Transition Metal-Decorated Mg12O12 Nanoclusters as Biosensors and Efficient Drug Carriers for the Metformin Anticancer Drug.

Drug carriers have been designed and investigated remarkably due to their effective use in the modern medication process. In this study, the decoration of the Mg12O12 nanocluster has been done with transition metals (Ni and Zn) for effective adsorption of metformin (anticancer drug). Decoration of Ni and Zn on a nanocluster allows two geometries, and similarly, the adsorption of metformin also provides two geometries. Density functional theory and time-dependent density functional theory have been employed at the B3LYP with 6-311G(d,p) level. The decoration of Ni and Zn offers good attachment and detachment of the drug, which is observed from their good adsorption energy values. Further, the reduction in the energy band gap is noted in the metformin-adsorbed nanocluster, which allows high charge transfer from a lower energy level to a high energy level. The drug carrier systems show an efficient working mechanism in a water solvent with the visible-light absorption range. Natural bonding orbital and dipole moment values suggested that the adsorption of the metformin causes charge separation in these systems. Moreover, low values of chemical softness with a high electrophilic index recommended that these systems are naturally stable with the least reactivity. Thus, we offer novel kinds of Ni- and Zn-decorated Mg12O12 nanoclusters as efficient carriers for metformin and also recommend them to experimentalists for the future development of drug carriers.

Designing efficient A-D-A1-D-A type fullerene free acceptor molecules with enhanced power conversion efficiency for solar cell applications.

The achievement of highly efficient power conversion efficiency (PCE) is a big concern for non-fullerene organic solar cells (NF-OSCs) because PCE can depend on numerous variables. Here, new five novel acceptor molecules without fullerenes were developed and investigated using DFT (density functional theory) and TD-DFT (time dependent-density functional theory). Compared to the recently synthesized molecule (PZ-dIDTC6), the developed molecules display a narrow optical band gap, exhibiting a red shift in the absorption spectrum. The developed molecules (YM1-YM5) express high mobility of electrons and holes in the active layer of OSCs (organic solar cells). In addition, high open-circuit voltage (Voc) values with maximum charge density shifting are noted in designed molecules. YM1-YM5 is also associated with low binding energy and excitation energy. This work proves that noncovalent conformational locking is favourable for improving PCE devices.

Nonfullerene Near-Infrared Sensitive Acceptors "Octacyclic Naphtho[1,2-b:5,6-b] Dithiophene Core" for Organic Solar Cell Applications: In Silico Molecular Engineering.

End-capped modification is an efficient approach for enhancing the power conversion efficiency of organic solar cells (OSCs). Herein, five novel acceptor molecules have been designed by end-capper modification of the recently synthesized molecule NTIC (R). Different geometric and photovoltaic properties like frontier molecular orbital analysis, absorption maximum, transition density matrix analysis, reorganizational energy, binding energy, oscillator strength, energy of excitation, and charge transfer analysis of designed and reference molecules have been computed by employing density functional theory and time-dependent density functional theory. Designed molecules expressed a narrow energy band gap (E g) with red-shifting in the absorption spectrum. Additionally, low excitation and binding energies are also noted in designed molecules. Excellent values of hole and electron reorganizational energies suggested that designed molecules are effective contributors to the development of the active layer of the organic solar cells. Further, a complex study is also performed for evaluation of charge transfer between the acceptor molecule and the donor polymer. Results of all analyses recommended that designed molecules are effective candidates for high-performance organic solar cell applications.

A Theoretical Framework of Zinc-Decorated Inorganic Mg12O12 Nanoclusters for Efficient COCl2 Adsorption: A Step Forward toward the Development of COCl2 Sensing Materials.

Gas sensors are widely explored due to their remarkable detection efficiency for pollutants. Phosgene is a toxic gas and its high concentration in the environment causes some serious health problems like swollen throat, a change in voice, late response of nervous systems, and many more. Therefore, the development of sensors for quick monitoring of COCl2 in the environment is the need of the time. In this aspect, we have explored the adsorption behavior of late transition metal-decorated Mg12O12 nanoclusters for COCl2. Density functional theory at the B3LYP/6-31G(d,p) level is used for optimization, frontier molecular orbital analysis, dipole moment, natural bonding orbitals, bond lengths, adsorption energies, and global reactivity descriptor analysis. Decoration of Zn on pure Mg12O12 delivered two geometries named as Y1 and Y2 with adsorption energy values of -388.91 and -403.11 kJ/mol, respectively. Adsorption of COCl2 on pure Mg12O12 also delivered two geometries (X1 and X2) with different orientations of COCl2. The computed adsorption energy values of X1 and X2 are -44.92 and -71.32 kJ/mol. However, adsorption of COCl2 on Zn-decorated Mg12O12 offered two geometries named as Z1 and Z2 with adsorption energy values of -455.22 and -419.04 kJ/mol, respectively. These adsorption energy values suggested that Zn decoration significantly enhances the adsorption capability of COCl2 gas. Further, the narrow band gap and large dipole moment values of COCl2-adsorbed Zn-decorated Mg12O12 nanoclusters suggested that designed systems are efficient candidates for COCl2 adsorption. Global reactivity indices unveil the great natural stability and least reactivity of designed systems. Results of all analyses suggested that Zn-decorated Mg12O12 nanoclusters are efficient aspirants for the development of high-performance COCl2 sensing materials.

In Silico Designing of Mg12O12 Nanoclusters with a Late Transition Metal for NO2 Adsorption: An Efficient Approach toward the Development of NO2 Sensing Materials.

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 Q NBO 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.

In Silico Modeling of New "Y-Series"-Based Near-Infrared Sensitive Non-Fullerene Acceptors for Efficient Organic Solar Cells.

This work was inspired by a previous report [Janjua, M. R. S. A. Inorg. Chem. 2012, 51, 11306-11314] in which the optoelectronic properties were improved with an acceptor bearing heteroaromatic rings. Herein, we have designed four novel Y-series non-fullerene acceptors (NFAs) by end-capped acceptor modifications of a recently synthesized 15% efficient Y21 molecule for better optoelectronic properties and their potential use in solar cell applications. Density functional theory (DFT) along with time-dependent density functional theory (TDDFT) at the B3LYP/6-31G(d,p) level of theory is used to calculate the band gap, exciton binding energy along with transition density matrix (TDM) analysis, reorganizational energy of electrons and holes, and absorption maxima and open-circuit voltage of investigated molecules. In addition, the PM6:YA1 complex is also studied to understand the charge shifting from the donor polymer PM6 to the NFA blend. Results of all parameters suggest that the DA'D electron-deficient core and effective end-capped acceptors in YA1-YA4 molecules form a perfect combination for effective tuning of optoelectronic properties by lowering frontier molecular orbital (FMO) energy levels, reorganization energy, and binding energy and increasing the absorption maximum and open-circuit voltage values in selected molecules (YA1-YA4). The combination of extended conjugation and excellent electron-withdrawing capability of the end-capped acceptor moiety in YA1 makes YA1 an excellent organic solar cell (OSC) candidate owing to promising photovoltaic properties including the lowest energy gap (1.924 eV), smallest electron mobility (λe = 0.0073 eV) and hole mobility (λh = 0.0083 eV), highest λmax values (783.36 nm (in gas) and 715.20 nm (in chloroform) with lowest transition energy values (E x) of 1.58 and 1.73 eV, respectively), and fine open-circuit voltage (V oc = 1.17 V) with respect to HOMOPM6-LUMOacceptor. Moreover, selected molecules are observed to have better photovoltaic properties than Y21, thus paving the way for experimentalists to look for future developments of Y-series-based highly efficient solar cells.