4.8 Article

Achiral Nanoparticle-Enhanced Chiral Twist and Thermal Stability of Blue Phase Liquid Crystals

期刊

ACS NANO
卷 16, 期 12, 页码 20577-20588

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c07321

关键词

liquid crystals; blue phases; gold nanoparticles; ligands; Bragg reflection; thermal stabilization

资金

  1. CB POB FOTECH-2 of the Warsaw University of Technology within the Excellence Initiative: Research University (IDUB) program
  2. National Science Center Poland [UMO-2019/35/B/ST5/04488, UMO-2019/35/B/ST5/04232, UMO-2019/35/B/ST3/04147 (07-079)]
  3. Polish Ministry of Education and Science [0112/DIA/2019/48]
  4. Military University of Technology [UGB 22-796]
  5. Ministry of Science and Technology, Taiwan [MOST 111-2628-E-110-001-MY2]
  6. nternational Visegrad Fund under the Visegrad-Taiwan [52190022]
  7. Scientific Council for Physics of the Warsaw University of Technology

向作者/读者索取更多资源

It has been demonstrated that small achiral gold nanoparticles (Au NPs) decorated with liquid crystal-like ligands can enhance the chiral twist and thermal stability of blue phase liquid crystals (BPLCs). The functionalization of Au NPs plays a critical role in the phase sequence of BPLCs.
Blue phase liquid crystals (BPLCs) are chiral mesophases with 3D order, which makes them a promising template for doping nanoparticles (NPs), yielding tunable nanomaterials attractive for microlasers and numerous microsensor applications. However, doping NPs to BPLCs causes BP lattice extension, which translates to elongation of operating wavelengths of light reflection. Here, it is demonstrated that small (2.4 nm diameter) achiral gold (Au) NPs decorated with designed LC-like ligands can enhance the chiral twist of BPLCs (i.e., reduce cell size of the single BP unit up to similar to 14% and similar to 7% for BPI and BPII, respectively), translating to a blue-shift of Bragg reflection. Doping NPs also significantly increases the thermal stability of BPs from 5.5 degrees C (for undoped BPLC) up to 22.8 degrees C (for doped BPLC). In line with our expectations, both effects are saturated, and their magnitude depends on the concentration of investigated nanodopants as well the BP phase type. Our research highlights the critical role of functionalization of Au NPs on the phase sequence of BPLCs. We show that inappropriate selection of surface ligands can destabilize BPs. Our BPLC and Au NPs are photochemically stable and exhibit great miscibility, preventing NP aggregation in the BPLC matrix over the long term. We believe that our findings will improve the fabrication of advanced nanomaterials into 3D periodic soft photonic structures.

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