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Asymmetric non-fullerene small molecules acceptor (as-NF-SMAs) exhibit greater vitality in photovoltaic materials compared to their symmetric counterparts due to their larger dipole moments and stronger intermolecular interactions, which facilitate exciton dissociation and charge transmission in organic solar cells (OSCs). Here, we introduced a new as-NF-SMAs, named IDT-TNIC, as the third component in ternary organic solar cells (TOSCs). The asymmetric IDT-TNIC used indacenodithiophene (IDT) as the central core, alkylthio-thiophene as a unilateral π-bridge and extended end groups as electron-withdrawing. Due to the non-covalent conformational lock (NCL) established between O⋅⋅⋅S and S⋅⋅⋅S, the IDT-TNIC molecule preserves its coplanar structure effectively. Furthermore, IDT-TNIC exhibits complementary absorption and excellent compatibility with donor and acceptor materials, as well as optimized ladder energy level arrangement, resulting in a higher and more balanced μ h /μ e value, more homogeneous and suitable phase separation morphology in TOSCs. Thus, the PCE of the TOSCs reached 17 % when the weight ratio of PM6 : Y6 : IDT-TNIC was 1 : 1.1 : 0.1, and it is noteworthy that when the device area was increased to 1 cm 2 , the PCE could still be maintained at over 14 %. Detailed studies and analysis indicate that IDT-TNIC has great potential as a third component in OSCs and for large-scale printing in the future., (© 2024 Wiley-VCH GmbH.)

The determination of molecular conformations of oligomeric acceptors (OAs) and their impact on molecular packing are crucial for understanding the photovoltaic performance of their resulting polymer solar cells (PSCs) but have not been well studied yet. Herein, we synthesized two dimeric acceptor materials, DIBP3F-Se and DIBP3F-S, which bridged two segments of Y6-derivatives by selenophene and thiophene, respectively. Theoretical simulation and experimental 1D and 2D NMR spectroscopic studies prove that both dimers exhibit O-shaped conformations other than S- or U-shaped counter-ones. Notably, this O-shaped conformation is likely governed by a distinctive "conformational lock" mechanism, arising from the intensified intramolecular π-π interactions among their two terminal groups within the dimers. PSCs based on DIBP3F-Se deliver a maximum efficiency of 18.09 %, outperforming DIBP3F-S-based cells (16.11 %) and ranking among the highest efficiencies for OA-based PSCs. This work demonstrates a facile method to obtain OA conformations and highlights the potential of dimeric acceptors for high-performance PSCs., (© 2023 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.)

The power conversion efficiency (PCE) of all-polymer solar cells (all-PSCs) has ascended rapidly arising from the development of polymerized small-molecule acceptor materials. However, numerous insulating long alkyl chains, which ensure the solubility of the polymer, result in inferior aggregation and charge mobility. Herein, this study proposes a facile random copolymerization strategy of two small molecule acceptor units with different lengths of alkyl side chains and synthesizes a series of polymer acceptors PYT-EHx, where x is the percentage of the short alkyl chain units. The aggregation strength and charge mobility of the acceptors rise linearly with increasing the proportion of short alkyl chain units. Thus, the PYT-EH20 reaches balanced aggregation with the star polymer donor PBDB-T, resulting in optimal morphology, fastest carrier transport, and reduced recombination and energy loss. Consequently, the PYT-EH20-based device yields a 14.8% PCE, a 16% improvement over the control PYT-EH0-based device, accompanied by an increase in open-circuit voltage (V oc ), short-circuit current density (J sc ), and fill factor (FF). This work demonstrates that the random copolymerization strategy with short alkyl chain insertion is an effective avenue for developing high-performance polymer acceptors, which facilitates further advances in the efficiency of all-PSCs., (© 2022 Wiley-VCH GmbH.)

