Search

Defects and disorder work as controlling parameters to alter the electronic structure of nanostructures and significantly influence their electronic, magnetic, and nonlinear optical (NLO) properties. In this study, we found that defect engineering is an effective strategy for tailoring the linear and nonlinear optical properties of Cu-doped titanium oxide (TiO2) flower-shaped nanostructures. The concentration of chemical doping of Cu in the TiO2 lattice creates intermediate defect states that impact electronic bandgap reduction and tunable defect luminescence. The estimation of the bandgap from density functional theory calculation follows the same trend of bandgap narrowing with Cu doping. The XPS study reveals that oxygen defects are responsible for bandgap narrowing and quenching of the PL intensity. A single-beam Z-scan technique with open and closed aperture configurations using ultrashort pulses centered at 532 nm excitation wavelength was used to study the NLO measurements. The open aperture reveals saturable absorption, whereas the closed aperture shows self-focusing behavior. The nonlinear absorption coefficient and refractive index extracted from NLO measurements demonstrate the linear dependence on the defect concentration and bandgap. The effects of heterogeneous dopants and lattice disorder on the nonlinear absorption behavior of these nanostructures are discussed in comparison with the figure of merit, non-linear refractive index, and absorption coefficient. The tunable NLO properties achieved by controlling such dopant-induced defects boost the scope of these nanostructures as optical limiting, optical switching, and optical photodiode applications. [ABSTRACT FROM AUTHOR]

We report temperature-dependent photoluminescence (PL) in the temperature range between 77 K and 300 K, and room temperature nonlinear optical (NLO) properties of solution processed lead-free Cs2NaBiI6 (CNBI) and Cs2KBiI6 (CKBI) perovskite films. The de-convolution analysis of temperature-dependent PL spectra showed thermal quenching behavior of free-exciton (FX) emission, an unusual blue-shift of PL emission, and line broadening with increasing temperature as a consequence of strong exciton–phonon interaction. The nonlinear refractive index (n2) and nonlinear absorption coefficient (β) of both the CNBI and CKBI films are determined using a closed aperture (CA) and open aperture (OA) Z-scan technique, respectively. Both the CNBI and CKBI perovskites exhibited features of saturable absorption (SA) with β ∼ −6.23 × 10−12 cm W−1, and −1.14× 10−12 cm W−1, respectively. The CA measurements depicted a self-defocusing effect in both the samples with n2 values ∼−1.06 × 10−14 cm2 W−1 and −1.337× 10−14 cm2 W−1, respectively. With such emission and NLO characteristics, CNBI and CKBI perovskite films can be used for designing eco-friendly optoelectronic and NLO devices. [ABSTRACT FROM AUTHOR]

Three-coordinated organoboron fluorophores bearing 3,5-diphenyl pyrazoles have been synthesized. The pyrazole anchored boron fluorophores show selective fluorescence quenching response to trinitrophenol (or) picric acid (PA) and have the ability to discriminate picric acid over other analytes. We investigated nonlinear optical (NLO) properties of these three-coordinated organoboron compounds (in solutions) in the presence and absence of PA. In absence of PA, the two-photon-absorption coefficient (β) of organoboron fluorophores exhibits a variation from 2 × 10−12 cm W−1 to 4 × 10−12 cm W−1. The results also reveal that the NLO characteristics of organoboron fluorophores exhibit a discernible variation with PA addition which has correlations with quenching observed in fluorescence measurements. [ABSTRACT FROM AUTHOR]

Intramolecular B ← N coordinated fluorophores have shown potential applications in optoelectronics and as sensors due to their unique photophysical properties. In this work, we report the synthesis and characterization of π-conjugated boron doped phenanthroimidazole dimers. All the π-conjugated B ← N coordinated phenanthroimidazole dimers exhibited high quantum yields in solution (up to 99%) and moderate quantum yields in the solid state (up to 51%). We investigated the nonlinear optical properties of phenanthroimidazole dimers and found that the measurement of two-photon-absorption cross-section is correlated with the conjugation length. [ABSTRACT FROM AUTHOR]

