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Functionally graded materials (FGMs) have spatial variations in structure or composition that result in gradients in their mechanical, thermal, swelling, or other properties. FGMs have garnered significant research interest because of their extensive applications in areas such as biomedical implants, sensors, and soft robotics. Recently, grayscale photopolymerization 3D printing has emerged as a promising technology for crafting complex and high‐resolution FGMs. This comprehensive work delves into various grayscale photopolymerization 3D printing techniques, offering insights into their ability to precisely control printing exposure energy and polymerization degree, which in turn influence material properties. Furthermore, this work highlights diverse applications of grayscale vat‐photopolymerization 3D printing. Finally, it offers perspectives on ways to enhance grayscale photopolymerization 3D printing, with a focus on improving printing feedstocks and grayscale strategies. [ABSTRACT FROM AUTHOR]

The optoelectronic properties of semiconductor nanoparticles make them valuable candidates for the long-term monitoring of transmembrane electric fields in excitable cells. In this work, we show that the electric field sensitivity of the fluorescence intensity of type-I and quasi-type-II quantum dots and quantum rods is enhanced under two-photon excitation compared to single-photon excitation. Based on the superior electric field sensitivity of the two-photon excited fluorescence, we demonstrate the ability of quantum dots and rods to track fast switching E-fields. These findings indicate the potential of semiconductor nanoparticles as cellular voltage probes in multiphoton imaging.

An original series of bipyrimidine‐based chromophores featuring alkoxystyryl donor groups bearing short chiral (S)‐2‐methylbutyl chains in positions 4, 3,4 and 3,5, connected to electron‐accepting 2,2‐bipyrimidine rings, has been developed. Their linear and non‐linear optical properties were studied using a variety of techniques, including one‐ and two‐photon absorption spectroscopy, fluorescence measurements, as well as Hyper‐Rayleigh scattering to determine the first hyperpolarizabilities. Their electronic and geometrical properties were rationalized by TD‐DFT calculations. The thermal properties of the compounds were also investigated by a combination of polarized light optical microscopy, differential scanning calorimetry measurements and small‐angle X‐ray scattering experiments. The derivatives were found not to have mesomorphic properties, but to exhibit melting temperatures or cold crystallization behavior that enabled the isolation of well‐organized thin films. The nonlinear optical properties of amorphous or crystalline thin films were studied by wide‐field second harmonic generation and multiphoton fluorescence imaging, confirming that non‐centrosymmetric crystal organization enables strong second and third harmonic generation. This new series confirms that our strategy of functionalizing 3D organic octupoles with short chiral chains to generate non‐centrosymmetric organized thin films enables the development of highly second order nonlinear optical active materials without the use of corona‐poling or tedious deposition techniques. [ABSTRACT FROM AUTHOR]

New phenyl and stilbene-bridged polyoxometalate (POM) charge-transfer chromophores with diphenylamino donor groups produce, respectively, the highest intrinsic and absolute quadratic hyperpolarisabilities measured for such species. The β0,zzz obtained for the phenyl bridge – at 180 × 10−30 esu – is remarkable for a short conjugated system while changing to the stilbene (260 × 10−30 esu) produces a substantial increase in non-linearity for a minimal red-shift in the absorption profile. Together with TD-DFT calculations, the results show that maximising conjugation in the π-bridge is vital to high performance in such "POMophores". [ABSTRACT FROM AUTHOR]

