Self-assembly Of Nanocrystals Research Articles

Chiroptical Nanocellulose Bio-Labels for Independent Multi-Channel Optical Encryption.

Advanced multiplexing optical labels with multiple information channels provide a powerful strategy for large-capacity and high-security information encryption. However, current optical labels face challenges of difficulty to realize independent multi-channel encryption, cumbersome design, and environmental pollution. Herein, multiplexing chiroptical bio-labels integrating with multiple optical elements, including structural color, photoluminescence (PL), circular polarized light activity, humidity-responsible color, and micro/nano physical patterns, are constructed in complex design based on host-guest self-assembly of cellulose nanocrystals and bio-gold nanoclusters. The thin nanocellulose labels exhibit tunable circular polarized structural color crossover the entire visible wavelength and circularly polarized PL with the highest-recorded dissymmetry factor up to 1.05 due to the well-ordered chiral organization of templated gold nanoclusters. Most importantly, these elements can independently encode customized anti-counterfeiting information to achieve five independent channels of high-level anti-counterfeiting, which are rarely achieved in traditional materials and design counterparts. Considering the exceptional seamless integration of five independent encryption channels and the recyclable features of labels, the bio-labels have great potential for the next generation anti-counterfeiting materials technology.

Adjusting Microscale to Atomic-Scale Structural Order in PbS Nanocrystal Superlattice for Enhanced Photodetector Performance.

An investigation is presented into the effect of the long-range order on the optoelectronic properties of PbS quantum dot (QD) superlattices, which form mesocrystals, for potential use in photodetector applications. By self-assembly of QD nanocrystals on an Si/SiOx substrate, a highly ordered and densely packed PbS QD superlattice with a microscale size is obtained. The results demonstrate that annealing treatment induces mesocrystalline superlattices with preferred growth orientation, achieved by dislodging ligands. The improved orientation and electronic coupling of the mesocrystalline superlattices exhibit superior photodetector performance compared to disordered QD structures and closely packed superlattices. This improved performance is attributed to atomic alignment between QDs, leading to enhanced electronic coupling. The findings suggest that these mesocrystalline superlattices have promising potential for the next generation of QD optoelectronic devices.

Sustainable, Insoluble, and Photonic Cellulose Nanocrystal Patches for Calcium Ion Sensing in Sweat.

Self-assembly of cellulose nanocrystals (CNCs) is invaluable for the development of sustainable optics and photonics. However, the functional failure of CNC-derived materials in humid or liquid environments inevitably impairs their development in biomedicine, membrane separation, environmental monitoring, and wearable devices. Here, a facile and robust method to fabricate insoluble hydrogels in a self-assembled CNC-polyvinyl alcohol (PVA) system is reported. Due to the reconstruction of inter- or intra-molecular hydrogen bond interactions, thermal dehydration makes an optimized CNC/PVA photonic film form a stable hydrogel network in an aqueous solution rather than dissolve. Notably, the resulting hydrogel exhibits superb mechanical performance (stress up to 3.3 Mpa and tough up to 0.73MJm-3 ) and reversible conversion between dry and wet states, enabling it convenient for specific functionalization. Sodium alginate (SA) can be adsorbed into the CNC photonic structure by swelling dry CNC/PVA film in a SA solution. The prepared hydrogel showcases the comprehensive properties of freezing resistance (-20°C), strong adhesion, satisfactory biocompatibility, and highly sensitive and selective Ca2+ sensing. The material could act as a portable wearable patch on the skin for the continuous analysis of calcium trends during different physical exercises, facilitating their development in precision nutrition and health monitoring.

Mosquito bite prevention through self-assembled cellulose nanocrystals.

Mosquitoes are the deadliest of all combined insects and animals affecting millions and killing hundreds or thousands of people each year. Existing protection methods however are limited and include volatile compounds that actively repel mosquitoes such as N,N-Diethyl-meta-toluamide (DEET) or different essential oils such as geraniol and citronella. Most are odorous compounds and require organic solvents for dispersion. This work investigates the barrier properties of cellulose nanocrystals (CNCs). CNCs are known to self-assemble in strong, transparent, chemical barrier films. They are fully bio-based, and their surface chemistry is ideal for aqueous dispersion of many compounds. This work saw a significant 80% decrease in feeding on human skin when a thin CNC coat was applied. The effect was further confirmed by artificial feeding on Aedes aegypti wherein CNC appears to act as a chemical camouflage to the many cues sought by the insects. The combined effect of CNC with indole reduced egg laying post exposure to mammalian blood close to null with 99.4% less eggs as compared to control. The chemical barrier effect was assessed through a simple headspace experiment showing that the same CNC coat blocked the passage of ammonium hydroxide vapor, a commonly used mosquito attractant, when applied on a filter paper membrane.