Developing organic solar cells based on a ternary active layer is one of the most effective approaches to improve their photovoltaic performance. However, limited success has been achieved in all-polymer solar cells (all-PSCs). In this study, a ternary all-PSC with improved efficiency and stability is realized by using J71 as the third component to adjust the host system of PBDB-T:PG1. The deeper highest occupied molecular orbital (HOMO) energy level of J71 downshifts the mixed HOMO energy levels of donors. The two polymer donors (P D s) have good miscibility and present Förster resonance energy transfer. When blended with PG1, the optimized morphology is obtained, showing enhanced crystallinity but meanwhile slightly reduced phase separation with improved exciton dissociation and collection efficiency, suppressed charge recombination, and reduced energy loss (0.55 eV). Combining the benefits mentioned above, the ternary all-PSC exhibits an excellent efficiency of 12.8% with simultaneously elevated open-circuit voltage (0.96 V), short-circuit current density (18.4 mA cm -2 ), and fill factor (72.2%). Moreover, the optimized ternary all-PSC shows improved storage and thermal stability. This study demonstrates that the utilization of a ternary all-polymer system based on two well-miscible P D s is an effective strategy to enhance the photovoltaic performance and stability of all-PSCs., (© 2022 Wiley-VCH GmbH.)

Despite more potential in realizing higher photovoltaic performance, the highest power conversion efficiency (PCE) of tandem organic photovoltaic (OPV) cells still lags behind that of state-of-the-art single-junction cells. In this work, highly efficient double-junction tandem OPV cells are fabricated by optimizing the photoactive layers with low voltage losses and developing an effective method to tune optical field distribution. The tandem OPV cells studied are structured as indium tin oxide (ITO)/ZnO/bottom photoactive layer/interconnecting layer (ICL)/top photoactive layer/MoO x /Ag, where the bottom and top photoactive layers are based on blends of PBDB-TF:ITCC and PBDB-TF:BTP-eC11, respectively, and ICL refers to interconnecting layer structured as MoO x /Ag/ZnO:PFN-Br. As these results indicate that there is not much room for optimizing the bottom photoactive layer, more effort is put into fine-tuning the top photoactive layer. By rationally modulating the composition and thickness of PBDB-TF:BTP-eC11 blend films, the 300 nm-thick PBDB-TF:BTP-eC11 film with 1:2 D/A ratio is found to be an ideal photoactive layer for the top sub-cell in terms of photovoltaic characteristics and light distribution control. For the optimized tandem cell, a PCE of 19.64% is realized, which is the highest result in the OPV field and certified as 19.50% by the National Institute of Metrology., (© 2021 Wiley-VCH GmbH.)

How to simultaneously achieve both high open-circuit voltage (V oc ) and high short-circuit current density (J sc ) is a big challenge for realising high power conversion efficiency (PCE) in all-small-molecule organic solar cells (all-SM OSCs). Herein, a novel small molecule (SM)-donor, namely FYSM-SiCl, with trialkylsilyl and chlorine substitutions was designed and synthesized. Compared to the original SM-donor FYSM-H, FYSM-Si with trialkylsilyl substitution showed a decreased crystallinity and lower highest occupied molecular orbital (HOMO) level, while FYSM-SiCl had an improved crystallinity, more ordered packing arrangement, significantly lower HOMO level, and predominant "face-on" orientation. Matched with a SM-acceptor Y6, the FYSM-SiCl-based all-SM OSCs exhibited both high V oc of 0.85 V and high J sc of 23.7 mA cm -2 , which is rare for all-SM OSCs and could be attributed to the low HOMO level of FYSM-SiCl donor and the delicate balance between high crystallinity and suitable blend morphology. As a result, FYSM-SiCl achieved a high PCE of 13.4 % in all-SM OSCs, which was much higher than those of the FYSM-H- (10.9 %) and FYSM-Si-based devices (12.2 %). This work demonstrated a promising method for the design of efficient SM-donors by a side-chain engineering strategy via the introduction of trialkylsilyl and chlorine substitutions., (© 2021 The Authors. ChemSusChem published by Wiley-VCH GmbH.)

In non-fullerene-based photovoltaic devices, it is unclear how excitons efficiently dissociate into charge carriers under small driving force. Here, we developed a modified method to estimate dielectric constants of PM6 donor and non-fullerene acceptors. Surprisingly, most non-fullerene acceptors and blend films showed higher dielectric constants. Moreover, they exhibited larger dielectric constants differences at the optical frequency. These results are likely bound to reduced exciton binding energy and bimolecular recombination. Besides, the overlap between the emission spectrum of donor and absorption spectra of non-fullerene acceptors allowed the energy transfer from donor to acceptors. Hence, based on the synergistic effect of dielectric property and energy transfer resulting in efficient charge separation, our finding paves an alternative path to elucidate the physical working mechanism in non-fullerene-based photovoltaic devices., (© 2021 Wiley-VCH GmbH.)

