Key words ternary organic solar cells - electron acceptors - indenoindene - power conversion efficiencies
Introduction
Bulk-heterojunction organic solar cells (BHJ-OSCs) as a promising technology for clean and renewable energy conversion have attracted increasing attention because of their great potential of light weight, semi-transparency, flexibility, and large-area production.[1 ] In recent years, nonfullerene electron acceptors with an acceptor–donor–acceptor (A–D–A) framework have aroused considerable interest because of their adjustable energy levels, tunable bandgaps, and feasible synthesis.[2 ] By elaborately designing nonfullerene acceptors and selecting appropriate polymer donors, a great progress has been achieved leading to high power conversion efficiencies (PCEs).[3 ]
The ternary organic photovoltaic technique of incorporating a third photoactive component is effective to address the intrinsic defect of BHJ-OSCs, which utilize binary active blends with insufficient sunlight collection capability due to their intrinsically narrow absorption of organic conjugated materials.[4 ] Ensuring that efficient exciton dissociation and charge collection are guaranteed, improved short-circuit current (J
sc ) and fill factor (FF) can be expected.[5 ] Moreover, emerging fused-ring electron acceptors (FREAs) with low open-circuit voltage (V
oc ) loss and highly tunable electronic structure represent a new opportunity to enriche ternary organic photovoltaics (OPVs). Blend combinations of donor/FREA/fullerene,[6 ] (donor)2/FREA,[7 ] and donor/(FREA)2[8 ] have been extensively explored leading to improved photovoltaic performance. Recently, fullerene-based acceptors such as [6,6]-phenyl-C61/71 -butyric acid methyl ester (PC61/71 BM), bis-adduct of phenyl-C71 -butyric-acid-methyl ester (bis-PC70 BM), and indene-C60 bisadduct (ICBA) have been introduced as third components into the nonfullerene binary OSCs for high photovoltaic performance. Hou et al fabricated high performance ternary OSCs, which for the 12.2% are based on polymer donor like poly[(2,6-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)-benzo[1,2-b:4,5-b′]dithiophene))-alt-(5,5-(1′,3′-di-2-thienyl-5′,7′-bis(2-ethylhexyl)benzo[1′,2′-c:4′,5′-c′]dithiophene-4,8-dione)] (PBDB-T), 2,2′-[[6,6,12,12-Tetrakis(4-hexylphenyl)-6,12-dihydrodithieno[2,3-d:2′,3′-d′]-s-indaceno[1,2-b:5,6-b′]dithiophene-2,8-diyl]bis[2-(5-methyl-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile] (IT-M), and bis[70]PCBM.[9 ] Chen and coworkers reported a small-bandgap FREA, 2,2′-[[6,6,12,12-Tetrakis(4-ethylhexylphenyl)-6,12-dihydrodithieno[2,3-d:2′,3′-d′]-s-indaceno[1,2-b:5,6-b′]dithiophene-2,8-diyl]bis[2-(5,6-difluoro-3-oxo-2-2,3-dihydro-1H-ioden-1-ylidene)malononitrile] (3TT-FIC),[10 ] which matched with a low-bandgap polymer donor, poly[4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b′]dithiophene-co-3-fluorothieno[3,4-b]thiophene-2-carboxylate] (PTB7-Th), achieving a high PCE of 12.21%. When PC71 BM was used as the third component, a much higher PCE of 13.54% is achieved in the ternary device. By using a wide-bandgap polymer PBT1-C as the donor, a crystalline FREA ITIC-2Cl, and an amorphous fullerene derivative ICBA as the acceptors, the blend morphology was optimized, Sun and coworkers obtained an impressive PCE of 13.4% with a high FF of 76.8%.[11 ] These results indicate that the cooperation of a fullerene-based acceptor and a nonfullerene acceptor to fabricate a ternary-blend device may be a promising way to controlling morphology and enhancing the performance of OSCs.
