A series of perylene diimide (PDI) dimers (PnTP, n = 0-3) with oligothiophenes as bridges were designed, theoretically calculated, synthesized, and developed as electron acceptors for polymer solar cells (PSCs). The effects of oligothiophene bridge length on the absorption, energy level, charge transport, morphology and photovoltaic properties of the molecules were investigated. These molecules exhibited good thermal stability with decomposition temperatures of 367-413 degrees C, broad and strong absorption in the visible region (400-700 nm), and appropriate HOMO (-5.74 to -5.61 eV) and LUMO (-3.84 to -3.72 eV) energy levels. When blending these PDI acceptors with a low bandgap polymer donor PBDTTT-C-T, the PSCs exhibited power conversion e...
Polymer acceptors based on perylene diimide (PDI) with three symmetrical S-heteroacene backbone unit...
Organic small molecule (SM) acceptors containing a perylene diimide (PDI) moiety, F2B-T2PDI and T2PD...
Perylene diimides (PDIs) are attractive alternatives to fullerenes as electron transporters because ...
Through cracking perylene diimide by inserting a single bond, small pi-conjugation unit thiophene an...
Herein we present the design of three perylene diimide (PDI) derivatives with different molecular ge...
The intermolecular stacking and crystallization of perylene diimides (<b>PDIs</b>) has become resear...
Herein we present the design of three perylene diimide (PDI) derivatives with different molecular ge...
The aggregate-induced limitation for high power-conversion efficiencies (PCEs) of perylene-diimide (...
Five copolymers, having 4,4,9,9-tetrakis(4-hexylphenyl)-indaceno[1,2-b: 5,6-b']-dithiophene as ...
The aggregate-induced limitation for high power-conversion efficiencies (PCEs) of perylene-diimide (...
The aggregate-induced limitation for high power-conversion efficiencies (PCEs) of perylene-diimide (...
A series of PDI dimers featuring various arylene linkers are developed as electron acceptors in orga...
The thrust towards energy conservation and reduced environmental footprint has fueled intensive res...
Two polymeric electron acceptors (PFPDI-2T and PFPDI-2FT) based on the fused perylene diimide (PDI) ...
We report a series of bay substituted perylene diimide based donor-acceptor-donor (D-A-D) type small...
Polymer acceptors based on perylene diimide (PDI) with three symmetrical S-heteroacene backbone unit...
Organic small molecule (SM) acceptors containing a perylene diimide (PDI) moiety, F2B-T2PDI and T2PD...
Perylene diimides (PDIs) are attractive alternatives to fullerenes as electron transporters because ...
Through cracking perylene diimide by inserting a single bond, small pi-conjugation unit thiophene an...
Herein we present the design of three perylene diimide (PDI) derivatives with different molecular ge...
The intermolecular stacking and crystallization of perylene diimides (<b>PDIs</b>) has become resear...
Herein we present the design of three perylene diimide (PDI) derivatives with different molecular ge...
The aggregate-induced limitation for high power-conversion efficiencies (PCEs) of perylene-diimide (...
Five copolymers, having 4,4,9,9-tetrakis(4-hexylphenyl)-indaceno[1,2-b: 5,6-b']-dithiophene as ...
The aggregate-induced limitation for high power-conversion efficiencies (PCEs) of perylene-diimide (...
The aggregate-induced limitation for high power-conversion efficiencies (PCEs) of perylene-diimide (...
A series of PDI dimers featuring various arylene linkers are developed as electron acceptors in orga...
The thrust towards energy conservation and reduced environmental footprint has fueled intensive res...
Two polymeric electron acceptors (PFPDI-2T and PFPDI-2FT) based on the fused perylene diimide (PDI) ...
We report a series of bay substituted perylene diimide based donor-acceptor-donor (D-A-D) type small...
Polymer acceptors based on perylene diimide (PDI) with three symmetrical S-heteroacene backbone unit...
Organic small molecule (SM) acceptors containing a perylene diimide (PDI) moiety, F2B-T2PDI and T2PD...
Perylene diimides (PDIs) are attractive alternatives to fullerenes as electron transporters because ...