Rao Aqil Shehzad

Bio: Rao Aqil Shehzad is an academic researcher from University of Agriculture, Faisalabad. The author has contributed to research in topics: Hyperpolarizability & Density functional theory. The author has an hindex of 8, co-authored 18 publications receiving 150 citations.

Benchmark study of the linear and nonlinear optical polarizabilities in proto-type NLO molecule of para-nitroaniline

Abstract: In the present investigation, for the first time, we have performed a thorough study about different functionals and basis sets for linear and nonlinear optical (NLO) properties of para-nitroanilin...

Tuning the optoelectronic properties of triphenylamine (TPA) based small molecules by modifying central core for photovoltaic applications

Abstract: Small donor molecules based on fused ring acceptors exhibit encouraging photovoltaic properties and expeditious advancement in organic solar cells. Central core modification of non-fullerene acceptor materials is a favorable methodology to enhance electronic properties and efficiency for OSCs. Herein, four new donor molecules, namely, BDTM1, PYRM2, ANTM3, and NM4 are designed with a strong donor moiety triphenylamine, tetracyanobutadiene as acceptor unit, and thiophene as spacer linked to a modified central core. Geometric parameters, optical, electrical properties, effect of central core modification on tailored molecules BDTM1-NM4 are investigated and compared with reference DPPR. DFT together with TDDFT approaches using MPW1PW91 functional is used to study key parameters like absorption maximum (λmax), frontier molecular approach, ionization potential, electron affinity, the density of states, transition density matrix along with open-circuit voltage (VOC), dipole moment and reorganization energy. Among all these molecules, BDTM1 shows maximum calculated absorption λmax (817 nm) and the lowest band gap (2.54 eV). This bathochromic shift in BDTM1 is due to the presence of 4,8-dimethoxy-2,6-di-2-thienylbenzodithiophene as a strong electron-withdrawing group. Computed reorganization energies (RE) shows that BDTM1 has the highest hole and electron mobility among all designed molecules. Combination of BDTM1 donor and PC61BM acceptor further verifies charge transfer and their interaction. The results illustrate that designed donor molecules (BDTM1-NM4) are better in performance and are recommended for experimentation to develop efficient OSCs. Four new donor molecules, namely, BDTM1, PYRM2, ANTM3, and NM4 are designed with a strong donor moiety triphenylamine, tetracyanobutadiene as acceptor unit and thiophene as spacer linked to a modified central core. Geometric parameters, optical, electrical properties, effect of central core modification on tailored molecules BDTM1-NM4 are investigated and compared with reference DPPR.

Molecular engineering of A–D–C–D–A configured small molecular acceptors (SMAs) with promising photovoltaic properties for high-efficiency fullerene-free organic solar cells

Abstract: Non fullerene small acceptor molecules in organic photovoltaics are proven beneficial than the traditional fullerene based acceptors for their fine contribution in organic solar cells. Researchers are constantly doing efforts for designing novel acceptor materials with promising photovoltaic properties. Designing of novel molecules by end-capped modifications is a convenient strategy to obtain high efficiency acceptor molecules for OSCs. Herein, we studied optoelectronic characteristics of five novel acceptor–donor–core–donor–acceptor configured small acceptor molecules (S1–S5) after end-capped modifications of recently synthesized DF-PCIC molecule. Designed molecules S1–S5 consist of 1,4-difluorobenzene (as central core), 4,4-bis(2-ethylhexyl)-2,6-dimethyl-4H-cyclopenta[1,2-b:5,4-b′]dithiophene as donor which directly attached with different end-capped acceptors. The electronic and optical properties of newly designed (S1–S5) molecules are examined and compared with reference molecule with the aid of DFT and TD-DFT. Certain key parameters like frontier molecular orbitals analysis, density of states, dipole moment, binding energy along with transition density matrix, excitation energy, charge mobility, absorption maxima and charge transfer analysis have been performed in order to explore the photo-physical, optoelectronic and photovoltaic properties of designed and reference molecule. Out of newly designed structures, S4 displayed lowest energy band-gap (2.25 eV) with red-shifting in absorption spectrum (λmax = 712.43 nm) in chloroform which disclosed the perfect relationship between end-capped acceptor with large electron withdrawing character through extended conjugation. Similarly, S1 exhibited highest value (1.53 V) of open circuit voltage (Voc) with respect to PTB7-Th donor material owing to lower values of λe. Designed molecules exhibit better electron and hole mobility as compared to reference molecule R. All molecules express better absorption maximum, open circuit voltage, low excitation energies, comparable binding energies, large dipole moment and efficient electron and hole transport as compared to reference molecules. So, results these parameters suggest that end-capped modification is a convenient strategy in order to enhance the efficiency of OSCs. Therefore, conceptualized molecules are recommended to experimentalist for out-looking future developments of highly efficient solar cells.

Tuning the optoelectronic properties of triphenylamine (TPA) based small molecules by modifying central core for photovoltaic applications

Abstract: Small donor molecules based on fused ring acceptors exhibit encouraging photovoltaic properties and expeditious advancement in organic solar cells. Central core modification of non-fullerene acceptor materials is a favorable methodology to enhance electronic properties and efficiency for OSCs. Herein, four new donor molecules, namely, BDTM1, PYRM2, ANTM3, and NM4 are designed with a strong donor moiety triphenylamine, tetracyanobutadiene as acceptor unit, and thiophene as spacer linked to a modified central core. Geometric parameters, optical, electrical properties, effect of central core modification on tailored molecules BDTM1-NM4 are investigated and compared with reference DPPR. DFT together with TDDFT approaches using MPW1PW91 functional is used to study key parameters like absorption maximum (λmax), frontier molecular approach, ionization potential, electron affinity, the density of states, transition density matrix along with open-circuit voltage (VOC), dipole moment and reorganization energy. Among all these molecules, BDTM1 shows maximum calculated absorption λmax (817 nm) and the lowest band gap (2.54 eV). This bathochromic shift in BDTM1 is due to the presence of 4,8-dimethoxy-2,6-di-2-thienylbenzodithiophene as a strong electron-withdrawing group. Computed reorganization energies (RE) shows that BDTM1 has the highest hole and electron mobility among all designed molecules. Combination of BDTM1 donor and PC61BM acceptor further verifies charge transfer and their interaction. The results illustrate that designed donor molecules (BDTM1-NM4) are better in performance and are recommended for experimentation to develop efficient OSCs. Four new donor molecules, namely, BDTM1, PYRM2, ANTM3, and NM4 are designed with a strong donor moiety triphenylamine, tetracyanobutadiene as acceptor unit and thiophene as spacer linked to a modified central core. Geometric parameters, optical, electrical properties, effect of central core modification on tailored molecules BDTM1-NM4 are investigated and compared with reference DPPR.