We recently reported two narrow bandgap acceptors NITI[12 ] and ZITI[13 ] consisting of indenoindene core. Both NITI and ZITI acceptors show excellent compatibility with donor materials and exhibit high performance. Using a combination of small-molecule donor benzodithiophene terthiophene rhodamine (BTR) with both the fullerene acceptor PC71 BM and NITI, we achieved a high PCE of 13.63% for ternary solar cells, which forms a hierarchical morphology consisting of a PCBM transporting highway and an intricate nonfullerene phase-separated pathway network.[14 ] In this work, we synthesized a nonfullerene acceptor ZITI-4F via the Knoevenagel reaction of INCN-2F and ZIT-CHO. ZITI-4F shows a very high molar extinction coefficient (ε ) of 2.46 × 105 M−1 cm−1 at 716 nm in solution with a low optical band of 1.47 eV. By matching with the wide-bandgap polymer donor PBDB-T, the optimized PBDB-T:ZITI-4F-based devices achieve a high PCE of 12.33% with an open-circuit voltage (V
oc ) of 0.80 V, a short circuit current density (J
sc ) of 21.17 mA cm−2 , and a FF of 73.27%. To further promote the OPV performance, PC71 BM was added into the device as a third component, and the ternary devices achieved a higher PCE of up to 13.40% with simultaneously elevated V
oc (0.82 V), J
sc (22.04 mA cm−2 ), and FF (74.24%). The recombination and morphology analyses indicate that the higher performance of ternary device can be attributed to the improved and more balanced charge mobility, reduced bimolecular recombination, and more favorable morphology.
Results and Discussion
The synthetic route of compound ZITI-4F is shown in [Figure S1 ] (see the Supporting Information). A dialdehyde precursor was prepared according to the reported procedure.[13 ] The target molecule ZITI-4F was synthesized via a Knoevenagel reaction between the dialdehyde and 2-(5,6-difluoro-3-oxo-2,3-dihydro-1H -inden-1-ylidene)malononitrile (2F-INCN-2F) in 76% yield as a black solid. ZITI-4F is fully characterized by conventional nuclear magnetic resonance (NMR), mass, and elemental analyses, and the detailed characterization data are given in the Supporting Information. ZITI-4F exhibits good solubility in commonly used device-processing solvents, such as chloroform, chlorobenzene, and o -dichlorobenzene. Thermal gravity analysis (TGA) of ZITI-4F under a nitrogen atmosphere shows good thermal stability with a high decomposition temperature of 321 °C (5% weight loss; see [Figure S2 ] in the Supporting Information).
The ultraviolet–visible–near infrared (UV–vis–NIR) absorption spectra of ZITI-4F in chloroform solution and in the film state are shown in [Figure 1b ]. ZITI-4F shows an absorption maximum at 716 nm with an extinction coefficient (ε ) of 2.46 × 105 M−1 cm−1 . In the film state, the absorption spectrum becomes broadened with the maximum absorption peak bathochromically shifted to 768 nm, which suggests that strong π–π intermolecular interactions are present in the solid state. The optical bandgap of ZITI-4F is calculated to be 1.47 eV according to the thin-film absorption onset (846 nm). ZITI-4F shows a perfect complementary absorption with the wide-bandgap polymer donor PBDB-T. Cyclic voltammetry measurement was carried out to evaluate the electrochemical property of ZITI-4F (see [Figure S2 ] in the Supporting Information) and the corresponding energy diagram is presented in [Figure 1c ]. The potential is calibrated by using ferrocene/ferrocenium (Fc/Fc+ ) redox couple (4.8 eV under vacuum energy level) as the reference. The HOMO and LUMO energy levels are estimated by the oxidation and reduction onsets to be −5.65 and −3.81 eV, respectively.
Fig. 1 (a) Molecular structures of PBDB-T and ZITI-4F. (b) UV–vis–NIR absorption spectra of ZITI-4F in chloroform and thin films and PBDB-T and PC71 BM in thin films. (c) Energy diagram of materials used in OPV devices.
