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Cited by 45 publications
(25 citation statements)
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“…The planarity as well as LUMO/HOMO of the D‐A copolymers can be fine tuned by the incorporation of the incorporation of C=N group in their backbone. Many D‐A copolymers using benzotriazole, benzothiadiazole, and quinoxaline as acceptors, have been designed and used as a donor for fullerene‐free PSCs 35–37 . Additionally, due to the absence of hydrogen atoms at 3‐ and 4‐positions, the size of TDz is a smaller as compared to thiophene 38–40 .…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…The planarity as well as LUMO/HOMO of the D‐A copolymers can be fine tuned by the incorporation of the incorporation of C=N group in their backbone. Many D‐A copolymers using benzotriazole, benzothiadiazole, and quinoxaline as acceptors, have been designed and used as a donor for fullerene‐free PSCs 35–37 . Additionally, due to the absence of hydrogen atoms at 3‐ and 4‐positions, the size of TDz is a smaller as compared to thiophene 38–40 .…”
Section: Introductionmentioning
confidence: 99%
“…Many D-A copolymers using benzotriazole, benzothiadiazole, and quinoxaline as acceptors, have been designed and used as a donor for fullerene-free PSCs. [35][36][37] Additionally, due to the absence of hydrogen atoms at 3-and 4-positions, the size of TDz is a smaller as compared to thiophene. [38][39][40] This compact structure of TDz compared to benzothiadiazole also provides a significant advantage in suppressing the torsion of the polymer backbone and also reduces the steric hindrance.…”
Section: Introductionmentioning
confidence: 99%
“…Enhancement in PCE is resulted from the improvement of light absorption ability of active layer materials. [ 6–8 ]…”
Section: Introductionmentioning
confidence: 99%
“…Enhancement in PCE is resulted from the improvement of light absorption ability of active layer materials. [6][7][8] Organic semi-conductors are good candidates for photovoltaic applications due to their high absorption coefficients but their higher exciton binding energies make them down. [9][10][11] Their strong electron-phonon coupling and low dielectric constants restricts the free charge generation.…”
Section: Introductionmentioning
confidence: 99%
“…[12][13][14] The lower molecular weight of small molecules causes high solubility. [15,16] In recent years, processing using green solvents has increased interest in small molecules due to their higher solubility in green solvents. Low-cost synthesis of small molecules is also increasing motivation to use them for OSCs.…”
mentioning
confidence: 99%