Quantum chemical study of new oxadiazoles as efficient optical and nonlinear optical and photovoltaic materials under gas, PCM and COSMO solvent effects

Abstract

The science of organic optical and nonlinear optical (NLO) materials has been captivating the scientific community owing to their extensive applications in optoelectronics, OLEDs, and telecommunications. This study presents the design and investigation of novel organic compounds of pyrene and 1,3,4-oxadiazole derivatives (1-oxza to 6-oxza), featuring various push–pull combinations. Quantum chemical calculations were employed to determine linear polarizabilities (α) and third-order NLO polarizabilities (γ). Notably, the largest average third-order NLO polarizability value was found to be 254.9 × 10⁻³⁶ esu for the finely tuned push–pull system 6-oxza, which is ∼35 times greater than that of the prototype NLO molecule of p-nitroaniline (p-NA). Among the derivatives, 1-oxza exhibits the highest linear isotropic polarizability (α_iso) value of 61.59 × 10⁻²⁴ esu, while 5-oxza displays the highest linear anisotropic polarizability (α_aniso) value of 60.09 × 10⁻²⁴ esu. A notable increase of approximately ∼1 to ∼2 times in < γ > is observed for selected compounds (1-oxza, 4-oxza, 6-oxza), indicating that the Conductor-like Screening Model (COSMO) overestimates the values compared to the polarizable continuum model (PCM) and gas phases. Solvent significantly enhances third-order NLO polarizability amplitudes depending upon solvent polarity and strength of substitution groups. We calculated the frequency-dependent third-order NLO polarizability of 6-oxza at laser wavelengths ranging from 1400 to 1970 nm. The second hyperpolarizability EFISHG process (γ(−2ω; ω, ω, 0)) was calculated at a laser wavelength of 1400 nm, and the γ-amplitude was found to be 400.1 × 10⁻³⁶ esu. The remarkable hyperpolarizability response in the gas phase is corroborated by TD-DFT calculations, which reveal a larger transition dipole moment of 3.062 and a lower transition energy of 3.780 eV as origin of larger hyperpolarizability for 6-oxza. A comprehensive analysis was performed based on FMOs for designed compounds to elucidate the intramolecular charge transfer (ICT) mechanisms and observed a notable reduction in energy band gap 4.89 eV for 6-oxza, which is responsible for enhanced NLO response. Additionally, DOS maps revealed the quantitative contributions of HOMOs and LUMOs for crucial electronic states related to the efficient ICT process. Additionally, we analyzed the photovoltaic properties and found that 6-oxza has the highest dye regeneration and the lowest open-circuit voltages of 1.89 eV and 2.22 eV, respectively. Our designed model compounds can put real-time such compounds under spotlight of scientific interests which seeks more efficient optical and NLO properties.