The photovoltaic performance of ZITI-4F was investigated and optimized based on a conventional device structure of indium tin oxide (ITO)/poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)(PEDOT:PSS)/active layer/PNDIT-F3N/Al, in which PBDB-T was used as the electron donor and PEDOT:PSS and PNDIT-F3N served as the anode and cathode buffer layers to promote charge collection at electrodes, respectively. The optimization procedures involved D:A ratios (from 1:0.8 to 1:1.2), thermal annealing temperature, and film thickness (see [Tables S1 ]
[S2 ]
[S3 ] in the Supporting Information). The devices were fabricated by a spin-coating method. Chloroform was utilized as the processing solvent with a total concentration of 17 mg/mL. The optimal D/A weight ratio was determined to be 1:1. The current density–voltage (J –V ) curves of both optimized devices are shown in [Figure 2a ]. The PBDB-T:ZITI-4F-based device after thermal annealing treatment at 110 °C for 10 min showed a high PCE of 12.33% with a V
oc of 0.80 V, a J
sc of 21.17 mA cm−2 , and a FF of 73.27%. By contrast, the PBDB-T:PC71 BM-based device yielded a moderate PCE of 7.82% due to the low J
sc of 12.32 mA cm−2 , regardless of a higher V
oc of 0.88 V and FF of 72.32%. Then, we added PC71 BM as the third component to construct ternary devices. Based on the same device structure wherein the ternary solar cells were constructed with the photoactive layer consisting of PBDB-T:ZITI-4F:PC71 BM (D:A1:A2), the D:A1 ratio was kept at 1:1 and the proportion of PC71 BM was carefully optimized. The devices with different PC71 BM contents exhibited consistent thicknesses of around 100 nm. We found that with the increase of the PC71 BM content, the V
oc and J
sc values improved slightly for all ternary devices. When the ratio of D:A1:A2 equals 1:1:0.4, the ternary device attained the highest PCE of 13.40%, with an increased V
oc of 0.82 V, J
sc of 22.04 mA cm−2 , and FF of 74.24%. Notably, the performance of ternary OSCs is less sensitive to the content of PC71 BM; even when the ratios of D:A1:A2 varies from 1:1:0.2 to 1:1:0.8, the resulting performances of ternary devices outperform with respect to the corresponding PBDB-T:ZITI-4F-based binary device ([Table 1 ] and [Figure 2a ]).
Fig. 2 (a) Characteristic J –V curves, (b) EQE curves, (c) J
ph vs. V
eff plots, and (d) correlation between J
sc and light intensity in the optimized PBDB-T:ZITI-4F- and PBDB-T:ZITI-4F:PC71 BM-based devices with different weight ratios.
Table 1
Photovoltaic parameters of PBDB-T:ZITI-4F:PC71 BM (D:A1:A2)-based devices with different weight ratios[a ]
D:A1:A2
V
oc (V)
J
sc (mA cm−2 )
J
cal (mA cm−2 )
FF (%)
PCEavg (PCEmax ) (%)
μ
h (cm2 V−1 s−1 )
μ
e (cm2 V−1 s−1 )
μ
h /μ
e
1:1:0
0.80
21.17
20.84
73.27
12.08 ± 0.16 (12.33)
2.04 × 10−4
3.09 × 10−4
1.51
1:1:0.2
0.81
21.86
21.31
72.87
12.76 ± 0.12 (12.88)
1.48 × 10−4
2.79 × 10−4
1.88
1:1:0.4
0.82
22.04
21.97
74.24
13.18 ± 0.15 (13.40)
2.53 × 10−4
2.94 × 10−4
1.16
1:1:0.6
0.82
21.92
21.36
72.77
12.88 ± 0.15 (13.11)
1.94 × 10−4
3.05 × 10−4
1.57
1:1:0.8
0.82
21.58
21.15
70.49
12.42 ± 0.13 (12.66)
1.26 × 10−4
2.82 × 10−4
2.24
1:0:1
0.88
12.32
11.94
72.23
7.58 ± 0.16 (7.82)
3.58 × 10−4
4.48 × 10−4
1.25
a Average values with standard deviations were obtained from 40 devices.
