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This quantum mechanical study focuses on the designing of twelve (MPAM1–MPAM12) bithieno thiophene (BTTI) central core-based small molecules to explore optoelectronic properties as donor candidates for organic solar cells (OSCs) and hole transport materials (HTMs) accompanied by enhanced charge mobility for perovskite solar cells (PSCs). MPAM1–MPAM6 have been designed by the substitution of thiophene-bridged end-capped acceptors on both side terminals of reference (MPAR). MPAM7–MPAM12 are tailored by adopting the same tactic on one side terminal only. MPW1PW91/6-311G (d,p) has been employed for all computational simulations. MPAM12 revealed the highest λmax at 639 nm in dichloromethane (DCM) solvent with the lowest Eg of 1.78 eV and dipole moment (20.74 D) in the solvent phase, showing excellent miscibility as compared to the reference. All designed chromophores (MPAM1–MPAM12) demonstrated higher estimated VOC and power conversion efficiency (PCE) when compared to MPAR, suggesting their prominent operational efficiency. Among all, MPAM4 manifested the highest PCE (47.86%). MPAM2 portrayed the highest electron mobility (0.0041573 eV) and MPAM3 exhibited the highest hole mobility (0.0047178 eV). The outcomes highlight the adequacy of the planned strategies, paving a new route for the development of small-molecule HTMs for PSCs and donor contributors for OSCs.

Gas sensors are widely used for detection of environmental pollution caused by various environmental factors such as road traffic and combustion of fossil fuels. Nitrogen dioxide (NO2) is one of the leading pollutants of the present age, which causes a number of serious health issues including acute bronchitis, cough, and phlegm, particularly in children. Nowadays, researchers are focused on designing new sensor materials for detection and removal of NO2 from the environment. In this line, we have made an attempt to design NO2 sensing materials by using theoretical techniques. Here, we have reported decoration of Mg12O12 nanoclusters with a late transition metal (Cu) by employing density functional theory at the B3LYP/6-31G(d,p) basis set. The decoration of metal on Mg12O12 gives two geometries (M1 and M2) with adsorption energies of -363.81 and -384.09 kJ/mol, respectively. Adsorption of NO2 on pristine Mg12O12 expressed an adsorption energy value of -62.36 kJ/mol. Adsorption of NO2 on Cu-decorated Mg12O12 nanocages delivered two geometries (N1 and N2) with adsorption energies of -442.56 and -447.64 kJ/mol. Metal-decorated Mg12O12 nanoclusters offer better adsorption of NO2 as compared to pristine Mg12O12 . Adsorption of NO2 on Cu-Mg12O12 nanoclusters also causes narrowing of band gap of magnesium oxide nanoclusters. Large dipole moment, high QNBO with large electrophilic index in NO2-Cu-Mg12O12 nanoclusters suggested that metal-decorated Mg12O12 nanoclusters are efficient candidates for NO2 adsorption. Different geometric parameters and results of global reactivity descriptors show that NO2-Cu-Mg12O12 nanoclusters are quite stable in nature with least reactivity. Thus, conceptualized systems are potential candidates for applications in NO2 sensing materials.