Two-Dimensional Self-assembly of Unconventional fcc Ru3Ir Nanocrystals for Efficient and Robust Acidic Water Oxidation

Acidic oxygen evolution reaction (OER) catalysts face the fundamental challenge of the trade-off between activity and durability that has not yet been well addressed. Herein, we integrate high activity of nanoparticles and good stability of bulk materials into a “macro-nano” catalyst through two-dimensional self-assembling of unconventional fcc phase Ru3Ir nanocrystals. Such catalysts deliver a low overpotential of 190 mV at 10 mA cm–2 and stably maintain this over 400 h or 10,000 potential cycles for acidic OER, surpassing previously reported metallic-based catalysts. Operando X-ray absorption spectroscopy and DFT calculations reveal that the high activity is derived from self-reconstructed surface Ru3IrOx species during OER, which are electronically modulated by the fcc-Ru3Ir substrate and lower the energy barrier of the potential-determining O* → OOH* step. Control experiments reveal that two-dimensional self-assembled structures significantly enhance the corrosion resistance ability of 2D fcc-Ru3Ir by inhibiting the excessive dissolution of surface Ru3IrOx species during the OER process. This nano-to-macro strategy may provide a guideline for designing efficient and robust catalysts for acidic OER and beyond.

Metal-Halide Perovskite Nanocrystal Superlattice: Self-Assembly and Optical Fingerprints.

Self-assembly of nanocrystals into superlattices is a fascinating process that not only changes geometric morphology, but also creates unique properties that considerably enrich the material toolbox for new applications. Numerous studies have driven the blossoming of superlattices from various aspects. These include precise control of size and morphology, enhancement of properties, exploitation of functions, andintegration of the material into miniature devices. The effective synthesis of metal-halide perovskite nanocrystals has advanced research on self-assembly of building blocks into micrometer-sized superlattices. More importantly, these materials exhibit abundant optical features,including highly coherent superfluorescence, amplified spontaneous laser emission, and adjustable spectral redshift, facilitating basic research and state-of-the-art applications. This review summarizes recent advances in the field of metal-halide perovskite superlattices. It begins with basic packing models and introduces various stacking configurations of superlattices. The potential of multiple capping ligands is also discussed and their crucial role in superlattice growth is highlighted, followed by detailed reviews of synthesis and characterization methods. How these optical features can be distinguished and present contemporary applications is then considered. This review concludes with a list of unanswered questions and an outlook on their potential use in quantum computing and quantum communications to stimulate further research in this area.

Regulatory Mechanism of Opposite Charges on Chiral Self-Assembly of Cellulose Nanocrystals.

The charge plays an important role in cellulose nanocrystal (CNC) self-assembly to form liquid crystal structures, which has rarely been systematically explored. In this work, a novel technique combining atomic force microscopy force and atomistic molecular dynamics simulations was addressed for the first time to systematically investigate the differences in the CNC self-assembly caused by external positive and negative charges at the microscopic level, wherein sodium polyacrylate (PAAS) and chitosan oligosaccharides (COS) were used as external positive and negative charge additives, respectively. The results show that although the two additives both make the color of CNC films shift blue and eventually disappear, their regulatory mechanisms are, respectively, related to the extrusion of CNC particles by PAAS and the reduction in CNC surface charge by COS. The two effects both decreased the spacing between CNC particles and further increased the cross angle of CNC stacking arrangement, which finally led to the color variations. Moreover, the disappearance of color was proved to be due to the kinetic arrest of CNC suspensions before forming chiral nematic structure with the addition of PAAS and COS. This work provides an updated theoretical basis for the detailed disclosure of the CNC self-assembly mechanism.

Organic Acid-Doped Cellulose Nanocrystals in Biocomposite Laminates as Chiral Nematic Photonic Films: Implications for Intelligent Packaging

The organic photonic film is one of the important materials in optical, bioengineering, and sensing applications. It is a task to achieve excellent mechanical properties and foldability of the biopolymer composites having chiral nematic structures without sacrificing their iridescence. Herein, we have proposed an approach to preserve and lock the self-assembled cellulose nanocrystal (CNC) films based on agro-waste between the layers of a poly(lactic acid) (PLA)/polycaprolactone (PCL) biocomposite. The photonic properties of the composites were tweaked by doping with different organic acids (OAs). The addition of OAs into CNCs has resulted in the generation of flexible films. The multilayer films were studied for interfacial interactions in the form of spherulite interlocking between CNCs and polymer blends through polarized optical microscopy and differential scanning calorimetry analysis. Composite films exhibited high mechanical strength and also showed reflection from the UV region to the near-IR region. The composite films displayed good visual color-sensing properties with moderate antibacterial activity for Escherichia coli bacteria. Such ordered nanocellulose–polymer biocomposites fabricated by a facile layer-by-layer approach may assist the growth of obtained photonic films as candidate materials having implications in bio-optical engineering and packaging.