The external quantum efficiency (EQE) curves of these devices are presented in [Figure 2b ]. The binary device based on PBDB-T:ZITI-4F shows a much broader and higher photo response than that based on PBDB-T:PC71 BM. The J
sc value of the optimized PBDB-T:ZITI-4F-based device calculated from integration of the EQE spectrum is 20.84 mA cm−2 . Compared with the binary devices, the ternary devices show higher EQE values over the whole spectral response range with the maximum value of around 81% at 840 nm, which accounts for the enhancement in photocurrents. The current densities integrated from the EQE curves are 21.31, 21.97, 21.36, and 21.15 mA cm−2 for PBDB-T:ZITI-4F:PC71 BM-based devices with weight ratios of 1:1:0.2, 1:1:0.4, 1:1:0.6, and 1:1:0.8, respectively ([Table 1 ]). These data are consistent with the J
sc values obtained from the J –V curves with small errors of 1 to 2%.
To unearth charge generation and extraction processes among these devices (binary devices and ternary devices), photocurrent analysis was performed. First, we measured the photocurrent density (J
ph ) versus the effective voltage (V
eff ) for the binary and ternary devices. The exciton dissociation probability can be calculated by P
diss = J
ph /J
sat . It can be seen that J
ph reaches saturation (J
sat ) when V
eff values reached ∼2 V, suggesting that the excitons inside those devices were dissociated. As shown in [Figure 2d ], all the devices exhibit high charge-extraction probability (P ) under the short-circuit conditions, which is 90% for binary devices. The P
diss is 91, 94, 92, 91% for PBDB-T:ZITI-4F:PC71 BM with weight ratios of 1:1:0.2, 1:1:0.4, 1:1:0.6, and 1:1:0.8, respectively. When the weight ration of D:A1:A2 is 1:1:0.4, P
diss is up to 94%, indicating more effective charge transport and exciton dissociation in the ternary device. Furthermore, the J
sc at different light intensities was inspected to determine the charge recombination dynamics. In principle, the recombination parameter (α ), defined by the equation J
sc ∝ Pα
, close to 1.0 suggests the neglectable bimolecular recombination. As shown in [Figure 2c ], the α values are greater than 0.94 for all the devices. Clearly, low or high contents of PC71 BM do not induce more recombination centers for our ternary system, suggesting that bimolecular recombination is efficiently suppressed. For the ternary devices, the α is 0.97 at the optimized ratio (D:A1:A2 = 1:1:0.4).
To understand the charge carrier transport property in binary and ternary devices, the J –V curves of the optimized single charge carrier devices were investigated using the space-charge-limited current (SCLC) method. The hole- and electron-only device structures are ITO/ZnO/active layer/Al and ITO/PEDOT:PSS/active layer/Au, respectively. The J –V curves are presented in [Figure S3 ] (see the Supporting Information), and the detailed data are summarized in [Table 1 ]. The hole (µ
h ) and electron mobilities (µ
e ) of the PBDB-T:ZITI-4F-based devices are 2.04 × 10−4 and 3.09 × 10−4 cm2 V−1 s−1 , respectively. The µ
h and µ
e values of ternary devices are 1.48 × 10−4 , 2.53 × 10−4 , 1.94 × 10−4 , 1.26 × 10−4 cm2 V−1 s−1 and 2.79 × 10−4 , 2.94 × 10−4 , 3.05 × 10−4 , 2.82 × 10−4 cm2 V−1 s−1 for devices based on PBDB-T:ZITI-4F:PC71 BM blends with weight ratios of 1:1:0.2, 1:1:0.4, 1:1:0.6, and 1:1:0.8, respectively. For the best ratio (D:A1:A2 = 1:1:0.4), the ternary blend shows the most balanced µ
h /µ
e ratio of 1.16. The increased balanced charge transporting property of ternary devices is one of the reasons for the improved FF values.
