Journal
OPTICAL AND QUANTUM ELECTRONICS
Volume 54, Issue 11, Pages -Publisher
SPRINGER
DOI: 10.1007/s11082-022-04074-z
Keywords
Benzothiazole; Alkyl chains; Doping; DFT; Photovoltaic
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This research focuses on the influence of heteroatoms (C, O, S) and the alkyl chain length (R = 2, 4, 6) on electron-acceptor fullerene-free benzothiazole material for improving the efficiency of photovoltaic cell devices. The results show that S-substituted benzothiazole exhibits the highest light-harvesting efficiency and short-circuit current density, indicating its potential application in organic solar cells.
Due to tremendous effort in the design of low-band-gap materials, fullerene-free organic solar cells exhibit excellent photovoltaic performances as compared to fullerene compounds. However, the theoretical modelling of wide-band-gap materials through material engineering to significantly enhance the photovoltaic properties remains a challenge. This research work focuses on the influence of heteroatoms (C, O, S) and the alkyl chain length (R = 2, 4, 6) on electron-acceptor fullerene-free benzothiazole material for improved efficiency of photovoltaic cell devices. The electronic excitation, frontier molecular orbitals, natural bond orbital, and photovoltaic properties have been discussed based on quantum chemical density functional theory calculations using the B3LYP/6-311 + + G (d,p) method. The HOMO-LUMO energy gap analysis revealed that O-atom doped benzothiazoles have higher reactivity relative to the C and S doped structures and the reactivity increases as the alkyl chain length increases. The photovoltaic results revealed the S-substituted benzothiazole has the highest light-harvesting efficiency and short-circuit current density (Jsc) of 0.9361 and 6.1026 respectively. This demonstrates the absorption and power converting potential of the S-doped benzothiazole relative to the C and O series dyes for application in organic solar cells.
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