The intrinsic electronic properties of donor (D) and acceptor (A) materials in coupling with morphological features dictate the output in organic solar cells (OSCs). New physical properties of intimate eutectic mixing are used in nonfullerene-acceptor-based D-A 1 -A 2 ternary blends to fine-tune the bulk heterojunction thin film morphology as well as their electronic properties. With enhanced thin film crystallinity and improved carrier transport, a significant J SC amplification is achieved due to the formation of eutectic fibrillar lamellae and reduced defects state density. Material wise, aligned cascading energy levels with much larger driving force, and suppressed recombination channels confirm efficient charge transfer and transport, enabling an improved power conversion efficiency (PCE) of 17.84%. These results reveal the importance of utilizing specific material interactions to control the crystalline habit in blended films to form a well-suited morphology in guiding superior performances, which is of high demand in the next episode of OSC fabrication toward 20% PCE., (© 2021 Wiley-VCH GmbH.)

Regulating molecular structure to optimize the active layer morphology is of considerable significance for improving the power conversion efficiencies (PCEs) in organic solar cells (OSCs). Herein, we demonstrated a simple ternary copolymerization approach to develop a terpolymer donor PM6-Tz20 by incorporating the 5,5'-dithienyl-2,2'-bithiazole (DTBTz, 20 mol%) unit into the backbone of PM6 (PM6-Tz00). This method can effectively tailor the molecular orientation and aggregation of the polymer, and then optimize the active layer morphology and the corresponding physical processes of devices, ultimately boosting FF and then PCE. Hence, the PM6-Tz20: Y6-based OSCs achieved a PCE of up to 17.1% with a significantly enhanced FF of 0.77. Using Ag (220 nm) instead of Al (100 nm) as cathode, the champion PCE was further improved to 17.6%. This work provides a simple and effective molecular design strategy to optimize the active layer morphology of OSCs for improving photovoltaic performance., (© 2020 Wiley-VCH GmbH.)

Developing high-performance donor polymers is important for nonfullerene organic solar cells (NF-OSCs), as state-of-the-art nonfullerene acceptors can only perform well if they are coupled with a matching donor with suitable energy levels. However, there are very limited choices of donor polymers for NF-OSCs, and the most commonly used ones are polymers named PM6 and PM7, which suffer from several problems. First, the performance of these polymers (particularly PM7) relies on precise control of their molecular weights. Also, their optimal morphology is extremely sensitive to any structural modification. In this work, a family of donor polymers is developed based on a random polymerization strategy. These polymers can achieve well-controlled morphology and high-performance with a variety of chemical structures and molecular weights. The polymer donors are D-A1-D-A2-type random copolymers in which the D and A1 units are monomers originating from PM6 or PM7, while the A2 unit comprises an electron-deficient core flanked by two thiophene rings with branched alkyl chains. Consequently, multiple cases of highly efficient NF-OSCs are achieved with efficiencies between 16.0% and 17.1%. As the electron-deficient cores can be changed to many other structural units, the strategy can easily expand the choices of high-performance donor polymers for NF-OSCs., (© 2020 Wiley-VCH GmbH.)

A non-conjugated polymer acceptor PF1-TS4 was firstly synthesized by embedding a thioalkyl segment in the mainchain, which shows excellent photophysical properties on par with a fully conjugated polymer, with a low optical band gap of 1.58 eV and a high absorption coefficient >10 5  cm -1 , a high LUMO level of -3.89 eV, and suitable crystallinity. Matched with the polymer donor PM6, the PF1-TS4-based all-PSC achieved a power conversion efficiency (PCE) of 8.63 %, which is ≈45 % higher than that of a device based on the small molecule acceptor counterpart IDIC16. Moreover, the PF1-TS4-based all-PSC has good thermal stability with ≈70 % of its initial PCE retained after being stored at 85 °C for 180 h, while the IDIC16-based device only retained ≈50 % of its initial PCE when stored at 85 °C for only 18 h. Our work provides a new strategy to develop efficient polymer acceptor materials by linkage of conjugated units with non-conjugated thioalkyl segments., (© 2020 The Authors. Published by Wiley-VCH GmbH.)

