this conundrum, the ionic conductivity, the mutual diffusion coefficient of the salt, and the steady-state current fraction of the block copolymer electrolytes were measured. These measurements enable predictions of limiting current with no adjustable parameters using the concentrated solution theory. We found quantitative agreement between experimentally measured limiting current densities and predictions based on the concentrated solution theory. This work sheds light on how to reliably measure and predict limiting current density in composite electrolytes.

Ultrastable liquid crystalline blue phase from molecular synergistic self-assembly

Fabricating functional materials via molecular self-assembly is a promising approach, and precisely controlling the molecular building blocks of nanostructures in the self-assembly process is an essential and challenging task. Blue phase liquid crystals are fascinating self-assembled three-dimensional nanomaterials because of their potential information displays and tuneable photonic applications. However, one of the main obstacles to their applications is their narrow temperature range of a few degrees centigrade, although many prior studies have broadened it to tens via molecular design. In this work, a series of tailored uniaxial rodlike mesogens disfavouring the formation of blue phases are introduced into a blue phase system comprising biaxial dimeric mesogens, a blue phase is observed continuously over a temperature range of 280 °C, and the range remains over 132.0 °C after excluding the frozen glassy state. The findings show that the molecular synergistic self-assembly behavior of biaxial and uniaxial mesogens may play a crucial role in achieving the ultrastable three-dimensional nanostructure of blue phases.