This work reports the first example of a single-chain protein computationally designed to contain four α-helical segments and fold to form a four-helix bundle encapsulating a supramolecular abiological chromophore that possesses exceptional nonlinear optical properties. The 109-residue protein, designated SCRPZ-1, binds and disperses an insoluble hyperpolarizable chromophore, ruthenium(II) [5-(4'-ethynyl-(2,2';6',2″-terpyridinyl))-10,20-bis(phenyl)porphinato]zinc(II)-(2,2';6',2″-terpyridine)(2+) (RuPZn) in aqueous buffer solution at a 1:1 stoichiometry. A 1:1 binding stoichiometry of the holoprotein is supported by electronic absorption and circular dichroism spectra, as well as equilibrium analytical ultracentrifugation and size exclusion chromatography. SCRPZ-1 readily dimerizes at micromolar concentrations, and an empirical redesign of the protein exterior produced a stable monomeric protein, SCRPZ-2, that also displayed a 1:1 protein:cofactor stoichiometry. For both proteins in aqueous buffer, the encapsulated cofactor displays photophysical properties resembling those exhibited by the dilute RuPZn cofactor in organic solvent: femtosecond, nanosecond, and microsecond time scale pump-probe transient absorption spectroscopic data evince intensely absorbing holoprotein excited states having large spectral bandwidth that penetrate deep in the near-infrared energy regime; the holoprotein electronically excited triplet state exhibits a microsecond time scale lifetime characteristic of the RuPZn chromophore. Hyper-Rayleigh light scattering measurements carried out at an incident irradiation wavelength of 1340 nm for these holoproteins demonstrate an exceptional dynamic hyperpolarizabilty (β1340 = 3100 × 10(-30) esu). X-ray reflectivity measurements establish that this de novo-designed hyperpolarizable protein can be covalently attached with high surface density to a silicon surface without loss of the cofactor, indicating that these assemblies provide a new approach to bioinspired materials that have unique electro-optic functionality.

In this review, we summarize the latest developments in research specifically derived from the unique properties of hollow microspheres, in particular, hollow silica spheres with uniform shells. We focus on applications in nanosphere (colloidal) lithography and nanophotonics. The lithography from a layer of hollow spheres can result in nanorings, from a multilayer in unique nano-architecture. In nanophotonics, disordered hollow spheres can result in antireflection coatings, while ordered colloidal crystals (CCs) of hollow spheres exhibit unique refractive index enhancement upon infiltration, ideal for optical sensing. Furthermore, whispering gallery mode (WGM) inside the shell of hollow spheres has also been demonstrated to enhance light absorption to improve the performance of solar cells. These applications differ from the classical applications of hollow spheres, based only on their low density and large surface area, such as catalysis and chemical sensing. We provide a brief overview of the synthesis and self-assembly approaches of the hollow spheres. We elaborate on their unique optical features leading to defect mode lasing, optomicrofluidics, and the existence of WGMs inside shell for light management. Finally, we provide a perspective on the direction towards which future research relevant to hollow spheres might be directed.

New synthesized bipyrimidine‐based chromophores presenting alkoxystyryl donor groups carrying aliphatic achiral and chiral chains in the 4 position, connected to electron‐accepting 2,2‐bipyrimidine cores have been synthesized. Their linear and nonlinear optical (NLO) properties were investigated as well as their mesomorphic properties by various techniques (light‐transmission measurements, polarized‐light optical microscopy, differential scanning calorimetry measurements and two‐photon excited fluorescence). The derivatives with achiral linear carbon chains were found to exhibit liquid‐crystal properties with the formation smectic phases over large temperature ranges, which were confirmed by small‐angle X‐ray scattering analysis via stacking models. The nonlinear optical properties in the solid state for derivatives with C14 and the citronellol chains have been studied by wide‐field second‐harmonic generation and multi‐photon fluorescence imaging, confirming centrosymmetry for these achiral mesogens and their excellent third‐order nonlinearity whereas the chiral compound exhibits non‐centrosymmetric organization resulting in a strong Second Harmonic Generation at the crystal state. [ABSTRACT FROM AUTHOR]

The question of size economy in the design of chromophores for nonlinear optics is addressed in this investigation. We have synthesized directly linked donor–acceptor dyads, which lack a π-conjugated linker, the presence of which is usually considered obligatory in materials designed for nonlinear optics. Correlating linear optical data, electrochemical data, computational data and hyper Rayleigh scattering (HRS) data on ferrocene (Fc) based dyads, we demonstrate that the first hyperpolarizability of such size economical chromophores is significantly better compared to that of Fc based, traditional, larger, donor–π–acceptor chromophores. Arguably, a larger π-conjugated linker decreases the electronic communication between the donor and the acceptor and weakens the intramolecular charge transfer in such chromophores. [ABSTRACT FROM AUTHOR]