Two wide-bandgap (WBG) conjugated polymers (PBPD-p and PBPD-m) based on phenyl-substituted benzodithiophene (BDT) with the different substitution position of the alkyl side chain and benzodithiophene-4,8-dione (BDD) units are designed and synthesized to investigate the influence of alkyl substitution position on the photovoltaic performance of polymers in polymer solar cells (PSCs). The thermogravimetric analysis, absorption spectroscopy, molecular energy level, X-ray diffraction, charge transport and photovoltaic performance of the polymers are systematically studied. Compared with PBPD-p, PBPD-m exhibits a slight blue-shift but a deeper highest occupied molecular orbital (HOMO) energy level, a tighter alkyl chain packing and a higher hole mobility. The PBPD-m-based PSCs blended with acceptor IT-4F shows a higher power conversion efficiency (PCE) of 11.95% with a high open-circuit voltage (V oc ) of 0.88 V, a short-circuit current density (J sc ) of 19.76 mA cm -2 and a fill factor (FF) of 68.7% when compared with the PCE of 6.97% with a V oc of 0.81 V, a J sc of 15.97 mA cm -2 and an FF of 53.9% for PBPD-p. These results suggest that it is a feasible and effective strategy to optimize photovoltaic properties of WBG polymers by changing the substitution position of alkyl side chain in PSCs., (© 2020 Wiley-VCH GmbH.)

Understanding the conformation effect on molecular packing, miscibility, and photovoltaic performance is important to open a new avenue for small-molecule acceptor (SMA) design. Herein, two novel acceptor-(donor-acceptor1-donor)-acceptor (A-DA1D-A)-type asymmetric SMAs are developed, namely C-shaped BDTP-4F and S-shaped BTDTP-4F. The BDTP-4F-based polymer solar cells (PSCs) with PM6 as donor, yields a power conversion efficiency (PCE) of 15.24%, significantly higher than that of the BTDTP-4F-based device (13.12%). The better PCE for BDTP-4F-based device is mainly attributed to more balanced charge transport, weaker bimolecular recombination, and more favorable morphology. Additionally, two traditional A-D-A-type SMAs (IDTP-4F and IDTTP-4F) are also synthesized to investigate the conformation effect on morphology and device performance. Different from the device result above, here, IDTP-4F with S-shape conformation outperforms than IDTTP-4F with C-shape conformation. Importantly, it is found that for these two different types of SMA, the better performing binary blend has similar morphological characteristics. Specifically, both PM6:BDTP-4F and PM6:IDTP-4F blend exhibit perfect nanofibril network structure with proper domain size, obvious face-on orientation and enhance donor-acceptor interactions, thereby better device performance. This work indicates tuning molecular conformation plays pivotal role in morphology and device effciciency, shining a light on the molecular design of the SMAs., (© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Over the past decade, organic solar cells (OSCs) have achieved a dramatic boost in their power conversion efficiencies from about 6 % to over 16 %. In addition to developments in device engineering, innovative photovoltaic materials, especially fluorinated donors and acceptors, have become the dominant factor for improved device performance. This minireview highlights fluorinated photovoltaic materials that enable efficient OSCs. Impressive OSCs have been obtained by developing some important molds of fluorinated donor and acceptor systems. The molecular design strategy and the matching principle of fluorinated donors and acceptors in OSCs are discussed. Finally, a concise summary and outlook are presented for advances in fluorinated materials to realize the practical application of OSCs., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Nonfullerene polymer solar cells (PSCs) are developed based on a fluorinated thienyl-based wide-bandgap (WBG) polymer PBBF as the electron donor and nonfullerene small molecule IDIC as the electron acceptor. PBBF exhibits a strong absorption in the range of 300-605 nm with a wide optical bandgap of 2.05 eV, which is complementary with that of IDIC. Meanwhile, it possesses a deeper highest occupied molecular orbital energy level of  -5.52 eV and a higher hole mobility of 7.3 × 10 -4  cm 2 V -1  s -1 compared to the nonfluorinated polymer PBDTT. The PSCs based on PBBF:IDIC without extra treatment show a power conversion efficiency (PCE) of 8.5% with a V oc of 0.95 V, a J sc of 15.3 mA cm -2 , and an FF of 58.8%, which is much higher than that of the devices based on PBDTT:IDIC (a PCE of 5.3% with a V oc of 0.88 V, a J sc of 13.7 mA cm -2 , and an FF of 43.9%). These results indicate that PBBF is a promising WBG polymer donor material for the photovoltaic applications in nonfullerene PSCs., (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

