The influence of various experimental parameters on the vertical deposition and structure formation of colloidal crystals on chemically patterned surfaces, with hydrophilic and hydrophobic areas, was investigated. The pattern dimensions range from about 4 to 400 microm, which is much larger than the individual particle size (255 nm), to control the microscopic crystal shape rather than influencing the crystal lattice geometry (as achieved in colloidal epitaxy). The deposition resolution and selectivity were tested by varying the particle concentration in the suspension, the substrate withdrawing speed, pattern size and orientation, and wetting contrast between the hydrophilic and hydrophobic regions. The evolution of colloidal crystal thickness with respect to the pattern dimensions and deposition parameters was further studied. Our results show that the pattern size has a rather strong influence on the deposited number of colloid layers and on the crystal quality. Better results are obtained when the lines of a stripe pattern are oriented parallel to the withdrawing direction rather than perpendicular. The deposition resolution (defined as the minimum feature size on which particles can be deposited) depends on the wetting contrast and increases with lower average hydrophobicity of the substrate.
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http://dx.doi.org/10.1021/la0489413 | DOI Listing |
Phys Rev Lett
December 2024
Department of Physics, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong, China.
The morphology and kinetics of the crystal growth front have been poorly explored at the particle level. Here, we experimentally observe the crystal growth front in liquid with single-particle kinetics using colloid systems and reveal a surface layer of polymorphic crystal near the solid-solid transition when the two crystals form a low-energy coherent interface. The thickness of the surface crystal can exceed 50 particles and grows logarithmically with the temperature as approaching the solid-solid transition which follows premelting theory.
View Article and Find Full Text PDFJ Chem Phys
January 2025
Department of Chemistry, Indian Institute of Science Education and Research (IISER) Tirupati, Tirupati, Andhra Pradesh 517619, India.
Although impurities are unavoidable in real-world and experimental systems, most numerical studies on nucleation focus on pure (impurity-free) systems. As a result, the role of impurities in phase transitions remains poorly understood, especially for systems with complex free energy landscapes featuring one or more intermediate metastable phases. In this study, we employed Monte Carlo simulations to investigate the effects of static impurities (quenched disorder) of varying length scales and surface morphologies on the crystal nucleation mechanism and kinetics in the Gaussian core model system-a representative model for soft colloidal systems.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Huaqiao University College of Materials Science and Engineering, No.668 Jimei Avenue, Xiamen, Fujian, 361021, Xiamen, CHINA.
The advancement of tin-based perovskite solar cells (TPSCs) has been severely hindered by the poor controllability of perovskite crystal growth and the energy level mismatch between the perovskite and fullerene-based electron transport layer (ETL). Here, we synthesized three cis-configured pyridyl-substituted fulleropyrrolidines (PPF), specifically 2-pyridyl (PPF2), 3-pyridyl (PPF3), and 4-pyridyl (PPF4), and utilized them as precursor additives to regulate the crystallization kinetics during film formation. The spatial distance between the two pyridine groups in PPF2, PPF3, and PPF4 increases sequentially, enabling PPF4 to interact with more perovskite colloidal particles.
View Article and Find Full Text PDFLangmuir
January 2025
State Key Laboratory of Digital Medical Engineering, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, People's Republic of China.
The protein carrier and encapsulation system based on polyelectrolytes plays crucial roles in drug research and development. Traditional methods such as isothermal titration calorimetry and molecular dynamics simulation have illuminated parts of this complex relationship. However, they fall short of capturing the full picture of the interaction during the carrier's fabrication and protein loading dynamics.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Institute of Chemistry, CAS, Laboratory of Colloid and Interface Scie, Zhong Guancun, 100080, Beijing, CHINA.
Here, we report the synthesis and self-assembly of a novel chiral 2,3:6,7‒naphthalenediimide-based triangular macrocycle (NDI-∆) and their chiroptical properties. The enantiomeric NDI-∆ is synthesized by condensation of (RR) or (SS)-trans-1,2-cyclohexanediamine and 2,3,6,7-naphthalenetetracarboxylic 2,3:6,7-dianhydride, in which the chirality of the macrocycles is controlled by the diamine. With the rigid outer π-surface, the macrocycle showed unique chiroptical properties and self-assembly modes.
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