As the morphology of the active layer is important for the device performance, which affects the charge transport and collection. Atomic force microscopy (AFM) and transmission electron microscopy (TEM) were used to investigate the superficial morphologies of the active layers and the influence of the PC71 BM ([Figure 3 ]). The root mean square (RMS) surface roughness of PBDB-T:ZITI-4F is 0.96 nm; the RMS roughness values of PBDB-T:ZITI-4F:PC71 BM (from 1:1:0.2 to 1:1:0.6) are almost the same, 1.01, 0.99, and 0.98 nm; when the ratio is 1:1:0.8, the RMS increases to 1.79 nm, which is closer to the RMS (2.19 nm) of the PBDB-T:PC71 BM blend. The higher RMS indicates oversized phase separation, which is responsible for the lower FF value and is in accordance with the slightly unbalanced hole and electron mobilities. In the TEM images, the ratios range from 1:1:0 to 1:1:0.6, the blend films exhibit similarly homogeneous and interpenetrating networks with nanoscale phase separation, and the domain sizes were gradually reduced. When further adding the PC71 BM component to a ratio of 1:1:0.8, the blend film shows a large phase aggregation and the domain sizes were increased, which is bad for exciton diffusion and agrees well with the slightly lower FF. The molecular packing of neat and blend films was investigated by two-dimensional grazing-incidence wide-angle X-ray scattering (2D-GIWAXS) measurements, and the corresponding in-plane (IP) and out-of-plane (OOP) line-cut profiles are shown in [Figure 4 ]. The ZITI-4F neat film shows a strong π − π stacking diffraction peak (010) at 1.81 Å−1 along the OOP direction and a sharp alkyl stacking packing (100) at 0.32 Å−1 along the in-plane (IP) direction, corresponding to a π − π stacking distance of 3.47 Å and a lamellar d -spacing of 19.2 Å, suggesting the good structural order of ZITI-4F. The PBDB-T neat film shows a broad (100) diffraction peak at 0.30 Å−1 (lamellar d -spacing of 21.3 Å) with wide azimuthal angle spreading and a (010) diffraction peak at 1.69 Å−1 (π − π stacking distance of 3.72 Å) in the OOP direction. For the ZITI-4F:PBDB-T binary blend, the (010) π − π stacking distance is 3.46 Å and the IP coherence length (CCL) is 7.2 nm. The increase of PC71 BM ratio clearly showed a typical diffuse reflection for at 1.35 Å−1 . When 40wt% PC71 BM was added to the binary blend, the (010) π − π stacking distance showed almost no change, but the IP CCL increased to 11.8 nm, suggesting that the introduction of PC71 BM can improve the material crystallinity, which may lead to the high J
sc and FF.
Fig. 3 AFM height images (top) and TEM (bottom) images of the blend films.
Fig. 4 (a) 2D GIWAXS patterns for PBDB-T:ZITI-4F:PC71 BM blend films with different weight ratios. (b) The corresponding line-cuts of GIWAXS patterns (solid line: out of plane, dash line: in-plane.)
Conclusion
We synthesized a small-molecule electron acceptor ZITI-4F based on the planar indenoindene–dithiophene core and 2F-INCN terminal. ZITI-4F has strong absorption (600–850 nm) with a high extinction coefficient of 2.46 × 105 M−1 cm−1 and a low bandgap of 1.47 eV. Using the wide-bandgap polymer PBDB-T as the electron donor, the PBDB-T:ZITI-4F-based binary device shows a PCE of 12.33%. By introducing PC71 BM as the third component, the ternary device exhibits an outstanding PCE of 13.40%. And AFM and GIWAXS studies indicate that the active-layer morphology was optimized by adding PC71 BM. Moreover, the ZITI that has been reported by our group[13 ] also showed a higher PCE of 13.66% for the PBDB-T:ZITI:PC71BM-based ternary device than that of the PBDB-T:ZITI-based OSC (13.03%; [Table 2 ]). We believe that combining fullerene derivatives and nonfullerene acceptors to construct ternary OSCs should be applicable and promising for the development of high-performance OSCs in future.