In this work, a nonfullerene polymer solar cell (PSC) based on a wide bandgap polymer donor PM6 containing fluorinated thienyl benzodithiophene (BDT-2F) unit and a narrow bandgap small molecule acceptor 2,2'-((2Z,2'Z)-((4,4,9,9-tetrahexyl-4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene-2,7-diyl)bis(methanylylidene))bis(3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile (IDIC) is developed. In addition to matched energy levels and complementary absorption spectrum with IDIC, PM6 possesses high crystallinity and strong π-π stacking alignment, which are favorable to charge carrier transport and hence suppress recombination in devices. As a result, the PM6:IDIC-based PSCs without extra treatments show an outstanding power conversion efficiency (PCE) of 11.9%, which is the record value for the as-cast PSC devices reported in the literature to date. Moreover, the device performances are insensitive to the active layer thickness (≈95-255 nm) and device area (0.20-0.81 cm 2 ) with PCEs of over 11%. Besides, the PM6:IDIC-based flexible PSCs with a large device area of 1.25 cm 2 exhibit a high PCE of 6.54%. These results indicate that the PM6:IDIC blend is a promising candidate for future roll-to-roll mass manufacturing and practical application of highly efficient PSCs., (© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

In this work, high-efficiency nonfullerene polymer solar cells (PSCs) are developed based on a thiazolothiazole-containing wide bandgap polymer PTZ1 as donor and a planar IDT-based narrow bandgap small molecule with four side chains (IDIC) as acceptor. Through thermal annealing treatment, a power conversion efficiency (PCE) of up to 11.5% with an open circuit voltage (V oc ) of 0.92 V, a short-circuit current density (J sc ) of 16.4 mA cm -2 , and a fill factor of 76.2% is achieved. Furthermore, the PSCs based on PTZ1:IDIC still exhibit a relatively high PCE of 9.6% with the active layer thickness of 210 nm and a superior PCE of 10.5% with the device area of up to 0.81 cm 2 . These results indicate that PTZ1 is a promising polymer donor material for highly efficient fullerene-free PSCs and large-scale devices fabrication., (© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

