Carbon nanodots (CNDs) are a class of green, photostable, luminescent nanomaterials with significant potential for optoelectronic applications.[1–9] However, their practical implementation is hampered by limited synthetic scalability, incompatibilit...
Carbon nanodots (CNDs) are a class of green, photostable, luminescent nanomaterials with significant potential for optoelectronic applications.[1–9] However, their practical implementation is hampered by limited synthetic scalability, incompatibility with functional soft material matrices, and the lack of controlled photoluminescence anisotropy. This dissertation addresses these fundamental challenges and demonstrates that anisotropic CNDs are viable electro-optical components for liquid-crystal-based photonic structures. Anisometric CNDs were synthesized through microwave-assisted carbonization of a calamitic nematic liquid-crystal precursor (5CB), yielding
nanoparticles that preserve the intrinsic shape anisotropy of their molecular template while exhibiting broad ultraviolet absorption, blue
photoluminescence, and exceptional dispersibility without requiring postsynthetic surface functionalization. The structural anisotropy and preferential π-domain orientation of these CNDs enable polarized visible emission when integrated into nematic host matrices, where their uniaxial alignment is governed by the host liquid-crystal director field. To realize multifunctional photonic materials, anisometric CNDs were incorporated within polymer network liquid crystals (PNLC), producing hybrid films with dual lightresponsive
functionality. These systems demonstrate electrically switchable light modulation between transparent (transmittance ≈ 93.1% and scattering
(transmittance ≈ 13.3%) states with ultrafast response kinetics (≈7.6 ms turnon,≈5.4 ms turn-off) alongside adjustable photoluminescence under ultraviolet excitation. Notably, the CNDs facilitate polymer network formation during photopolymerization, enabling efficient light scattering at ultralow polymer concentrations, a capability absent in CND-free controls. The synergistic alignment of CNDs with the nematic director produces linearly polarized photoluminescence with an emission dichroic ratio of ≈1.63, establishing direct structure-function relationships wherein particle anisotropy governs macroscopic photonic response. This work establishes a design paradigm for soft photonic materials through anisometric nanocarbon integration in liquid-crystal-templated architectures, enabling dualresponsive,
polarized, electrically switchable systems applicable to smart windows, adaptive optical shutters, ultraviolet-protection coatings, and
polarization-based security devices while providing fundamental insights into nanocarbon-enabled photoluminescence phenomena.