Conquering the solubility barrier of di-n-octylamine as structure-directing agent in hierarchical silicoaluminophosphate synthesis by using phase-transfer synthesis

Silicoaluminophosphates (SAPOs) are a class of microporous solids employed as solid acid catalysts or adsorbents in petrochemical and coal chemical processes, which are often generated in hydrothermal synthesis using water-soluble organic structure-directing agents (OSDA), resulting in the formation of micron sized, rod-like crystals running along pore-channel direction for unidimensional SAPOs. The use of a low-cost, barely soluble di-n-octylamine (DOA) as OSDA in a water/toluene biphasic media to crystallize SAPO-31 is reported. The product is disclosed to be a hierarchically porous material built up of self-assembled nanocrystals (∼110 nm) with enhanced diffusion property and preserved acidity comparable to that of a standard sample derived using di-n-hexylamine as OSDA. The formation is mediated by the formation of a Pickering emulsion structure that favors crystal nucleation over growth, thus overcoming the solubility barrier of candidate OSDA. The obtained material exhibited higher isomer yield in catalytic hydroisomerization of n-dodecane compared to the control sample. Product distribution analysis discloses that mono-branched isomers are generated mainly inside the micropores, while di-branched isomers are produced via key-lock catalysis on pore-mouth sites. The increase in isomerization selectivity is attributed to the formation of more mono-branched isomers and their lowered cracking probability associated with enhanced diffusion property. This new synthetic protocol expands the toolkit of candidate OSDAs towards hydrophobic molecules and exemplifies porogen-free fabrication of hierarchical SAPOs. The uncovered origin of shape-selectivity offers a guidance towards manipulating hydroisomerization product slates.

Self-assembly of Au nanocrystals into large-area 3-D ordered flexible superlattice nanostructures arrays for ultrasensitive trace multi-hazard detection.

Plasmonic nanoparticles that self-assemble into highly ordered superlattice nanostructures hold substantial promise for facilitating ultra-trace surface-enhanced Raman scattering (SERS) detection. Herein, we propose a boiling-point evaporation method to synthesize ordered monocrystal-like superlattice Au nanostructures (OML-Au NTs) with a polyhedral morphology. Combined with thermal nanoimprint technology, OML-Au NTs were directly transferred to impact-resistant polystyrene (IPS) flexible SERS substrates, the obtained flexible substrates (donated as OML-Au NTs/IPS) detection limit for R6G molecules as low as 10-13 M. These results were confirmed by simulating the electromagnetic field distribution of ordered/unordered two-dimensional single-layer and three-dimensional aggregated gold nanostructures. The OML-Au NTs/IPS substrates were successfully used to detect and quantify three commonly-used agricultural pesticides, achieving detection limits as low as 10-11 M and 10-12 M, and in situ real-time detection limit reached 0.24pg/cm2 for thiram on apple peels, which was 3 orders of magnitude lower than the current detection limit. In addition, the Raman intensity from multiple locations showed a relative standard deviation lower than 7 %, exhibiting the reliability necessary for practical applications. As a result, this research demonstrates a highly reproducible method to enable the development of plasmonic nanomaterials with flexible superstructures.

A General Approach to Stabilize Nanocrystal Superlattices by Covalently Bonded Ligands

Self-assembled inorganic nanocrystal (NC) superlattices are powerful material platforms with diverse structures and emergent functionalities. However, their applications suffer from the low structural stability against solvents and other stimuli, due to the weak interparticle interactions. Existing strategies to stabilize NC superlattices typically require the design and incorporation of special ligands prior to self-assembly and are only applicable to superlattices of certain NCs, ligands, and structures. Here we report a general method to stabilize superlattices of various NC compositions and structures via strong, covalently bonded ligands. The core is the use of light-triggered, nitrene-based cross-linkers that do not interfere the self-assembly process while nonspecifically and effectively bonding the native ligands of NCs. The stabilized 2D and 3D superlattices of metal, semiconductor, and magnetic NCs retain their structures when being exposed to solvents of different polarities (from toluene to water) and show high thermal stability and mechanical rigidity. This can further stabilize binary NC superlattices, beyond those achievable in previous methods. Stabilized superlattices show robust and reproducible functionalities, for instance, when serving as reusable substrates for surface enhanced Raman spectroscopy. These results create more possibilities in exploiting the impressive library of NC superlattices in a broad scope of applications.

