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Enhancement of air stability and photovoltaic performance in organic solar cells by structural modulation of bis‐amide‐based donor‐acceptor copolymers: A computational insight
Author(s) -
Bhattacharya Labanya,
Sharma Sagar,
Sahu Sridhar
Publication year - 2021
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/qua.26524
Subject(s) - copolymer , acceptor , density functional theory , heteroatom , materials science , homo/lumo , organic solar cell , thiophene , amide , porphyrin , molecular orbital , photochemistry , chemistry , molecule , computational chemistry , organic chemistry , polymer , ring (chemistry) , physics , composite material , condensed matter physics
The effect of structural modulation on a series of donor‐acceptor (D‐A) copolymers ( 1 ‐ 7 ), comprising of thieno[3,2‐ b ]thiophene (TT) donor and thiazole‐flanked different bis‐amide‐functionalized acceptor units, has been explored. Structural functionalization has been performed by incorporating aromatic rings in the bis‐amide‐functionalized bipyrrolylidene‐2,2′(1 H ,1′ H )‐dione (BPD) ( 1 ) acceptor unit, and six D‐A copolymers containing isoindigo ( 2 ), azaisoindigo ( 3 ), benzoisoindigo ( 4 ), benzoazaisoindigo ( 5 ), 1,5‐naphthyridine‐BPD ( 6 ), and 1,8‐naphthyridine‐BPD ( 7 ) as acceptor units are designed. Density functional theory has been employed to understand the impact of structural modulation on geometrical, optoelectronic, charge transport, and photovoltaic properties of the copolymers. The higher proportion of N‐heteroatom in copolymers 3 , 6 , and 7 leads to low‐lying highest occupied molecular orbital (lowest unoccupied molecular orbital) levels and thus improves their air stability and open‐circuit voltage. The computed optical absorption in the visible range (602‐754 nm) ensures that the studied compounds can efficiently harvest photon energy. The ratio of charge transfer rate ( K CT ) and charge recombination rate ( K CR ) at donor/PC 61 BM interfaces of structurally tuned copolymers are found to be ∼10 7 to 10 22 times higher than 1 /PC 61 BM. The maximum predicted power conversion efficiency by Scharber diagram could reach up to ∼8% for 3 , 6 , and 7 . The calculated results shed light on the fact that the structural modulation of bis‐amide‐functionalized D‐A copolymers can efficaciously lead to enhanced air stability and photovoltaic performance.