Experimental Section
Materials and General Methods
All reactions involving air- or moisture-sensitive compounds were carried out in a dry reaction vessel under a positive pressure of nitrogen. Unless stated otherwise, starting materials were obtained from Adamas, Aldrich, or J&K and were used without further purification. Anhydrous THF and toluene were distilled over Na/benzophenone prior to use. Anhydrous DMF was distilled over CaH2 prior to use. Compounds 1 and methyl 2-bromothiophene-3-carboxylate were prepared according to published procedures. 1 H and 13 C NMR spectra were measured with Bruker Fourier 300, or Bruker Avance 400 spectrometers. Chemical shifts for hydrogens are reported in parts per million (ppm, scale) downfield from tetramethylsilane and are referenced to the residual protons in the NMR solvent (CDCl3 : 7.26). 13 C NMR spectra were recorded at 100 MHz. Chemical shifts for carbons are reported in parts per million (ppm, scale) downfield from tetramethylsilane and are referenced to the carbon resonance of the solvent (CDCl3 : 77.2). The data are presented as follows: chemical shift, multiplicity (s = singlet, d = doublet, t = triplet, m = multiplet and/or multiple resonances, br = broad), coupling constant in hertz (Hz), and integration. MALDI measurements were performed with a MALDI-FT 9.4 T, Bruker solariX, or MALDI-TOF MS Bruker Autoflex III. Elemental analyses were performed with a Flash EA 1112 Series from ThermoQuest. UV-vis was recorded with Jasco V-570 spectrometers. Cyclic voltammetry (CV) was performed with a CHI620D potentiostat. All measurements were carried out in a one-compartment cell under a nitrogen atmosphere, equipped with a glassy-carbon electrode, a platinum counter-electrode, and an Ag/Ag+ reference electrode with a scan rate of 100 mV/s. The supporting electrolyte was a 0.1 mol/L dichloromethane solution of tetrabutylammonium perchlorate (TBAP). All potentials were corrected against Fc/Fc+ . CV was measured with a scan rate of 100 mV/s. Thermogravimetric analysis (TGA) was performe d with a Shimadzu DTG 60 instrument at a heating rate of 10 °C min−1 under a nitrogen atmosphere with runs recorded from room temperature to 510 °C.
Fabrication of Organic Solar Cells
The device structures were: ITO/PEDOT:PSS/PBDB-T:ZITI-4F (or PBDB-T:ZITI-4F:PC71 BM)/PNDIT-F3N/Al. Organic solar cell devices were fabricated using ITO-coated glass substrates (15 Ω sq−1 ), which were cleaned with de-ionized water, acetone, and isopropyl alcohol in successive 20 min sonication steps applying a final 20 min oxygen plasma treatment to eliminate any remaining organic component. A thin layer (ca. 30 nm) of PEDOT:PSS (Bayer Baytron 4083) was first spin-coated on the pre-cleaned ITO-coated glass substrates at 3000 rpm and baked at 150 °C for 15 min under ambient conditions. The substrates were then transferred into a nitrogen-filled glovebox. Subsequently, The active layers were spin coated from chloroform solution with the same optimal donor/acceptor (D/A) weight ratios of 1:1 for both PBDB-T:ZITI-4F (or PBDB-T:ZITI-4F:PC71 BM) blends with a total concentration of 17 mg/mL and then treated with thermal annealing at 110 °C for 10 min. Then PNDIT-F3 N as the electron transporting layer was spin-coated on the active layer by 3000 rpm from alcohol solution. At the final stage, the substrates were pumped down in high vacuum, and aluminum (100 nm) was thermally evaporated onto the active layer. Shadow masks were used to define the OSC active area (0.05 cm2 ) of the devices.
Device Characterization
The current density–voltage (J–V) characteristics of unencapsulated photovoltaic devices were measured under N2 using a Keithley 2400 source meter. A 300 W xenon arc solar simulator (Oriel) with an AM 1.5 global filter operated at 100 mW cm−2 was used to simulate the AM 1.5G solar irradiation. The illumination intensity was corrected by using a silicon photodiode with a protective KG5 filter calibrated by the National Renewable Energy Laboratory (NREL). The external quantum efficiency (EQE) was performed using certified IPCE equipment (Zolix Instruments, Inc, SolarCellScan100).