Self-assembled photosensitive carbon nanocrystals with broad-spectrum antibacterial bioactivity

Synthesis and antibacterial applications of self-assembled carbon nanocrystals.

Self-assembly of cellulose nanocrystals confined to square capillaries.

Biological systems exploit restricted degrees of freedom to drive self-assembly of nano- and microarchitectures. Simplified systems, such as colloidal nanoparticles that behave as lyotropic liquid crystalline mesophases in confined geometric spaces, may be used to mimic biological structures. Cellulose nanocrystals (CNCs) are colloidally stable nanoparticles that self-assemble into chiral nematic (ChN) liquid crystalline mesophases. To date, the self-assembly of ChN mesophases of CNCs has been studied under confinement conditions within curved surfaces or under drying conditions that impose curvatures that can be exploited to control ChN ordering; however, their self-assembly has not been investigated in geometries with square cross-sections under static conditions. Here, we show that because of surface anchoring on perpendicular surfaces, the ChN CNC phase is unable to bend with the 90° angle of the square capillary under increasing confinement. Instead, the ChN phase forms radial layers in the shape of concentric squircle shells. With increasing layer distance from the capillary wall, the squircles transition into concentric cylinder shells. In larger capillaries, the radial shell layers appear as a continuous spiral pattern that engulfs fragmented ChN pseudolayers, a defect to accommodate the cylindrical confinement of the mesophase. These results are useful for understanding the fundamentals of self-assembling systems and development of new technologies.

Microfluidic synthesis of monodisperse and size-tunable CsPbBr3 supraparticles.

The highly controlled, microfluidic template-assisted self-assembly of CsPbBr3 nanocrystals into spherical supraparticles is presented, achieving precise control over average supraparticle size through the variation of nanocrystal concentration and droplet size; thus facilitating the synthesis of highly monodisperse, sub-micron supraparticles (with diameters between 280 and 700 nm).

A study across scales to unveil microstructural regimes in the multivalent metal driven self-assembly of cellulose nanocrystals.

Understanding the behaviour of self-assembled systems, from nanoscale building blocks to bulk materials, is a central theme for the rational design of high-performance materials. Herein, we revealed, at different length scales, how the self-assembly of TEMPO-oxidised cellulose nanocrystals (TOCNCs) into rod fractal gels is directed by the complexation of Fe3+ ions on the surface of colloidal particles. Different specificities in Fe3+ binding on the TOCNC surface and conformational changes of the nanocellulose chain were unveiled by paramagnetic NMR spectroscopy. The macroscopic properties of systems presenting different concentrations of TOCNCs and Fe3+ ions were investigated by rheology and microscopy, demonstrating the tunability of the self-assembly of cellulose nanorods driven by Fe3+ complexation. Near-atomistic coarse-grained molecular dynamics simulations were developed to gain microscopic insight into the behaviour of this colloidal system. We found that the formation of different self-assembled architectures is driven by metal-nanocellulose complexation combined with the attenuation of electrostatic repulsion and water structuration around cellulose, leading to different microstructural regimes, from isolated nanorods to disconnected rod fractal clusters and rod fractal gels. These findings lay the foundation to unlock the full potential of cellulose nanocrystals as sustainable building blocks to develop self-assembled materials with defined structural control for a range of advanced applications.

Enantioselective disruption of cellulose nanocrystal self-assembly into chiral nematic phases in D-alanine solutions.

The chiral environment of enantiomerically pure D-alanine solutions is observed to disrupt and modify the entropy-driven assembly of cellulose nanocrystals (CNCs) into a chiral nematic mesophase. The effect is specific to D-alanine and cannot be attributed to the adsorption of alanine molecules (neither D- nor L-alanine) onto the CNC particles.

