Cholesteric liquid crystals (CLCs), also known as chiral nematic LCs, show a photonic stopband, which is promising for various optical applications. In particular, CLCs confined in microcompartments are useful for sensing, lasing, and optical barcoding at the microscale. The integration of distinct CLCs into single microstructures can provide advanced functionality. In this work, CLC multishells with multiple stopbands are created by liquid-liquid phase separation (LLPS) in a simple yet highly controlled manner. A homogeneous ternary mixture of LC, hydrophilic liquid, and co-solvent is microfluidically emulsified to form uniform oil-in-water drops, which undergo LLPS to form onion-like drops composed of alternating CLC-rich and CLC-depleted layers. The multiplicity is controlled from one to five by adjusting the initial composition of the ternary mixture, which dictates the number of consecutive steps of LLPS. Interestingly, the concentration of the chiral dopant becomes reduced from the outermost to the innermost CLC drop due to uneven partitioning during LLPS, which results in multiple stopbands. Therefore, the photonic multishells show multiple structural colors. In addition, dye-doped multishells provide band-edge lasing at two different wavelengths. This new class of photonic multishells will provide new opportunities for advanced optical applications.

Download full-text PDF

Source
http://dx.doi.org/10.1002/adma.202002166DOI Listing

Publication Analysis

Top Keywords

photonic multishells
12
cholesteric liquid
8
liquid crystals
8
phase separation
8
optical applications
8
multishells multiple
8
multiple stopbands
8
ternary mixture
8
photonic
4
multishells composed
4

Similar Publications

Engineering of hollow particles with tunable internal structures often requires complicated processes and/or invasive cleavage. Halogen-bond driven 3D confined-assembly of block copolymers has shed light on the engineering of polymer organization along with the fabricating of unique nanostructures. Herein, a family of multilevel hollow-structured particles (e.

View Article and Find Full Text PDF

Fluorine Doping Mediated Epitaxial Growth of NaREF on TiO for Boosting NIR Light Utilization in Bioimaging and Photodynamic Therapy.

Angew Chem Int Ed Engl

October 2024

Department of Chemistry, Shanghai Stomatological Hospital & School of Stomatology, State Key Laboratory of Molecular Engineering of Polymers, iChem (Collaborative Innovation Center of Chemistry for Energy Materials), Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai, 200433, China.

By integrating TiO with rare earth upconversion nanocrystals (NaREF), efficient energy transfer can be achieved between the two subunits under near-infrared (NIR) excitation, which hold tremendous potential in the fields of photocatalysis, photodynamic therapy (PDT), etc. However, in the previous studies, the combination of TiO with NaREF is a non-epitaxial random blending mode, resulting in a diminished energy transfer efficiency between the NaREF and TiO. Herein, we present a fluorine doping-mediated epitaxial growth strategy for the synthesis of TiO-NaREF heteronanocrystals (HNCs).

View Article and Find Full Text PDF

Strategy to Achieve a Pure Red/Green/Blue-Emitting Upconversion Luminescence for Full-Color Displays.

ACS Appl Mater Interfaces

July 2024

Materials Architecturing Research Center, Korea Institute of Science and Technology, 5, Hwarang-ro 14-gil, Seongbuk-gu, Seoul 02792, Republic of Korea.

Multicolor tunable upconversion nanoparticles (UCNPs) have garnered attention owing to their diverse applications such as displays, imaging, and security. Typically, achieving multicolor emission from UCNPs requires complicated core/multishell nanostructures comprising a core with at least five shells. Here, we propose a strategy to achieve bright and orthogonal red (R), green (G), and blue (B) upconversion (UC) luminescence without synthesizing complicated core/quintuple-shell or core/sextuple-shell nanostructures.

View Article and Find Full Text PDF

Multishell Silver Indium Selenide-Based Quantum Dots and Their Poly(methyl methacrylate) Composites for Application in Red-Light-Emitting Diodes.

ACS Appl Mater Interfaces

July 2024

School of Chemistry, CRANN and AMBER Research Centres, Trinity College Dublin, College Green, Dublin 2 D02 PN40, Ireland.

In this work, the production of novel multishell silver indium selenide quantum dots (QDs) shelled with zinc selenide and zinc sulfide through a multistep synthesis precisely designed to develop high-quality red-emitting QDs is explored. The formation of the multishell nanoheterostructure significantly improves the photoluminescence quantum yield of the nanocrystals from 3% observed for the silver indium selenide core to 27 and 46% after the deposition of the zinc selenide and zinc sulfide layers, respectively. Moreover, the incorporation of the multishelled QDs in a poly(methyl methacrylate) (PMMA) matrix via in situ radical polymerization is investigated, and the role of thiol ligand passivation is proven to be fundamental for the stabilization of the QDs during the polymerization step, preventing their decomposition and the relative luminescence quenching.

View Article and Find Full Text PDF

Lanthanide-doped nanocrystals that convert near-infrared (NIR) irradiation into shorter wavelength emission (ultraviolet-C) offer many exciting opportunities for biomedicine, bioimaging, and environmental catalysis. However, developing lanthanide-doped nanocrystals with high UVC brightness for efficient photocatalysis is a formidable challenge due to the complexity of the multiphoton process. Here, we report a series of heterogeneous core-multishell structures based on a co-sensitization strategy with multi-band enhanced emission profiles under 980 nm excitation.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!