A series of triaryl pyrazole B ← N coordinate dimers with different π-conjugated (spacer) bridges (compound 4 (no spacer); compound 7 (2,5-bis(hexyloxy)benzene); compound 8 (9,9-dihexyl-9H-fluorene); compound 9 (9-hexyl-9H-carbazole); compound 10 (thiophene); compound 11 (2,2′-bithiophene)) has been synthesized from simple triaryl pyrazoles. Three different synthetic protocols were applied to synthesize the desired B ← N coordinate pyrazole dimers. All the B ← N coordinate pyrazole dimers exhibit absorption maxima between 337 and 399 nm with good molar absorption coefficients (12 000 to 22 100 M−1 cm−1 in CH2Cl2). They are highly emissive in the solution state with quantum yields of up to 0.94. Due to a substantial change in the excited state dipole moment, B ← N coordinate pyrazole dimers exhibit versatile and appreciably large nonlinear optical (NLO) properties. The dimer symmetry and the presence of donor or acceptor moieties affect the two-photon-absorption (TPA) cross-section substantially. In addition, the investigation reveals that the dimer π-conjugation length in all dimer variants has a remarkable impact on the NLO characteristics. [ABSTRACT FROM AUTHOR]

Defects and disorder work as controlling parameters to alter the electronic structure of nanostructures and significantly influence their electronic, magnetic, and nonlinear optical (NLO) properties. In this study, we found that defect engineering is an effective strategy for tailoring the linear and nonlinear optical properties of Cu-doped titanium oxide (TiO 2 ) flower-shaped nanostructures. The concentration of chemical doping of Cu in the TiO 2 lattice creates intermediate defect states that impact electronic bandgap reduction and tunable defect luminescence. The estimation of the bandgap from density functional theory calculation follows the same trend of bandgap narrowing with Cu doping. The XPS study reveals that oxygen defects are responsible for bandgap narrowing and quenching of the PL intensity. A single-beam Z-scan technique with open and closed aperture configurations using ultrashort pulses centered at 532 nm excitation wavelength was used to study the NLO measurements. The open aperture reveals saturable absorption, whereas the closed aperture shows self-focusing behavior. The nonlinear absorption coefficient and refractive index extracted from NLO measurements demonstrate the linear dependence on the defect concentration and bandgap. The effects of heterogeneous dopants and lattice disorder on the nonlinear absorption behavior of these nanostructures are discussed in comparison with the figure of merit, non-linear refractive index, and absorption coefficient. The tunable NLO properties achieved by controlling such dopant-induced defects boost the scope of these nanostructures as optical limiting, optical switching, and optical photodiode applications.

Three-coordinated organoboron fluorophores bearing 3,5-diphenyl pyrazoles have been synthesized. The pyrazole anchored boron fluorophores show selective fluorescence quenching response to trinitrophenol (or) picric acid (PA) and have the ability to discriminate picric acid over other analytes. We investigated nonlinear optical (NLO) properties of these three-coordinated organoboron compounds (in solutions) in the presence and absence of PA. In absence of PA, the two-photon-absorption coefficient (β) of organoboron fluorophores exhibits a variation from 2 × 10-12 cm W-1 to 4 × 10-12 cm W-1. The results also reveal that the NLO characteristics of organoboron fluorophores exhibit a discernible variation with PA addition which has correlations with quenching observed in fluorescence measurements.

Intramolecular B ← N coordinated fluorophores have shown potential applications in optoelectronics and as sensors due to their unique photophysical properties. In this work, we report the synthesis and characterization of π-conjugated boron doped phenanthroimidazole dimers. All the π-conjugated B ← N coordinated phenanthroimidazole dimers exhibited high quantum yields in solution (up to 99%) and moderate quantum yields in the solid state (up to 51%). We investigated the nonlinear optical properties of phenanthroimidazole dimers and found that the measurement of two-photon-absorption cross-section is correlated with the conjugation length.