SCLC Mobility Measurements
Space charge-limited currents were tested in electron-only devices with a configuration of ITO/ZnO/ PBDB-T:ZITI-4F (or PBDB-T:ZITI-4F:PC71 BM)/Al and hole-only devices with a configuration of ITO/PEDOT:PSS/ PBDB-T:ZITI-4F (or PBDB-T:ZITI-4F:PC71 BM)/Au. The devices were prepared following the same procedure described in the experimental section for photovoltaic devices, except for the metal electrode. The mobilities were determined by fitting the dark current to the model of a single carrier SCLC current with field dependent mobility, which is described as
where J is the current, μ
0 is the zero-field mobility, ε0 is the permittivity of free space, εr is the relative permittivity of the material, V is the effective voltage, and L is the thickness of the active layer.
Microstructure Investigation
Atomic force microscopy (AFM) images of the thin films were obtained on a NanoscopeIIIa AFM (Digital Instruments) operating platform in tapping mode. Transmission electron microscopy (TEM) observation was performed on JEOL 2200FS at 160 kV accelerating voltage. Grazing incidence X-ray diffraction characterization of the thin films was performed at the SSRL on beamline 11-3, Standford Synchrotron Radiation Lab. Thin film samples were spin-casted on to PEDOT:PSS covered SiO2 wafers. The scattering signal was recorded on a 2D detector (MarCCD). The samples were ≈15 mm long in the direction of the beam path, and the detector was located at a distance of ≈300 mm from the sample center (distance calibrated using a silver behenate standard). The incidence angle of 0.16° was chosen which gave the optimized signal-to-background ratio. The beam energy was 8 keV. All GIWAXS experiments were done in helium atmosphere. The data was processed and analyzed using waxdiff software package.
Synthetic Part
Compound ZITI-4F. INCN-2F (83 mg, 0.36 mmol) and ZIT-CHO (100 mg, 0.09 mmol) were added to a solvent mixture of chloroform (10 mL) and pyridine (0.2 mL). The reaction was placed in an oil bath at 75 °C and was stirred overnight. The mixture was directly purified on a silica-gel column chromatography using trichloromethane as eluent to give 106 mg of ZITI-4F as black solid (76%). ZITI-4F: 1 H NMR (400 MHz, CDCl3 ): 8.96 (s, 2H), 8.55 (m, 2H), 7.92 (s, 2H), 7.79 (s, 2H), 7.68 (t, 3J = 7.6 Hz, 2H), 7.57 (s, 2H), 3.88 (s, 4H), 2.13 (s, 8H), 1.30 0.50 (m, 92H); 13 C NMR (150 MHz, CDCl3 ): 185.5, 164.5, 158.4, 158.2, 156.5, 154.8, 154.7, 153.0, 152.9, 147.9, 142.1, 139.4, 138.1, 136.1, 134.1, 133.9, 119.5, 116.8, 116.4, 114.5, 114.3, 114.1, 114.0, 112.0, 111.8, 76.5, 76.3, 68.1, 53.7, 42.6, 42.4, 34.7, 34.4, 34.1, 33.4, 33.1, 31.5, 31.3, 31.3, 29.3, 29.2, 27.9, 27.2, 27.1, 25.6, 25.6, 24.8, 24.7, 22.6, 22.3, 22.1, 22.1, 13.5, 13.5, 13.3; HRMS (MALDI-TOF) calcd for C100 H116 F4 N4 O2 S2 [M]+ : 1544.8470, found, 1544.8479. Anal. Calcd for C100 H116 F4 N4 O2 S2 (%): C, 77.68; H, 7.56; N, 3.62; found: C, 77.38; H, 7.53; N, 3.77.
Table 2
Photovoltaic performance of PBDB-T:ZITI:PC71 BM-based solar cells
V
oc (V)
J
sc (mA cm−2 )
J
cal (mA cm−2 )
FF (%)
PCEavg (PCEmax ) (%)[a ]
PBDB-T:ZITI
0.89
19.80
19.68
74.04
12.87 ± 0.10 (13.03)
PBDB-T:ZITI:PC71 BM
0.89
20.36
20.24
74.83
13.48 ± 0.14 (13.66)
a Average values with standard deviations were obtained from 25 devices.