Self-Assembled CuCo2S4 Nanoparticles for Efficient Chemo-Photothermal Therapy of Arterial Inflammation

Cardiovascular disease caused by atherosclerosis (AS) seriously affects human health. Photothermal therapy (PTT) brings hope to the diagnosis and treatment of AS, with the development of nanotechnology. To improve treatment efficiency, self-assembled CuCo2S4 nanocrystals (NCs) were developed as a drug-delivery nanocarrier, triggered by near-infrared (NIR) light for efficient chemophotothermal therapy of arterial inflammation. The as-prepared self-assembled CuCo2S4 NCs exhibited excellent biocompatibility and a very high chloroquine (CL)-loading content. In addition, the self-assembled CuCo2S4 NCs/CL nanocomposites showed good photothermal performance, due to strong absorption in the NIR region, and the release of CL from the NCs/CL nanocomposites was driven by NIR light. When illuminated by NIR light, both PTT from the NCs and chemotherapy from the CL were simultaneously triggered, resulting in killing macrophages with a synergistic effect. Moreover, chemo-photothermal therapy with CuCo2S4 NCs/CL nanocomposites showed an effective therapeutic effect for arterial inflammation, in vivo. Our work demonstrated that chemo-photothermal therapy could be a promising strategy for the treatment of arterial inflammation against atherosclerosis.

Controlling superstructure formation and macro-scale adhesion via confined evaporation of cellulose nanocrystals

The self-assembly of cellulose nanocrystals can tether their interfacial interactions and the associated properties of their constructs. For instance, assemblies of highly aligned cellulose nanocrystals (CNCs) bear improved mechanical strength, barrier properties, and piezoelectric response. In this study, the self-assembly of CNC superstructure was assessed under various confinement geometries, enabling optimization of the long-range order within the microstructures formed. The confinement involved the planar capillary (with a rectangular cross-section)formed between two glass substrates with silicone boundaries. The impact of temperature, width and thickness of the capillary plane on self-assembly of the micro-scaled lamellar structures was evaluated. Thinner capillaries and lower temperatures were found to considerably improve long-range order and increase the frequency of the periodic microstructures formed. The drying process was monitored by rheological analysis, which showed an initial fast drying followed by slow drying due to the hindered diffusion through lamellae. The adhesive properties of the formed superstructures were evaluated. The shear strength was shown to depend on the orientation of the superstructures and therefore of the CNCs. About 4 MPa adhesion strength was obtained when the lamellar superstructures were perpendicularly aligned with respect to the in-plane force applied, while ca. 3 MPa adhesion was obtained for parallel alignment. The experimental framework described herein enabled the evaluation of the impact of the dimensions of a drying meniscus on self-assembly of anisometric colloids while also linking cellulosic assemblies with their interfacial supramolecular interactions. This simple framework brings forward the possibility to correlate the behavior of nanometric objects with micro- and macro-scaled observations, e.g., macro-scaled mechanics of adhesion.

A miRNA-based gene therapy nanodrug synergistically enhances pro-inflammatory antitumor immunity against melanoma

MicroRNA (miRNA)-based gene therapy is a robust approach to treating human cancers. However, the low target specificity and safety issues associated with viral vectors have limited the clinical use of miRNA therapeutics. In the present study, we aimed to develop a biocompatible nanocarrier to deliver the tumor suppressor miR-30a-5p for gene therapy of ocular melanoma. The quasi-mesoporous magnetic nanospheres (MMNs) were prepared by polyelectrolytes-mediated self-assembling Fe3O4 nanocrystals; the cationic polymer capped quasi-mesoporous inner tunnels of the MMNs facilitate high miRNA loading and protect from nuclease degradation. Then, the outer layer of the MMNs was modified with a disulfide bond bridged very low molecular weight polyethyleneimine (PEI) network to form redox-responsive nanospheres (rMMNs) that enhance the miRNA payload and enable miRNA release under glutathione-dominant tumor microenvironment. The miR-30a-5p loaded rMMNs nanodrug (miR-30a-5p@rMMNs) upregulated miR-30a-5p level and inhibited malignant phenotypes of ocular melanoma by targeting the transcription factor E2F7 both in vitro and in vivo. Additionally, rMMNs act as an enhancer to increase cancer cell apoptosis by modulating M1-like macrophage polarization and activating Fenton reaction. Thus, the rMMNs is a promising miRNA carrier for gene therapy and could enhance pro-inflammatory immunity in melanoma and other cancers. Statement of significance• miR-30a-5p@rMMNs inhibited malignant phenotypes of ocular melanoma both in vitro and in vivo.• The rMMNs promoted M1 macrophage polarization thus synergistically enhancing pro-inflammatory anti-tumor immunity against melanoma.• The rMMNs showed no obvious toxicity under the injection dose.

WP Nanocrystals on N,P Dual-Doped Carbon Nanosheets with Deeply Analyzed Catalytic Mechanisms for Lithium–Sulfur Batteries

WP Nanocrystals on N,P Dual-Doped Carbon Nanosheets with Deeply Analyzed Catalytic Mechanisms for Lithium–Sulfur Batteries