High-performance ternary organic solar cells are fabricated by using a wide-bandgap polymer donor (bithienyl-benzodithiophene-alt-fluorobenzotriazole copolymer, J52) and two well-miscible nonfullerene acceptors, methyl-modified nonfullerene acceptor (IT-M) and 2,2'-((2Z,2'Z)-((5,5'-(4,4,9,9-tetrakis(4-hexylphenyl)-4,9-dihydros-indaceno[1,2-b:5,6-b']dithiophene-2,7-diyl)bis(4-((2-ethylhexyl)oxy)thiophene-5,2-diyl))bis(methanylylidene))bis(3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile (IEICO). The two acceptors with complementary absorption spectra and similar lowest unoccupied molecular orbital levels show excellent compatibility in the blend due to their very similar chemical structures. Consequently, the obtained ternary organic solar cells (OSC) exhibits a high efficiency of 11.1%, with an enhanced short-circuit current density of 19.7 mA cm -2 and a fill factor of 0.668. In this ternary system, broadened absorption, similar output voltages, and compatible morphology are achieved simultaneously, demonstrating a promising strategy to further improve the performance of ternary OSCs., (© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Five polymer donors with distinct chemical structures and different electronic properties are surveyed in a planar and narrow-bandgap fused-ring electron acceptor (IDIC)-based organic solar cells, which exhibit power conversion efficiencies of up to 11%., (© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A new broad bandgap and 2D-conjugated D-A copolymer, PBDTBTz-T, based on bithienyl-benzodithiophene donor unit and bithiazole (BTz) acceptor unit, is designed and synthesized for the application as donor material in polymer solar cells (PSCs). The polymer possesses highly coplanar and crystalline structure with a higher hole mobility and lower HOMO energy level which is beneficial to achieve higher open circuit voltage (Voc ) of the PSCs with the polymer as donor. The PSCs based on PBDTBTz-T:PC71 BM blend film with a lower PC71 BM content of 40% demonstrate a power conversion efficiency (PCE) of 6.09% with a relatively higher Voc of 0.92 V. These results indicate that the lower HOMO energy level of the BTz-based D-A copolymer is beneficial to a high Voc of the PSCs. The polymer, with highly coplanar and crystalline structure, can effectively reduce the content of fullerene acceptor in the active layer and can enhance the absorption and PCE of the PSCs., (© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A new 2D-conjugated small molecule with alkylthio-thienyl-conjugated side chains (BDTT-S-TR) is synthesized for application as a donor material in organic solar cells (OSCs). The OSCs based on BDTT-S-TR/PC70 BM demonstrate a power conversion efficiency (PCE) of 9.20% without extra treatment. Moreover, an encouraging PCE of 6.68% is achieved from the device with active area of 144 mm(2)., (© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A new copolymer PM6 based on fluorothienyl-substituted benzodithiophene is synthesized and characterized. The inverted polymer solar cells based on PM6 exhibit excellent performance with Voc of 0.98 V and power conversion efficiency (PCE) of 9.2% for a thin-film thickness of 75 nm. Furthermore, the single-junction semitransparent device shows a high PCE of 5.7%., (© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Highly efficient polymer solar cells with a tandem structure are fabricated by using two excellent photovoltaic polymers and a highly transparent intermediate recombination layer. Power conversion -efficiencies over 10% can be realized with a photovoltaic response within 800 nm., (© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A polythiophene derivative called PDCBT, which has a backbone of thiophene units and just carboxylate functional groups to modulate its properties, exhibits properties superior to those of poly(3-hexylthiophene), the classic polythiophene derivative, when used as an electron donor in polymer solar cells (PSCs). The best device, based on PDCBT/PC71BM (1:1), develops a good power conversion efficiency of 7.2%., (© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

For the blend film of PBDTTT-C-T:PC71 BM, the use of 1,8-diiodooctane as the solvent additive enriches the polymer at the top surface, so that a power conversion efficiency of 9.13% is recorded in the inverted polymer solar cell based on the blend, which is much higher than that of the device with conventional structure., (© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Attaching meta-alkoxy-phenyl groups as conjugated side chains is an easy and effective way to modulate the molecular energy level of D-A polymer for photovoltaic application, and the polymer solar cells based on the polymer consisting meta-alkoxy-phenyl groups as conjugated side chain, PBT-OP, shows an enhanced open circuit voltage and thus higher efficiency of 7.50%, under the illumination of AM 1.5G, 100 mW/cm(2) ., (© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The synergistic effect of fluorination on molecular energy level modulation is realized by introducing fluorine atoms onto both the donor and the acceptor moieties in a D-A polymer, and as a result, the polymer solar cell device based on the trifluorinated polymer, PBT-3F, shows a high efficiency of 8.6%, under illumination of AM 1.5G, 100 mW cm(-) (2) ., (© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A new copolymer PBDTP-DTBT based on benzothiadiazole and alkylphenyl substituted benzodithiophene is synthesized and characterized. The correlation of the evolution of the morphology and photovoltaic performance is investigated. The power conversion efficiency of the polymer solar cells based on PBDTP-DTBT/PC71 BM (1:1.5, w/w) reaches up to 8.07%, under the irradiation of AM 1.5G, 100 mW/cm(2) ., (Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The correlation among molecular conformation, the crystallinity of the morphology, propensity for π-π stacking, J- versus H-aggregation, and photovoltaic performance have been studied based on two newly designed polymers, PBDTTT-S-T and PDT-S-T. The results show that more linear backbone structure is helpful to improve photovoltaic properties of the polymer, and therefore, molecular conformation should be considered for molecular design of photovoltaic polymers., (Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A new copolymer PIDTDTQx based on indacenodithiophene and quinoxaline is synthesized and characterized. The correlation between the D/A ratio, mobility, and photovoltaic properties, as well as morphology of the D/A blend based on a PIDTDTQx:PC(70) BM system is investigated. The power conversion efficiency of the polymer solar cells based on PIDTDTQx/PC(70) BM (1:4, w/w) reaches 7.51%., (Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)